Richard Myers | Profiles RNS

Richard H. Myers, PhD

Professor Emeritus

Boston University Chobanian & Avedisian School of Medicine

Neurology

PhD, Georgia State University
MA, Georgia State University
MEd, Georgia State University
BA, University of Kansas

Websites

	Google Scholar
	ResearchGate
	LinkedIn

ORCID : 0000-0002-8365-2674

Dr. Richard H. Myers retired in 2020 and is now Emeritus Professor of Neurology at Chobanian and Avedisian School of Medicine. He is no longer accepting students or post-doctoral fellows. The phone number listed in my contact information is not active. I no longer have a phone at BUSM.

Dr. Myers' professional interests focused upon the application of genetic research methods for the investigation of adult onset diseases with complex etiology (Parkinson’s disease, coronary heart disease, Alzheimer’s disease, pulmonary function, osteoarthritis, osteoporosis etc.). Dr. Myers has had a long-standing interest in Huntington’s disease and has participated in a wide range of research investigations for this disease. He was a member of the New England Huntington’s disease "Center Without Walls" since its inception in 1980. His HD studies are best characterized as ‘Neurobiological Studies’ in that they include studies into the mechanisms of disease expression, including complex genetic modifier studies and a series of neuropathological studies of effects of disease expression in the brain. Additional interests include ethical issues influencing utilization of genetic test procedures.
Dr. Myers been involved in a number of studies in positional cloning. He also participated in the cloning of the gene for Huntington’s disease in 1993. He initiated the genome scan project in the Framingham Study, and a genome scan in Parkinson’s disease. Dr. Myers' Parkinson’s disease genetic linkage study, known as the "GenePD" study, involved an international collaboration of twenty clinical centers in Parkinson’s disease. The study sought genetic loci involved in risk for PD. From 1993 he has participated in genetic linkage studies for hypertension (the HyperGEN study, one of the NHLBI Family Blood Pressure Program Project studies), and the genome scan in the NHLBI Family Heart Study.

Dr. Myers has published more than 250 peer reviewed articles, 38 individual NIH funded grants, and mentored many extraordinarily talented students and post-docs.

Boston Medical Center

BU Research
NIH RePORTER Research

Cyclin G-associated kinase as a novel target for Parkinson's disease
01/01/2017 - 12/31/2019 (PI)
Ellison Foundation

Functional analysis of Disease associated risk alleles in sporadic Parkinson's disease
09/23/2014 - 06/30/2019 (Multi-PI)
PI: Richard H. Myers, PhD
Whitehead Institute for Biomedical Research NIH NINDS
5R01NS088538-05

Probing the Dark Matter of the Genome in the NHLBI Family Heart Study
07/01/2016 - 06/30/2018 (Subcontract PI)
The Washington University NIH NHLBI
4R01HL117078-04

Epigenetic Markers in Huntington's Disease Brain
07/01/2011 - 04/30/2017 (PI)
NIH/National Institute of Neurological Disorders & Stroke
3R01NS073947-05S1

Probing the Dark Matter of the Genome in the NHLBI Family Heart Study
07/22/2013 - 06/30/2016 (Subcontract PI)
The Washington University NIH NHLBI
5R01HL117078-03

Epigenetic Markers of Huntington Disease Brain
07/01/2011 - 04/30/2016 (PI)
NIH/National Institute of Neurological Disorders & Stroke
1 R01 NS073947 01

Characterization of the role of cyclin G-associated kinase in Parkinson disease
09/01/2011 - 04/30/2015 (PI)
NIH/National Institute of Neurological Disorders & Stroke
5R01NS076843-03

Genomic Scan for Atherosclerosis Pathway Genes in African Americans from FHS Scan
05/15/2008 - 04/30/2013 (Subcontract PI)
The Washington University NIH NHLBI
5R01HL088215-04

Identifying Susceptibility Genes for Metabolic Syndrome
01/29/2007 - 12/31/2011 (Subcontract PI)
Regents of the University of Minnesota NIH NIDDK
5R01DK068320-03

Mapping Adiposity QTLs in the NHLBI Family Heart Study
09/20/2004 - 06/30/2009 (PI)
Washington University, St Louis NIH NIDDK

Showing 10 of 12 results. Show All Results

Title

Yr	Title	Project-Sub Proj	Pubs
2018	An iPSC based platform for functionally assessing genetic and environmental risk	5R01NS088538-05	32
2017	An iPSC based platform for functionally assessing genetic and environmental risk	5R01NS088538-04	32
2016	An iPSC based platform for functionally assessing genetic and environmental risk	5R01NS088538-03	32
2015	An iPSC based platform for functionally assessing genetic and environmental risk	5R01NS088538-02	32
2015	Epigenetic Markers in Huntington's disease Brain	3R01NS073947-05S1	33
2015	Epigenetic Markers in Huntington's disease Brain	5R01NS073947-05	33
2014	An iPSC based platform for functionally assessing genetic and environmental risk	1R01NS088538-01	32
2014	Epigenetic Markers in Huntington's disease Brain	5R01NS073947-04	33
2013	Characterization of the role of cyclin G-associated kinase in Parkinson disease	5R01NS076843-03	14
2013	Epigenetic Markers in Huntington's disease Brain	5R01NS073947-03	33

Showing 10 of 34 results. Show All Results

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.

iCite Analysis Copy PMIDs To Clipboard

Lee JM, McLean ZL, Correia K, Shin JW, Lee S, Jang JH, Lee Y, Kim KH, Choi DE, Long JD, Lucente D, Seong IS, Pinto RM, Giordano JV, Mysore JS, Siciliano J, Elezi E, Ruliera J, Gillis T, Wheeler VC, MacDonald ME, Gusella JF, Gatseva A, Ciosi M, Lomeikaite V, Loay H, Monckton DG, Wills C, Massey TH, Jones L, Holmans P, Kwak S, Sampaio C, Orth M, Bernhard Landwehrmeyer G, Paulsen JS, Ray Dorsey E, Myers RH. Genetic modifiers of somatic expansion and clinical phenotypes in Huntington's disease reveal shared and tissue-specific effects. bioRxiv. 2024 Jun 18. PMID: 38948755; PMCID: PMC11212857; DOI: 10.1101/2024.06.10.597797;

Nazeen S, Wang X, Zielinski D, Lam I, Hallacli E, Xu P, Ethier E, Strom R, Zanella CA, Nithianandam V, Ritter D, Henderson A, Saurat N, Afroz J, Nutter-Upham A, Benyamini H, Copty J, Ravishankar S, Morrow A, Mitchel J, Neavin D, Gupta R, Farbehi N, Grundman J, Myers RH, Scherzer CR, Trojanowski JQ, Van Deerlin VM, Cooper AA, Lee EB, Erlich Y, Lindquist S, Peng J, Geschwind DH, Powell J, Studer L, Feany MB, Sunyaev SR, Khurana V. Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathies. bioRxiv. 2024 Mar 07. PMID: 38496508; PMCID: PMC10942362; DOI: 10.1101/2024.03.03.583145;

Koromina M, Ravi A, Panagiotaropoulou G, Schilder BM, Humphrey J, Braun A, Bidgeli T, Chatzinakos C, Coombes B, Kim J, Liu X, Terao C, O 'Connell KS, Adams M, Adolfsson R, Alda M, Alfredsson L, Andlauer TFM, Andreassen OA, Antoniou A, Baune BT, Bengesser S, Biernacka J, Boehnke M, Bosch R, Cairns M, Carr VJ, Casas M, Catts S, Cichon S, Corvin A, Craddock N, Dafnas K, Dalkner N, Dannlowski U, Degenhardt F, Di Florio A, Dikeos D, Fellendorf FT, Ferentinos P, Forstner AJ, Forty L, Frye M, Fullerton JM, Gawlik M, Gizer IR, Gordon-Smith K, Green MJ, Grigoroiu-Serbanescu M, Guzman-Parra J, Hahn T, Henskens F, Hillert J, Jablensky AV, Jones L, Jones I, Jonsson L, Kelsoe JR, Kircher T, Kirov G, Kittel-Schneider S, Kogevinas M, Landén M, Leboyer M, Lenger M, Lissowska J, Lochner C, Loughland C, MacIntyre D, Martin NG, Maratou E, Mathews CA, Mayoral F, McElroy SL, McGregor NW, McIntosh A, McQuillin A, Michie P, Milanova V, Mitchell PB, Moutsatsou P, Mowry B, Müller-Myhsok B, Myers R, Nenadic I, Nöthen MM, O'Donovan C, O'Donovan M, Ophoff RA, Owen MJ, Pantelis C, Pato C, Pato MT, Patrinos GP, Pawlak JM, Perlis RH, Porichi E, Posthuma D, Ramos-Quiroga JA, Reif A, Reininghaus EZ, Ribasés M, Rietschel M, Schall U, Schulze TG, Scott L, Scott RJ, Serretti A, Weickert CS, Smoller JW, Artigas MS, Stein DJ, Streit F, Toma C, Tooney P, Vieta E, Vincent JB, Waldman ID, Weickert T, Witt SH, Hong KS, Ikeda M, Iwata N, Swiatkowska B, Won HH, Edenberg HJ, Ripke S, Raj T, Coleman JRI, Mullins N. Fine-mapping genomic loci refines bipolar disorder risk genes. medRxiv. 2024 Feb 13. PMID: 38405768; PMCID: PMC10889003; DOI: 10.1101/2024.02.12.24302716;

Hyeon SJ, Park J, Yoo J, Kim SH, Hwang YJ, Kim SC, Liu T, Shim HS, Kim Y, Cho Y, Woo J, Kim KS, Myers RH, Ryu HL, Kowall NW, Song EJ, Hwang EM, Seo H, Lee J, Ryu H. Dysfunction of X-linked inhibitor of apoptosis protein (XIAP) triggers neuropathological processes via altered p53 activity in Huntington's disease. Prog Neurobiol. 2021 09; 204:102110.View Related Profiles.

Ryu, Hoon
Lee, Junghee
Kowall, Neil
Myers, Richard

PMID: 34166773; PMCID: PMC8364511; DOI: 10.1016/j.pneurobio.2021.102110;

Lai D, Alipanahi B, Fontanillas P, Schwantes-An TH, Aasly J, Alcalay RN, Beecham GW, Berg D, Bressman S, Brice A, Brockman K, Clark L, Cookson M, Das S, Van Deerlin V, Follett J, Farrer MJ, Trinh J, Gasser T, Goldwurm S, Gustavsson E, Klein C, Lang AE, Langston JW, Latourelle J, Lynch T, Marder K, Marras C, Martin ER, McLean CY, Mejia-Santana H, Molho E, Myers RH, Nuytemans K, Ozelius L, Payami H, Raymond D, Rogaeva E, Rogers MP, Ross OA, Samii A, Saunders-Pullman R, Schüle B, Schulte C, Scott WK, Tanner C, Tolosa E, Tomkins JE, Vilas D, Trojanowski JQ, Uitti R, Vance JM, Visanji NP, Wszolek ZK, Zabetian CP, Mirelman A, Giladi N, Orr Urtreger A, Cannon P, Fiske B, Foroud T. Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease. Ann Neurol. 2021 07; 90(1):76-88.View Related Profiles.

Latourelle, Jeanne
Myers, Richard

PMID: 33938021; PMCID: PMC8252519; DOI: 10.1002/ana.26094;

Raghunathan R, Hogan JD, Labadorf A, Myers RH, Zaia J. A glycomics and proteomics study of aging and Parkinson's disease in human brain. Sci Rep. 2020 07 30; 10(1):12804.View Related Profiles.

Labadorf, Adam
Zaia, Joseph
Raghunathan, Rekha
Myers, Richard

PMID: 32733076; PMCID: PMC7393382; DOI: 10.1038/s41598-020-69480-3;

Ellis N, Tee A, McAllister B, Massey T, McLauchlan D, Stone T, Correia K, Loupe J, Kim KH, Barker D, Hong EP, Chao MJ, Long JD, Lucente D, Vonsattel JPG, Pinto RM, Elneel KA, Ramos EM, Mysore JS, Gillis T, Wheeler VC, Medway C, Hall L, Kwak S, Sampaio C, Ciosi M, Maxwell A, Chatzi A, Monckton DG, Orth M, Landwehrmeyer GB, Paulsen JS, Shoulson I, Myers RH, van Duijn E, Rickards H, MacDonald ME, Lee JM, Gusella JF, Jones L, Holmans P. Genetic Risk Underlying Psychiatric and Cognitive Symptoms in Huntington's Disease. Biol Psychiatry. 2020 05 01; 87(9):857-865. PMID: 32087949; PMCID: PMC7156911; DOI: 10.1016/j.biopsych.2019.12.010;

Agus F, Crespo D, Myers RH, Labadorf A. The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington's disease brain. BMC Med Genomics. 2019 10 16; 12(1):137.View Related Profiles.

Labadorf, Adam
Myers, Richard

PMID: 31619230; PMCID: PMC6796419; DOI: 10.1186/s12920-019-0581-9;

Wyss AB, Sofer T, Lee MK, Terzikhan N, Nguyen JN, Lahousse L, Latourelle JC, Smith AV, Bartz TM, Feitosa MF, Gao W, Ahluwalia TS, Tang W, Oldmeadow C, Duan Q, de Jong K, Wojczynski MK, Wang XQ, Noordam R, Hartwig FP, Jackson VE, Wang T, Obeidat M, Hobbs BD, Huan T, Gui H, Parker MM, Hu D, Mogil LS, Kichaev G, Jin J, Graff M, Harris TB, Kalhan R, Heckbert SR, Paternoster L, Burkart KM, Liu Y, Holliday EG, Wilson JG, Vonk JM, Sanders JL, Barr RG, de Mutsert R, Menezes AMB, Adams HHH, van den Berge M, Joehanes R, Levin AM, Liberto J, Launer LJ, Morrison AC, Sitlani CM, Celedón JC, Kritchevsky SB, Scott RJ, Christensen K, Rotter JI, Bonten TN, Wehrmeister FC, Bossé Y, Xiao S, Oh S, Franceschini N, Brody JA, Kaplan RC, Lohman K, McEvoy M, Province MA, Rosendaal FR, Taylor KD, Nickle DC, Williams LK, Burchard EG, Wheeler HE, Sin DD, Gudnason V, North KE, Fornage M, Psaty BM, Myers RH, O'Connor G, Hansen T, Laurie CC, Cassano PA, Sung J, Kim WJ, Attia JR, Lange L, Boezen HM, Thyagarajan B, Rich SS, Mook-Kanamori DO, Horta BL, Uitterlinden AG, Im HK, Cho MH, Brusselle GG, Gharib SA, Dupuis J, Manichaikul A, London SJ. Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Nat Commun. 2018 07 30; 9(1):2976.View Related Profiles.

O'Connor, George
Latourelle, Jeanne
Dupuis, Josee
Myers, Richard

PMID: 30061609; PMCID: PMC6065313; DOI: 10.1038/s41467-018-05369-0;

Labadorf A, Choi SH, Myers RH. Evidence for a Pan-Neurodegenerative Disease Response in Huntington's and Parkinson's Disease Expression Profiles. Front Mol Neurosci. 2017; 10:430.View Related Profiles.

Labadorf, Adam
Myers, Richard
Choi, Seung Hoan

PMID: 29375298; PMCID: PMC5768647; DOI: 10.3389/fnmol.2017.00430;

Showing 10 of 347 results. Show More

Hui KY, Fernandez-Hernandez H, Hu J, Schaffner A, Pankratz N, Hsu NY, Chuang LS, Carmi S, Villaverde N, Li X, Rivas M, Levine AP, Bao X, Labrias PR, Haritunians T, Ruane D, Gettler K, Chen E, Li D, Schiff ER, Pontikos N, Barzilai N, Brant SR, Bressman S, Cheifetz AS, Clark LN, Daly MJ, Desnick RJ, Duerr RH, Katz S, Lencz T, Myers RH, Ostrer H, Ozelius L, Payami H, Peter Y, Rioux JD, Segal AW, Scott WK, Silverberg MS, Vance JM, Ubarretxena-Belandia I, Foroud T, Atzmon G, Pe'er I, Ioannou Y, McGovern DPB, Yue Z, Schadt EE, Cho JH, Peter I. Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease. Sci Transl Med. 2018 01 10; 10(423). PMID: 29321258; PMCID: PMC6028002; DOI: 10.1126/scitranslmed.aai7795;

Reed ER, Latourelle JC, Bockholt JH, Bregu J, Smock J, Paulsen JS, Myers RH. MicroRNAs in CSF as prodromal biomarkers for Huntington disease in the PREDICT-HD study. Neurology. 2018 01 23; 90(4):e264-e272.View Related Profiles.

Reed, Eric
Latourelle, Jeanne
Myers, Richard

PMID: 29282329; PMCID: PMC5798654; DOI: 10.1212/WNL.0000000000004844;

Lee JM, Chao MJ, Harold D, Abu Elneel K, Gillis T, Holmans P, Jones L, Orth M, Myers RH, Kwak S, Wheeler VC, MacDonald ME, Gusella JF. A modifier of Huntington's disease onset at the MLH1 locus. Hum Mol Genet. 2017 Oct 01; 26(19):3859-3867. PMID: 28934397; PMCID: PMC6455020; DOI: 10.1093/hmg/ddx286;

Chao MJ, Gillis T, Atwal RS, Mysore JS, Arjomand J, Harold D, Holmans P, Jones L, Orth M, Myers RH, Kwak S, Wheeler VC, MacDonald ME, Gusella JF, Lee JM. Haplotype-based stratification of Huntington's disease. Eur J Hum Genet. 2017 Nov; 25(11):1202-1209. PMID: 28832564; PMCID: PMC5643960; DOI: 10.1038/ejhg.2017.125;

Neueder A, Landles C, Ghosh R, Howland D, Myers RH, Faull RLM, Tabrizi SJ, Bates GP. The pathogenic exon 1 HTT protein is produced by incomplete splicing in Huntington's disease patients. Sci Rep. 2017 05 02; 7(1):1307. PMID: 28465506; PMCID: PMC5431000; DOI: 10.1038/s41598-017-01510-z;

Choi SH, Labadorf AT, Myers RH, Lunetta KL, Dupuis J, DeStefano AL. Evaluation of logistic regression models and effect of covariates for case-control study in RNA-Seq analysis. BMC Bioinformatics. 2017 Feb 06; 18(1):91.View Related Profiles.

Labadorf, Adam
DeStefano, Anita
Dupuis, Josee
Lunetta, Kathryn
Myers, Richard
Choi, Seung Hoan

PMID: 28166718; PMCID: PMC5294900; DOI: 10.1186/s12859-017-1498-y;

Labadorf A, Hoss AG, Myers RH. Neuroimmune Pharmacology. Huntington’s Disease. 2017. View Publication

Wake C, Labadorf A, Dumitriu A, Hoss AG, Bregu J, Albrecht KH, DeStefano AL, Myers RH. Novel microRNA discovery using small RNA sequencing in post-mortem human brain. BMC Genomics. 2016 Oct 04; 17(1):776.View Related Profiles.

Labadorf, Adam
Hoss, Andrew
DeStefano, Anita
Albrecht, Kenneth
Myers, Richard

PMID: 27716130; PMCID: PMC5050850; DOI: 10.1186/s12864-016-3114-3;

Trinh J, Gustavsson EK, Vilariño-Güell C, Bortnick S, Latourelle J, McKenzie MB, Tu CS, Nosova E, Khinda J, Milnerwood A, Lesage S, Brice A, Tazir M, Aasly JO, Parkkinen L, Haytural H, Foroud T, Myers RH, Sassi SB, Hentati E, Nabli F, Farhat E, Amouri R, Hentati F, Farrer MJ. DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study. Lancet Neurol. 2016 Nov; 15(12):1248-1256.View Related Profiles.

Latourelle, Jeanne
Myers, Richard

PMID: 27692902; DOI: 10.1016/S1474-4422(16)30203-4;

Nielson CM, Liu CT, Smith AV, Ackert-Bicknell CL, Reppe S, Jakobsdottir J, Wassel C, Register TC, Oei L, Alonso N, Oei EH, Parimi N, Samelson EJ, Nalls MA, Zmuda J, Lang T, Bouxsein M, Latourelle J, Claussnitzer M, Siggeirsdottir K, Srikanth P, Lorentzen E, Vandenput L, Langefeld C, Raffield L, Terry G, Cox AJ, Allison MA, Criqui MH, Bowden D, Ikram MA, Mellström D, Karlsson MK, Carr J, Budoff M, Phillips C, Cupples LA, Chou WC, Myers RH, Ralston SH, Gautvik KM, Cawthon PM, Cummings S, Karasik D, Rivadeneira F, Gudnason V, Orwoll ES, Harris TB, Ohlsson C, Kiel DP, Hsu YH. Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2. J Bone Miner Res. 2016 Dec; 31(12):2085-2097.View Related Profiles.

Liu, Ching-Ti
Latourelle, Jeanne
Cupples, L
Myers, Richard

PMID: 27476799; PMCID: PMC5477772; DOI: 10.1002/jbmr.2913;

Nagle MW, Latourelle JC, Labadorf A, Dumitriu A, Hadzi TC, Beach TG, Myers RH. The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane. PLoS One. 2016; 11(8):e0160925.View Related Profiles.

Labadorf, Adam
Latourelle, Jeanne
Myers, Richard

PMID: 27508417; PMCID: PMC4980018; DOI: 10.1371/journal.pone.0160925;

Labadorf A, Hoss AG, Lagomarsino V, Latourelle JC, Hadzi TC, Bregu J, MacDonald ME, Gusella JF, Chen JF, Akbarian S, Weng Z, Myers RH. Correction: RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression. PLoS One. 2016; 11(7):e0160295.View Related Profiles.

Labadorf, Adam
Latourelle, Jeanne
Myers, Richard

PMID: 27454300; PMCID: PMC4959683; DOI: 10.1371/journal.pone.0160295;

Soldner F, Stelzer Y, Shivalila CS, Abraham BJ, Latourelle JC, Barrasa MI, Goldmann J, Myers RH, Young RA, Jaenisch R. Parkinson-associated risk variant in distal enhancer of a-synuclein modulates target gene expression. Nature. 2016 May 5; 533(7601):95-9.View Related Profiles.

Latourelle, Jeanne
Myers, Richard

PMID: 27096366; PMCID: PMC5042324; DOI: 10.1038/nature17939;

Hoss AG, Labadorf A, Beach TG, Latourelle JC, Myers RH. microRNA Profiles in Parkinson's Disease Prefrontal Cortex. Front Aging Neurosci. 2016; 8:36.View Related Profiles.

Labadorf, Adam
Hoss, Andrew
Latourelle, Jeanne
Myers, Richard

PMID: 26973511; PMCID: PMC4772525; DOI: 10.3389/fnagi.2016.00036;

Kilpeläinen TO, Carli JF, Skowronski AA, Sun Q, Kriebel J, Feitosa MF, Hedman ÅK, Drong AW, Hayes JE, Zhao J, Pers TH, Schick U, Grarup N, Kutalik Z, Trompet S, Mangino M, Kristiansson K, Beekman M, Lyytikäinen LP, Eriksson J, Henneman P, Lahti J, Tanaka T, Luan J, Del Greco M F, Pasko D, Renström F, Willems SM, Mahajan A, Rose LM, Guo X, Liu Y, Kleber ME, Pérusse L, Gaunt T, Ahluwalia TS, Ju Sung Y, Ramos YF, Amin N, Amuzu A, Barroso I, Bellis C, Blangero J, Buckley BM, Böhringer S, I Chen YD, de Craen AJ, Crosslin DR, Dale CE, Dastani Z, Day FR, Deelen J, Delgado GE, Demirkan A, Finucane FM, Ford I, Garcia ME, Gieger C, Gustafsson S, Hallmans G, Hankinson SE, Havulinna AS, Herder C, Hernandez D, Hicks AA, Hunter DJ, Illig T, Ingelsson E, Ioan-Facsinay A, Jansson JO, Jenny NS, Jørgensen ME, Jørgensen T, Karlsson M, Koenig W, Kraft P, Kwekkeboom J, Laatikainen T, Ladwig KH, LeDuc CA, Lowe G, Lu Y, Marques-Vidal P, Meisinger C, Menni C, Morris AP, Myers RH, Männistö S, Nalls MA, Paternoster L, Peters A, Pradhan AD, Rankinen T, Rasmussen-Torvik LJ, Rathmann W, Rice TK, Brent Richards J, Ridker PM, Sattar N, Savage DB, Söderberg S, Timpson NJ, Vandenput L, van Heemst D, Uh HW, Vohl MC, Walker M, Wichmann HE, Widén E, Wood AR, Yao J, Zeller T, Zhang Y, Meulenbelt I, Kloppenburg M, Astrup A, Sørensen TI, Sarzynski MA, Rao DC, Jousilahti P, Vartiainen E, Hofman A, Rivadeneira F, Uitterlinden AG, Kajantie E, Osmond C, Palotie A, Eriksson JG, Heliövaara M, Knekt PB, Koskinen S, Jula A, Perola M, Huupponen RK, Viikari JS, Kähönen M, Lehtimäki T, Raitakari OT, Mellström D, Lorentzon M, Casas JP, Bandinelli S, März W, Isaacs A, van Dijk KW, van Duijn CM, Harris TB, Bouchard C, Allison MA, Chasman DI, Ohlsson C, Lind L, Scott RA, Langenberg C, Wareham NJ, Ferrucci L, Frayling TM, Pramstaller PP, Borecki IB, Waterworth DM, Bergmann S, Waeber G, Vollenweider P, Vestergaard H, Hansen T, Pedersen O, Hu FB, Eline Slagboom P, Grallert H, Spector TD, Jukema JW, Klein RJ, Schadt EE, Franks PW, Lindgren CM, Leibel RL, Loos RJ. Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. Nat Commun. 2016; 7:10494.View Related Profiles.

Pradhan, Aruna
Myers, Richard

PMID: 26833098; PMCID: PMC4740377; DOI: 10.1038/ncomms10494;

Dumitriu A, Golji J, Labadorf AT, Gao B, Beach TG, Myers RH, Longo KA, Latourelle JC. Integrative analyses of proteomics and RNA transcriptomics implicate mitochondrial processes, protein folding pathways and GWAS loci in Parkinson disease. BMC Med Genomics. 2016; 9:5.View Related Profiles.

Labadorf, Adam
Latourelle, Jeanne
Myers, Richard

PMID: 26793951; PMCID: PMC4722694; DOI: 10.1186/s12920-016-0164-y;

Bates G, Osborne GF, Ali N, Benjamin C, Papadopoulou A, Howland D, Tabrizi SJ, Faull RLM, Myers RH, Landles C, Neueder A. B4 Detection of the aberrantly spliced exon 1 – intron 1 htt mRNA in HD patient post mortem brain tissue and fibroblast lines. Journal of Neurology Neurosurgery & Psychiatry. 2016; 87(Suppl 1):A10.2-A10. View Publication

Biglan KM, Shoulson I, Kieburtz K, Oakes D, Kayson E, Shinaman MA, Zhao H, Romer M, Young A, Hersch S, Penney J, Marder K, Paulsen J, Quaid K, Siemers E, Tanner C, Mallonee W, Suter G, Dubinsky R, Gray C, Nance M, Bundlie S, Radtke D, Kostyk S, Baic C, Caress J, Walker F, Hunt V, O'Neill C, Chouinard S, Factor S, Greenamyre T, Wood-Siverio C, Corey-Bloom J, Song D, Peavy G, Moskowitz C, Wesson M, Samii A, Bird T, Lipe H, Blindauer K, Marshall F, Zimmerman C, Goldstein J, Rosas D, Novak P, Caviness J, Adler C, Duffy A, Wheelock V, Tempkin T, Richman D, Seeberger L, Albin R, Chou KL, Racette B, Perlmutter JS, Perlman S, Bordelon Y, Martin W, Wieler M, Leavitt B, Raymond L, Decolongon J, Clarke L, Jankovic J, Hunter C, Hauser RA, Sanchez-Ramos J, Furtado S, Suchowersky O, Klimek ML, Guttman M, Sethna R, Feigin A, Cox M, Shannon B, Percy A, Dure L, Harrison M, Johnson W, Higgins D, Molho E, Nickerson C, Evans S, Hobson D, Singer C, Galvez-Jimenez N, Shannon K, Comella C, Ross C, Saint-Hilaire MH, Testa C, Rosenblatt A, Hogarth P, Weiner W, Como P, Kumar R, Cotto C, Stout J, Brocht A, Watts A, Eberly S, Weaver C, Foroud T, Gusella J, MacDonald M, Myers R, Fahn S, Shults C. Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials. JAMA Neurol. 2016 Jan; 73(1):102-10.View Related Profiles.

Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 26569098; DOI: 10.1001/jamaneurol.2015.2736;

Labadorf A, Hoss AG, Lagomarsino V, Latourelle JC, Hadzi TC, Bregu J, MacDonald ME, Gusella JF, Chen JF, Akbarian S, Weng Z, Myers RH. RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression. PLoS One. 2015; 10(12):e0143563.View Related Profiles.

Labadorf, Adam
Hoss, Andrew
Latourelle, Jeanne
Chen, Jiang-Fan
Myers, Richard

PMID: 26636579; PMCID: PMC4670106; DOI: 10.1371/journal.pone.0143563;

Dong X, Tsuji J, Labadorf A, Roussos P, Chen JF, Myers RH, Akbarian S, Weng Z. The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington's Disease. PLoS One. 2015; 10(12):e0144398.View Related Profiles.

Labadorf, Adam
Myers, Richard

PMID: 26636336; PMCID: PMC4670094; DOI: 10.1371/journal.pone.0144398;

Hoss AG, Lagomarsino VN, Frank S, Hadzi TC, Myers RH, Latourelle JC. Study of plasma-derived miRNAs mimic differences in Huntington's disease brain. Mov Disord. 2015 Dec; 30(14):1961-4.View Related Profiles.

Hoss, Andrew
Latourelle, Jeanne
Myers, Richard
Frank, Samuel

PMID: 26573701; PMCID: PMC4715548; DOI: 10.1002/mds.26457;

Labadorf AT, Myers RH. Evidence of Extensive Alternative Splicing in Post Mortem Human Brain HTT Transcription by mRNA Sequencing. PLoS One. 2015; 10(10):e0141298.View Related Profiles.

Labadorf, Adam
Myers, Richard

PMID: 26496077; PMCID: PMC4619731; DOI: 10.1371/journal.pone.0141298;

Lee JM, Kim KH, Shin A, Chao MJ, Abu Elneel K, Gillis T, Mysore JS, Kaye JA, Zahed H, Kratter IH, Daub AC, Finkbeiner S, Li H, Roach JC, Goodman N, Hood L, Myers RH, MacDonald ME, Gusella JF. Sequence-Level Analysis of the Major European Huntington Disease Haplotype. Am J Hum Genet. 2015 Sep 3; 97(3):435-44. PMID: 26320893; PMCID: PMC4564985; DOI: 10.1016/j.ajhg.2015.07.017;

Identification of Genetic Factors that Modify Clinical Onset of Huntington's Disease. Cell. 2015 Jul 30; 162(3):516-26. PMID: 26232222; PMCID: PMC4524551; DOI: 10.1016/j.cell.2015.07.003;

Joshi PK, Esko T, Mattsson H, Eklund N, Gandin I, Nutile T, Jackson AU, Schurmann C, Smith AV, Zhang W, Okada Y, Stancáková A, Faul JD, Zhao W, Bartz TM, Concas MP, Franceschini N, Enroth S, Vitart V, Trompet S, Guo X, Chasman DI, O'Connel JR, Corre T, Nongmaithem SS, Chen Y, Mangino M, Ruggiero D, Traglia M, Farmaki AE, Kacprowski T, Bjonnes A, van der Spek A, Wu Y, Giri AK, Yanek LR, Wang L, Hofer E, Rietveld CA, McLeod O, Cornelis MC, Pattaro C, Verweij N, Baumbach C, Abdellaoui A, Warren HR, Vuckovic D, Mei H, Bouchard C, Perry JR, Cappellani S, Mirza SS, Benton MC, Broeckel U, Medland SE, Lind PA, Malerba G, Drong A, Yengo L, Bielak LF, Zhi D, van der Most PJ, Shriner D, Mägi R, Hemani G, Karaderi T, Wang Z, Liu T, Demuth I, Zhao JH, Meng W, Lataniotis L, van der Laan SW, Bradfield JP, Wood AR, Bonnefond A, Ahluwalia TS, Hall LM, Salvi E, Yazar S, Carstensen L, de Haan HG, Abney M, Afzal U, Allison MA, Amin N, Asselbergs FW, Bakker SJ, Barr RG, Baumeister SE, Benjamin DJ, Bergmann S, Boerwinkle E, Bottinger EP, Campbell A, Chakravarti A, Chan Y, Chanock SJ, Chen C, Chen YD, Collins FS, Connell J, Correa A, Cupples LA, Smith GD, Davies G, Dörr M, Ehret G, Ellis SB, Feenstra B, Feitosa MF, Ford I, Fox CS, Frayling TM, Friedrich N, Geller F, Scotland G, Gillham-Nasenya I, Gottesman O, Graff M, Grodstein F, Gu C, Haley C, Hammond CJ, Harris SE, Harris TB, Hastie ND, Heard-Costa NL, Heikkilä K, Hocking LJ, Homuth G, Hottenga JJ, Huang J, Huffman JE, Hysi PG, Ikram MA, Ingelsson E, Joensuu A, Johansson Å, Jousilahti P, Jukema JW, Kähönen M, Kamatani Y, Kanoni S, Kerr SM, Khan NM, Koellinger P, Koistinen HA, Kooner MK, Kubo M, Kuusisto J, Lahti J, Launer LJ, Lea RA, Lehne B, Lehtimäki T, Liewald DC, Lind L, Loh M, Lokki ML, London SJ, Loomis SJ, Loukola A, Lu Y, Lumley T, Lundqvist A, Männistö S, Marques-Vidal P, Masciullo C, Matchan A, Mathias RA, Matsuda K, Meigs JB, Meisinger C, Meitinger T, Menni C, Mentch FD, Mihailov E, Milani L, Montasser ME, Montgomery GW, Morrison A, Myers RH, Nadukuru R, Navarro P, Nelis M, Nieminen MS, Nolte IM, O'Connor GT, Ogunniyi A, Padmanabhan S, Palmas WR, Pankow JS, Patarcic I, Pavani F, Peyser PA, Pietilainen K, Poulter N, Prokopenko I, Ralhan S, Redmond P, Rich SS, Rissanen H, Robino A, Rose LM, Rose R, Sala C, Salako B, Salomaa V, Sarin AP, Saxena R, Schmidt H, Scott LJ, Scott WR, Sennblad B, Seshadri S, Sever P, Shrestha S, Smith BH, Smith JA, Soranzo N, Sotoodehnia N, Southam L, Stanton AV, Stathopoulou MG, Strauch K, Strawbridge RJ, Suderman MJ, Tandon N, Tang ST, Taylor KD, Tayo BO, Töglhofer AM, Tomaszewski M, Tšernikova N, Tuomilehto J, Uitterlinden AG, Vaidya D, van Hylckama Vlieg A, van Setten J, Vasankari T, Vedantam S, Vlachopoulou E, Vozzi D, Vuoksimaa E, Waldenberger M, Ware EB, Wentworth-Shields W, Whitfield JB, Wild S, Willemsen G, Yajnik CS, Yao J, Zaza G, Zhu X, Salem RM, Melbye M, Bisgaard H, Samani NJ, Cusi D, Mackey DA, Cooper RS, Froguel P, Pasterkamp G, Grant SF, Hakonarson H, Ferrucci L, Scott RA, Morris AD, Palmer CN, Dedoussis G, Deloukas P, Bertram L, Lindenberger U, Berndt SI, Lindgren CM, Timpson NJ, Tönjes A, Munroe PB, Sørensen TI, Rotimi CN, Arnett DK, Oldehinkel AJ, Kardia SL, Balkau B, Gambaro G, Morris AP, Eriksson JG, Wright MJ, Martin NG, Hunt SC, Starr JM, Deary IJ, Griffiths LR, Tiemeier H, Pirastu N, Kaprio J, Wareham NJ, Pérusse L, Wilson JG, Girotto G, Caulfield MJ, Raitakari O, Boomsma DI, Gieger C, van der Harst P, Hicks AA, Kraft P, Sinisalo J, Knekt P, Johannesson M, Magnusson PK, Hamsten A, Schmidt R, Borecki IB, Vartiainen E, Becker DM, Bharadwaj D, Mohlke KL, Boehnke M, van Duijn CM, Sanghera DK, Teumer A, Zeggini E, Metspalu A, Gasparini P, Ulivi S, Ober C, Toniolo D, Rudan I, Porteous DJ, Ciullo M, Spector TD, Hayward C, Dupuis J, Loos RJ, Wright AF, Chandak GR, Vollenweider P, Shuldiner AR, Ridker PM, Rotter JI, Sattar N, Gyllensten U, North KE, Pirastu M, Psaty BM, Weir DR, Laakso M, Gudnason V, Takahashi A, Chambers JC, et al. DirectionalView Related Profiles.

O'Connor, George
Dupuis, Josee
Cupples, L
Heard-Costa, Nancy
Myers, Richard
Seshadri, Sudha

PMID: 26131930; PMCID: PMC4516141; DOI: 10.1038/nature14618;

Hoss AG, Labadorf A, Latourelle JC, Kartha VK, Hadzi TC, Gusella JF, MacDonald ME, Chen JF, Akbarian S, Weng Z, Vonsattel JP, Myers RH. miR-10b-5p expression in Huntington's disease brain relates to age of onset and the extent of striatal involvement. BMC Med Genomics. 2015; 8:10.View Related Profiles.

Labadorf, Adam
Hoss, Andrew
Latourelle, Jeanne
Chen, Jiang-Fan
Myers, Richard

PMID: 25889241; PMCID: PMC4349621; DOI: 10.1186/s12920-015-0083-3;

Labadorf A, Hoss AG, Hadzi T, Myers RH. Immune Function and Neuro-inflammation are Implicated by mRNA Transcriptomics in Huntington Disease. Neurotherapeutics. 2015; 12(1):273.
Hoss AG, Kartha VK, Labadorf A, Latourelle JC, Myers RH. microRNAs Expressed in Huntington Disease Brains Relate to Age of Onset and the Extent of Striatal Degeneration. Neurotherapeutics. 2015; 12(1):273.

Correia K, Harold D, Kim KH, Holmans P, Jones L, Orth M, Myers RH, Kwak S, Wheeler VC, MacDonald ME, Gusella JF, Lee JM. The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease. J Huntingtons Dis. 2015; 4(3):279-84. PMID: 26444025; PMCID: PMC4753529; DOI: 10.3233/JHD-150169;

Bai G, Cheung I, Shulha HP, Coelho JE, Li P, Dong X, Jakovcevski M, Wang Y, Grigorenko A, Jiang Y, Hoss A, Patel K, Zheng M, Rogaev E, Myers RH, Weng Z, Akbarian S, Chen JF. Epigenetic dysregulation of hairy and enhancer of split 4 (HES4) is associated with striatal degeneration in postmortem Huntington brains. Hum Mol Genet. 2015 Mar 1; 24(5):1441-56.View Related Profiles.

Hoss, Andrew
Myers, Richard

PMID: 25480889; PMCID: PMC4321450; DOI: 10.1093/hmg/ddu561;

Bharadwaj R, Peter CJ, Jiang Y, Roussos P, Vogel-Ciernia A, Shen EY, Mitchell AC, Mao W, Whittle C, Dincer A, Jakovcevski M, Pothula V, Rasmussen TP, Giakoumaki SG, Bitsios P, Sherif A, Gardner PD, Ernst P, Ghose S, Sklar P, Haroutunian V, Tamminga C, Myers RH, Futai K, Wood MA, Akbarian S. Conserved higher-order chromatin regulates NMDA receptor gene expression and cognition. Neuron. 2014 Dec 3; 84(5):997-1008. PMID: 25467983; PMCID: PMC4258154; DOI: 10.1016/j.neuron.2014.10.032;

Nalls MA, Pankratz N, Lill CM, Do CB, Hernandez DG, Saad M, DeStefano AL, Kara E, Bras J, Sharma M, Schulte C, Keller MF, Arepalli S, Letson C, Edsall C, Stefansson H, Liu X, Pliner H, Lee JH, Cheng R, Ikram MA, Ioannidis JP, Hadjigeorgiou GM, Bis JC, Martinez M, Perlmutter JS, Goate A, Marder K, Fiske B, Sutherland M, Xiromerisiou G, Myers RH, Clark LN, Stefansson K, Hardy JA, Heutink P, Chen H, Wood NW, Houlden H, Payami H, Brice A, Scott WK, Gasser T, Bertram L, Eriksson N, Foroud T, Singleton AB. Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Nat Genet. 2014 Sep; 46(9):989-93.View Related Profiles.

DeStefano, Anita
Myers, Richard
Seshadri, Sudha

PMID: 25064009; PMCID: PMC4146673; DOI: 10.1038/ng.3043;

Hoss AG, Kartha VK, Dong X, Latourelle JC, Dumitriu A, Hadzi TC, Macdonald ME, Gusella JF, Akbarian S, Chen JF, Weng Z, Myers RH. MicroRNAs located in the Hox gene clusters are implicated in huntington's disease pathogenesis. PLoS Genet. 2014 Feb; 10(2):e1004188.View Related Profiles.

Dumitriu, Alexandra
Hoss, Andrew
Latourelle, Jeanne
Myers, Richard

PMID: 24586208; PMCID: PMC3937267; DOI: 10.1371/journal.pgen.1004188;

McCusker EA, Myers RH. Feasibility of Huntington disease trials in the disease prodrome. Neurology. 2014 Mar 11; 82(10):824-5. PMID: 24510495; DOI: 10.1212/WNL.0000000000000197;

Jones L, Gusella JF, MacDonald ME, Wheeler V, Lee JM, Myers RH, Latourelle JC, Harold D, Holmans P, Orth M, Kwak S. A03 Genetic Modifiers Affecting The Age At Motor Onset In Huntington's Disease. Journal of Neurology Neurosurgery & Psychiatry. 2014; 85(Suppl 1):A1-A2. View Publication

Hendricks AE, Dupuis J, Logue MW, Myers RH, Lunetta KL. Correction for multiple testing in a gene region. Eur J Hum Genet. 2014 Mar; 22(3):414-8.View Related Profiles.

Dupuis, Josee
Lunetta, Kathryn
Logue, Mark
Myers, Richard

PMID: 23838599; PMCID: PMC3925272; DOI: 10.1038/ejhg.2013.144;

Pichler I, Del Greco M F, Gögele M, Lill CM, Bertram L, Do CB, Eriksson N, Foroud T, Myers RH, Nalls M, Keller MF, Benyamin B, Whitfield JB, Pramstaller PP, Hicks AA, Thompson JR, Minelli C. Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study. PLoS Med. 2013; 10(6):e1001462. PMID: 23750121; PMCID: PMC3672214; DOI: 10.1371/journal.pmed.1001462;

Ramos EM, Latourelle JC, Gillis T, Mysore JS, Squitieri F, Di Pardo A, Di Donato S, Gellera C, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Gomez-Tortosa E, Ayuso C, Suchowersky O, Trent RJ, McCusker E, Novelletto A, Frontali M, Jones R, Ashizawa T, Frank S, Saint-Hilaire MH, Hersch SM, Rosas HD, Lucente D, Harrison MB, Zanko A, Abramson RK, Marder K, Gusella JF, Lee JM, Alonso I, Sequeiros J, Myers RH, Macdonald ME. Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onset. Neurogenetics. 2013 Nov; 14(3-4):173-9.View Related Profiles.

Latourelle, Jeanne
Saint-Hilaire, Marie-Helene
Myers, Richard
Frank, Samuel

PMID: 23644918; PMCID: PMC3825533; DOI: 10.1007/s10048-013-0364-y;

Dumitriu A, Myers RH, Mckee A, Seshadri S, Destefano A. RNA-sequencing evaluation of fresh frozen and formaldehyde-fixed prefrontal cortex brain tissue for the study of Alzheimer's disease. Alzheimer's and Dementia. 2013; 9(4):P177. View Publication

Shulha HP, Crisci JL, Reshetov D, Tushir JS, Cheung I, Bharadwaj R, Chou HJ, Houston IB, Peter CJ, Mitchell AC, Yao WD, Myers RH, Chen JF, Preuss TM, Rogaev EI, Jensen JD, Weng Z, Akbarian S. Human-specific histone methylation signatures at transcription start sites in prefrontal neurons. PLoS Biol. 2012; 10(11):e1001427.View Related Profiles.

Chen, Jiang-Fan
Myers, Richard

PMID: 23185133; PMCID: PMC3502543; DOI: 10.1371/journal.pbio.1001427;

Latourelle JC, Dumitriu A, Hadzi TC, Beach TG, Myers RH. Evaluation of Parkinson disease risk variants as expression-QTLs. PLoS One. 2012; 7(10):e46199.View Related Profiles.

Dumitriu, Alexandra
Latourelle, Jeanne
Myers, Richard

PMID: 23071545; PMCID: PMC3465315; DOI: 10.1371/journal.pone.0046199;

Hadzi TC, Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Gillis T, Mysore JS, Gusella JF, MacDonald ME, Myers RH, Vonsattel JP. Assessment of cortical and striatal involvement in 523 Huntington disease brains. Neurology. 2012 Oct 16; 79(16):1708-15.View Related Profiles.

Latourelle, Jeanne
Lunetta, Kathryn
Cupples, L
Myers, Richard

PMID: 23035064; PMCID: PMC3468776; DOI: 10.1212/WNL.0b013e31826e9a5d;

Wilk JB, Shrine NR, Loehr LR, Zhao JH, Manichaikul A, Lopez LM, Smith AV, Heckbert SR, Smolonska J, Tang W, Loth DW, Curjuric I, Hui J, Cho MH, Latourelle JC, Henry AP, Aldrich M, Bakke P, Beaty TH, Bentley AR, Borecki IB, Brusselle GG, Burkart KM, Chen TH, Couper D, Crapo JD, Davies G, Dupuis J, Franceschini N, Gulsvik A, Hancock DB, Harris TB, Hofman A, Imboden M, James AL, Khaw KT, Lahousse L, Launer LJ, Litonjua A, Liu Y, Lohman KK, Lomas DA, Lumley T, Marciante KD, McArdle WL, Meibohm B, Morrison AC, Musk AW, Myers RH, North KE, Postma DS, Psaty BM, Rich SS, Rivadeneira F, Rochat T, Rotter JI, Artigas MS, Starr JM, Uitterlinden AG, Wareham NJ, Wijmenga C, Zanen P, Province MA, Silverman EK, Deary IJ, Palmer LJ, Cassano PA, Gudnason V, Barr RG, Loos RJ, Strachan DP, London SJ, Boezen HM, Probst-Hensch N, Gharib SA, Hall IP, O'Connor GT, Tobin MD, Stricker BH. Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. Am J Respir Crit Care Med. 2012 Oct 1; 186(7):622-32.View Related Profiles.

O'Connor, George
Latourelle, Jeanne
Dupuis, Josee
Myers, Richard

PMID: 22837378; PMCID: PMC3480517; DOI: 10.1164/rccm.201202-0366OC;

Ramos EM, Latourelle JC, Lee JH, Gillis T, Mysore JS, Squitieri F, Di Pardo A, Di Donato S, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Gomez-Tortosa E, Ayuso C, Suchowersky O, Trent RJ, McCusker E, Novelletto A, Frontali M, Jones R, Ashizawa T, Frank S, Saint-Hilaire MH, Hersch SM, Rosas HD, Lucente D, Harrison MB, Zanko A, Marder K, Gusella JF, Lee JM, Alonso I, Sequeiros J, Myers RH, Macdonald ME. Population stratification may bias analysis of PGC-1a as a modifier of age at Huntington disease motor onset. Hum Genet. 2012 Dec; 131(12):1833-40.View Related Profiles.

Latourelle, Jeanne
Saint-Hilaire, Marie-Helene
Myers, Richard
Frank, Samuel

PMID: 22825315; PMCID: PMC3492689; DOI: 10.1007/s00439-012-1205-z;

Lee JH, Lee JM, Ramos EM, Gillis T, Mysore JS, Kishikawa S, Hadzi T, Hendricks AE, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Squitieri F, Gellera C, Gomez-Tortosa E, Ayuso C, Suchowersky O, Trent RJ, McCusker E, Novelletto A, Frontali M, Jones R, Ashizawa T, Frank S, Saint-Hilaire MH, Hersch SM, Rosas HD, Lucente D, Harrison MB, Zanko A, Abramson RK, Marder K, Sequeiros J, Landwehrmeyer GB, Shoulson I, Myers RH, MacDonald ME, Gusella JF. TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease. Biochem Biophys Res Commun. 2012 Aug 3; 424(3):404-8.View Related Profiles.

Saint-Hilaire, Marie-Helene
Myers, Richard
Frank, Samuel

PMID: 22771793; PMCID: PMC3752397; DOI: 10.1016/j.bbrc.2012.06.120;

Dumitriu A, Latourelle JC, Hadzi TC, Pankratz N, Garza D, Miller JP, Vance JM, Foroud T, Beach TG, Myers RH. Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation. PLoS Genet. 2012 Jun; 8(6):e1002794.View Related Profiles.

Dumitriu, Alexandra
Latourelle, Jeanne
Myers, Richard

PMID: 22761592; PMCID: PMC3386245; DOI: 10.1371/journal.pgen.1002794;

Lill CM, Roehr JT, McQueen MB, Kavvoura FK, Bagade S, Schjeide BM, Schjeide LM, Meissner E, Zauft U, Allen NC, Liu T, Schilling M, Anderson KJ, Beecham G, Berg D, Biernacka JM, Brice A, DeStefano AL, Do CB, Eriksson N, Factor SA, Farrer MJ, Foroud T, Gasser T, Hamza T, Hardy JA, Heutink P, Hill-Burns EM, Klein C, Latourelle JC, Maraganore DM, Martin ER, Martinez M, Myers RH, Nalls MA, Pankratz N, Payami H, Satake W, Scott WK, Sharma M, Singleton AB, Stefansson K, Toda T, Tung JY, Vance J, Wood NW, Zabetian CP, Young P, Tanzi RE, Khoury MJ, Zipp F, Lehrach H, Ioannidis JP, Bertram L. Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. PLoS Genet. 2012; 8(3):e1002548.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Myers, Richard

PMID: 22438815; PMCID: PMC3305333; DOI: 10.1371/journal.pgen.1002548;

Dumitriu A, Moser C, Hadzi TC, Williamson SL, Pacheco CD, Hendricks AE, Latourelle JC, Wilk JB, Destefano AL, Myers RH. Postmortem Interval Influences a-Synuclein Expression in Parkinson Disease Brain. Parkinsons Dis. 2012; 2012:614212.View Related Profiles.

Dumitriu, Alexandra
DeStefano, Anita
Pacheco, Christopher
Latourelle, Jeanne
Myers, Richard

PMID: 22530163; PMCID: PMC3317023; DOI: 10.1155/2012/614212;

Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, Mayeux R, Ross OA, Scherzer CR, Simon DK, Tanner C, Vance JM, Wszolek ZK, Zabetian CP, Myers RH, Payami H, Scott WK, Foroud T. Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Ann Neurol. 2012 Mar; 71(3):370-84.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Myers, Richard

PMID: 22451204; PMCID: PMC3354734; DOI: 10.1002/ana.22687;

Lee JM, Gillis T, Mysore JS, Ramos EM, Myers RH, Hayden MR, Morrison PJ, Nance M, Ross CA, Margolis RL, Squitieri F, Griguoli A, Di Donato S, Gomez-Tortosa E, Ayuso C, Suchowersky O, Trent RJ, McCusker E, Novelletto A, Frontali M, Jones R, Ashizawa T, Frank S, Saint-Hilaire MH, Hersch SM, Rosas HD, Lucente D, Harrison MB, Zanko A, Abramson RK, Marder K, Sequeiros J, MacDonald ME, Gusella JF. Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region. Am J Hum Genet. 2012 Mar 9; 90(3):434-44.View Related Profiles.

Saint-Hilaire, Marie-Helene
Myers, Richard
Frank, Samuel

PMID: 22387017; PMCID: PMC3309179; DOI: 10.1016/j.ajhg.2012.01.005;

Lee JM, Ramos EM, Lee JH, Gillis T, Mysore JS, Hayden MR, Warby SC, Morrison P, Nance M, Ross CA, Margolis RL, Squitieri F, Orobello S, Di Donato S, Gomez-Tortosa E, Ayuso C, Suchowersky O, Trent RJ, McCusker E, Novelletto A, Frontali M, Jones R, Ashizawa T, Frank S, Saint-Hilaire MH, Hersch SM, Rosas HD, Lucente D, Harrison MB, Zanko A, Abramson RK, Marder K, Sequeiros J, Paulsen JS, Landwehrmeyer GB, Myers RH, MacDonald ME, Gusella JF. CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion. Neurology. 2012 Mar 6; 78(10):690-5.View Related Profiles.

Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 22323755; PMCID: PMC3306163; DOI: 10.1212/WNL.0b013e318249f683;

Sebastiani P, Solovieff N, Dewan AT, Walsh KM, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Hoh J, Perls TT. Genetic signatures of exceptional longevity in humans. PLoS One. 2012; 7(1):e29848.View Related Profiles.

Baldwin, Clinton
Steinberg, Martin
Montano, Monty
Sebastiani, Paola
Myers, Richard
Andersen, Stacy
Perls, Thomas

PMID: 22279548; PMCID: PMC3261167; DOI: 10.1371/journal.pone.0029848;

Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI, Smith AV, Tobin MD, Verwoert GC, Hwang SJ, Pihur V, Vollenweider P, O'Reilly PF, Amin N, Bragg-Gresham JL, Teumer A, Glazer NL, Launer L, Zhao JH, Aulchenko Y, Heath S, Sõber S, Parsa A, Luan J, Arora P, Dehghan A, Zhang F, Lucas G, Hicks AA, Jackson AU, Peden JF, Tanaka T, Wild SH, Rudan I, Igl W, Milaneschi Y, Parker AN, Fava C, Chambers JC, Fox ER, Kumari M, Go MJ, van der Harst P, Kao WH, Sjögren M, Vinay DG, Alexander M, Tabara Y, Shaw-Hawkins S, Whincup PH, Liu Y, Shi G, Kuusisto J, Tayo B, Seielstad M, Sim X, Nguyen KD, Lehtimäki T, Matullo G, Wu Y, Gaunt TR, Onland-Moret NC, Cooper MN, Platou CG, Org E, Hardy R, Dahgam S, Palmen J, Vitart V, Braund PS, Kuznetsova T, Uiterwaal CS, Adeyemo A, Palmas W, Campbell H, Ludwig B, Tomaszewski M, Tzoulaki I, Palmer ND, Aspelund T, Garcia M, Chang YP, O'Connell JR, Steinle NI, Grobbee DE, Arking DE, Kardia SL, Morrison AC, Hernandez D, Najjar S, McArdle WL, Hadley D, Brown MJ, Connell JM, Hingorani AD, Day IN, Lawlor DA, Beilby JP, Lawrence RW, Clarke R, Hopewell JC, Ongen H, Dreisbach AW, Li Y, Young JH, Bis JC, Kähönen M, Viikari J, Adair LS, Lee NR, Chen MH, Olden M, Pattaro C, Bolton JA, Köttgen A, Bergmann S, Mooser V, Chaturvedi N, Frayling TM, Islam M, Jafar TH, Erdmann J, Kulkarni SR, Bornstein SR, Grässler J, Groop L, Voight BF, Kettunen J, Howard P, Taylor A, Guarrera S, Ricceri F, Emilsson V, Plump A, Barroso I, Khaw KT, Weder AB, Hunt SC, Sun YV, Bergman RN, Collins FS, Bonnycastle LL, Scott LJ, Stringham HM, Peltonen L, Perola M, Vartiainen E, Brand SM, Staessen JA, Wang TJ, Burton PR, Soler Artigas M, Dong Y, Snieder H, Wang X, Zhu H, Lohman KK, Rudock ME, Heckbert SR, Smith NL, Wiggins KL, Doumatey A, Shriner D, Veldre G, Viigimaa M, Kinra S, Prabhakaran D, Tripathy V, Langefeld CD, Rosengren A, Thelle DS, Corsi AM, Singleton A, Forrester T, Hilton G, McKenzie CA, Salako T, Iwai N, Kita Y, Ogihara T, Ohkubo T, Okamura T, Ueshima H, Umemura S, Eyheramendy S, Meitinger T, Wichmann HE, Cho YS, Kim HL, Lee JY, Scott J, Sehmi JS, Zhang W, Hedblad B, Nilsson P, Smith GD, Wong A, Narisu N, Stancáková A, Raffel LJ, Yao J, Kathiresan S, O'Donnell CJ, Schwartz SM, Ikram MA, Longstreth WT, Mosley TH, Seshadri S, Shrine NR, Wain LV, Morken MA, Swift AJ, Laitinen J, Prokopenko I, Zitting P, Cooper JA, Humphries SE, Danesh J, Rasheed A, Goel A, Hamsten A, Watkins H, Bakker SJ, van Gilst WH, Janipalli CS, Mani KR, Yajnik CS, Hofman A, Mattace-Raso FU, Oostra BA, Demirkan A, Isaacs A, Rivadeneira F, Lakatta EG, Orru M, Scuteri A, Ala-Korpela M, Kangas AJ, Lyytikäinen LP, Soininen P, Tukiainen T, Würtz P, Ong RT, Dörr M, Kroemer HK, Völker U, Völzke H, Galan P, Hercberg S, Lathrop M, Zelenika D, Deloukas P, Mangino M, Spector TD, Zhai G, Meschia JF, Nalls MA, Sharma P, Terzic J, Kumar MV, Denniff M, Zukowska-Szczechowska E, Wagenknecht LE, Fowkes FG, Charchar FJ, Schwarz PE, Hayward C, Guo X, Rotimi C, Bots ML, Brand E, Samani NJ, Polasek O, Talmud PJ, Nyberg F, Kuh D, Laan M, Hveem K, Palmer LJ, van der Schouw YT, Casas JP, Mohlke KL, Vineis P, Raitakari O, Ganesh SK, Wong TY, Tai ES, Cooper RS, Laakso M, Rao DC, Harris TB, Morris RW, Dominiczak AF, Kivimaki M, Marmot MG, Miki T, Saleheen D, Chandak GR, Coresh J, Navis G, Salomaa V, Han BG, Zhu X, Kooner JS, Melander O, Ridker PM, Bandinelli S, Gyllensten UB, Wright AF, Wilson JF, Ferrucci L, Farrall M, Tuomilehto J, Pramstaller PP, Elosua R, Soranzo N, Sijbrands EJ, Altshuler D, Loos RJ, Shuldiner AR, Gieger C, Meneton P, Uitterlinden AG, Wareham NJ, Gudnason V, Rotter JI, Rettig R, Uda M, Strachan DP, Witteman JC, Hartikainen AL, Beckmann JS, Boerwinkle E, Vasan RS, Boehnke M, Larson MG, Järvelin MR, Psaty BM, Abecasis GR, Chakravarti A, Elliott P, van Duijn CM, Newton-Cheh C, Levy D, Caulfield MJ, Johnson T. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 2011 Oct 6; 478(7367):103-9.View Related Profiles.

O'Donnell, Christopher
Cupples, L
Larson, Martin
Chen, Ming-Huei
Myers, Richard
Hwang, Shih-Jen
Seshadri, Sudha
Ramachandran, Vasan

PMID: 21909115; PMCID: PMC3340926; DOI: 10.1038/nature10405;

Pankratz N, Dumitriu A, Hetrick KN, Sun M, Latourelle JC, Wilk JB, Halter C, Doheny KF, Gusella JF, Nichols WC, Myers RH, Foroud T, DeStefano AL. Copy number variation in familial Parkinson disease. PLoS One. 2011; 6(8):e20988.View Related Profiles.

Dumitriu, Alexandra
DeStefano, Anita
Latourelle, Jeanne
Myers, Richard

PMID: 21829596; PMCID: PMC3149037; DOI: 10.1371/journal.pone.0020988;

Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Retraction. Science. 2011 Jul 22; 333(6041):404.View Related Profiles.

Baldwin, Clinton
Steinberg, Martin
Sebastiani, Paola
Myers, Richard
Andersen, Stacy
Perls, Thomas

PMID: 21778381; DOI: 10.1126/science.333.6041.404-a;

Soldner F, Laganière J, Cheng AW, Hockemeyer D, Gao Q, Alagappan R, Khurana V, Golbe LI, Myers RH, Lindquist S, Zhang L, Guschin D, Fong LK, Vu BJ, Meng X, Urnov FD, Rebar EJ, Gregory PD, Zhang HS, Jaenisch R. Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations. Cell. 2011 Jul 22; 146(2):318-31. PMID: 21757228; PMCID: PMC3155290; DOI: 10.1016/j.cell.2011.06.019;

Latourelle JC, Hendricks AE, Pankratz N, Wilk JB, Halter C, Nichols WC, Gusella JF, Destefano AL, Myers RH, Foroud T. Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease. Mov Disord. 2011 Sep; 26(11):2039-44.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Myers, Richard

PMID: 21661047; PMCID: PMC3346677; DOI: 10.1002/mds.23781;

Dumitriu A, Pacheco CD, Wilk JB, Strathearn KE, Latourelle JC, Goldwurm S, Pezzoli G, Rochet JC, Lindquist S, Myers RH. Cyclin-G-associated kinase modifies a-synuclein expression levels and toxicity in Parkinson's disease: results from the GenePD Study. Hum Mol Genet. 2011 Apr 15; 20(8):1478-87.View Related Profiles.

Dumitriu, Alexandra
Pacheco, Christopher
Latourelle, Jeanne
Myers, Richard

PMID: 21258085; PMCID: PMC3063983; DOI: 10.1093/hmg/ddr026;

Sebastiani P, Solovieff N, Puca A, Perls T, Myers RH et. al. Editorial Expression of Concern (Retraction of vol 330, pg 912, 2010). Science. 2011; 333(6041):404.

Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Lango Allen H, Lindgren CM, Luan J, Mägi R, Randall JC, Vedantam S, Winkler TW, Qi L, Workalemahu T, Heid IM, Steinthorsdottir V, Stringham HM, Weedon MN, Wheeler E, Wood AR, Ferreira T, Weyant RJ, Segrè AV, Estrada K, Liang L, Nemesh J, Park JH, Gustafsson S, Kilpeläinen TO, Yang J, Bouatia-Naji N, Esko T, Feitosa MF, Kutalik Z, Mangino M, Raychaudhuri S, Scherag A, Smith AV, Welch R, Zhao JH, Aben KK, Absher DM, Amin N, Dixon AL, Fisher E, Glazer NL, Goddard ME, Heard-Costa NL, Hoesel V, Hottenga JJ, Johansson A, Johnson T, Ketkar S, Lamina C, Li S, Moffatt MF, Myers RH, Narisu N, Perry JR, Peters MJ, Preuss M, Ripatti S, Rivadeneira F, Sandholt C, Scott LJ, Timpson NJ, Tyrer JP, van Wingerden S, Watanabe RM, White CC, Wiklund F, Barlassina C, Chasman DI, Cooper MN, Jansson JO, Lawrence RW, Pellikka N, Prokopenko I, Shi J, Thiering E, Alavere H, Alibrandi MT, Almgren P, Arnold AM, Aspelund T, Atwood LD, Balkau B, Balmforth AJ, Bennett AJ, Ben-Shlomo Y, Bergman RN, Bergmann S, Biebermann H, Blakemore AI, Boes T, Bonnycastle LL, Bornstein SR, Brown MJ, Buchanan TA, Busonero F, Campbell H, Cappuccio FP, Cavalcanti-Proença C, Chen YD, Chen CM, Chines PS, Clarke R, Coin L, Connell J, Day IN, den Heijer M, Duan J, Ebrahim S, Elliott P, Elosua R, Eiriksdottir G, Erdos MR, Eriksson JG, Facheris MF, Felix SB, Fischer-Posovszky P, Folsom AR, Friedrich N, Freimer NB, Fu M, Gaget S, Gejman PV, Geus EJ, Gieger C, Gjesing AP, Goel A, Goyette P, Grallert H, Grässler J, Greenawalt DM, Groves CJ, Gudnason V, Guiducci C, Hartikainen AL, Hassanali N, Hall AS, Havulinna AS, Hayward C, Heath AC, Hengstenberg C, Hicks AA, Hinney A, Hofman A, Homuth G, Hui J, Igl W, Iribarren C, Isomaa B, Jacobs KB, Jarick I, Jewell E, John U, Jørgensen T, Jousilahti P, Jula A, Kaakinen M, Kajantie E, Kaplan LM, Kathiresan S, Kettunen J, Kinnunen L, Knowles JW, Kolcic I, König IR, Koskinen S, Kovacs P, Kuusisto J, Kraft P, Kvaløy K, Laitinen J, Lantieri O, Lanzani C, Launer LJ, Lecoeur C, Lehtimäki T, Lettre G, Liu J, Lokki ML, Lorentzon M, Luben RN, Ludwig B, Manunta P, Marek D, Marre M, Martin NG, McArdle WL, McCarthy A, McKnight B, Meitinger T, Melander O, Meyre D, Midthjell K, Montgomery GW, Morken MA, Morris AP, Mulic R, Ngwa JS, Nelis M, Neville MJ, Nyholt DR, O'Donnell CJ, O'Rahilly S, Ong KK, Oostra B, Paré G, Parker AN, Perola M, Pichler I, Pietiläinen KH, Platou CG, Polasek O, Pouta A, Rafelt S, Raitakari O, Rayner NW, Ridderstråle M, Rief W, Ruokonen A, Robertson NR, Rzehak P, Salomaa V, Sanders AR, Sandhu MS, Sanna S, Saramies J, Savolainen MJ, Scherag S, Schipf S, Schreiber S, Schunkert H, Silander K, Sinisalo J, Siscovick DS, Smit JH, Soranzo N, Sovio U, Stephens J, Surakka I, Swift AJ, Tammesoo ML, Tardif JC, Teder-Laving M, Teslovich TM, Thompson JR, Thomson B, Tönjes A, Tuomi T, van Meurs JB, van Ommen GJ, Vatin V, Viikari J, Visvikis-Siest S, Vitart V, Vogel CI, Voight BF, Waite LL, Wallaschofski H, Walters GB, Widen E, Wiegand S, Wild SH, Willemsen G, Witte DR, Witteman JC, Xu J, Zhang Q, Zgaga L, Ziegler A, Zitting P, Beilby JP, Farooqi IS, Hebebrand J, Huikuri HV, James AL, Kähönen M, Levinson DF, Macciardi F, Nieminen MS, Ohlsson C, Palmer LJ, Ridker PM, Stumvoll M, Beckmann JS, Boeing H, Boerwinkle E, Boomsma DI, Caulfield MJ, Chanock SJ, Collins FS, Cupples LA, Smith GD, Erdmann J, Froguel P, Grönberg H, Gyllensten U, Hall P, Hansen T, Harris TB, Hattersley AT, Hayes RB, Heinrich J, Hu FB, Hveem K, Illig T, Jarvelin MR, Kaprio J, Karpe F, Khaw KT, Kiemeney LA, Krude H, Laakso M, Lawlor DA, Metspalu A, Munroe PB, Ouwehand WH, Pedersen O, Penninx BW, Peters A, Pramstaller PP, Quertermous T, Reinehr T, Rissanen A, Rudan I, Samani NJ, Schwarz PE, Shuldiner AR, Spector TD, Tuomilehto J, Uda M, Uitterlinden A, Valle TT, Wabitsch M, Waeber G, Wareham NJ, Watkins H, Wilson JF, Wright AF, Zillikens MC, Chatterjee N, McCarroll SA, Purcell S, Schadt EE, Visscher PM, et al. AssocView Related Profiles.

O'Donnell, Christopher
Cupples, L
Atwood, Larry
Heard-Costa, Nancy
Glazer, Nicole
Myers, Richard

PMID: 20935630; PMCID: PMC3014648; DOI: 10.1038/ng.686;

Lanoue AC, Dumitriu A, Myers RH, Soghomonian JJ. Decreased glutamic acid decarboxylase mRNA expression in prefrontal cortex in Parkinson's disease. Exp Neurol. 2010 Nov; 226(1):207-17.View Related Profiles.

Dumitriu, Alexandra
Soghomonian, Jean-Jacques
Myers, Richard

PMID: 20832408; PMCID: PMC3108022; DOI: 10.1016/j.expneurol.2010.09.001;

Latourelle JC, Dybdahl M, Destefano AL, Myers RH, Lash TL. Estrogen-related and other disease diagnoses preceding Parkinson's disease. Clin Epidemiol. 2010; 2:153-70.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Myers, Richard

PMID: 20865113; PMCID: PMC2943181; DOI: 10.2147/clep.s9621;

Sebastiani P, Solovieff N, Puca A, Hartley SW, Melista E, Andersen S, Dworkis DA, Wilk JB, Myers RH, Steinberg MH, Montano M, Baldwin CT, Perls TT. Genetic signatures of exceptional longevity in humans. Science. 2010 Jul 1; 2010.View Related Profiles.

Baldwin, Clinton
Steinberg, Martin
Montano, Monty
Sebastiani, Paola
Myers, Richard
Andersen, Stacy
Perls, Thomas

PMID: 20595579; DOI: 10.1126/science.1190532;

Latourelle JC, Dybdahl M, Destefano AL, Myers RH, Lash TL. Risk of Parkinson's disease after tamoxifen treatment. BMC Neurol. 2010; 10:23.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Myers, Richard

PMID: 20385012; PMCID: PMC2862029; DOI: 10.1186/1471-2377-10-23;

Hendricks A, Myers RH, Lunetta K. Retaining Power: Is it Possible to Simply and Effectively Adjust for Multiple Comparisons in a Candidate Gene Region?. 19th Annual Meeting of the International-Genetic-Epidemiology-Society. 2010; 34.

Latourelle JC, Pankratz N, Dumitriu A, Wilk JB, Goldwurm S, Pezzoli G, Mariani CB, DeStefano AL, Halter C, Gusella JF, Nichols WC, Myers RH, Foroud T. Genomewide association study for onset age in Parkinson disease. BMC Med Genet. 2009; 10:98.View Related Profiles.

Dumitriu, Alexandra
DeStefano, Anita
Latourelle, Jeanne
Myers, Richard

PMID: 19772629; PMCID: PMC2758866; DOI: 10.1186/1471-2350-10-98;

Hendricks AE, Latourelle JC, Lunetta KL, Cupples LA, Wheeler V, MacDonald ME, Gusella JF, Myers RH. Estimating the probability of de novo HD cases from transmissions of expanded penetrant CAG alleles in the Huntington disease gene from male carriers of high normal alleles (27-35 CAG). Am J Med Genet A. 2009 Jul; 149A(7):1375-81.View Related Profiles.

Latourelle, Jeanne
Lunetta, Kathryn
Cupples, L
Myers, Richard

PMID: 19507258; PMCID: PMC2724761; DOI: 10.1002/ajmg.a.32901;

Feitosa MF, North KE, Myers RH, Pankow JS, Borecki IB. Evidence for three novel QTLs for adiposity on chromosome 2 with epistatic interactions: the NHLBI Family Heart Study. Obesity (Silver Spring). 2009 Dec; 17(12):2190-5. PMID: 19521348; PMCID: PMC4976636; DOI: 10.1038/oby.2009.181;

Swami M, Hendricks AE, Gillis T, Massood T, Mysore J, Myers RH, Wheeler VC. Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset. Hum Mol Genet. 2009 Aug 15; 18(16):3039-47. PMID: 19465745; PMCID: PMC2714728; DOI: 10.1093/hmg/ddp242;

Laramie JM, Wilk JB, Williamson SL, Nagle MW, Latourelle JC, Tobin JE, Province MA, Borecki IB, Myers RH. Multiple genes influence BMI on chromosome 7q31-34: the NHLBI Family Heart Study. Obesity (Silver Spring). 2009 Dec; 17(12):2182-9.View Related Profiles.

Latourelle, Jeanne
Myers, Richard

PMID: 19461589; DOI: 10.1038/oby.2009.141;

Wilk JB, Chen TH, Gottlieb DJ, Walter RE, Nagle MW, Brandler BJ, Myers RH, Borecki IB, Silverman EK, Weiss ST, O'Connor GT. A genome-wide association study of pulmonary function measures in the Framingham Heart Study. PLoS Genet. 2009 Mar; 5(3):e1000429.View Related Profiles.

O'Connor, George
Myers, Richard
Chen, Ting-hsu

PMID: 19300500; PMCID: PMC2652834; DOI: 10.1371/journal.pgen.1000429;

Franceschini N, North KE, Arnett D, Pankow JS, Chung JH, Baird L, Leppert MF, Eckfeldt JH, Boerwinkle E, Gu CC, Lewis CE, Myers RH, Turner ST, Weder A, Kao WH, Mosley TH, Chakravarti A, Kramer H, Zhang J, Hunt SC. The association of cell cycle checkpoint 2 variants and kidney function: findings of the Family Blood Pressure Program and the Atherosclerosis Risk In Communities study. Am J Hypertens. 2009 May; 22(5):552-8. PMID: 19265784; PMCID: PMC2727134; DOI: 10.1038/ajh.2009.41;

Ma D, Feitosa MF, Wilk JB, Laramie JM, Yu K, Leiendecker-Foster C, Myers RH, Province MA, Borecki IB. Leptin is associated with blood pressure and hypertension in women from the National Heart, Lung, and Blood Institute Family Heart Study. Hypertension. 2009 Mar; 53(3):473-9. PMID: 19204185; PMCID: PMC2668693; DOI: 10.1161/HYPERTENSIONAHA.108.118133;

Latourelle JC, Hendricks A, Wilk JB, DeStefano AL, Pankratz N, Foroud T, Myers RH. Rare Variants with Recessive Effects identified in a Genome-wide Association Study of Parkinson's Disease. 18th Annual Meeting of the International-Genetic-Epidemiology-Society. 2009.

Wu J, Pankow JS, Tracy RP, North KE, Myers RH, Feitosa ME, Province MA, Borecki IB. A QTL on 12q influencing an inflammation marker and obesity in white women: the NHLBI Family Heart Study. Obesity (Silver Spring). 2009 Mar; 17(3):525-31. PMID: 19238141; PMCID: PMC4962615; DOI: 10.1038/oby.2008.556;

Shi G, Gu CC, Kraja AT, Arnett DK, Myers RH, Pankow JS, Hunt SC, Rao DC. Genetic effect on blood pressure is modulated by age: the Hypertension Genetic Epidemiology Network Study. Hypertension. 2009 Jan; 53(1):35-41. PMID: 19029486; PMCID: PMC2633773; DOI: 10.1161/HYPERTENSIONAHA.108.120071;

Pankratz N, Wilk JB, Latourelle JC, DeStefano AL, Halter C, Pugh EW, Doheny KF, Gusella JF, Nichols WC, Foroud T, Myers RH. Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Hum Genet. 2009 Jan; 124(6):593-605.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Myers, Richard

PMID: 18985386; PMCID: PMC2627511; DOI: 10.1007/s00439-008-0582-9;

Latourelle JC, Sun M, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, Shill HA, Singer C, Goldwurm S, Pezzoli G, Zini M, Saint-Hilaire MH, Hendricks AE, Williamson S, Nagle MW, Wilk JB, Massood T, Huskey KW, Laramie JM, DeStefano AL, Baker KB, Itin I, Litvan I, Nicholson G, Corbett A, Nance M, Drasby E, Isaacson S, Burn DJ, Chinnery PF, Pramstaller PP, Al-hinti J, Moller AT, Ostergaard K, Sherman SJ, Roxburgh R, Snow B, Slevin JT, Cambi F, Gusella JF, Myers RH. The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study. BMC Med. 2008; 6:32.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 18986508; PMCID: PMC2596771; DOI: 10.1186/1741-7015-6-32;

Feitosa MF, Myers RH, Pankow JS, Province MA, Borecki IB. LIPC variants in the promoter and intron 1 modify HDL-C levels in a sex-specific fashion. Atherosclerosis. 2009 May; 204(1):171-7. PMID: 19101670; PMCID: PMC2710035; DOI: 10.1016/j.atherosclerosis.2008.09.007;

McNicoll CF, Latourelle JC, MacDonald ME, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts RL, Guttman M, Racette BA, Perlmutter JS, Ahmed A, Shill HA, Singer C, Saint-Hilaire MH, Massood T, Huskey KW, DeStefano AL, Gillis T, Mysore J, Goldwurm S, Pezzoli G, Baker KB, Itin I, Litvan I, Nicholson G, Corbett A, Nance M, Drasby E, Isaacson S, Burn DJ, Chinnery PF, Pramstaller PP, Al-Hinti J, Moller AT, Ostergaard K, Sherman SJ, Roxburgh R, Snow B, Slevin JT, Cambi F, Gusella JF, Myers RH. Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study. Mov Disord. 2008 Aug 15; 23(11):1596-601.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 18649400; PMCID: PMC2655323; DOI: 10.1002/mds.22186;

DeStefano AL, Latourelle J, Lew MF, Suchowersky O, Klein C, Golbe LI, Mark MH, Growdon JH, Wooten GF, Watts R, Guttman M, Racette BA, Perlmutter JS, Marlor L, Shill HA, Singer C, Goldwurm S, Pezzoli G, Saint-Hilaire MH, Hendricks AE, Gower A, Williamson S, Nagle MW, Wilk JB, Massood T, Huskey KW, Baker KB, Itin I, Litvan I, Nicholson G, Corbett A, Nance M, Drasby E, Isaacson S, Burn DJ, Chinnery PF, Pramstaller PP, Al-Hinti J, Moller AT, Ostergaard K, Sherman SJ, Roxburgh R, Snow B, Slevin JT, Cambi F, Gusella JF, Myers RH. Replication of association between ELAVL4 and Parkinson disease: the GenePD study. Hum Genet. 2008 Aug; 124(1):95-9.View Related Profiles.

Gower, Adam
DeStefano, Anita
Latourelle, Jeanne
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 18587682; PMCID: PMC2716559; DOI: 10.1007/s00439-008-0526-4;

Tobin JE, Latourelle JC, Lew MF, Klein C, Suchowersky O, Shill HA, Golbe LI, Mark MH, Growdon JH, Wooten GF, Racette BA, Perlmutter JS, Watts R, Guttman M, Baker KB, Goldwurm S, Pezzoli G, Singer C, Saint-Hilaire MH, Hendricks AE, Williamson S, Nagle MW, Wilk JB, Massood T, Laramie JM, DeStefano AL, Litvan I, Nicholson G, Corbett A, Isaacson S, Burn DJ, Chinnery PF, Pramstaller PP, Sherman S, Al-hinti J, Drasby E, Nance M, Moller AT, Ostergaard K, Roxburgh R, Snow B, Slevin JT, Cambi F, Gusella JF, Myers RH. Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology. 2008 Jul 1; 71(1):28-34.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Saint-Hilaire, Marie-Helene
Moss, Mark
Myers, Richard

PMID: 18509094; PMCID: PMC2654275; DOI: 10.1212/01.wnl.0000304051.01650.23;

Laramie JM, Wilk JB, Williamson SL, Nagle MW, Latourelle JC, Tobin JE, Province MA, Borecki IB, Myers RH. Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; the NHLBI Family Heart Study. BMC Med Genet. 2008; 9:46.View Related Profiles.

Latourelle, Jeanne
Myers, Richard

PMID: 18498660; PMCID: PMC2409301; DOI: 10.1186/1471-2350-9-46;

Zhang Q, Lewis CE, Wagenknecht LE, Myers RH, Pankow JS, Hunt SC, North KE, Hixson JE, Jeffrey Carr J, Shimmin LC, Borecki I, Province MA. Genome-wide admixture mapping for coronary artery calcification in African Americans: the NHLBI Family Heart Study. Genet Epidemiol. 2008 Apr; 32(3):264-72. PMID: 18200599; DOI: 10.1002/gepi.20301;

Wilk JB, Laramie JM, Latourelle JC, Williamson S, Nagle MW, Tobin JE, Foster CL, Eckfeldt JH, Province MA, Borecki IB, Myers RH. NYD-SP18 is associated with obesity in the NHLBI Family Heart Study. Int J Obes (Lond). 2008 Jun; 32(6):930-5.View Related Profiles.

Latourelle, Jeanne
Myers, Richard

PMID: 18317470; PMCID: PMC2667232; DOI: 10.1038/ijo.2008.23;

Massood T, Latourelle JC, Srinidhi Mysore J, Fossale E, Gillis T, Gusella JF, MacDonald ME, Myers RH. HD Repeat Determines the Rate of Neuropathological Change. Neurotherapeutics. 2008; 5(2):367. View Publication
Moser K, Biglan K, Ross CA, EHDN Working Group 'Symptomatic Treatment'. Inaugural Huntington Disease Clinical Research Symposium Organized by the Huntington Study Group. Neurotherapeutics. 2008; 5(2):363-375. View Publication
Feitosa MF, An P, Ketkar S, Myers RH, Pankow JS, Province M, Borecki I. Association of promoter LIPC variants with fat distribution and HDL level: The NHLBI Family Heart Study (FHS). 17th Annual Meeting of the International-Genetic-Epidemiology-Society. 2008.
Shi G, Gu CC, Kraja AT, Arnett DK, Myers RH, Pankow JS, Hunt SC, Thirupathi Rao DC. Modeling Age Variation in QTL Effects Leads to Substantially Improved Linkage Evidence for Blood Pressure in the HyperGEN Study. 17th Annual Meeting of the International-Genetic-Epidemiology-Society. 2008.

Bielinski SJ, Pankow JS, Foster CL, Miller MB, Hopkins PN, Eckfeldt JH, Hixson J, Liu Y, Register T, Myers RH, Arnett DK. Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: the NHLBI Family Heart Study follow-up examination. Atherosclerosis. 2008 Jul; 199(1):172-8. PMID: 18045607; PMCID: PMC2517220; DOI: 10.1016/j.atherosclerosis.2007.10.006;

Bielinski SJ, Pankow JS, Miller MB, Hopkins PN, Eckfeldt JH, Hixson J, Liu Y, Register T, Myers RH, Arnett DK. Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: the NHLBI family heart study follow-up examination. Genes Immun. 2007 Dec; 8(8):684-90. PMID: 17917677

Dupré N, Rivière JB, Myers RH, Provencher P, Pourcher E, Emond F, Rouleau GA. LRRK2 is not a significant cause of Parkinson's disease in French-Canadians. Can J Neurol Sci. 2007 Aug; 34(3):333-5. PMID: 17803032

Wheeler VC, Persichetti F, McNeil SM, Mysore JS, Mysore SS, MacDonald ME, Myers RH, Gusella JF, Wexler NS. Factors associated with HD CAG repeat instability in Huntington disease. J Med Genet. 2007 Nov; 44(11):695-701. PMID: 17660463; PMCID: PMC2705129; DOI: 10.1136/jmg.2007.050930;

Laramie JM, Wilk JB, DeStefano AL, Myers RH. HaploBuild: an algorithm to construct non-contiguous associated haplotypes in family based genetic studies. Bioinformatics. 2007 Aug 15; 23(16):2190-2.View Related Profiles.

DeStefano, Anita
Myers, Richard

PMID: 17586827; PMCID: PMC2665175; DOI: 10.1093/bioinformatics/btm316;

Litvan I, Chesselet MF, Gasser T, Di Monte DA, Parker D, Hagg T, Hardy J, Jenner P, Myers RH, Price D, Hallett M, Langston WJ, Lang AE, Halliday G, Rocca W, Duyckaerts C, Dickson DW, Ben-Shlomo Y, Goetz CG, Melamed E. The etiopathogenesis of Parkinson disease and suggestions for future research. Part II. J Neuropathol Exp Neurol. 2007 May; 66(5):329-36. PMID: 17483689

Litvan I, Halliday G, Hallett M, Goetz CG, Rocca W, Duyckaerts C, Ben-Shlomo Y, Dickson DW, Lang AE, Chesselet MF, Langston WJ, Di Monte DA, Gasser T, Hagg T, Hardy J, Jenner P, Melamed E, Myers RH, Parker D, Price DL. The etiopathogenesis of Parkinson disease and suggestions for future research. Part I. J Neuropathol Exp Neurol. 2007 Apr; 66(4):251-7. PMID: 17413315

Greenwood TA, Libiger O, Kardia S, Hanis C, Morrison AC, Gu CC, Rice T, Miller M, Turner ST, Myers RH, Grove J, Hsiao CF, Weder AB, Schork NJ. Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program. Genet Epidemiol. 2007 Apr; 31(3):195-210. PMID: 17266112

Tobin JE, Cui J, Wilk JB, Latourelle JC, Laramie JM, McKee AC, Guttman M, Karamohamed S, DeStefano AL, Myers RH. Sepiapterin reductase expression is increased in Parkinson's disease brain tissue. Brain Res. 2007 Mar 30; 1139:42-7.View Related Profiles.

DeStefano, Anita
McKee, Ann
Latourelle, Jeanne
Myers, Richard

PMID: 17270157; PMCID: PMC1868471; DOI: 10.1016/j.brainres.2007.01.001;

Borecki I, Feitosa MF, Ma D, North KE, Williamson S, Laramie J, Myers RH. The general transcription factor FOXO1A on 13q14 is associated with obesity. 15th Annual Meeting of the International-Genetic-Epidemiology-Society. 2007; 31.
Feitosa MF, North K, Myers RH, Pankow JS, Borecki I. Lipid and dietary factors confound detection of a QTL on 2p24-p25 for adiposity: the NHLBI-Family Heart Study. 15th Annual Meeting of the International-Genetic-Epidemiology-Society. 2007; 31.
Feitosa MF, Myers RH, Province M, Borecki I. Genetic variation in the hepatic lipase gene is associated with HDL-cholesterol levels in the NHLB Family Heart Study. 16th Annual Meeting of the International-Genetic-Epidemiology-Society. 2007; 31.

North KE, Franceschini N, Borecki IB, Gu CC, Heiss G, Province MA, Arnett DK, Lewis CE, Miller MB, Myers RH, Hunt SC, Freedman BI. Genotype-by-sex interaction on fasting insulin concentration: the HyperGEN study. Diabetes. 2007 Jan; 56(1):137-42. PMID: 17192475

Wilk JB, Tobin JE, Suchowersky O, Shill HA, Klein C, Wooten GF, Lew MF, Mark MH, Guttman M, Watts RL, Singer C, Growdon JH, Latourelle JC, Saint-Hilaire MH, DeStefano AL, Prakash R, Williamson S, Berg CJ, Sun M, Goldwurm S, Pezzoli G, Racette BA, Perlmutter JS, Parsian A, Baker KB, Giroux ML, Litvan I, Pramstaller PP, Nicholson G, Burn DJ, Chinnery PF, Vieregge P, Slevin JT, Cambi F, MacDonald ME, Gusella JF, Myers RH, Golbe LI. Herbicide exposure modifies GSTP1 haplotype association to Parkinson onset age: the GenePD Study. Neurology. 2006 Dec 26; 67(12):2206-10.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 17190945

Andresen JM, Gayán J, Djoussé L, Roberts S, Brocklebank D, Cherny SS, Cardon LR, Gusella JF, MacDonald ME, Myers RH, Housman DE, Wexler NS. The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset. Ann Hum Genet. 2007 May; 71(Pt 3):295-301. PMID: 17181545

Kraja AT, Borecki IB, North K, Tang W, Myers RH, Hopkins PN, Arnett D, Corbett J, Adelman A, Province MA. Longitudinal and age trends of metabolic syndrome and its risk factors: the Family Heart Study. Nutr Metab (Lond). 2006; 3:41. PMID: 17147796; PMCID: PMC1697811; DOI: 10.1186/1743-7075-3-41;

Kishikawa S, Li JL, Gillis T, Hakky MM, Warby S, Hayden M, MacDonald ME, Myers RH, Gusella JF. Brain-derived neurotrophic factor does not influence age at neurologic onset of Huntington's disease. Neurobiol Dis. 2006 Nov; 24(2):280-5. PMID: 16962786

Zeng W, Gillis T, Hakky M, Djoussé L, Myers RH, MacDonald ME, Gusella JF. Genetic analysis of the GRIK2 modifier effect in Huntington's disease. BMC Neurosci. 2006; 7:62. PMID: 16959037; PMCID: PMC1618398; DOI: 10.1186/1471-2202-7-62;

Wilk JB, Myers RH, Pankow JS, Hunt SC, Leppert MF, Freedman BI, Province MA, Ellison RC. Adrenergic receptor polymorphisms associated with resting heart rate: the HyperGEN Study. Ann Hum Genet. 2006 Sep; 70(Pt 5):566-73.View Related Profiles.

Myers, Richard
Ellison, Robert

PMID: 16907703

Li JL, Hayden MR, Warby SC, Durr A, Morrison PJ, Nance M, Ross CA, Margolis RL, Rosenblatt A, Squitieri F, Frati L, Gómez-Tortosa E, García CA, Suchowersky O, Klimek ML, Trent RJ, McCusker E, Novelletto A, Frontali M, Paulsen JS, Jones R, Ashizawa T, Lazzarini A, Wheeler VC, Prakash R, Xu G, Djoussé L, Mysore JS, Gillis T, Hakky M, Cupples LA, Saint-Hilaire MH, Cha JH, Hersch SM, Penney JB, Harrison MB, Perlman SL, Zanko A, Abramson RK, Lechich AJ, Duckett A, Marder K, Conneally PM, Gusella JF, MacDonald ME, Myers RH. Genome-wide significance for a modifier of age at neurological onset in Huntington's disease at 6q23-24: the HD MAPS study. BMC Med Genet. 2006; 7:71.View Related Profiles.

Garcia, Carmen
Cupples, L
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 16914060; PMCID: PMC1586197; DOI: 10.1186/1471-2350-7-71;

Avery CL, Freedman BI, Kraja AT, Borecki IB, Miller MB, Pankow JS, Arnett D, Lewis CE, Myers RH, Hunt SC, North KE. Genotype-by-sex interaction in the aetiology of type 2 diabetes mellitus: support for sex-specific quantitative trait loci in Hypertension Genetic Epidemiology Network participants. Diabetologia. 2006 Oct; 49(10):2329-36. PMID: 16906437

Myers RH. Considerations for genomewide association studies in Parkinson disease. Am J Hum Genet. 2006 Jun; 78(6):1081-2. PMID: 16685659; PMCID: PMC1474090; DOI: 10.1086/504730;

Sun M, Latourelle JC, Wooten GF, Lew MF, Klein C, Shill HA, Golbe LI, Mark MH, Racette BA, Perlmutter JS, Parsian A, Guttman M, Nicholson G, Xu G, Wilk JB, Saint-Hilaire MH, DeStefano AL, Prakash R, Williamson S, Suchowersky O, Labelle N, Growdon JH, Singer C, Watts RL, Goldwurm S, Pezzoli G, Baker KB, Pramstaller PP, Burn DJ, Chinnery PF, Sherman S, Vieregge P, Litvan I, Gillis T, MacDonald ME, Myers RH, Gusella JF. Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study. Arch Neurol. 2006 Jun; 63(6):826-32.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 16769863

Lloret A, Dragileva E, Teed A, Espinola J, Fossale E, Gillis T, Lopez E, Myers RH, MacDonald ME, Wheeler VC. Genetic background modifies nuclear mutant huntingtin accumulation and HD CAG repeat instability in Huntington's disease knock-in mice. Hum Mol Genet. 2006 Jun 15; 15(12):2015-24. PMID: 16687439

Feitosa MF, Province MA, Heiss G, Arnett DK, Myers RH, Pankow JS, Hopkins PN, Borecki IB. Evidence of QTL on 15q21 for high-density lipoprotein cholesterol: the National Heart, Lung, and Blood Institute Family Heart Study (NHLBI FHS). Atherosclerosis. 2007 Jan; 190(1):232-7. PMID: 16529751

Laramie JM, Wilk JB, Hunt SC, Ellison RC, Chakravarti A, Boerwinkle E, Myers RH. Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program. BMC Med Genet. 2006; 7:17.View Related Profiles.

Myers, Richard
Ellison, Robert

PMID: 16509988; PMCID: PMC1413518; DOI: 10.1186/1471-2350-7-17;

An P, Freedman BI, Rich SS, Mandel SA, Arnett DK, Myers RH, Chen YD, Hunt SC, Rao DC. Quantitative trait loci on chromosome 8q24 for pancreatic beta-cell function and 7q11 for insulin sensitivity in obese nondiabetic white and black families: evidence from genome-wide linkage scans in the NHLBI Hypertension Genetic Epidemiology Network (HyperGEN) study. Diabetes. 2006 Feb; 55(2):551-8. PMID: 16443794

North KE, Avery CL, Lange LA, Borecki I, Myers RH. Evidence for association between a SNP at 12q24.3 and body fat and BMI under a chromosome 12 linkage peak: The HyperGEN study. 46th Annual Conference on Cardiovascular Disease Epidemiology. 2006; 113.
Bielinski S, Pankow JS, Hopkins P, Eckfeldt JH, Hixon J, Liu YM, Register TC, Myers RH, Arnett DK. Genome-wide scans for loci affecting MCP-1 and ICAM-1 levels in the NHLBI family heart study follow-up examination. 46th Annual Conference on Cardiovascular Disease Epidemiology. 2006.

Karamohamed S, Latourelle JC, Racette BA, Perlmutter JS, Wooten GF, Lew M, Klein C, Shill H, Golbe LI, Mark MH, Guttman M, Nicholson G, Wilk JB, Saint-Hilaire M, DeStefano AL, Prakash R, Tobin S, Williamson J, Suchowersky O, Labell N, Growdon BN, Singer C, Watts R, Goldwurm S, Pezzoli G, Baker KB, Giroux ML, Pramstaller PP, Burn DJ, Chinnery P, Sherman S, Vieregge P, Litvan I, Gusella JF, Myers RH, Parsian A. BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study. Neurology. 2005 Dec 13; 65(11):1823-5.View Related Profiles.

DeStefano, Anita
Latourelle, Jeanne
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 16344533

Kraja AT, Hunt SC, Pankow JS, Myers RH, Heiss G, Lewis CE, Rao DC, Province MA. Quantitative trait loci for metabolic syndrome in the Hypertension Genetic Epidemiology Network study. Obes Res. 2005 Nov; 13(11):1885-90. PMID: 16339118

Karamohamed S, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, Liu J, Shoemaker CM, Wilk JB, DeStefano AL, Latourelle JC, Xu G, Watts R, Growdon J, Lew M, Waters C, Vieregge P, Pramstaller PP, Klein C, Racette BA, Perlmutter JS, Parsian A, Singer C, Montgomery E, Baker K, Gusella JF, Herbert A, Myers RH. Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ-1 (T497C) genes in familial Parkinson's disease from the GenePD study. Mov Disord. 2005 Sep; 20(9):1188-91.View Related Profiles.

Herbert, Alan
DeStefano, Anita
Latourelle, Jeanne
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 15966003

Seong IS, Ivanova E, Lee JM, Choo YS, Fossale E, Anderson M, Gusella JF, Laramie JM, Myers RH, Lesort M, MacDonald ME. HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism. Hum Mol Genet. 2005 Oct 1; 14(19):2871-80. PMID: 16115812

Yu K, Zhang S, Borecki I, Kraja A, Xiong C, Myers R, Province M. A haplotype similarity based transmission/disequilibrium test under founder heterogeneity. Ann Hum Genet. 2005 Jul; 69(Pt 4):455-67. PMID: 15996173

Friedman JH, Trieschmann ME, Myers RH, Fernandez HH. Monozygotic twins discordant for Huntington disease after 7 years. Arch Neurol. 2005 Jun; 62(6):995-7. PMID: 15956172

Lin JP, Myers RH, Almasy L, Coon HH, Arnett DK, Hong Y, Hunt SC. Linkage of the cholesterol 7alpha-hydroxylase gene and low-density lipoprotein cholesterol conditional on apolipoprotein E association: the National Heart, Lung, and Blood Institute Family Heart Study. Chin Med J (Engl). 2005 Mar 5; 118(5):362-9. PMID: 15780204

Kraja AT, Hunt SC, Pankow JS, Myers RH, Heiss G, Lewis CE, Rao D, Province MA. An evaluation of the metabolic syndrome in the HyperGEN study. Nutr Metab (Lond). 2005 Jan 18; 2(1):2. PMID: 15656912; PMCID: PMC549210; DOI: 10.1186/1743-7075-2-2;

North KE, Myers RH, Feitosa MF, Tang W, Lewis C, Hopkins P, Hixson J, Wagenknecht L, Kraja A, Borecki I. Genetic architecture of adiposity: Evidence for epistatic interactions on chromosomes 7 and 13 in the NHLBI Family Heart Study (FHS). 14th Annual Meeting of the International-Genetic-Epidemiology-Society. 2005.
Feitosa MF, Province M, Heiss G, Arnett DK, Myers RH, Pankow JS, Hopkins P, Borecki I. A QTL on 15q21 influences HDL-cholesterol: NHLB-FHS. 14th Annual Meeting of the International-Genetic-Epidemiology-Society. 2005.

Avery CL, Freedman BI, Heiss G, Kraja A, Rice T, Arnett D, Miller MB, Pankow JS, Lewis CE, Myers RH, Hunt SC, Almasy L, North KE. Linkage analysis of diabetes status among hypertensive families: the Hypertension Genetic Epidemiology Network study. Diabetes. 2004 Dec; 53(12):3307-12. PMID: 15561964

Djoussé L, Pankow JS, Arnett DK, Eckfeldt JH, Myers RH, Ellison RC. Apolipoprotein E polymorphism modifies the alcohol-HDL association observed in the National Heart, Lung, and Blood Institute Family Heart Study. Am J Clin Nutr. 2004 Dec; 80(6):1639-44.View Related Profiles.

Myers, Richard
Ellison, Robert

PMID: 15585780

Wilk JB, Djousse L, Arnett DK, Hunt SC, Province MA, Heiss G, Myers RH. Genome-wide linkage analyses for age at diagnosis of hypertension and early-onset hypertension in the HyperGEN study. Am J Hypertens. 2004 Sep; 17(9):839-44. PMID: 15363829

Jiang Y, Wilk JB, Borecki I, Williamson S, DeStefano AL, Xu G, Liu J, Ellison RC, Province M, Myers RH. Common variants in the 5' region of the leptin gene are associated with body mass index in men from the National Heart, Lung, and Blood Institute Family Heart Study. Am J Hum Genet. 2004 Aug; 75(2):220-30.View Related Profiles.

DeStefano, Anita
Myers, Richard
Ellison, Robert

PMID: 15197684; PMCID: PMC1216056

Myers RH. Huntington's disease genetics. NeuroRx. 2004 Apr; 1(2):255-62. PMID: 15717026; PMCID: PMC534940

Djoussé L, Knowlton B, Hayden MR, Almqvist EW, Brinkman RR, Ross CA, Margolis RL, Rosenblatt A, Durr A, Dode C, Morrison PJ, Novelletto A, Frontali M, Trent RJ, McCusker E, Gómez-Tortosa E, Mayo Cabrero D, Jones R, Zanko A, Nance M, Abramson RK, Suchowersky O, Paulsen JS, Harrison MB, Yang Q, Cupples LA, Mysore J, Gusella JF, MacDonald ME, Myers RH. Evidence for a modifier of onset age in Huntington disease linked to the HD gene in 4p16. Neurogenetics. 2004 Jun; 5(2):109-14.View Related Profiles.

Cupples, L
Yang, Qiong
Myers, Richard

PMID: 15029481; PMCID: PMC1866166

Herrera VL, Didishvili T, Lopez LV, Myers RH, Ruiz-Opazo N. Genome-wide scan identifies novel QTLs for cholesterol and LDL levels in F2[Dahl RxS]-intercross rats. Circ Res. 2004 Mar 5; 94(4):446-52.View Related Profiles.

Ruiz-Opazo, Nelson
Myers, Richard
Herrera, Victoria

PMID: 14739155

Djousse L, Pankow JS, Arnett DK, Eckfeldt JH, Myers RH, Ellison RC. Apolipoprotein E polymorphism modifies the alcohol-HDL association in the NHLBI Family Heart Study. 44th Annual Conference on Cardiovascular Disease Epidemiology. 2004; 109.
Trieschmann MM, Friedman JH, Myers RH, Fernandez H. Monozygotic twins discordant for Huntington's disease after seven years. 8th International Congress of Parkinsons Disease and Movement Disoders. 2004.
Avery CL, Freedman BI, Heiss G, North KE, Myers RH et al. Linkage analysis of diabetes susceptibility among hypertensive families: The HyperGEN Study. Conference: 44th Annual Conference on Cardiovascular Disease Epidemiology. 2004; 109.

Karamohamed S, DeStefano AL, Wilk JB, Shoemaker CM, Golbe LI, Mark MH, Lazzarini AM, Suchowersky O, Labelle N, Guttman M, Currie LJ, Wooten GF, Stacy M, Saint-Hilaire M, Feldman RG, Sullivan KM, Xu G, Watts R, Growdon J, Lew M, Waters C, Vieregge P, Pramstaller PP, Klein C, Racette BA, Perlmutter JS, Parsian A, Singer C, Montgomery E, Baker K, Gusella JF, Fink SJ, Myers RH, Herbert A. A haplotype at the PARK3 locus influences onset age for Parkinson's disease: the GenePD study. Neurology. 2003 Dec 9; 61(11):1557-61.View Related Profiles.

Herbert, Alan
DeStefano, Anita
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 14663042

Tang W, Miller MB, Rich SS, North KE, Pankow JS, Borecki IB, Myers RH, Hopkins PN, Leppert M, Arnett DK. Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. Diabetes. 2003 Nov; 52(11):2840-7. PMID: 14578304

Gagnon DR, Glickman ME, Myers RH, Cupples LA. The analysis of survival data with a non-susceptible fraction and dual censoring mechanisms. Stat Med. 2003 Oct 30; 22(20):3249-62.View Related Profiles.

Gagnon, David
Cupples, L
Glickman, Mark
Myers, Richard

PMID: 14518026

Wilk JB, DeStefano AL, Joost O, Myers RH, Cupples LA, Slater K, Atwood LD, Heard-Costa NL, Herbert A, O'Connor GT, Gottlieb DJ. Linkage and association with pulmonary function measures on chromosome 6q27 in the Framingham Heart Study. Hum Mol Genet. 2003 Nov 1; 12(21):2745-51.View Related Profiles.

Herbert, Alan
DeStefano, Anita
O'Connor, George
Cupples, L
Heard-Costa, Nancy
Myers, Richard

PMID: 12966033

Li JL, Hayden MR, Almqvist EW, Brinkman RR, Durr A, Dodé C, Morrison PJ, Suchowersky O, Ross CA, Margolis RL, Rosenblatt A, Gómez-Tortosa E, Cabrero DM, Novelletto A, Frontali M, Nance M, Trent RJ, McCusker E, Jones R, Paulsen JS, Harrison M, Zanko A, Abramson RK, Russ AL, Knowlton B, Djoussé L, Mysore JS, Tariot S, Gusella MF, Wheeler VC, Atwood LD, Cupples LA, Saint-Hilaire M, Cha JH, Hersch SM, Koroshetz WJ, Gusella JF, MacDonald ME, Myers RH. A genome scan for modifiers of age at onset in Huntington disease: The HD MAPS study. Am J Hum Genet. 2003 Sep; 73(3):682-7.View Related Profiles.

Cupples, L
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 12900792; PMCID: PMC1180695

Djoussé L, Knowlton B, Hayden M, Almqvist EW, Brinkman R, Ross C, Margolis R, Rosenblatt A, Durr A, Dode C, Morrison PJ, Novelletto A, Frontali M, Trent RJ, McCusker E, Gómez-Tortosa E, Mayo D, Jones R, Zanko A, Nance M, Abramson R, Suchowersky O, Paulsen J, Harrison M, Yang Q, Cupples LA, Gusella JF, MacDonald ME, Myers RH. Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease. Am J Med Genet A. 2003 Jun 15; 119A(3):279-82.View Related Profiles.

Cupples, L
Yang, Qiong
Myers, Richard

PMID: 12784292

Wheelock VL, Tempkin T, Marder K, Nance M, Myers RH, Zhao H, Kayson E, Orme C, Shoulson I. Predictors of nursing home placement in Huntington disease. Neurology. 2003 Mar 25; 60(6):998-1001. PMID: 12654967

Panhuysen CI, Cupples LA, Wilson PW, Herbert AG, Myers RH, Meigs JB. A genome scan for loci linked to quantitative insulin traits in persons without diabetes: the Framingham Offspring Study. Diabetologia. 2003 Apr; 46(4):579-87.View Related Profiles.

Herbert, Alan
Cupples, L
Myers, Richard

PMID: 12739029

Wilk JB, DeStefano AL, Arnett DK, Rich SS, Djousse L, Crapo RO, Leppert MF, Province MA, Cupples LA, Gottlieb DJ, Myers RH. A genome-wide scan of pulmonary function measures in the National Heart, Lung, and Blood Institute Family Heart Study. Am J Respir Crit Care Med. 2003 Jun 1; 167(11):1528-33.View Related Profiles.

DeStefano, Anita
Cupples, L
Myers, Richard

PMID: 12637344

Wu X, Cooper RS, Boerwinkle E, Turner ST, Hunt S, Myers R, Olshen RA, Curb D, Zhu X, Kan D, Luke A. Combined analysis of genomewide scans for adult height: results from the NHLBI Family Blood Pressure Program. Eur J Hum Genet. 2003 Mar; 11(3):271-4. PMID: 12673281

DeStefano AL, Gates GA, Heard-Costa N, Myers RH, Baldwin CT. Genomewide linkage analysis to presbycusis in the Framingham Heart Study. Arch Otolaryngol Head Neck Surg. 2003 Mar; 129(3):285-9.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Heard-Costa, Nancy
Myers, Richard

PMID: 12622536

Mukhopadhyay N, Finegold DN, Larson MG, Cupples LA, Myers RH, Weeks DE. A genome-wide scan for loci affecting normal adult height in the Framingham Heart Study. Hum Hered. 2003; 55(4):191-201.View Related Profiles.

Cupples, L
Larson, Martin
Myers, Richard

PMID: 14566097

Gasser T, Bressman S, Dürr A, Higgins J, Klockgether T, Myers RH. State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis. Mov Disord. 2003 Jan; 18(1):3-18. PMID: 12518296

Van Laer L, DeStefano AL, Myers RH, Flothmann K, Thys S, Fransen E, Gates GA, Van Camp G, Baldwin CT. Is DFNA5 a susceptibility gene for age-related hearing impairment? Eur J Hum Genet. 2002 Dec; 10(12):883-6.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Myers, Richard

PMID: 12461698

Djoussé L, Knowlton B, Cupples LA, Marder K, Shoulson I, Myers RH. Weight loss in early stage of Huntington's disease. Neurology. 2002 Nov 12; 59(9):1325-30.View Related Profiles.

Cupples, L
Myers, Richard

PMID: 12427878

Karasik D, Myers RH, Hannan MT, Gagnon D, McLean RR, Cupples LA, Kiel DP. Mapping of quantitative ultrasound of the calcaneus bone to chromosome 1 by genome-wide linkage analysis. Osteoporos Int. 2002 Oct; 13(10):796-802.View Related Profiles.

Gagnon, David
Myers, Richard

PMID: 12378368

Karasik D, Myers RH, Cupples LA, Hannan MT, Gagnon DR, Herbert A, Kiel DP. Genome screen for quantitative trait loci contributing to normal variation in bone mineral density: the Framingham Study. J Bone Miner Res. 2002 Sep; 17(9):1718-27.View Related Profiles.

Gagnon, David
Myers, Richard

PMID: 12211443

Coon H, Eckfeldt JH, Leppert MF, Myers RH, Arnett DK, Heiss G, Province MA, Hunt SC. A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study. Hum Genet. 2002 Sep; 111(3):263-9. PMID: 12215839

Wilk JB, Myers RH, Zhang Y, Lewis CE, Atwood L, Hopkins PN, Ellison RC. Evidence for a gene influencing heart rate on chromosome 4 among hypertensives. Hum Genet. 2002 Aug; 111(2):207-13.View Related Profiles.

Myers, Richard
Ellison, Robert
Zhang, Yuqing

PMID: 12189495

Coady SA, Jaquish CE, Fabsitz RR, Larson MG, Cupples LA, Myers RH. Genetic variability of adult body mass index: a longitudinal assessment in framingham families. Obes Res. 2002 Jul; 10(7):675-81.View Related Profiles.

Cupples, L
Larson, Martin
Myers, Richard

PMID: 12105290

Maher NE, Currie LJ, Lazzarini AM, Wilk JB, Taylor CA, Saint-Hilaire MH, Feldman RG, Golbe LI, Wooten GF, Myers RH. Segregation analysis of Parkinson disease revealing evidence for a major causative gene. Am J Med Genet. 2002 May 1; 109(3):191-7.View Related Profiles.

Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 11977177

Djoussé L, Myers RH, Province MA, Hunt SC, Eckfeldt JH, Evans G, Peacock JM, Ellison RC. Influence of apolipoprotein E, smoking, and alcohol intake on carotid atherosclerosis: National Heart, Lung, and Blood Institute Family Heart Study. Stroke. 2002 May; 33(5):1357-61.View Related Profiles.

Myers, Richard
Ellison, Robert

PMID: 11988615

Demissie S, Cupples LA, Myers R, Aliabadi P, Levy D, Felson DT. Genome scan for quantity of hand osteoarthritis: the Framingham Study. Arthritis Rheum. 2002 Apr; 46(4):946-52.View Related Profiles.

Levy, Daniel
Felson, David
Cupples, L
Myers, Richard
Demissie, Serkalem

PMID: 11953971

DeStefano AL, Lew MF, Golbe LI, Mark MH, Lazzarini AM, Guttman M, Montgomery E, Waters CH, Singer C, Watts RL, Currie LJ, Wooten GF, Maher NE, Wilk JB, Sullivan KM, Slater KM, Saint-Hilaire MH, Feldman RG, Suchowersky O, Lafontaine AL, Labelle N, Growdon JH, Vieregge P, Pramstaller PP, Klein C, Hubble JP, Reider CR, Stacy M, MacDonald ME, Gusella JF, Myers RH. PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study. Am J Hum Genet. 2002 May; 70(5):1089-95.View Related Profiles.

DeStefano, Anita
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 11920285; PMCID: PMC447587

Joost O, Wilk JB, Cupples LA, Harmon M, Shearman AM, Baldwin CT, O'Connor GT, Myers RH, Gottlieb DJ. Genetic loci influencing lung function: a genome-wide scan in the Framingham Study. Am J Respir Crit Care Med. 2002 Mar 15; 165(6):795-9.View Related Profiles.

Baldwin, Clinton
O'Connor, George
Cupples, L
Myers, Richard

PMID: 11897646

Meigs JB, Panhuysen CI, Myers RH, Wilson PW, Cupples LA. A genome-wide scan for loci linked to plasma levels of glucose and HbA(1c) in a community-based sample of Caucasian pedigrees: The Framingham Offspring Study. Diabetes. 2002 Mar; 51(3):833-40.View Related Profiles.

Cupples, L
Myers, Richard

PMID: 11872688

Maher NE, Golbe LI, Lazzarini AM, Mark MH, Currie LJ, Wooten GF, Saint-Hilaire M, Wilk JB, Volcjak J, Maher JE, Feldman RG, Guttman M, Lew M, Waters CH, Schuman S, Suchowersky O, Lafontaine AL, Labelle N, Vieregge P, Pramstaller PP, Klein C, Hubble J, Reider C, Growdon J, Watts R, Montgomery E, Baker K, Singer C, Stacy M, Myers RH. Epidemiologic study of 203 sibling pairs with Parkinson's disease: the GenePD study. Neurology. 2002 Jan 8; 58(1):79-84.View Related Profiles.

Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 11781409

Baldwin CT, Cupples LA, Joost O, Demissie S, Chaisson C, Mcalindon T, Myers RH, Felson D. Absence of linkage or association for osteoarthritis with the vitamin D receptor/type II collagen locus: the Framingham Osteoarthritis Study. J Rheumatol. 2002 Jan; 29(1):161-5.View Related Profiles.

Chaisson, Christine
Baldwin, Clinton
Felson, David
Cupples, L
Myers, Richard
Demissie, Serkalem

PMID: 11824954

Karasik D, Hannan MT, Cupples LA, Myers RH, Kiel DP. Chromosomal mapping of quantitative trait loci for bone mineral density: The Framingham study. Osteoporosis International. 2002; 12:S11.
Karasik D, Hannan MT, Myers RH, Kiel DP. Stratified genome screen for quantitative trait loci contributing to normal bone mineral density (BMD) in the Framingham Study. American Journal of Human Biology. 2002; 14(1):117-118.

Coon H, Leppert MF, Eckfeldt JH, Oberman A, Myers RH, Peacock JM, Province MA, Hopkins PN, Heiss G. Genome-wide linkage analysis of lipids in the Hypertension Genetic Epidemiology Network (HyperGEN) Blood Pressure Study. Arterioscler Thromb Vasc Biol. 2001 Dec; 21(12):1969-76. PMID: 11742872

Feitosa MF, Borecki IB, Rich SS, Arnett DK, Sholinsky P, Myers RH, Leppert M, Province MA. Quantitative-trait loci influencing body-mass index reside on chromosomes 7 and 13: the National Heart, Lung, and Blood Institute Family Heart Study. Am J Hum Genet. 2002 Jan; 70(1):72-82. PMID: 11713718; PMCID: PMC384905

Gottlieb DJ, Wilk JB, Harmon M, Evans JC, Joost O, Levy D, O'Connor GT, Myers RH. Heritability of longitudinal change in lung function. The Framingham study. Am J Respir Crit Care Med. 2001 Nov 1; 164(9):1655-9.View Related Profiles.

Levy, Daniel
O'Connor, George
Myers, Richard

PMID: 11719305

Peacock JM, Arnett DK, Atwood LD, Myers RH, Coon H, Rich SS, Province MA, Heiss G. Genome scan for quantitative trait loci linked to high-density lipoprotein cholesterol: The NHLBI Family Heart Study. Arterioscler Thromb Vasc Biol. 2001 Nov; 21(11):1823-8. PMID: 11701472

DeStefano AL, Golbe LI, Mark MH, Lazzarini AM, Maher NE, Saint-Hilaire M, Feldman RG, Guttman M, Watts RL, Suchowersky O, Lafontaine AL, Labelle N, Lew MF, Waters CH, Growdon JH, Singer C, Currie LJ, Wooten GF, Vieregge P, Pramstaller PP, Klein C, Hubble JP, Stacy M, Montgomery E, MacDonald ME, Gusella JF, Myers RH. Genome-wide scan for Parkinson's disease: the GenePD Study. Neurology. 2001 Sep 25; 57(6):1124-6.View Related Profiles.

DeStefano, Anita
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 11571351

Glorioso N, Filigheddu F, Troffa C, Soro A, Parpaglia PP, Tsikoudakis A, Myers RH, Herrera VL, Ruiz-Opazo N. Interaction of alpha(1)-Na,K-ATPase and Na,K,2Cl-cotransporter genes in human essential hypertension. Hypertension. 2001 Aug; 38(2):204-9.View Related Profiles.

Ruiz-Opazo, Nelson
Myers, Richard
Herrera, Victoria

PMID: 11509477

O'Donnell CJ, Larson MG, Feng D, Sutherland PA, Lindpaintner K, Myers RH, D'Agostino RA, Levy D, Tofler GH. Genetic and environmental contributions to platelet aggregation: the Framingham heart study. Circulation. 2001 Jun 26; 103(25):3051-6.View Related Profiles.

O'Donnell, Christopher
Larson, Martin
Myers, Richard

PMID: 11425767

Hunt SC, Kronenberg F, Eckfeldt JH, Hopkins PN, Myers RH, Heiss G. Association of plasma bilirubin with coronary heart disease and segregation of bilirubin as a major gene trait: the NHLBI family heart study. Atherosclerosis. 2001 Feb 15; 154(3):747-54. PMID: 11257278

Nance MA, Myers RH. Juvenile onset Huntington's disease--clinical and research perspectives. Ment Retard Dev Disabil Res Rev. 2001; 7(3):153-7. PMID: 11553930

Heard-Costa NL, Demissie S, DeStefano AL, Knowlton BA, Maher NE, Myers RH, Volcjak JS, Wilk JB, Cupples LA. Influence of marker heterozygosity and genetic heterogeneity on fine mapping. Genet Epidemiol. 2001; 21 Suppl 1:S467-72.View Related Profiles.

DeStefano, Anita
Cupples, L
Heard-Costa, Nancy
Myers, Richard
Demissie, Serkalem

PMID: 11793720

Wilk JB, Volcjak JS, Myers RH, Maher NE, Knowlton BA, Heard-Costa NL, Demissie S, Cupples LA, DeStefano AL. Family-based association tests for qualitative and quantitative traits using single-nucleotide polymorphism and microsatellite data. Genet Epidemiol. 2001; 21 Suppl 1:S364-9.View Related Profiles.

DeStefano, Anita
Heard-Costa, Nancy
Myers, Richard
Demissie, Serkalem

PMID: 11793700

Gómez-Tortosa E, MacDonald ME, Friend JC, Taylor SA, Weiler LJ, Cupples LA, Srinidhi J, Gusella JF, Bird ED, Vonsattel JP, Myers RH. Quantitative neuropathological changes in presymptomatic Huntington's disease. Ann Neurol. 2001 Jan; 49(1):29-34. PMID: 11198293

Myers RH, Cupples LA, Taylor CA, Saint-Hilaire MH, Auerbach S, Feldman RG, Farrer LA. . The genetic component in Parkinson’s disease is half that of Alzheimer’s disease. Alzheimer’s Reports. 2001; 4:9-15.

Zee RY, Myers RH, Hannan MT, Wilson PW, Ordovas JM, Schaefer EJ, Lindpaintner K, Kiel DP. Absence of linkage for bone mineral density to chromosome 12q12-14 in the region of the vitamin D receptor gene. Calcif Tissue Int. 2000 Dec; 67(6):434-9. PMID: 11289690

Levy D, DeStefano AL, Larson MG, O'Donnell CJ, Lifton RP, Gavras H, Cupples LA, Myers RH. Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study. Hypertension. 2000 Oct; 36(4):477-83.View Related Profiles.

DeStefano, Anita
O'Donnell, Christopher
Gavras, Haralambos
Larson, Martin
Myers, Richard

PMID: 11040222

Coon H, Myers RH, Borecki IB, Arnett DK, Hunt SC, Province MA, Djousse L, Leppert MF. Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study. Arterioscler Thromb Vasc Biol. 2000 Oct; 20(10):2275-80. PMID: 11031215

Djoussé L, Myers RH, Coon H, Arnett DK, Province MA, Ellison RC. Smoking influences the association between apolipoprotein E and lipids: the National Heart, Lung, and Blood Institute Family Heart Study. Lipids. 2000 Aug; 35(8):827-31.View Related Profiles.

Myers, Richard
Ellison, Robert

PMID: 10984105

Wilk JB, Djousse L, Arnett DK, Rich SS, Province MA, Hunt SC, Crapo RO, Higgins M, Myers RH. Evidence for major genes influencing pulmonary function in the NHLBI family heart study. Genet Epidemiol. 2000 Jul; 19(1):81-94. PMID: 10861898

Salomaa V, Pankow J, Heiss G, Cakir B, Eckfeldt JH, Ellison RC, Myers RH, Hiller KM, Brantley KR, Morris TL, Weston BW. Genetic background of Lewis negative blood group phenotype and its association with atherosclerotic disease in the NHLBI family heart study. J Intern Med. 2000 Jun; 247(6):689-98.View Related Profiles.

Myers, Richard
Ellison, Robert

PMID: 10886491

Shearman AM, Ordovas JM, Cupples LA, Schaefer EJ, Harmon MD, Shao Y, Keen JD, DeStefano AL, Joost O, Wilson PW, Housman DE, Myers RH. Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham study. Hum Mol Genet. 2000 May 22; 9(9):1315-20.View Related Profiles.

DeStefano, Anita
Myers, Richard

PMID: 10814713

Wilk JB, Djousse L, Borecki I, Atwood LD, Hunt SC, Rich SS, Eckfeldt JH, Arnett DK, Rao DC, Myers RH. Segregation analysis of serum uric acid in the NHLBI Family Heart Study. Hum Genet. 2000 Mar; 106(3):355-9.View Related Profiles.

Rao, Dinesh
Myers, Richard

PMID: 10798367

Kronenberg F, Rich SS, Sholinsky P, Arnett DK, Province ME, Myers RH, Eckfeldt JH, Williams RR, Hunt SC. Insulin and hypertension in the NHLBI Family Heart Study: a sibpair approach to a controversial issue. Am J Hypertens. 2000 Mar; 13(3):240-50. PMID: 10777027

Hong Y, Leppert MF, Lin J, Hunt SC, Rich SS, Arnett DK, Myers RH, Eckfeldt J, Williams RR, Province MA. No evidence of linkage between the very-low-density lipoprotein receptor gene and fasting serum insulin or homeostasis model assessment insulin resistance index: the National Heart, Lung, and Blood Institute Family Heart Study. Metabolism. 2000 Mar; 49(3):293-7. PMID: 10726903

Marder K, Zhao H, Myers RH, Cudkowicz M, Kayson E, Kieburtz K, Orme C, Paulsen J, Penney JB, Siemers E, Shoulson I. Rate of functional decline in Huntington's disease. Huntington Study Group. Neurology. 2000 Jan 25; 54(2):452-8. PMID: 10668713

Feitosa MF, Borecki I, Rich S, Arnett DK, Sholinsky P, Myers RH, Province M. Genome scan for body mass index in the National Heart, Lung, and Blood Institute Family Heart Study. The American Journal of Human Genetics. 2000; 67(4):49.
Myers RH . Genetic modifiers and predictive testing in Huntington’s disease. NeuroScience News. Editor: Patrick McGeer. 2000; 3:23-29.
Province M, Hunt SC, Shannon W, Myers RH, Arnett DK, Pankow J, Lewis CE, Thirupathil Rao DC. Resolution of linkage heterogeneity in complex traits: regression tree linkage analysis of blood pressure in the NHLBI-HyperGEN study. The American Journal of Human Genetics. 2000; 67(4):52.
Wheelock V, Tempkin T, Marder K, Nance M, Myers RH, Zhao H. Do motor, behavioral or psychiatric correlates predict the need for institutional care in patients with Huntington's disease?. Annals of Neurology. 2000; 48(3):467.
Peacock JM, Atwood LD, Arnett DK, Borecki I, Hunt SC, Myers RH, Panklow JS, Hong YL, Rich S. Gene-environment interactions in the prediction of HDL cholesterol: Influence of waist-hip ratio. Circulation. 2000; 101(6):732.

Taylor CA, Saint-Hilaire MH, Cupples LA, Thomas CA, Burchard AE, Feldman RG, Myers RH. Environmental, medical, and family history risk factors for Parkinson's disease: a New England-based case control study. Am J Med Genet. 1999 Dec 15; 88(6):742-9.View Related Profiles.

Thomas, Cathi-Ann
Cupples, L
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 10581500

Zhang Y, Kreger BE, Dorgan JF, Cupples LA, Myers RH, Splansky GL, Schatzkin A, Ellison RC. Parental age at child's birth and son's risk of prostate cancer. The Framingham Study. Am J Epidemiol. 1999 Dec 1; 150(11):1208-12.View Related Profiles.

Kreger, Bernard
Cupples, L
Myers, Richard
Ellison, Robert
Zhang, Yuqing

PMID: 10588081

Ellison RC, Myers RH, Zhang Y, Djoussé L, Knox S, Williams RR, Province MA. Effects of similarities in lifestyle habits on familial aggregation of high density lipoprotein and low density lipoprotein cholesterol: the NHLBI Family Heart Study. Am J Epidemiol. 1999 Nov 1; 150(9):910-8.View Related Profiles.

Myers, Richard
Ellison, Robert
Zhang, Yuqing

PMID: 10547136

MacDonald ME, Vonsattel JP, Shrinidhi J, Couropmitree NN, Cupples LA, Bird ED, Gusella JF, Myers RH. Evidence for the GluR6 gene associated with younger onset age of Huntington's disease. Neurology. 1999 Oct 12; 53(6):1330-2. PMID: 10522893

Coon H, Leppert MF, Kronenberg F, Province MA, Myers RH, Arnett DK, Eckfeldt JH, Heiss G, Williams RR, Hunt SC. Evidence for a major gene accounting for mild elevation in LDL cholesterol: the NHLBI Family Heart Study. Ann Hum Genet. 1999 Sep; 63(Pt 5):401-12. PMID: 10735582

Joost O, Taylor CA, Thomas CA, Cupples LA, Saint-Hilaire MH, Feldman RG, Baldwin CT, Myers RH. Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease. Mov Disord. 1999 Jul; 14(4):590-5.View Related Profiles.

Thomas, Cathi-Ann
Baldwin, Clinton
Cupples, L
Saint-Hilaire, Marie-Helene
Myers, Richard

PMID: 10435495

Gates GA, Couropmitree NN, Myers RH. Genetic associations in age-related hearing thresholds. Arch Otolaryngol Head Neck Surg. 1999 Jun; 125(6):654-9. PMID: 10367922

Feng D, Lindpaintner K, Larson MG, Rao VS, O'Donnell CJ, Lipinska I, Schmitz C, Sutherland PA, Silbershatz H, D'Agostino RB, Muller JE, Myers RH, Levy D, Tofler GH. Increased platelet aggregability associated with platelet GPIIIa PlA2 polymorphism: the Framingham Offspring Study. Arterioscler Thromb Vasc Biol. 1999 Apr; 19(4):1142-7.View Related Profiles.

O'Donnell, Christopher
Larson, Martin
D'Agostino, Ralph
Myers, Richard

PMID: 10195947

Ellison RC, Zhang Y, Myers RH, Swanson JL, Higgins M, Eckfeldt J. Lewis blood group phenotype as an independent risk factor for coronary heart disease (the NHLBI Family Heart Study). Am J Cardiol. 1999 Feb 1; 83(3):345-8.View Related Profiles.

Myers, Richard
Ellison, Robert
Zhang, Yuqing

PMID: 10072221

Wilk JB, Premkumar S, Nicolaou M, Myers RH, Maher NE, Harmon MD, Farrer LA, DeStefano AL, Cupples LA, Couropmitree NN. Stratification techniques to explore genotype environment interactions. Genet Epidemiol. 1999; 17 Suppl 1:S761-6.View Related Profiles.

DeStefano, Anita
Farrer, Lindsay
Myers, Richard

PMID: 10597527

Karluk D, Myers RH, DiFiglia M, Vonsattel JP et al. Nonagenarians with Huntington disease (HD) have low CAG repeats. Journal of Neuropathology and Experimental Neurology. 1999; 58(5). View Publication

Sieradzan KA, Mann DM. On the pathological progression of Huntington's disease. Ann Neurol. 1998 Jul; 44(1):148-9. PMID: 9667607

Pocovi M, Cenarro A, Civeira F, Torralba MA, Perez-Calvo JI, Mozas P, Giraldo P, Giralt M, Myers RH, Cupples LA, Ordovas JM. Beta-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypo-alpha-lipoproteinaemia. Lancet. 1998 Jun 27; 351(9120):1919-23. PMID: 9654259

Felson DT, Couropmitree NN, Chaisson CE, Hannan MT, Zhang Y, McAlindon TE, LaValley M, Levy D, Myers RH. Evidence for a Mendelian gene in a segregation analysis of generalized radiographic osteoarthritis: the Framingham Study. Arthritis Rheum. 1998 Jun; 41(6):1064-71.View Related Profiles.

Chaisson, Christine
Felson, David
LaValley, Michael
Myers, Richard
Zhang, Yuqing

PMID: 9627016

O'Donnell CJ, Lindpaintner K, Larson MG, Rao VS, Ordovas JM, Schaefer EJ, Myers RH, Levy D. Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framingham Heart Study. Circulation. 1998 May 12; 97(18):1766-72.View Related Profiles.

O'Donnell, Christopher
Larson, Martin
Myers, Richard

PMID: 9603529

Givelber RJ, Couropmitree NN, Gottlieb DJ, Evans JC, Levy D, Myers RH, O'Connor GT. Segregation analysis of pulmonary function among families in the Framingham Study. Am J Respir Crit Care Med. 1998 May; 157(5 Pt 1):1445-51.View Related Profiles.

O'Connor, George
Myers, Richard

PMID: 9603122

Jenkins BG, Rosas HD, Chen YC, Makabe T, Myers R, MacDonald M, Rosen BR, Beal MF, Koroshetz WJ. 1H NMR spectroscopy studies of Huntington's disease: correlations with CAG repeat numbers. Neurology. 1998 May; 50(5):1357-65. PMID: 9595987

ACMG/ASHG statement. Laboratory guidelines for Huntington disease genetic testing. The American College of Medical Genetics/American Society of Human Genetics Huntington Disease Genetic Testing Working Group. Am J Hum Genet. 1998 May; 62(5):1243-7. PMID: 9545416; PMCID: PMC1377103

Arnett DK, Borecki IB, Ludwig EH, Pankow JS, Myers R, Evans G, Folsom AR, Heiss G, Higgins M. Angiotensinogen and angiotensin converting enzyme genotypes and carotid atherosclerosis: the atherosclerosis risk in communities and the NHLBI family heart studies. Atherosclerosis. 1998 May; 138(1):111-6. PMID: 9678776

Ewbank DC. Effects of age and ethnicity on the link between APOE epsilon4 and Alzheimer disease. JAMA. 1998 Feb 25; 279(8):580-1; author reply 581-2. PMID: 9486746

Myers RH, Marans K, MacDonald ME . Huntington’s Disease. In: Genetic Instabilities and Hereditary Neurological Diseases. Editors: Stephen T. Warren and Robert T. Wells. Academic Press. 1998; 301-323.
Feng DL, Lindpaintner K, Larson MG, O'Donnell C, Silbershatz H, Lipinska I, Sutherland PA, Muller JE, D'Agostino RB, Myers RH, Tofler GH . Factor VII gene polymorphism and cardiovascular disease: The Framingham Heart Study Circulation. 1998; 98: 2410-.
O'Donnell CJ, Larson MG, Feng DL, Myers RH, Levy D, Tofler GH. Heritability of platelet aggregation in the Framingham Heart Study. Circulation. 1998; 97(8):830.

Post WS, Larson MG, Myers RH, Galderisi M, Levy D. Heritability of left ventricular mass: the Framingham Heart Study. Hypertension. 1997 Nov; 30(5):1025-8.View Related Profiles.

Larson, Martin
Myers, Richard

PMID: 9369250

Farrer LA, Cupples LA, Haines JL, Hyman B, Kukull WA, Mayeux R, Myers RH, Pericak-Vance MA, Risch N, van Duijn CM. Effects of age, sex, and ethnicity on the association between apolipoprotein E genotype and Alzheimer disease. A meta-analysis. APOE and Alzheimer Disease Meta Analysis Consortium. JAMA. 1997 Oct 22-29; 278(16):1349-56.View Related Profiles.

Cupples, L
Farrer, Lindsay
Myers, Richard

PMID: 9343467

Liao D, Myers R, Hunt S, Shahar E, Paton C, Burke G, Province M, Heiss G. Familial history of stroke and stroke risk. The Family Heart Study. Stroke. 1997 Oct; 28(10):1908-12. PMID: 9341694

Kiel DP, Myers RH, Cupples LA, Kong XF, Zhu XH, Ordovas J, Schaefer EJ, Felson DT, Rush D, Wilson PW, Eisman JA, Holick MF. The BsmI vitamin D receptor restriction fragment length polymorphism (bb) influences the effect of calcium intake on bone mineral density. J Bone Miner Res. 1997 Jul; 12(7):1049-57.View Related Profiles.

Felson, David
Holick, Michael
Myers, Richard

PMID: 9200004

Taylor CA, Myers RH. Long-term impact of Huntington disease linkage testing. Am J Med Genet. 1997 Jun 27; 70(4):365-70. PMID: 9182776

Penney JB, Vonsattel JP, MacDonald ME, Gusella JF, Myers RH. CAG repeat number governs the development rate of pathology in Huntington's disease. Ann Neurol. 1997 May; 41(5):689-92. PMID: 9153534

McNeil SM, Novelletto A, Srinidhi J, Barnes G, Kornbluth I, Altherr MR, Wasmuth JJ, Gusella JF, MacDonald ME, Myers RH. Reduced penetrance of the Huntington's disease mutation. Hum Mol Genet. 1997 May; 6(5):775-9. PMID: 9158152

Vonsattel JPG, Zhao Y, Lenzi S, Hedley-Whyte ET, Myers RH et. al. ALZHEIMER DISEASE DOES NOT PROTECT THE NEOSTRIATUM IN COMBINED CASES OF HUNTINGTON (HD) AND ALZHEIMER DISEASE (AD). Journal of Neuropathology and Experimental Neurology. 1997; 56(5).
Liao DP, Myers RH, Burke G, Province M, Shahar E, Paton C, Hunt S, Heiss G. Parental history of stroke and stroke risk - The FHS study. Stroke. 1997; 28(1):70.
Vasterling J, White RF, Marans K, Myers RH, Sax D. Neuropsychological functioning in juvenile/adolescent onset Huntington's disease: A case series. Archives of Clinical Neuropsychology. 1997; 12(4):421. View Publication

DeStefano AL, Cupples LA, Myers RH, Farrer LA. Detecting linkage for a complex disease using simulated extended pedigrees. Genet Epidemiol. 1997; 14(6):981-6.View Related Profiles.

DeStefano, Anita
Farrer, Lindsay
Myers, Richard

PMID: 9433611

Sax DS, Powsner R, Kim A, Tilak S, Bhatia R, Cupples LA, Myers RH. Evidence of cortical metabolic dysfunction in early Huntington's disease by single-photon-emission computed tomography. Mov Disord. 1996 Nov; 11(6):671-7.View Related Profiles.

Cupples, L
Powsner, Rachel
Myers, Richard

PMID: 8914093

Pocovi M, Cenarro A, Civeira F, Myers RH, Casao E, Esteban M, Ordovas JM. Incomplete dominance of type III hyperlipoproteinemia is associated with the rare apolipoprotein E2 (Arg136-->Ser) variant in multigenerational pedigree studies. Atherosclerosis. 1996 Apr 26; 122(1):33-46. PMID: 8724110

Lindpaintner K, Lee M, Larson MG, Rao VS, Pfeffer MA, Ordovas JM, Schaefer EJ, Wilson AF, Wilson PW, Vasan RS, Myers RH, Levy D. Absence of association or genetic linkage between the angiotensin-converting-enzyme gene and left ventricular mass. N Engl J Med. 1996 Apr 18; 334(16):1023-8.View Related Profiles.

Larson, Martin
Myers, Richard
Ramachandran, Vasan

PMID: 8598840

Myers RH, Schaefer EJ, Wilson PW, D'Agostino R, Ordovas JM, Espino A, Au R, White RF, Knoefel JE, Cobb JL, McNulty KA, Beiser A, Wolf PA. Apolipoprotein E epsilon4 association with dementia in a population-based study: The Framingham study. Neurology. 1996 Mar; 46(3):673-7.View Related Profiles.

Beiser, Alexa
Sullivan, Kimberly
Wolf, Philip
D'Agostino, Ralph
Au, Rhoda
Myers, Richard
White, Roberta

PMID: 8618665

Podgor MJ, Hiller R. Associations of types of lens opacities between and within eyes of individuals: an application of second-order generalized estimating equations. The Framingham Eye Studies Group. Stat Med. 1996 Jan 30; 15(2):145-56. PMID: 8614751

Gusella JF, McNeil S, Persichetti F, Srinidhi J, Novelletto A, Bird E, Faber P, Vonsattel JP, Myers RH, MacDonald ME. Huntington's disease. Cold Spring Harb Symp Quant Biol. 1996; 61:615-26. PMID: 9246488

Statement on use of apolipoprotein E testing for Alzheimer disease. American College of Medical Genetics/American Society of Human Genetics Working Group on ApoE and Alzheimer disease. JAMA. 1995 Nov 22-29; 274(20):1627-9.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 7474250

Leeflang EP, Zhang L, Tavaré S, Hubert R, Srinidhi J, MacDonald ME, Myers RH, de Young M, Wexler NS, Gusella JF, et al. Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum. Hum Mol Genet. 1995 Sep; 4(9):1519-26. PMID: 8541834

Persichetti F, Ambrose CM, Ge P, McNeil SM, Srinidhi J, Anderson MA, Jenkins B, Barnes GT, Duyao MP, Kanaley L, et al. Normal and expanded Huntington's disease gene alleles produce distinguishable proteins due to translation across the CAG repeat. Mol Med. 1995 May; 1(4):374-83. PMID: 8521295; PMCID: PMC2230005

Myers RH . Genetic testing for Huntington's disease. Scientific American; Science & Medicine. March/April. 1995; 4.
Ellison RC, Myers RH. Genetic and Familial Aspects of Disease. In: Introduction to Clinical Medicine. Mosby Yearbook. 1995; 9-12.
Myers RH, Schaefer EJ, Wilson PWF, D'Agostino R, Bachman DL, Ordovas JM, Au R, Cobb JL, Wolf PA . Apolipoprotein E allele 4 is associated with dementia in the Framingham study. In: Research Advances in Alzheimer’s Disease and Related Disorders. Editors: Iqbal K, Mortimer J, Winblad B, Wisniewski H. John Wiley & Sons, Ltd. Chichester England. 1995; 63-70.
Levy D, Lindpaintner K, Larson MG, Ramachandran VS, Myers RH, Pfeffer MA, Ordovas JM, Schaefer EJ, Wilson PWF. 729-4 Left Ventricular Hypertrophy and the Deletion-Insertion Polymorphism of the Angiotensin Converting Enzyme Gene. Journal of the American College of Cardiology. 1995; 25(2). View Publication
Ramachandran VS, Levy D, Larson MG, Ordovas JM, Schaefer EJ, Myers RH, Lindpaintner K, Wilson PWF. 901-81 Association of a Molecular Variant of the Angiotensinogen Gene and Hypertension. Journal of the American College of Cardiology. 1995; 25(2). View Publication

Wilson PW, Myers RH, Larson MG, Ordovas JM, Wolf PA, Schaefer EJ. Apolipoprotein E alleles, dyslipidemia, and coronary heart disease. The Framingham Offspring Study. JAMA. 1994 Dec 7; 272(21):1666-71.View Related Profiles.

Larson, Martin
Wolf, Philip
Myers, Richard

PMID: 7966894

Persichetti F, Srinidhi J, Kanaley L, Ge P, Myers RH, D'Arrigo K, Barnes GT, MacDonald ME, Vonsattel JP, Gusella JF, et al. Huntington's disease CAG trinucleotide repeats in pathologically confirmed post-mortem brains. Neurobiol Dis. 1994 Dec; 1(3):159-66. PMID: 9173995

Familial aggregation of lens opacities: the Framingham Eye Study and the Framingham Offspring Eye Study. Am J Epidemiol. 1994 Sep 15; 140(6):555-64. PMID: 8067349

Multani P, Myers RH, Blume HW, Schomer DL, Sotrel A. Neocortical dendritic pathology in human partial epilepsy: a quantitative Golgi study. Epilepsia. 1994 Jul-Aug; 35(4):728-36. PMID: 7521835

Lazzarini AM, Myers RH, Zimmerman TR, Mark MH, Golbe LI, Sage JI, Johnson WG, Duvoisin RC. A clinical genetic study of Parkinson's disease: evidence for dominant transmission. Neurology. 1994 Mar; 44(3 Pt 1):499-506. PMID: 8145922

Myers RH, Friend JC, Cupples LA. Oligodendroglial proliferation in presymptomatic Huntington`s disease. 1994.
Gaston S, Myers RH, White RF, Tanzi R, Feldman RG. Clinical phenotype of chromosome 14q24 associated FAD in the Italian-American (Feldman FAD Family) pedigree. Neurobiology of Aging. 1994; 15:S9. View Publication

MacDonald ME, Barnes G, Srinidhi J, Duyao MP, Ambrose CM, Myers RH, Gray J, Conneally PM, Young A, Penney J, et al. Gametic but not somatic instability of CAG repeat length in Huntington's disease. J Med Genet. 1993 Dec; 30(12):982-6. PMID: 8133508; PMCID: PMC1016628

Myers RH, MacDonald ME, Gusella JF. Discrepancy resolved. Nat Genet. 1993 Nov; 5(3):215. PMID: 8110292

Myers RH, MacDonald ME, Koroshetz WJ, Duyao MP, Ambrose CM, Taylor SA, Barnes G, Srinidhi J, Lin CS, Whaley WL, et al. De novo expansion of a (CAG)n repeat in sporadic Huntington's disease. Nat Genet. 1993 Oct; 5(2):168-73. PMID: 8252042

Sotrel A, Williams RS, Kaufmann WE, Myers RH. Evidence for neuronal degeneration and dendritic plasticity in cortical pyramidal neurons of Huntington's disease: a quantitative Golgi study. Neurology. 1993 Oct; 43(10):2088-96. PMID: 8413971

Kiely DK, Wolf PA, Cupples LA, Beiser AS, Myers RH. Familial aggregation of stroke. The Framingham Study. Stroke. 1993 Sep; 24(9):1366-71.View Related Profiles.

Beiser, Alexa
Cupples, L
Wolf, Philip
Myers, Richard

PMID: 8362432

Duyao M, Ambrose C, Myers R, Novelletto A, Persichetti F, Frontali M, Folstein S, Ross C, Franz M, Abbott M, et al. Trinucleotide repeat length instability and age of onset in Huntington's disease. Nat Genet. 1993 Aug; 4(4):387-92. PMID: 8401587

Farrer LA, Cupples LA, Wiater P, Conneally PM, Gusella JF, Myers RH. The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HD. Am J Hum Genet. 1993 Jul; 53(1):125-30.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 8317477; PMCID: PMC1682222

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group. Cell. 1993 Mar 26; 72(6):971-83. PMID: 8458085

Cupples LA, Myers RH. Segregation analysis for high density lipoprotein in the Berkeley data. Genet Epidemiol. 1993; 10(6):629-34.View Related Profiles.

Cupples, L
Myers, Richard

PMID: 8314072

Koroshetz WJ, Myers RH, Martin JB. Neurology of Huntington's disease. In: The Molecular and Genetic Basis of Neurological Disease. Editors: Rosenberg RN, Prusiner SB, DiMauro S, Barchi RL, Kunkel LM. Butterworth & Heinemann. Boston,MA. 1993; 737-751.
Sotrel A, Myers RH. CORTICAL PATHOLOGY IN HUNTINGTONS-DISEASE - MORPHOMETRIC AND OBSERVATIONAL STUDY. Journal of Neuropathology and Experimental Neurology. 1993; 52(3):280.
Sotrel A, Myers RH. CORTICAL PATHOLOGY IN HUNTINGTON'S DISEASE. Journal of Neuropathology and Experimental Neurology. 1993; 52(3). View Publication

Diamond R, White RF, Myers RH, Mastromauro C, Koroshetz WJ, Butters N, Rothstein DM, Moss MB, Vasterling J. Evidence of presymptomatic cognitive decline in Huntington's disease. J Clin Exp Neuropsychol. 1992 Nov; 14(6):961-75.View Related Profiles.

Vasterling, Jennifer
Moss, Mark
Myers, Richard
White, Roberta

PMID: 1452640

Ogawa T, Matson WR, Beal MF, Myers RH, Bird ED, Milbury P, Saso S. Kynurenine pathway abnormalities in Parkinson's disease. Neurology. 1992 Sep; 42(9):1702-6. PMID: 1513457

Genest JJ, Martin-Munley SS, McNamara JR, Ordovas JM, Jenner J, Myers RH, Silberman SR, Wilson PW, Salem DN, Schaefer EJ. Familial lipoprotein disorders in patients with premature coronary artery disease. Circulation. 1992 Jun; 85(6):2025-33. PMID: 1534286

MacDonald ME, Novelletto A, Lin C, Tagle D, Barnes G, Bates G, Taylor S, Allitto B, Altherr M, Myers R, et al. The Huntington's disease candidate region exhibits many different haplotypes. Nat Genet. 1992 May; 1(2):99-103. PMID: 1302016

Farrer LA, Cupples LA, Kiely DK, Conneally PM, Myers RH. Inverse relationship between age at onset of Huntington disease and paternal age suggests involvement of genetic imprinting. Am J Hum Genet. 1992 Mar; 50(3):528-35.View Related Profiles.

Cupples, L
Farrer, Lindsay
Myers, Richard

PMID: 1531729; PMCID: PMC1684271

Brand FN, Kiely DK, Kannel WB, Myers RH. Family patterns of coronary heart disease mortality: the Framingham Longevity Study. J Clin Epidemiol. 1992 Feb; 45(2):169-74. PMID: 1573433

Farrer LA, Myers RH, Cupples LA. Segregation analysis of total nevus density and estimation of lifetime risk and average onset age of melanoma. Cytogenet Cell Genet. 1992; 59(2-3):197-9.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 1737499

White RF, Vasterling J, Koroshetz W, Myers RH . Neuropsychology of Huntington's disease. In: Clinical Syndromes in Adult Neuropsychology: The Practitioner's Handbook. Editor: White RF. Elsevier. Amsterdam. 1992; 213-251.
Koroshetz WJ, Myers RH, Martin JB. The Neurology of Huntington's disease. In: Movement Disorders in Neurology and Neuropsychiatry. Editors: Joseph AR and Young RR. Blackwell Scientific Publications. Cambridge,MA. 1992; 167-177.

Vonsattel JP, Myers RH, Bird ED, Ge P, Richardson EP. [Huntington disease: 7 cases with relatively preserved neostriatal islets]. Rev Neurol (Paris). 1992; 148(2):107-16. PMID: 1534925

Farrer L, Adrienne Cupples L, Myers RH, Connor L, Growdon JH. Reply to Tzourio et al. The American Journal of Human Genetics. 1992; 50(3).
Adrienne Cupples L, Risch N, Farrer L, Myers RH. Reply to Krawczak and Bockel. The American Journal of Human Genetics. 1992; 50(3).

Vonsattel JP, Myers RH, Hedley-Whyte ET, Ropper AH, Bird ED, Richardson EP. Cerebral amyloid angiopathy without and with cerebral hemorrhages: a comparative histological study. Ann Neurol. 1991 Nov; 30(5):637-49. PMID: 1763890

Myers RH, Vonsattel JP, Paskevich PA, Kiely DK, Stevens TJ, Cupples LA, Richardson EP, Bird ED. Decreased neuronal and increased oligodendroglial densities in Huntington's disease caudate nucleus. J Neuropathol Exp Neurol. 1991 Nov; 50(6):729-42.View Related Profiles.

Cupples, L
Myers, Richard

PMID: 1836225

Myers RH, Sax DS, Koroshetz WJ, Mastromauro C, Cupples LA, Kiely DK, Pettengill FK, Bird ED. Factors associated with slow progression in Huntington's disease. Arch Neurol. 1991 Aug; 48(8):800-4.View Related Profiles.

Cupples, L
Myers, Richard

PMID: 1832854

Cupples LA, Risch N, Farrer LA, Myers RH. Estimation of morbid risk and age at onset with missing information. Am J Hum Genet. 1991 Jul; 49(1):76-87.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 1829582; PMCID: PMC1683228

Sotrel A, Paskevich PA, Kiely DK, Bird ED, Williams RS, Myers RH. Morphometric analysis of the prefrontal cortex in Huntington's disease. Neurology. 1991 Jul; 41(7):1117-23. PMID: 1829794

Meissen GJ, Mastromauro CA, Kiely DK, McNamara DS, Myers RH. Understanding the decision to take the predictive test for Huntington disease. Am J Med Genet. 1991 Jun 15; 39(4):404-10. PMID: 1678928

Farrer LA, Myers RH, Connor L, Cupples LA, Growdon JH. Segregation analysis reveals evidence of a major gene for Alzheimer disease. Am J Hum Genet. 1991 Jun; 48(6):1026-33.View Related Profiles.

Cupples, L
Farrer, Lindsay
Myers, Richard

PMID: 2035523; PMCID: PMC1683119

Doolittle TH, Myers RH, Lehrich JR, Birnbaum G, Sheremata W, Franklin GM, Nelson LM, Hauser SL. Multiple sclerosis sibling pairs: clustered onset and familial predisposition. Neurology. 1990 Oct; 40(10):1546-52. PMID: 2215946

Myers RH, Kiely DK, Cupples LA, Kannel WB. Parental history is an independent risk factor for coronary artery disease: the Framingham Study. Am Heart J. 1990 Oct; 120(4):963-9.View Related Profiles.

Cupples, L
Myers, Richard

PMID: 2220549

St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, McLachlan DR, Orr H, Bruni AC, Sorbi S, Rainero I, Foncin JF, Pollen D, Cantu JM, Tupler R, Voskresenskaya N, Mayeux R, Growden J, Fried VA, Myers RH, Nee L, Backhovens H, Martin JJ, Rossor M, Owen MJ, Mullan M, Percy ME, Karlinsky H, Rich S, Heston L, Montesi M, Mortilla M, Nacmias N, Gusella JF, Hardy JA, et al. Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder. Nature. 1990 Sep 13; 347(6289):194-7.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 2395471

Farrer LA, Myers RH, Cupples LA, St George-Hyslop PH, Bird TD, Rossor MN, Mullan MJ, Polinsky R, Nee L, Heston L, et al. Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneity. Neurology. 1990 Mar; 40(3 Pt 1):395-403.View Related Profiles.

Cupples, L
Farrer, Lindsay
Myers, Richard

PMID: 2314579

Breitner JCS, Farrer L, Myers RH, Adrienne Cupples L, Growdon JH. Estimation of familial risk in Alzheimer's disease. Annals of Neurology. 1990; 27(3). View Publication

St George-Hyslop PH, Haines JL, Polinsky RJ, Tanzi RE, Farrer L, Myers RH, Gusella JF. Molecular genetics of familial Alzheimer's disease. Can J Neurol Sci. 1989 Nov; 16(4 Suppl):465-7.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 2680005

Sax DS, Bird ED, Gusella JF, Myers RH. Phenotypic variation in 2 Huntington's disease families with linkage to chromosome 4. Neurology. 1989 Oct; 39(10):1332-6. PMID: 2529452

Myers RH, Leavitt J, Farrer LA, Jagadeesh J, McFarlane H, Mastromauro CA, Mark RJ, Gusella JF. Homozygote for Huntington disease. Am J Hum Genet. 1989 Oct; 45(4):615-8.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 2535231; PMCID: PMC1683503

Schildkraut JM, Myers RH, Cupples LA, Kiely DK, Kannel WB. Coronary risk associated with age and sex of parental heart disease in the Framingham Study. Am J Cardiol. 1989 Sep 15; 64(10):555-9. PMID: 2782245

MacDonald ME, Cheng SV, Zimmer M, Haines JL, Poustka A, Allitto B, Smith B, Whaley WL, Romano DM, Jagadeesh J, et al. Clustering of multiallele DNA markers near the Huntington's disease gene. J Clin Invest. 1989 Sep; 84(3):1013-6. PMID: 2569477; PMCID: PMC329749

St George-Hyslop PH, Myers RH, Haines JL, Farrer LA, Tanzi RE, Abe K, James MF, Conneally PM, Polinsky RJ, Gusella JF. Familial Alzheimer's disease: progress and problems. Neurobiol Aging. 1989 Sep-Oct; 10(5):417-25.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 2682321

Conneally PM, Haines JL, Tanzi RE, Wexler NS, Penchaszadeh GK, Harper PS, Folstein SE, Cassiman JJ, Myers RH, Young AB, et al. Huntington disease: no evidence for locus heterogeneity. Genomics. 1989 Aug; 5(2):304-8. PMID: 2571579

Mastromauro CA, Meissen GJ, Cupples LA, Kiely DK, Berkman B, Myers RH. Estimation of fertility and fitness in Huntington disease in New England. Am J Med Genet. 1989 Jun; 33(2):248-54.View Related Profiles.

Cupples, L
Myers, Richard

PMID: 2527461

Farrer LA, O'Sullivan DM, Cupples LA, Growdon JH, Myers RH. Assessment of genetic risk for Alzheimer's disease among first-degree relatives. Ann Neurol. 1989 May; 25(5):485-93.View Related Profiles.

Cupples, L
Farrer, Lindsay
Myers, Richard

PMID: 2774490

Cupples LA, Terrin NC, Myers RH, D'Agostino RB. Using survival methods to estimate age-at-onset distributions for genetic diseases with an application to Huntington disease. Genet Epidemiol. 1989; 6(2):361-71.View Related Profiles.

Cupples, L
D'Agostino, Ralph
Myers, Richard

PMID: 2524419

St George-Hyslop PH, Tanzi RE, Haines JL, Polinsky RJ, Farrer L, Myers RH, Gusella JF. Molecular genetics of familial Alzheimer's disease. Eur Neurol. 1989; 29 Suppl 3:25-7.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 2693103

Haines JL, Farrer LA, Myers RH. Linkage map of anonymous loci near the CF gene. Prog Clin Biol Res. 1989; 329:29-34.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 2622958

St George-Hyslop PH, Myers RH, Haines JI, Farrer L, Tanzi R, Conneally PM, Polinsky RJ, Gusella JF. Authors' response to commentaries. Neurobiology of Aging. 1989; 10(5):446-448. View Publication

Farrer LA, Myers RH, Cupples LA, Conneally PM. Considerations in using linkage analysis as a presymptomatic test for Huntington's disease. J Med Genet. 1988 Sep; 25(9):577-88.View Related Profiles.

Cupples, L
Farrer, Lindsay
Myers, Richard

PMID: 2903248; PMCID: PMC1051534

Meissen GJ, Myers RH, Mastromauro CA, Koroshetz WJ, Klinger KW, Farrer LA, Watkins PA, Gusella JF, Bird ED, Martin JB. Predictive testing for Huntington's disease with use of a linked DNA marker. N Engl J Med. 1988 Mar 3; 318(9):535-42.View Related Profiles.

Farrer, Lindsay
Myers, Richard

PMID: 2893260

Myers RH, Vonsattel JP, Stevens TJ, Cupples LA, Richardson EP, Martin JB, Bird ED. Clinical and neuropathologic assessment of severity in Huntington's disease. Neurology. 1988 Mar; 38(3):341-7. PMID: 2964565

Farrer L, Haines J, Gusella J, Myers RH et al. Genetics and Alzheimer’s Disease. Molecular Genetic Strategies in Familial Alzheimer’s Disease: Theoretical and Practical Considerations. 1988; 109-115. View Publication

Gilliam TC, Bucan M, MacDonald ME, Zimmer M, Haines JL, Cheng SV, Pohl TM, Meyers RH, Whaley WL, Allitto BA, et al. A DNA segment encoding two genes very tightly linked to Huntington's disease. Science. 1987 Nov 13; 238(4829):950-2. PMID: 2890209

St George-Hyslop PH, Tanzi RE, Polinsky RJ, Neve RL, Pollen D, Drachman D, Growdon J, Cupples LA, Nee L, Myers RH, et al. Absence of duplication of chromosome 21 genes in familial and sporadic Alzheimer's disease. Science. 1987 Oct 30; 238(4827):664-6. PMID: 2890206

St George-Hyslop PH, Tanzi RE, Polinsky RJ, Haines JL, Nee L, Watkins PC, Myers RH, Feldman RG, Pollen D, Drachman D, et al. The genetic defect causing familial Alzheimer's disease maps on chromosome 21. Science. 1987 Feb 20; 235(4791):885-90. PMID: 2880399

Mastromauro C, Myers RH, Berkman B. Attitudes toward presymptomatic testing in Huntington disease. Am J Med Genet. 1987 Feb; 26(2):271-82. PMID: 2949611

Myers RH. Genetic linkage test for Huntington's disease. The Genetic Resource. 1987; 4:15-18.
Vonsattel JP, Myers RH, Stevens TJ, Ferrante RJ, Paskevich PA, Bird ED, Richardson EP. Huntington's disease: Neuropathological grading. In: The Basal Ganglia: Structure and Function. Editors: Carpenter MB, Jayaraman A. Plenum Press. New York,NY. 1987; 515-531.
Gusella JF, St. George-Hyslop PH, Tanzi RE, Polinsky RJ, Haines JL, Nee L, Watkins PC, Steward GD, Neve R, Bruns GA, Myers RH, Feldman RG, Pollen D, Drachman D, Bruni A, Foncin JF, Frommelt P, Amaducci L, Conneally PM. . Genetic Linkage analysis of familial Alzheimer's disease. In: Molecular Neuropathology of Aging. Davies P, Finch CE (Editors). Banbury Report 27, Cold Spring Harbor Laboratory. 1987; 425-442.
Vonsattel JP, Myers RH, Stevens TJ, Bird ED et al. The Basal Ganglia II: Structure and Function—Current Concepts. Huntington’s Disease: Neuropathological Grading. 1987; 515-531. View Publication

St George-Hyslop P, Polinsky R, Haines J, Nee L, Tanzi R, Conneally P, Growdon J, Myers R, Pollen D, Drachman D, et al. Search for the familial Alzheimer's disease gene. J Neural Transm Suppl. 1987; 24:13-21. PMID: 2890708

Mastromauro C, Myers RH, Berkman B. Change in attitudes toward presymptomatic testing in Huntington disease. Am J Med Genet. 1986 Jun; 24(2):369-71. PMID: 3013007

Falek A, Myers RH, Craddick R. Prediction in the onset and detection of Huntington's disease. In: Life Span Research on the Prediction of Psychopathology. Editors: Erlenmayer-Kimling L, Miller N, Dohrenwend BS. Erlbaum Publishers. New York,NY. 1986; 275-285.

Vonsattel JP, Myers RH, Stevens TJ, Ferrante RJ, Bird ED, Richardson EP. Neuropathological classification of Huntington's disease. J Neuropathol Exp Neurol. 1985 Nov; 44(6):559-77. PMID: 2932539

Myers RH, Sax DS, Schoenfeld M, Bird ED, Wolf PA, Vonsattel JP, White RF, Martin JB. Late onset of Huntington's disease. J Neurol Neurosurg Psychiatry. 1985 Jun; 48(6):530-4.View Related Profiles.

Wolf, Philip
Myers, Richard

PMID: 3159849; PMCID: PMC1028368

Myers RH, Cupples LA, Schoenfeld M, D'Agostino RB, Terrin NC, Goldmakher N, Wolf PA. Maternal factors in onset of Huntington disease. Am J Hum Genet. 1985 May; 37(3):511-23.View Related Profiles.

Wolf, Philip
D'Agostino, Ralph
Myers, Richard

PMID: 3159258; PMCID: PMC1684593

Myers RH, Schoenfeld M, Bird ED. Huntington's disease: genetics, chemical pathology, and management. Prog Med Genet. 1985; 6:91-122. PMID: 2873625

Shafer DA, Myers RH, Saltzman D. Siabon (Siamang-Gibbon) Hybrids. In: The Lesser Apes: Evolutionary and Behavioral Biology. Editors: Preushoft H, Chivers D, Brockelman W, Creel N. Edinburgh University Press. Edinburgh. 1985.

Schoenfeld M, Myers RH, Cupples LA, Berkman B, Sax DS, Clark E. Increased rate of suicide among patients with Huntington's disease. J Neurol Neurosurg Psychiatry. 1984 Dec; 47(12):1283-7. PMID: 6239910; PMCID: PMC1028135

Schoenfeld M, Myers RH, Berkman B, Clark E. Potential impact of a predictive test on the gene frequency of Huntington disease. Am J Med Genet. 1984 Jul; 18(3):423-9. PMID: 6236692

Schoenfeld M, Berkman B, Myers RH, Clark E. Attitudes toward marriage and childbearing of individuals at risk for Huntington's disease. Soc Work Health Care. 1984; 9(4):73-81. PMID: 6237443

Savage D, Padgett S, Myers R, Anderson S, Levy D, Plehn J, Finizola B, Castelli W. Noninvasive cardiology tools and endpoints in genetic epidemiology: the Framingham Study. Prog Clin Biol Res. 1984; 147:407-17. PMID: 6539918

Sudarsky L, Myers RH, Walshe TM. Huntington's disease in monozygotic twins reared apart. J Med Genet. 1983 Dec; 20(6):408-11. PMID: 6228662; PMCID: PMC1049168

Myers RH, Goldman D, Bird ED, Sax DS, Merril CR, Schoenfeld M, Wolf PA. Maternal transmission in Huntington's disease. Lancet. 1983 Jan 29; 1(8318):208-10.View Related Profiles.

Wolf, Philip
Myers, Richard

PMID: 6130245

Myers RH, Growdon JH, Bird ED, Feldman RG, Martin JB. False-negative results with levodopa for early detection of Huntington's disease. N Engl J Med. 1982 Aug 26; 307(9):561-2. PMID: 6212764

Myers RH, Madden JJ, Teague JL, Falek A. Factors related to onset age of Huntington disease. Am J Hum Genet. 1982 May; 34(3):481-8. PMID: 6211092; PMCID: PMC1685335

Myers RH, Martin JB. Huntington's Disease. Seminars in Neurology. 1982; 2:365-372.

Sinex FM, Myers RH. Alzheimer's disease, Down's syndrome, and aging: the genetic approach. Ann N Y Acad Sci. 1982; 396:3-13. PMID: 6217775

Wolkin JR, Myers RH . Characteristics of a Gibbon-Siamang hybrid ape. International Journal of Primatology. 1980; 1:203-221.

Myers RH, Falek A. Quantification of muscle tremor of Huntington's disease patients and their offspring in an early detection study. Biol Psychiatry. 1979 Oct; 14(5):777-89. PMID: 159079

Myers RH, Shafer DA. Hybrid ape offspring of a mating of gibbon and siamang. Science. 1979 Jul 20; 205(4403):308-10. PMID: 451603

Myers RH. The chromosome connection: the theory of evolution is evolving. The Sciences. 1979; 20(5):18-20.

Myers RH, De Castro JM. Learned aversions to intracerebral carbachol. Physiol Behav. 1977 Oct; 19(4):467-72. PMID: 613337

Myers RH, Hobbs ME, Gross PM. Regularities in the Densities of Dilute Solutions of Some Monochlorobenzotrihalides1. Journal of the American Chemical Society. 1954; 76(18). View Publication

This graph shows the total number of publications by year, by first, middle/unknown, or last author.

Bar chart showing 342 publications over 42 distinct years, with a maximum of 17 publications in 2002

Bar chart showing 342 publications over 42 distinct years, with a maximum of 17 publications in 2002

Year	Publications
1980	1
1982	4
1983	2
1984	4
1985	5
1986	2
1987	9
1988	4
1989	13
1990	5
1991	7
1992	12
1993	12
1994	7
1995	8
1996	6
1997	11
1998	12
1999	11
2000	16
2001	13
2002	17
2003	13
2004	10
2005	10
2006	16
2007	13
2008	15
2009	9
2010	6
2011	7
2012	13
2013	4
2014	6
2015	11
2016	11
2017	6
2018	3
2019	2
2020	1
2021	2
2024	3

In addition to these self-described keywords below, a list of MeSH based concepts is available here.

coronary heart disease
genetic testing
Huntington's disease
Neurogenetics
Parkinson's disease
risk factors

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