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PhD, Boston University
MS, Northwestern University

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Research
Publications

BU Research
NIH RePORTER Research

Personnel agreement for research services of Eftymia Melista
04/01/2013 - 08/31/2013 (PI)
VA Boston Healthcare System

Personnel Agreement for Research Services of Clinton Baldwin
04/01/2013 - 08/31/2013 (PI)
VA Boston Healthcare System

Evaluation of iPS Stem Cells as a Model of Alzheimer Disease
09/15/2011 - 08/31/2013 (PI)
NIH/National Institute on Aging
5R21AG039489-02

Title

Yr	Title	Project-Sub Proj	Pubs
2012	Evaluation of iPS Stem Cells as a Model of Alzheimer Disease	5R21AG039489-02
2011	Evaluation of iPS Stem Cells as a Model of Alzheimer Disease	1R21AG039489-01A1
2009	GENETIC FACTORS CAUSING LONGEVITY IN CENTENARIANS	2R56AG027216-04	2
2008	GENETIC FACTORS CAUSING LONGEVITY IN CENTENARIANS AND THEIR OFFSPRING	5R01AG027216-03	4
2007	GENETIC FACTORS CAUSING LONGEVITY IN CENTENARIANS AND THEIR OFFSPRING	5R01AG027216-02	4
2006	GENETIC FACTORS CAUSING LONGEVITY IN CENTENARIANS AND THEIR OFFSPRING	1R01AG027216-01A1	4
1998	GENE DEFECTS CAUSING OSTEOARTHRITIS	5R01AR043858-04	1
1997	GENE DEFECTS CAUSING OSTEOARTHRITIS	5R01AR043858-03	1
1996	GENE DEFECTS CAUSING OSTEOARTHRITIS	5R01AR043858-02	1
1995	GENE DEFECTS CAUSING OSTEOARTHRITIS	1R01AR043858-01	1

Showing 10 of 17 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

Logue MW, Solovieff N, Leussis MP, Wolf EJ, Melista E, Baldwin C, Koenen KC, Petryshen TL, Miller MW. The ankyrin-3 gene is associated with posttraumatic stress disorder and externalizing comorbidity. Psychoneuroendocrinology. 2013 Oct; 38(10):2249-57.View Related Profiles.

Baldwin, Clinton
Wolf, Erika
Logue, Mark
Miller, Mark

PMID: 23796624; PMCID: PMC3775967; DOI: 10.1016/j.psyneuen.2013.04.013;

Alsultan A, Ngo D, Bae H, Sebastiani P, Baldwin CT, Melista E, Suliman AM, Albuali WH, Nasserullah Z, Luo HY, Chui DH, Steinberg MH, Al-Ali AK. Genetic studies of fetal hemoglobin in the Arab-Indian haplotype sickle cell-ß(0) thalassemia. Am J Hematol. 2013 Jun; 88(6):531-2.View Related Profiles.

Baldwin, Clinton
Chui, David
Ngo, Duyen
Steinberg, Martin
Sebastiani, Paola

PMID: 23483609; DOI: 10.1002/ajh.23434;

Reitz C, Jun G, Naj A, Rajbhandary R, Vardarajan BN, Wang LS, Valladares O, Lin CF, Larson EB, Graff-Radford NR, Evans D, De Jager PL, Crane PK, Buxbaum JD, Murrell JR, Raj T, Ertekin-Taner N, Logue M, Baldwin CT, Green RC, Barnes LL, Cantwell LB, Fallin MD, Go RC, Griffith P, Obisesan TO, Manly JJ, Lunetta KL, Kamboh MI, Lopez OL, Bennett DA, Hendrie H, Hall KS, Goate AM, Byrd GS, Kukull WA, Foroud TM, Haines JL, Farrer LA, Pericak-Vance MA, Schellenberg GD, Mayeux R. Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ?4,and the risk of late-onset Alzheimer disease in African Americans. JAMA. 2013 Apr 10; 309(14):1483-92.View Related Profiles.

Baldwin, Clinton
Jun, Gyungah
Lunetta, Kathryn
Farrer, Lindsay
Logue, Mark

PMID: 23571587; PMCID: PMC3667653; DOI: 10.1001/jama.2013.2973;

Ngo D, Bae H, Steinberg MH, Sebastiani P, Solovieff N, Baldwin CT, Melista E, Safaya S, Farrer LA, Al-Suliman AM, Albuali WH, Al Bagshi MH, Naserullah Z, Akinsheye I, Gallagher P, Luo HY, Chui DH, Farrell JJ, Al-Ali AK, Alsultan A. Fetal hemoglobin in sickle cell anemia: genetic studies of the Arab-Indian haplotype. Blood Cells Mol Dis. 2013 Jun; 51(1):22-6.View Related Profiles.

Baldwin, Clinton
Chui, David
Ngo, Duyen
Luo, Hong
Farrer, Lindsay
Steinberg, Martin
Sebastiani, Paola

PMID: 23465615; PMCID: PMC3647015; DOI: 10.1016/j.bcmd.2012.12.005;

Vardarajan B, Vergote D, Tissir F, Logue M, Yang J, Daude N, Ando K, Rogaeva E, Lee J, Cheng R, Brion JP, Ghani M, Shi B, Baldwin CT, Kar S, Mayeux R, Fraser P, Goffinet AM, George-Hyslop PS, Farrer LA, Westaway D. Role of p73 in Alzheimer disease: lack of association in mouse models or in human cohorts. Mol Neurodegener. 2013; 8:10.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay
Logue, Mark

PMID: 23414597; PMCID: PMC3614544; DOI: 10.1186/1750-1326-8-10;

Milton JN, Rooks H, Drasar E, McCabe EL, Baldwin CT, Melista E, Gordeuk VR, Nouraie M, Kato GR, Minniti C, Taylor J, Campbell A, Luchtman-Jones L, Rana S, Castro O, Zhang Y, Thein SL, Sebastiani P, Gladwin MT, Steinberg MH. Genetic determinants of haemolysis in sickle cell anaemia. Br J Haematol. 2013 Apr; 161(2):270-8.View Related Profiles.

Baldwin, Clinton
Hicks, Jacqueline
Steinberg, Martin
Sebastiani, Paola

PMID: 23406172; PMCID: PMC4129543; DOI: 10.1111/bjh.12245;

Whitcomb DC, LaRusch J, Krasinskas AM, Klei L, Smith JP, Brand RE, Neoptolemos JP, Lerch MM, Tector M, Sandhu BS, Guda NM, Orlichenko L, Alkaade S, Amann ST, Anderson MA, Baillie J, Banks PA, Conwell D, Coté GA, Cotton PB, DiSario J, Farrer LA, Forsmark CE, Johnstone M, Gardner TB, Gelrud A, Greenhalf W, Haines JL, Hartman DJ, Hawes RA, Lawrence C, Lewis M, Mayerle J, Mayeux R, Melhem NM, Money ME, Muniraj T, Papachristou GI, Pericak-Vance MA, Romagnuolo J, Schellenberg GD, Sherman S, Simon P, Singh VP, Slivka A, Stolz D, Sutton R, Weiss FU, Wilcox CM, Zarnescu NO, Wisniewski SR, O'Connell MR, Kienholz ML, Roeder K, Barmada MM, Yadav D, Devlin B. Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Nat Genet. 2012 Dec; 44(12):1349-54.View Related Profiles.

Baldwin, Clinton
Jun, Gyungah
Lunetta, Kathryn
Farrer, Lindsay
Kowall, Neil
Stern, Robert

PMID: 23143602; PMCID: PMC3510344; DOI: 10.1038/ng.2466;

Bae HT, Baldwin CT, Sebastiani P, Telen MJ, Ashley-Koch A, Garrett M, Hooper WC, Bean CJ, Debaun MR, Arking DE, Bhatnagar P, Casella JF, Keefer JR, Barron-Casella E, Gordeuk V, Kato GJ, Minniti C, Taylor J, Campbell A, Luchtman-Jones L, Hoppe C, Gladwin MT, Zhang Y, Steinberg MH. Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans. Blood. 2012 Aug 30; 120(9):1961-2.View Related Profiles.

Baldwin, Clinton
Steinberg, Martin
Sebastiani, Paola

PMID: 22936743; PMCID: PMC3433099; DOI: 10.1182/blood-2012-06-432849;

Logue MW, Baldwin C, Guffanti G, Melista E, Wolf EJ, Reardon AF, Uddin M, Wildman D, Galea S, Koenen KC, Miller MW. A genome-wide association study of post-traumatic stress disorder identifies the retinoid-related orphan receptor alpha (RORA) gene as a significant risk locus. Mol Psychiatry. 2013 Aug; 18(8):937-42.View Related Profiles.

Baldwin, Clinton
Wolf, Erika
Logue, Mark
Miller, Mark
Galea, Sandro

PMID: 22869035; PMCID: PMC3494788; DOI: 10.1038/mp.2012.113;

Melville SA, Buros J, Parrado AR, Vardarajan B, Logue MW, Shen L, Risacher SL, Kim S, Jun G, DeCarli C, Lunetta KL, Baldwin CT, Saykin AJ, Farrer LA. Multiple loci influencing hippocampal degeneration identified by genome scan. Ann Neurol. 2012 Jul; 72(1):65-75.View Related Profiles.

Baldwin, Clinton
Jun, Gyungah
Lunetta, Kathryn
Farrer, Lindsay
Logue, Mark
Melville, Scott

PMID: 22745009; PMCID: PMC3405172; DOI: 10.1002/ana.23644;

Showing 10 of 110 results. Show More

Alsultan A, Ngo DA, Farrell JJ, Akinsheye I, Solovieff N, Ghabbour HA, Al-Ali A, Alsuliman A, Al-Baghshi M, Albu-Ali W, Alabdulaali M, Baldwin CT, Farrer LA, Luo H, Melista E, Safaya S, Nwaru M, Chui DH, Steinberg MH. A functional promoter polymorphism of the d-globin gene is a specific marker of the Arab-Indian haplotype. Am J Hematol. 2012 Aug; 87(8):824-6.View Related Profiles.

Baldwin, Clinton
Chui, David
Ngo, Duyen
Farrer, Lindsay
Steinberg, Martin

PMID: 22641479; DOI: 10.1002/ajh.23239;

Kamboh MI, Demirci FY, Wang X, Minster RL, Carrasquillo MM, Pankratz VS, Younkin SG, Saykin AJ, Jun G, Baldwin C, Logue MW, Buros J, Farrer L, Pericak-Vance MA, Haines JL, Sweet RA, Ganguli M, Feingold E, Dekosky ST, Lopez OL, Barmada MM. Genome-wide association study of Alzheimer's disease. Transl Psychiatry. 2012; 2:e117.View Related Profiles.

Baldwin, Clinton
Jun, Gyungah
Farrer, Lindsay
Logue, Mark

PMID: 22832961; PMCID: PMC3365264; DOI: 10.1038/tp.2012.45;

Milton JN, Sebastiani P, Solovieff N, Hartley SW, Bhatnagar P, Arking DE, Dworkis DA, Casella JF, Barron-Casella E, Bean CJ, Hooper WC, DeBaun MR, Garrett ME, Soldano K, Telen MJ, Ashley-Koch A, Gladwin MT, Baldwin CT, Steinberg MH, Klings ES. A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. PLoS One. 2012; 7(4):e34741.View Related Profiles.

Baldwin, Clinton
Klings, Elizabeth
Hicks, Jacqueline
Steinberg, Martin
Sebastiani, Paola

PMID: 22558097; PMCID: PMC3338756; DOI: 10.1371/journal.pone.0034741;

Conneely KN, Capell BC, Erdos MR, Sebastiani P, Solovieff N, Swift AJ, Baldwin CT, Budagov T, Barzilai N, Atzmon G, Puca AA, Perls TT, Geesaman BJ, Boehnke M, Collins FS. Human longevity and common variations in the LMNA gene: a meta-analysis. Aging Cell. 2012 Jun; 11(3):475-81.View Related Profiles.

Baldwin, Clinton
Sebastiani, Paola
Perls, Thomas

PMID: 22340368; PMCID: PMC3350595; DOI: 10.1111/j.1474-9726.2012.00808.x;

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;

Sebastiani P, Riva A, Montano M, Pham P, Torkamani A, Scherba E, Benson G, Milton JN, Baldwin CT, Andersen S, Schork NJ, Steinberg MH, Perls TT. Whole genome sequences of a male and female supercentenarian, ages greater than 114?years. Front Genet. 2011; 2:90.View Related Profiles.

Baldwin, Clinton
Hicks, Jacqueline
Steinberg, Martin
Montano, Monty
Sebastiani, Paola
Andersen, Stacy
Perls, Thomas

PMID: 22303384; PMCID: PMC3262222; DOI: 10.3389/fgene.2011.00090;

Logue MW, Schu M, Vardarajan BN, Buros J, Green RC, Go RC, Griffith P, Obisesan TO, Shatz R, Borenstein A, Cupples LA, Lunetta KL, Fallin MD, Baldwin CT, Farrer LA. A comprehensive genetic association study of Alzheimer disease in African Americans. Arch Neurol. 2011 Dec; 68(12):1569-79.View Related Profiles.

Baldwin, Clinton
Lunetta, Kathryn
Cupples, L
Farrer, Lindsay
Logue, Mark

PMID: 22159054; PMCID: PMC3356921; DOI: 10.1001/archneurol.2011.646;

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;

Alsultan A, Solovieff N, Aleem A, AlGahtani FH, Al-Shehri A, Osman ME, Kurban K, Bahakim H, Al-Momen AK, Baldwin CT, Chui DH, Steinberg MH. Fetal hemoglobin in sickle cell anemia: Saudi patients from the Southwestern province have similar HBB haplotypes but higher HbF levels than African Americans. Am J Hematol. 2011 Jul; 86(7):612-4.View Related Profiles.

Baldwin, Clinton
Chui, David
Steinberg, Martin

PMID: 21630302; DOI: 10.1002/ajh.22032;

Solovieff N, Hartley SW, Baldwin CT, Klings ES, Gladwin MT, Taylor JG, Kato GJ, Farrer LA, Steinberg MH, Sebastiani P. Ancestry of African Americans with sickle cell disease. Blood Cells Mol Dis. 2011 Jun 15; 47(1):41-5.View Related Profiles.

Baldwin, Clinton
Klings, Elizabeth
Farrer, Lindsay
Steinberg, Martin
Sebastiani, Paola

PMID: 21546286; PMCID: PMC3116635; DOI: 10.1016/j.bcmd.2011.04.002;

Akinsheye I, Alsultan A, Solovieff N, Ngo D, Baldwin CT, Sebastiani P, Chui DH, Steinberg MH. Fetal hemoglobin in sickle cell anemia. Blood. 2011 Jul 7; 118(1):19-27.View Related Profiles.

Baldwin, Clinton
Chui, David
Ngo, Duyen
Steinberg, Martin
Sebastiani, Paola

PMID: 21490337; PMCID: PMC3139383; DOI: 10.1182/blood-2011-03-325258;

Naj AC, Jun G, Beecham GW, Wang LS, Vardarajan BN, Buros J, Gallins PJ, Buxbaum JD, Jarvik GP, Crane PK, Larson EB, Bird TD, Boeve BF, Graff-Radford NR, De Jager PL, Evans D, Schneider JA, Carrasquillo MM, Ertekin-Taner N, Younkin SG, Cruchaga C, Kauwe JS, Nowotny P, Kramer P, Hardy J, Huentelman MJ, Myers AJ, Barmada MM, Demirci FY, Baldwin CT, Green RC, Rogaeva E, St George-Hyslop P, Arnold SE, Barber R, Beach T, Bigio EH, Bowen JD, Boxer A, Burke JR, Cairns NJ, Carlson CS, Carney RM, Carroll SL, Chui HC, Clark DG, Corneveaux J, Cotman CW, Cummings JL, DeCarli C, DeKosky ST, Diaz-Arrastia R, Dick M, Dickson DW, Ellis WG, Faber KM, Fallon KB, Farlow MR, Ferris S, Frosch MP, Galasko DR, Ganguli M, Gearing M, Geschwind DH, Ghetti B, Gilbert JR, Gilman S, Giordani B, Glass JD, Growdon JH, Hamilton RL, Harrell LE, Head E, Honig LS, Hulette CM, Hyman BT, Jicha GA, Jin LW, Johnson N, Karlawish J, Karydas A, Kaye JA, Kim R, Koo EH, Kowall NW, Lah JJ, Levey AI, Lieberman AP, Lopez OL, Mack WJ, Marson DC, Martiniuk F, Mash DC, Masliah E, McCormick WC, McCurry SM, McDavid AN, McKee AC, Mesulam M, Miller BL, Miller CA, Miller JW, Parisi JE, Perl DP, Peskind E, Petersen RC, Poon WW, Quinn JF, Rajbhandary RA, Raskind M, Reisberg B, Ringman JM, Roberson ED, Rosenberg RN, Sano M, Schneider LS, Seeley W, Shelanski ML, Slifer MA, Smith CD, Sonnen JA, Spina S, Stern RA, Tanzi RE, Trojanowski JQ, Troncoso JC, Van Deerlin VM, Vinters HV, Vonsattel JP, Weintraub S, Welsh-Bohmer KA, Williamson J, Woltjer RL, Cantwell LB, Dombroski BA, Beekly D, Lunetta KL, Martin ER, Kamboh MI, Saykin AJ, Reiman EM, Bennett DA, Morris JC, Montine TJ, Goate AM, Blacker D, Tsuang DW, Hakonarson H, Kukull WA, Foroud TM, Haines JL, Mayeux R, Pericak-Vance MA, Farrer LA, Schellenberg GD. Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Nat Genet. 2011 May; 43(5):436-41.View Related Profiles.

McKee, Ann
Baldwin, Clinton
Jun, Gyungah
Lunetta, Kathryn
Farrer, Lindsay
Kowall, Neil
Stern, Robert

PMID: 21460841; PMCID: PMC3090745; DOI: 10.1038/ng.801;

Farrell JJ, Sherva RM, Chen ZY, Luo HY, Chu BF, Ha SY, Li CK, Lee AC, Li RC, Li CK, Yuen HL, So JC, Ma ES, Chan LC, Chan V, Sebastiani P, Farrer LA, Baldwin CT, Steinberg MH, Chui DH. A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression. Blood. 2011 May 5; 117(18):4935-45.View Related Profiles.

Baldwin, Clinton
Chui, David
Luo, Hong
Farrer, Lindsay
Steinberg, Martin
Sebastiani, Paola
Sherva, Richard

PMID: 21385855; PMCID: PMC3100700; DOI: 10.1182/blood-2010-11-317081;

Dworkis DA, Klings ES, Solovieff N, Li G, Milton JN, Hartley SW, Melista E, Parente J, Sebastiani P, Steinberg MH, Baldwin CT. Severe sickle cell anemia is associated with increased plasma levels of TNF-R1 and VCAM-1. Am J Hematol. 2011 Feb; 86(2):220-3.View Related Profiles.

Baldwin, Clinton
Klings, Elizabeth
Hicks, Jacqueline
Steinberg, Martin
Sebastiani, Paola

PMID: 21264913; PMCID: PMC3078643; DOI: 10.1002/ajh.21928;

Sherva R, Baldwin CT, Inzelberg R, Vardarajan B, Cupples LA, Lunetta K, Bowirrat A, Naj A, Pericak-Vance M, Friedland RP, Farrer LA. Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data. J Alzheimers Dis. 2011; 23(2):349-59.View Related Profiles.

Baldwin, Clinton
Lunetta, Kathryn
Cupples, L
Farrer, Lindsay
Sherva, Richard

PMID: 21098978; PMCID: PMC3819807; DOI: 10.3233/JAD-2010-100714;

Solovieff N, Hartley SW, Baldwin CT, Perls TT, Steinberg MH, Sebastiani P. Clustering by genetic ancestry using genome-wide SNP data. BMC Genet. 2010; 11:108.View Related Profiles.

Baldwin, Clinton
Steinberg, Martin
Sebastiani, Paola
Perls, Thomas

PMID: 21143920; PMCID: PMC3018397; DOI: 10.1186/1471-2156-11-108;

Erlich PM, Lunetta KL, Cupples LA, Abraham CR, Green RC, Baldwin CT, Farrer LA. Serum paraoxonase activity is associated with variants in the PON gene cluster and risk of Alzheimer disease. Neurobiol Aging. 2012 May; 33(5):1015.e7-23.View Related Profiles.

Abraham, Carmela
Baldwin, Clinton
Lunetta, Kathryn
Cupples, L
Farrer, Lindsay

PMID: 20980077; PMCID: PMC3034817; DOI: 10.1016/j.neurobiolaging.2010.08.003;

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;

Sebastiani P, Solovieff N, Hartley SW, Milton JN, Riva A, Dworkis DA, Melista E, Klings ES, Garrett ME, Telen MJ, Ashley-Koch A, Baldwin CT, Steinberg MH. Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study. Am J Hematol. 2010 Jan; 85(1):29-35.View Related Profiles.

Baldwin, Clinton
Klings, Elizabeth
Hicks, Jacqueline
Steinberg, Martin
Sebastiani, Paola

PMID: 20029952; PMCID: PMC2903007; DOI: 10.1002/ajh.21572;

Solovieff N, Milton JN, Hartley SW, Sherva R, Sebastiani P, Dworkis DA, Klings ES, Farrer LA, Garrett ME, Ashley-Koch A, Telen MJ, Fucharoen S, Ha SY, Li CK, Chui DH, Baldwin CT, Steinberg MH. Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster. Blood. 2010 Mar 4; 115(9):1815-22.View Related Profiles.

Baldwin, Clinton
Chui, David
Klings, Elizabeth
Hicks, Jacqueline
Farrer, Lindsay
Steinberg, Martin
Sebastiani, Paola
Sherva, Richard

PMID: 20018918; PMCID: PMC2832816; DOI: 10.1182/blood-2009-08-239517;

Sebastiani P, Montano M, Puca A, Solovieff N, Kojima T, Wang MC, Melista E, Meltzer M, Fischer SE, Andersen S, Hartley SH, Sedgewick A, Arai Y, Bergman A, Barzilai N, Terry DF, Riva A, Anselmi CV, Malovini A, Kitamoto A, Sawabe M, Arai T, Gondo Y, Steinberg MH, Hirose N, Atzmon G, Ruvkun G, Baldwin CT, Perls TT. RNA editing genes associated with extreme old age in humans and with lifespan in C. elegans. PLoS One. 2009; 4(12):e8210.View Related Profiles.

Baldwin, Clinton
Terry, Dellara
Steinberg, Martin
Montano, Monty
Sebastiani, Paola
Andersen, Stacy
Perls, Thomas

PMID: 20011587; PMCID: PMC2788130; DOI: 10.1371/journal.pone.0008210;

Cuenco KT, Friedland R, Baldwin CT, Guo J, Vardarajan B, Lunetta KL, Cupples LA, Green RC, DeCarli C, Farrer LA. Association of TTR polymorphisms with hippocampal atrophy in Alzheimer disease families. Neurobiol Aging. 2011 Feb; 32(2):249-56.View Related Profiles.

Baldwin, Clinton
Lunetta, Kathryn
Cupples, L
Farrer, Lindsay

PMID: 19328595; PMCID: PMC2930090; DOI: 10.1016/j.neurobiolaging.2009.02.014;

Zhao Z, Timofeev N, Hartley SW, Chui DH, Fucharoen S, Perls TT, Steinberg MH, Baldwin CT, Sebastiani P. Imputation of missing genotypes: an empirical evaluation of IMPUTE. BMC Genet. 2008; 9:85.View Related Profiles.

Baldwin, Clinton
Chui, David
Steinberg, Martin
Sebastiani, Paola
Perls, Thomas

PMID: 19077279; PMCID: PMC2636842; DOI: 10.1186/1471-2156-9-85;

T Cuenco K, Lunetta KL, Baldwin CT, McKee AC, Guo J, Cupples LA, Green RC, St George-Hyslop PH, Chui H, DeCarli C, Farrer LA. Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease. Arch Neurol. 2008 Dec; 65(12):1640-8.View Related Profiles.

McKee, Ann
Baldwin, Clinton
Lunetta, Kathryn
Cupples, L
Farrer, Lindsay

PMID: 19064752; PMCID: PMC2719762; DOI: 10.1001/archneur.65.12.1640;

Sedgewick AE, Timofeev N, Sebastiani P, So JC, Ma ES, Chan LC, Fucharoen G, Fucharoen S, Barbosa CG, Vardarajan BN, Farrer LA, Baldwin CT, Steinberg MH, Chui DH. BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies. Blood Cells Mol Dis. 2008 Nov-Dec; 41(3):255-8.View Related Profiles.

Baldwin, Clinton
Chui, David
Farrer, Lindsay
Steinberg, Martin
Sebastiani, Paola

PMID: 18691915; PMCID: PMC4100606; DOI: 10.1016/j.bcmd.2008.06.007;

Sebastiani P, Wang L, Nolan VG, Melista E, Ma Q, Baldwin CT, Steinberg MH. Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations. Am J Hematol. 2008 Mar; 83(3):189-95.View Related Profiles.

Baldwin, Clinton
Steinberg, Martin
Sebastiani, Paola

PMID: 17918249

Sebastiani P, Zhao Z, Abad-Grau MM, Riva A, Hartley SW, Sedgewick AE, Doria A, Montano M, Melista E, Terry D, Perls TT, Steinberg MH, Baldwin CT. A hierarchical and modular approach to the discovery of robust associations in genome-wide association studies from pooled DNA samples. BMC Genet. 2008; 9:6.View Related Profiles.

Baldwin, Clinton
Terry, Dellara
Steinberg, Martin
Montano, Monty
Sebastiani, Paola
Perls, Thomas

PMID: 18194558; PMCID: PMC2248205; DOI: 10.1186/1471-2156-9-6;

Lee DS, Larson MG, Lunetta KL, Dupuis J, Rong J, Keaney JF, Lipinska I, Baldwin CT, Vasan RS, Benjamin EJ. Clinical and genetic correlates of soluble P-selectin in the community. J Thromb Haemost. 2008 Jan; 6(1):20-31.View Related Profiles.

Baldwin, Clinton
Benjamin, Emelia
Dupuis, Josee
Lunetta, Kathryn
Larson, Martin
Ramachandran, Vasan

PMID: 17944986

Sebastiani P, Nolan VG, Baldwin CT, Abad-Grau MM, Wang L, Adewoye AH, McMahon LC, Farrer LA, Taylor JG, Kato GJ, Gladwin MT, Steinberg MH. A network model to predict the risk of death in sickle cell disease. Blood. 2007 Oct 1; 110(7):2727-35.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay
Steinberg, Martin
Sebastiani, Paola

PMID: 17600133; PMCID: PMC1988954; DOI: 10.1182/blood-2007-04-084921;

Nolan VG, Ma Q, Cohen HT, Adewoye A, Rybicki AC, Baldwin C, Mahabir RN, Homan EP, Wyszynski DF, Fabry ME, Nagel RL, Farrer LA, Steinberg MH. Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B. Am J Hematol. 2007 Mar; 82(3):179-84.View Related Profiles.

Baldwin, Clinton
Cohen, Herbert
Farrer, Lindsay
Steinberg, Martin

PMID: 17034027

Ma Q, Wyszynski DF, Farrell JJ, Kutlar A, Farrer LA, Baldwin CT, Steinberg MH. Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea. Pharmacogenomics J. 2007 Dec; 7(6):386-94.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay
Steinberg, Martin

PMID: 17299377

Rogaeva E, Meng Y, Lee JH, Gu Y, Kawarai T, Zou F, Katayama T, Baldwin CT, Cheng R, Hasegawa H, Chen F, Shibata N, Lunetta KL, Pardossi-Piquard R, Bohm C, Wakutani Y, Cupples LA, Cuenco KT, Green RC, Pinessi L, Rainero I, Sorbi S, Bruni A, Duara R, Friedland RP, Inzelberg R, Hampe W, Bujo H, Song YQ, Andersen OM, Willnow TE, Graff-Radford N, Petersen RC, Dickson D, Der SD, Fraser PE, Schmitt-Ulms G, Younkin S, Mayeux R, Farrer LA, St George-Hyslop P. The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease. Nat Genet. 2007 Feb; 39(2):168-77.View Related Profiles.

Baldwin, Clinton
Lunetta, Kathryn
Cupples, L
Farrer, Lindsay

PMID: 17220890; PMCID: PMC2657343; DOI: 10.1038/ng1943;

Terry DF, Wyszynski DF, Nolan VG, Atzmon G, Schoenhofen EA, Pennington JY, Andersen SL, Wilcox MA, Farrer LA, Barzilai N, Baldwin CT, Asea A. Serum heat shock protein 70 level as a biomarker of exceptional longevity. Mech Ageing Dev. 2006 Nov; 127(11):862-8.View Related Profiles.

Baldwin, Clinton
Terry, Dellara
Farrer, Lindsay
Andersen, Stacy

PMID: 17027907; PMCID: PMC1781061; DOI: 10.1016/j.mad.2006.08.007;

Adewoye AH, Nolan VG, Ma Q, Baldwin C, Wyszynski DF, Farrell JJ, Farrer LA, Steinberg MH. Association of polymorphisms of IGF1R and genes in the transforming growth factor- beta /bone morphogenetic protein pathway with bacteremia in sickle cell anemia. Clin Infect Dis. 2006 Sep 1; 43(5):593-8.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay
Steinberg, Martin

PMID: 16886151

Akomolafe A, Lunetta KL, Erlich PM, Cupples LA, Baldwin CT, Huyck M, Green RC, Farrer LA. Genetic association between endothelial nitric oxide synthase and Alzheimer disease. Clin Genet. 2006 Jul; 70(1):49-56.View Related Profiles.

Baldwin, Clinton
Lunetta, Kathryn
Farrer, Lindsay

PMID: 16813604

Nolan VG, Adewoye A, Baldwin C, Wang L, Ma Q, Wyszynski DF, Farrell JJ, Sebastiani P, Farrer LA, Steinberg MH. Sickle cell leg ulcers: associations with haemolysis and SNPs in Klotho, TEK and genes of the TGF-beta/BMP pathway. Br J Haematol. 2006 Jun; 133(5):570-8.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay
Steinberg, Martin
Sebastiani, Paola

PMID: 16681647; PMCID: PMC1679888; DOI: 10.1111/j.1365-2141.2006.06074.x;

Meng Y, Baldwin CT, Bowirrat A, Waraska K, Inzelberg R, Friedland RP, Farrer LA. Association of polymorphisms in the Angiotensin-converting enzyme gene with Alzheimer disease in an Israeli Arab community. Am J Hum Genet. 2006 May; 78(5):871-7.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay

PMID: 16642441; PMCID: PMC1474030; DOI: 10.1086/503687;

Koenen KC, Saxe G, Purcell S, Smoller JW, Bartholomew D, Miller A, Hall E, Kaplow J, Bosquet M, Moulton S, Baldwin C. Polymorphisms in FKBP5 are associated with peritraumatic dissociation in medically injured children. Mol Psychiatry. 2005 Dec; 10(12):1058-9. PMID: 16088328

Erlich PM, Lunetta KL, Cupples LA, Huyck M, Green RC, Baldwin CT, Farrer LA. Polymorphisms in the PON gene cluster are associated with Alzheimer disease. Hum Mol Genet. 2006 Jan 1; 15(1):77-85.View Related Profiles.

Baldwin, Clinton
Lunetta, Kathryn
Cupples, L
Farrer, Lindsay

PMID: 16319130

Faraone SV, Skol AD, Tsuang DW, Young KA, Haverstock SL, Prabhudesai S, Mena F, Menon AS, Leong L, Sautter F, Baldwin C, Bingham S, Weiss D, Collins J, Keith T, Vanden Eng JL, Boehnke M, Tsuang MT, Schellenberg GD. Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14. Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5; 139B(1):91-100. PMID: 16152571

Russo CJ, Melista E, Cui J, DeStefano AL, Bakris GL, Manolis AJ, Gavras H, Baldwin CT. Association of NEDD4L ubiquitin ligase with essential hypertension. Hypertension. 2005 Sep; 46(3):488-91.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Gavras, Haralambos

PMID: 16103266

Baldwin C, Nolan VG, Wyszynski DF, Ma QL, Sebastiani P, Embury SH, Bisbee A, Farrell J, Farrer L, Steinberg MH. Association of klotho, bone morphogenic protein 6, and annexin A2 polymorphisms with sickle cell osteonecrosis. Blood. 2005 Jul 1; 106(1):372-5.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay
Steinberg, Martin
Sebastiani, Paola

PMID: 15784727; PMCID: PMC1895132; DOI: 10.1182/blood-2005-02-0548;

Sebastiani P, Ramoni MF, Nolan V, Baldwin CT, Steinberg MH. Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia. Nat Genet. 2005 Apr; 37(4):435-40.View Related Profiles.

Baldwin, Clinton
Steinberg, Martin
Sebastiani, Paola

PMID: 15778708; PMCID: PMC2896308; DOI: 10.1038/ng1533;

Bowirrat A, Cui J, Waraska K, Friedland RP, Oscar-Berman M, Farrer LA, Korczyn A, Baldwin CT. Lack of association between angiotensin-converting enzyme and dementia of the Alzheimer's type in an elderly Arab population in Wadi Ara, Israel. Neuropsychiatr Dis Treat. 2005 Mar; 1(1):73-6.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay
Berman, Marlene

PMID: 18568123; PMCID: PMC2426814; DOI: 10.2147/nedt.1.1.73.52302;

Zhou XF, Cui J, DeStefano AL, Chazaro I, Farrer LA, Manolis AJ, Gavras H, Baldwin CT. Polymorphisms in the promoter region of catalase gene and essential hypertension. Dis Markers. 2005; 21(1):3-7.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Gavras, Haralambos
Farrer, Lindsay

PMID: 15735318; PMCID: PMC3851957; DOI: 10.1155/2005/487014;

Cui J, Melista E, Chazaro I, Zhang Y, Zhou X, Manolis AJ, Baldwin CT, Destefano AL, Gavras H. Sequence variation of bradykinin receptors B1 and B2 and association with hypertension. J Hypertens. 2005 Jan; 23(1):55-62.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Gavras, Haralambos

PMID: 15643125

Nolan VG, Baldwin C, Ma Q, Wyszynski DF, Amirault Y, Farrell JJ, Bisbee A, Embury SH, Farrer LA, Steinberg MH. Association of single nucleotide polymorphisms in klotho with priapism in sickle cell anaemia. Br J Haematol. 2005 Jan; 128(2):266-72.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay
Steinberg, Martin

PMID: 15638863

Saleh M, Vaillancourt JP, Graham RK, Huyck M, Srinivasula SM, Alnemri ES, Steinberg MH, Nolan V, Baldwin CT, Hotchkiss RS, Buchman TG, Zehnbauer BA, Hayden MR, Farrer LA, Roy S, Nicholson DW. Differential modulation of endotoxin responsiveness by human caspase-12 polymorphisms. Nature. 2004 May 6; 429(6987):75-9.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay
Steinberg, Martin

PMID: 15129283

Wyszynski DF, Baldwin CT, Cleves MA, Amirault Y, Nolan VG, Farrell JJ, Bisbee A, Kutlar A, Farrer LA, Steinberg MH. Polymorphisms near a chromosome 6q QTL area are associated with modulation of fetal hemoglobin levels in sickle cell anemia. Cell Mol Biol (Noisy-le-grand). 2004 Feb; 50(1):23-33.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay
Steinberg, Martin

PMID: 15040424

Cui J, Zhou X, Chazaro I, DeStefano AL, Manolis AJ, Baldwin CT, Gavras H. Association of polymorphisms in the promoter region of the PNMT gene with essential hypertension in African Americans but not in whites. Am J Hypertens. 2003 Oct; 16(10):859-63.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Gavras, Haralambos

PMID: 14553966

Nguyen GH, Bouchard J, Boselli MG, Tolstoi LG, Keith L, Baldwin C, Nguyen NC, Schultz M, Herrera VL, Smith CL. DNA stability and schizophrenia in twins. Am J Med Genet B Neuropsychiatr Genet. 2003 Jul 1; 120B(1):1-10.View Related Profiles.

Baldwin, Clinton
Herrera, Victoria

PMID: 12815731

Erlich PM, Cui J, Chazaro I, Farrer LA, Baldwin CT, Gavras H, DeStefano AL. Genetic variants of WNK4 in whites and African Americans with hypertension. Hypertension. 2003 Jun; 41(6):1191-5.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Gavras, Haralambos
Farrer, Lindsay

PMID: 12719438

Skol AD, Young KA, Tsuang DW, Faraone SV, Haverstock SL, Bingham S, Prabhudesai S, Mena F, Menon AS, Yu CE, Rundell P, Pepple J, Sauter F, Baldwin C, Weiss D, Collins J, Keith T, Boehnke M, Schellenberg GD, Tsuang MT. Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large Veterans Affairs Cooperative Study sample. Am J Med Genet B Neuropsychiatr Genet. 2003 Apr 1; 118B(1):8-15. PMID: 12627457

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

Farrer LA, Bowirrat A, Friedland RP, Waraska K, Korczyn AD, Baldwin CT. Identification of multiple loci for Alzheimer disease in a consanguineous Israeli-Arab community. Hum Mol Genet. 2003 Feb 15; 12(4):415-22.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay

PMID: 12566388

Farrer LA, Friedland RP, Bowirrat A, Waraska K, Korczyn A, Baldwin CT. Genetic and environmental epidemiology of Alzheimer's disease in arabs residing in Israel. J Mol Neurosci. 2003; 20(3):207-12.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay

PMID: 14500999

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

Bowirrat A, Friedland RP, Farrer L, Baldwin C, Korczyn A. Genetic and environmental risk factors for Alzheimer's disease in Israeli Arabs. J Mol Neurosci. 2002 Aug-Oct; 19(1-2):239-45.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay

PMID: 12212789

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

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

Tsuang DW, Skol AD, Faraone SV, Bingham S, Young KA, Prabhudesai S, Haverstock SL, Mena F, Menon AS, Bisset D, Pepple J, Sauter F, Baldwin C, Weiss D, Collins J, Boehnke M, Schellenberg GD, Tsuang MT. Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample. Am J Med Genet. 2001 Dec 8; 105(8):662-8. PMID: 11803512

Merchant SN, McKenna MJ, Baldwin CT, Milunsky A, Nadol JB. Otopathology in a case of type I Waardenburg's syndrome. Ann Otol Rhinol Laryngol. 2001 Sep; 110(9):875-82.View Related Profiles.

Milunsky, Aubrey
Baldwin, Clinton

PMID: 11558766

DeStefano AL, Gavras H, Heard-Costa N, Bursztyn M, Manolis A, Farrer LA, Baldwin CT, Gavras I, Schwartz F. Maternal component in the familial aggregation of hypertension. Clin Genet. 2001 Jul; 60(1):13-21.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Gavras, Haralambos
Gavras, Irene
Farrer, Lindsay
Heard-Costa, Nancy

PMID: 11531965

Tsuang MT, Faraone SV, Bingham S, Young K, Prabhudesai S, Haverstock SL, Mena F, Menon AS, Pepple J, Johnson J, Baldwin C, Weiss D, Collins J. Department of Veterans Affairs Cooperative Studies Program genetic linkage study of schizophrenia: ascertainment methods and sample description. Am J Med Genet. 2000 Jun 12; 96(3):342-7. PMID: 10898912

Nicolaou M, DeStefano AL, Gavras I, Cupples LA, Manolis AJ, Baldwin CT, Gavras H, Farrer LA. Genetic predisposition to stroke in relatives of hypertensives. Stroke. 2000 Feb; 31(2):487-92.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Gavras, Haralambos
Gavras, Irene
Cupples, L
Farrer, Lindsay

PMID: 10657427

Schwartz F, Baldwin CT, Baima J, Gavras H. Mitochondrial DNA mutations in patients with orthostatic hypotension. Am J Med Genet. 1999 Sep 10; 86(2):145-50.View Related Profiles.

Baldwin, Clinton
Gavras, Haralambos

PMID: 10449650

Baldwin CT, Schwartz F, Baima J, Burzstyn M, DeStefano AL, Gavras I, Handy DE, Joost O, Martel T, Manolis A, Nicolaou M, Bresnahan M, Farrer L, Gavras H. Identification of a polymorphic glutamic acid stretch in the alpha2B-adrenergic receptor and lack of linkage with essential hypertension. Am J Hypertens. 1999 Sep; 12(9 Pt 1):853-7.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Gavras, Haralambos
Gavras, Irene
Farrer, Lindsay

PMID: 10509541

Milunsky A, Huang XL, Milunsky J, DeStefano A, Baldwin CT. A locus for autosomal recessive achromatopsia on human chromosome 8q. Clin Genet. 1999 Jul; 56(1):82-5.View Related Profiles.

DeStefano, Anita
Milunsky, Aubrey
Baldwin, Clinton

PMID: 10466422

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

Baima J, Nicolaou M, Schwartz F, DeStefano AL, Manolis A, Gavras I, Laffer C, Elijovich F, Farrer L, Baldwin CT, Gavras H. Evidence for linkage between essential hypertension and a putative locus on human chromosome 17. Hypertension. 1999 Jul; 34(1):4-7.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Gavras, Haralambos
Gavras, Irene
Farrer, Lindsay

PMID: 10406815

DeStefano AL, Baldwin CT, Burzstyn M, Gavras I, Handy DE, Joost O, Martel T, Nicolaou M, Schwartz F, Streeten DH, Farrer LA, Gavras H. Autosomal dominant orthostatic hypotensive disorder maps to chromosome 18q. Am J Hum Genet. 1998 Nov; 63(5):1425-30.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Gavras, Haralambos
Gavras, Irene
Farrer, Lindsay

PMID: 9792870; PMCID: PMC1377553

Milunsky J, Huang XL, Baldwin CT, Farah MG, Milunsky A. Evidence for genetic heterogeneity of the Carney complex (familial atrial myxoma syndromes). Cancer Genet Cytogenet. 1998 Oct 15; 106(2):173-6.View Related Profiles.

Milunsky, Aubrey
Baldwin, Clinton

PMID: 9797786

DeStefano AL, Cupples LA, Arnos KS, Asher JH, Baldwin CT, Blanton S, Carey ML, da Silva EO, Friedman TB, Greenberg J, Lalwani AK, Milunsky A, Nance WE, Pandya A, Ramesar RS, Read AP, Tassabejhi M, Wilcox ER, Farrer LA. Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations. Hum Genet. 1998 May; 102(5):499-506.View Related Profiles.

DeStefano, Anita
Milunsky, Aubrey
Baldwin, Clinton
Cupples, L
Farrer, Lindsay

PMID: 9654197

Milunsky J, DeStefano AL, Huang XL, Baldwin CT, Michels VV, Jako G, Milunsky A. Familial paragangliomas: linkage to chromosome 11q23 and clinical implications. Am J Med Genet. 1997 Oct 3; 72(1):66-70.View Related Profiles.

DeStefano, Anita
Milunsky, Aubrey
Baldwin, Clinton

PMID: 9295078

Bjarnason I, Sharpstone DR, Francis N, Marker A, Taylor C, Barrett M, Macpherson A, Baldwin C, Menzies IS, Crane RC, Smith T, Pozniak A, Gazzard BG. Intestinal inflammation, ileal structure and function in HIV. AIDS. 1996 Oct; 10(12):1385-91. PMID: 8902068

Lautenschlager NT, Milunsky A, DeStefano A, Farrer L, Baldwin CT. A novel mutation in the MITF gene causes Waardenburg syndrome type 2. Genet Anal. 1996 Jul; 13(2):43-4.View Related Profiles.

DeStefano, Anita
Milunsky, Aubrey
Baldwin, Clinton
Farrer, Lindsay

PMID: 8880147

Bonné-Tamir B, DeStefano AL, Briggs CE, Adair R, Franklyn B, Weiss S, Korostishevsky M, Frydman M, Baldwin CT, Farrer LA. Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3. Am J Hum Genet. 1996 Jun; 58(6):1254-9.View Related Profiles.

DeStefano, Anita
Baldwin, Clinton
Farrer, Lindsay

PMID: 8651303; PMCID: PMC1915077

Baldwin CT, Weiss S, Farrer LA, De Stefano AL, Adair R, Franklyn B, Kidd KK, Korostishevsky M, Bonné-Tamir B. Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population. Hum Mol Genet. 1995 Sep; 4(9):1637-42.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay

PMID: 8541853

Baldwin CT, Hoth CF, Macina RA, Milunsky A. Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature. Am J Med Genet. 1995 Aug 28; 58(2):115-22.View Related Profiles.

Milunsky, Aubrey
Baldwin, Clinton

PMID: 8533800

Van Camp G, Van Thienen MN, Handig I, Van Roy B, Rao VS, Milunsky A, Read AP, Baldwin CT, Farrer LA, Bonduelle M, et al. Chromosome 13q deletion with Waardenburg syndrome: further evidence for a gene involved in neural crest function on 13q. J Med Genet. 1995 Jul; 32(7):531-6.View Related Profiles.

Milunsky, Aubrey
Baldwin, Clinton
Farrer, Lindsay

PMID: 7562965; PMCID: PMC1050545

Baldwin CT, Farrer LA, Adair R, Dharmavaram R, Jimenez S, Anderson L. Linkage of early-onset osteoarthritis and chondrocalcinosis to human chromosome 8q. Am J Hum Genet. 1995 Mar; 56(3):692-7.View Related Profiles.

Baldwin, Clinton
Farrer, Lindsay

PMID: 7887424; PMCID: PMC1801178

Farrer LA, Arnos KS, Asher JH, Baldwin CT, Diehl SR, Friedman TB, Greenberg J, Grundfast KM, Hoth C, Lalwani AK, et al. Locus heterogeneity for Waardenburg syndrome is predictive of clinical subtypes. Am J Hum Genet. 1994 Oct; 55(4):728-37.View Related Profiles.

Milunsky, Aubrey
Baldwin, Clinton
Grundfast, Kenneth
Farrer, Lindsay

PMID: 7942851; PMCID: PMC1918288

Baldwin CT, Lipsky NR, Hoth CF, Cohen T, Mamuya W, Milunsky A. Mutations in PAX3 associated with Waardenburg syndrome type I. Hum Mutat. 1994; 3(3):205-11.View Related Profiles.

Milunsky, Aubrey
Baldwin, Clinton

PMID: 8019556

Dharmavaram RM, Baldwin CT, Reginato AM, Jimenez SA. Amplification of cDNAs for human cartilage-specific types II, IX and XI collagens from chondrocytes and Epstein-Barr virus-transformed lymphocytes. Matrix. 1993 Mar; 13(2):125-33. PMID: 8388073

Hoth CF, Milunsky A, Lipsky N, Sheffer R, Clarren SK, Baldwin CT. Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I). Am J Hum Genet. 1993 Mar; 52(3):455-62.View Related Profiles.

Milunsky, Aubrey
Baldwin, Clinton

PMID: 8447316; PMCID: PMC1682157

Wu BL, Milunsky A, Wyandt H, Hoth C, Baldwin C, Skare J. In situ hybridization applied to Waardenburg syndrome. Cytogenet Cell Genet. 1993; 63(1):29-32.View Related Profiles.

Milunsky, Aubrey
Baldwin, Clinton

PMID: 8449034

Strobel D, Tsuneyoshi T, Kuivaniemi H, Tromp G, Spotila LD, Baldwin CT, Constantinou CD, Ganguly A, Sereda L, Sokolov BP, et al. Three new polymorphisms at the COL1A2 locus. Matrix. 1992 Apr; 12(2):87-91. PMID: 1603040

Baldwin CT, Hoth CF, Amos JA, da-Silva EO, Milunsky A. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Nature. 1992 Feb 13; 355(6361):637-8.View Related Profiles.

Milunsky, Aubrey
Baldwin, Clinton

PMID: 1347149

Williams CJ, Harrison DA, Hopkinson I, Baldwin CT, Ahmad NN, Ala-Kokko L, Korn RM, Buxton PG, Dimascio J, Considine EL, et al. Detection of sequence variants in the gene for human type II procollagen (COL2A1) by direct sequencing of polymerase chain reaction-amplified genomic DNA. Hum Mutat. 1992; 1(5):403-16. PMID: 1301950

Ganguly A, Baldwin CT, Strobel D, Conway D, Horton W, Prockop DJ. Heterozygous mutation in the G+5 position of intron 33 of the pro-alpha 2(I) gene (COL1A2) that causes aberrant RNA splicing and lethal osteogenesis imperfecta. Use of carbodiimide methods that decrease the extent of DNA sequencing necessary to define an unusual mutation. J Biol Chem. 1991 Jun 25; 266(18):12035-40. PMID: 1711048

Ala-Kokko L, Baldwin CT, Moskowitz RW, Prockop DJ. Single base mutation in the type II procollagen gene (COL2A1) as a cause of primary osteoarthritis associated with a mild chondrodysplasia. Proc Natl Acad Sci U S A. 1990 Sep; 87(17):6565-8. PMID: 1975693; PMCID: PMC54577

Prockop DJ, Baldwin CT, Constantinou CD. Mutations in type I procollagen genes that cause osteogenesis imperfecta. Adv Hum Genet. 1990; 19:105-32. PMID: 2193488

Baldwin CT, Silbert JE, Humphries DE, Cogburn JN, Smith BD. Increased proteoglycan synthesis following the differentiation of F9 embryonal carcinoma cells: formation of a differentiation-specific proteoheparan sulfate. Matrix. 1989 Nov; 9(5):389-96.View Related Profiles.

Smith, Barbara
Baldwin, Clinton

PMID: 2615695

Baldwin CT, Reginato AM, Prockop DJ. A new epidermal growth factor-like domain in the human core protein for the large cartilage-specific proteoglycan. Evidence for alternative splicing of the domain. J Biol Chem. 1989 Sep 25; 264(27):15747-50. PMID: 2789216

Baldwin CT, Reginato AM, Smith C, Jimenez SA, Prockop DJ. Structure of cDNA clones coding for human type II procollagen. The alpha 1(II) chain is more similar to the alpha 1(I) chain than two other alpha chains of fibrillar collagens. Biochem J. 1989 Sep 1; 262(2):521-8. PMID: 2803268; PMCID: PMC1133299

Ala-Kokko L, Kontusaari S, Baldwin CT, Kuivaniemi H, Prockop DJ. Structure of cDNA clones coding for the entire prepro alpha 1 (III) chain of human type III procollagen. Differences in protein structure from type I procollagen and conservation of codon preferences. Biochem J. 1989 Jun 1; 260(2):509-16. PMID: 2764886; PMCID: PMC1138697

Baldwin CT, Constantinou CD, Dumars KW, Prockop DJ. A single base mutation that converts glycine 907 of the alpha 2(I) chain of type I procollagen to aspartate in a lethal variant of osteogenesis imperfecta. The single amino acid substitution near the carboxyl terminus destabilizes the whole triple helix. J Biol Chem. 1989 Feb 15; 264(5):3002-6. PMID: 2914942

Fazio MJ, Olsen DR, Kauh EA, Baldwin CT, Indik Z, Ornstein-Goldstein N, Yeh H, Rosenbloom J, Uitto J. Cloning of full-length elastin cDNAs from a human skin fibroblast recombinant cDNA library: further elucidation of alternative splicing utilizing exon-specific oligonucleotides. J Invest Dermatol. 1988 Nov; 91(5):458-64. PMID: 3171221

Smith BD, Baldwin CT. Undifferentiated F9 embryonal carcinoma cells produce a short-chain collagen molecule. Biochem J. 1988 Oct 1; 255(1):85-9.View Related Profiles.

Smith, Barbara
Baldwin, Clinton

PMID: 2848513; PMCID: PMC1135193

Tromp G, Kuivaniemi H, Stacey A, Shikata H, Baldwin CT, Jaenisch R, Prockop DJ. Structure of a full-length cDNA clone for the prepro alpha 1(I) chain of human type I procollagen. Biochem J. 1988 Aug 1; 253(3):919-22. PMID: 3178743; PMCID: PMC1149391

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