L. Adrienne Cupples, PhD
Professor
Boston University School of Public Health
Dept of Biostatistics

PhD, Boston University
MA, Boston University




L. Adrienne Cupples, Ph.D. is Professor of Biostatistics and of Epidemiology. She has a long standing interest in statistical methods for epidemiologic studies, for survival data analysis and for genetic epidemiology. She has taught for thirty years at both the introductory and advanced levels. She developed several of the courses in the Biostatistics curriculum, including Statistical Methods for Epidemiology (BS852) and has received numerous teaching awards, including the Norman A Scotch Award for Excellence in Teaching at the School of Public Health. For her efforts in research she received the BUSPH Faculty Career Award in Research & Scholarship as the First Recipient. And she received the Janet L. Norwood Award for Outstanding Achievement by a Woman in the Statistical Sciences as the ninth recipient in 2010 and the 2012 L. Adrienne Cupples Award for Excellence in Teaching, Research and Service in Biostatistics. In 2014 she received the AHA Richard Remington Lecturer and in 2017 she received the International Genetic Epidemiology Society Leadership Award. She has collaborated in the Framingham Heart Study for more than 30 years on a variety of topics from risk factors for sudden death, nutritional epidemiology and most recently the genetic etiology of cardiovascular disease and its risk factors. She has served as Co-Principal Investigator of the NHLBI Contract to Boston University for the Framingham Heart Study and Co-Chair of the Framingham Genetics Steering Committee. She also has a long history with the study of the genetic etiology of Alzheimer’s disease in the MIRAGE Study (Multi-Institutional Research of Alzheimer’s Genetic Epidemiology) and of Huntington disease. She has been actively involved in genetic risk prediction and evaluation of how people interpret and respond to such predictions, particularly in the context of Alzheimer's disease through the REVEAL (Risk Evaluation and Education for Alzheimer's Disease) Study. She has directly mentored 15 students on their doctoral research and has served on many thesis committees.

Professor
Boston University School of Public Health
Epidemiology


Investigator
Framingham Heart Study


Boston Medical Center


Member
Boston University
Genome Science Institute



2017 International Genetic Epidemiology Society : International Genetic Epidemiology Society Leadership Award
2014 American Heart Association: EPI/NPAM 2014 Richard Remington Lecturer
2012 Boston University, Department of Biostatistics, School of Public Health: L. Adrienne Cupples Award for Excellence in Teaching, Research, and Service in Biostatistics
2010 Boston University School of Public Health: Faculty Career Award in Research & Scholarship, First Recipient
2010 University of Alabama: Janet L. Norwood Award for Outstanding Achievement by a Woman in the Statistical Sciences, 9th award
2007 National U of Singapore: Visiting Professor
2006 University of Leeds, UK: Visiting Professor
1995 Boston University School of Public Health: Norman Scotch Award for Excellence in Teaching


Impact of Disclosing Amyloid Imaging Results to Cognitively Normal Individuals(REVEAL 5)
08/20/2015 - 05/31/2020 (Subcontract PI)
The Brigham and Women's Hospital, Inc. NIH NIA
3RF1AG047866-01A1S4

Mechanism and Clinical Importance of Hyperkyphosis: The Framingham Study
09/30/2011 - 05/31/2017 (Subcontract PI)
Hebrew Rehabilitation Center For Aged, Inc. NIH NIA
5R01AG041658-04

DCC Supplement for Rare Variants and NHLBI Traits
04/01/2015 - 03/31/2017 (Subcontract PI)
University of Washington NIH NHLBI
5R01HL120393-03

Whole Genome Sequence Imputation in Families for Echocardiographic Traits
09/20/2013 - 07/31/2016 (PI)
NIH/National Heart, Lung, and Blood Institute
5R21HL121589-02

Rare Variants and NHLBI Traits in Deeply Phenotyped Cohorts
04/01/2015 - 03/31/2016 (Subcontract PI)
University of Washington NIH NHLBI
5R01HL120393-02

A Multi-Ethnic Study of Gene-Lifestyle Interactions in Cardiovascular Traits
01/01/2015 - 12/31/2015 (Subcontract PI)
The Washington University NIH NHLBI
5R01HL118305-02

Interdisciplinary Training for Biostatisticians
07/01/2010 - 06/30/2015 (PI of Sub-Project / SP)
PI: Paola Sebastiani, PhD
NIH/National Institute of General Medical Sciences
5T32GM074905-10

The Role of Eicosanoids in Renal Function Project 5: Human Hypertension and P450 Omega/Omega-1 Hydroxylases and Epoxygenases
07/01/2009 - 06/30/2015 (Subcontract PI)
Vanderbilt University NIH NIDDK
3P01DK038226-27S1

Rare Variants and NHLBI Traits in Deeply Phenotyped Cohorts
04/01/2014 - 03/31/2015 (Subcontract PI)
University of Washington NIH NHLBI
1R01HL120393-01A1

A Multi-Ethnic Study of Gene-Lifestyle Interactions in Cardiovascular Traits
01/15/2014 - 12/31/2014 (Subcontract PI)
The Washington University NIH NHLBI
1R01HL118305-01A1

Showing 10 of 30 results. Show All Results


Title


Yr Title Project-Sub Proj Pubs
2015 Genetic Architecture of Adiposity in Multiple Large Cohorts 5R01DK089256-06 72
2014 Whole Genome Sequence Imputation in Families for Echocardioagraphic Traits 5R21HL121589-02 1
2014 Genetic Architecture of Adiposity in Multiple Large Cohorts 2R01DK089256-05 72
2013 Whole Genome Sequence Imputation in Families for Echocardioagraphic Traits 1R21HL121589-01 1
2013 Genetic Architecture of Adiposity in Multiple Large Cohorts 5R01DK089256-04 72
2012 Genetic Architecture of Adiposity in Multiple Large Cohorts 5R01DK089256-03 72
2011 Genetic Architecture of Adiposity in Multiple Large Cohorts 5R01DK089256-02 72
2011 Interdisciplinary Training for Biostatisticians 5T32GM074905-07 104
2010 Genetic Architecture of Adiposity in Multiple Large Cohorts 1R01DK089256-01 72
2010 Interdisciplinary Training for Biostatisticians 2T32GM074905-06 104
Showing 10 of 16 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.

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  1. Fisher V, Sebastiani P, Cupples LA, Liu CT. ANNORE: Genetic fine mapping with functional annotation. Hum Mol Genet. 2021 Jul 24.View Related Profiles. PMID: 34302344
     
  2. Sarnowski C, Chen H, Biggs ML, Wassertheil-Smoller S, Bressler J, Irvin MR, Ryan KA, Karasik D, Arnett DK, Cupples LA, Fardo DW, Gogarten SM, Heavner BD, Jain D, Kang HM, Kooperberg C, Mainous AG, Mitchell BD, Morrison AC, O'Connell JR, Psaty BM, Rice K, Smith AV, Vasan RS, Windham BG, Kiel DP, Murabito JM, Lunetta KL. Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. PLoS One. 2021; 16(7):e0253611.View Related Profiles. PMID: 34214102; PMCID: PMC8253404; DOI: 10.1371/journal.pone.0253611;
     
  3. Feofanova EV, Lim E, Chen H, Lee M, Liu CT, Cupples LA, Boerwinkle E. Exome sequence association study of levels and longitudinal change of cardiovascular risk factor phenotypes in European Americans and African Americans from the Atherosclerosis Risk in Communities Study. Genet Epidemiol. 2021 Jun 24.View Related Profiles. PMID: 34167169
     
  4. Keramati AR, Chen MH, Rodriguez BAT, Yanek LR, Bhan A, Gaynor BJ, Ryan K, Brody JA, Zhong X, Wei Q, Kammers K, Kanchan K, Iyer K, Kowalski MH, Pitsillides AN, Cupples LA, Li B, Schlaeger TM, Shuldiner AR, O'Connell JR, Ruczinski I, Mitchell BD, Faraday N, Taub MA, Becker LC, Lewis JP, Mathias RA, Johnson AD. Genome sequencing unveils a regulatory landscape of platelet reactivity. Nat Commun. 2021 06 15; 12(1):3626. PMID: 34131117
     
  5. Sofer T, Zheng X, Laurie CA, Gogarten SM, Brody JA, Conomos MP, Bis JC, Thornton TA, Szpiro A, O'Connell JR, Lange EM, Gao Y, Cupples LA, Psaty BM, Rice KM. Variant-specific inflation factors for assessing population stratification at the phenotypic variance level. Nat Commun. 2021 06 09; 12(1):3506. PMID: 34108454
     
  6. Kwong AM, Blackwell TW, LeFaive J, de Andrade M, Barnard J, Barnes KC, Blangero J, Boerwinkle E, Burchard EG, Cade BE, Chasman DI, Chen H, Conomos MP, Cupples LA, Ellinor PT, Eng C, Gao Y, Guo X, Irvin MR, Kelly TN, Kim W, Kooperberg C, Lubitz SA, Mak ACY, Manichaikul AW, Mathias RA, Montasser ME, Montgomery CG, Musani S, Palmer ND, Peloso GM, Qiao D, Reiner AP, Roden DM, Shoemaker MB, Smith JA, Smith NL, Su JL, Tiwari HK, Weeks DE, Weiss ST, Scott LJ, Smith AV, Abecasis GR, Boehnke M, Kang HM. Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries. Genetics. 2021 May 17; 218(1).View Related Profiles. PMID: 33720349; PMCID: PMC8128395; DOI: 10.1093/genetics/iyab044;
     
  7. Liu CT, Karasik D, Xu H, Zhou Y, Broe K, Cupples LA, Cpgm de Groot L, Ham A, Hannan MT, Hsu YH, Jacques P, McLean RR, Paul L, Selhub J, Trajanoska K, van der Velde N, van Schoor N, Kiel DP. Genetic variants modify the associations of concentrations of methylmalonic acid, vitamin B-12, vitamin B-6, and folate with bone mineral density. Am J Clin Nutr. 2021 May 08.View Related Profiles. PMID: 33964857
     
  8. Stilp AM, Emery LS, Broome JG, Buth EJ, Khan AT, Laurie CA, Wang FF, Wong Q, Chen D, D'Augustine CM, Heard-Costa NL, Hohensee CR, Johnson WC, Juarez LD, Liu J, Mutalik KM, Raffield LM, Wiggins KL, de Vries PS, Kelly TN, Kooperberg C, Natarajan P, Peloso GM, Peyser PA, Reiner AP, Arnett DK, Aslibekyan S, Barnes KC, Bielak LF, Bis JC, Cade BE, Chen MH, Correa A, Cupples LA, de Andrade M, Ellinor PT, Fornage M, Franceschini N, Gan W, Ganesh SK, Graffelman J, Grove ML, Guo X, Hawley NL, Hsu WL, Jackson RD, Jaquish CE, Johnson AD, Kardia SLR, Kelly S, Lee J, Mathias RA, McGarvey ST, Mitchell BD, Montasser ME, Morrison AC, North KE, Nouraie SM, Oelsner EC, Pankratz N, Rich SS, Rotter JI, Smith JA, Taylor KD, Vasan RS, Weeks DE, Weiss ST, Wilson CG, Yanek LR, Psaty BM, Heckbert SR, Laurie CC. A System for Phenotype Harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program. Am J Epidemiol. 2021 Apr 16.View Related Profiles. PMID: 33861317
     
  9. Natarajan P, Pampana A, Graham SE, Ruotsalainen SE, Perry JA, de Vries PS, Broome JG, Pirruccello JP, Honigberg MC, Aragam K, Wolford B, Brody JA, Antonacci-Fulton L, Arden M, Aslibekyan S, Assimes TL, Ballantyne CM, Bielak LF, Bis JC, Cade BE, Do R, Doddapaneni H, Emery LS, Hung YJ, Irvin MR, Khan AT, Lange L, Lee J, Lemaitre RN, Martin LW, Metcalf G, Montasser ME, Moon JY, Muzny D, O'Connell JR, Palmer ND, Peralta JM, Peyser PA, Stilp AM, Tsai M, Wang FF, Weeks DE, Yanek LR, Wilson JG, Abecasis G, Arnett DK, Becker LC, Blangero J, Boerwinkle E, Bowden DW, Chang YC, Chen YI, Choi WJ, Correa A, Curran JE, Daly MJ, Dutcher SK, Ellinor PT, Fornage M, Freedman BI, Gabriel S, Germer S, Gibbs RA, He J, Hveem K, Jarvik GP, Kaplan RC, Kardia SLR, Kenny E, Kim RW, Kooperberg C, Laurie CC, Lee S, Lloyd-Jones DM, Loos RJF, Lubitz SA, Mathias RA, Martinez KAV, McGarvey ST, Mitchell BD, Nickerson DA, North KE, Palotie A, Park CJ, Psaty BM, Rao DC, Redline S, Reiner AP, Seo D, Seo JS, Smith AV, Tracy RP, Vasan RS, Kathiresan S, Cupples LA, Rotter JI, Morrison AC, Rich SS, Ripatti S, Willer C, Peloso GM. Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices. Nat Commun. 2021 04 12; 12(1):2182.View Related Profiles. PMID: 33846329; PMCID: PMC8042019; DOI: 10.1038/s41467-021-22339-1;
     
  10. Graff M, Justice AE, Young KL, Marouli E, Zhang X, Fine RS, Lim E, Buchanan V, Rand K, Feitosa MF, Wojczynski MK, Yanek LR, Shao Y, Rohde R, Adeyemo AA, Aldrich MC, Allison MA, Ambrosone CB, Ambs S, Amos C, Arnett DK, Atwood L, Bandera EV, Bartz T, Becker DM, Berndt SI, Bernstein L, Bielak LF, Blot WJ, Bottinger EP, Bowden DW, Bradfield JP, Brody JA, Broeckel U, Burke G, Cade BE, Cai Q, Caporaso N, Carlson C, Carpten J, Casey G, Chanock SJ, Chen G, Chen M, Chen YI, Chen WM, Chesi A, Chiang CWK, Chu L, Coetzee GA, Conti DV, Cooper RS, Cushman M, Demerath E, Deming SL, Dimitrov L, Ding J, Diver WR, Duan Q, Evans MK, Falusi AG, Faul JD, Fornage M, Fox C, Freedman BI, Garcia M, Gillanders EM, Goodman P, Gottesman O, Grant SFA, Guo X, Hakonarson H, Haritunians T, Harris TB, Harris CC, Henderson BE, Hennis A, Hernandez DG, Hirschhorn JN, McNeill LH, Howard TD, Howard B, Hsing AW, Hsu YH, Hu JJ, Huff CD, Huo D, Ingles SA, Irvin MR, John EM, Johnson KC, Jordan JM, Kabagambe EK, Kang SJ, Kardia SL, Keating BJ, Kittles RA, Klein EA, Kolb S, Kolonel LN, Kooperberg C, Kuller L, Kutlar A, Lange L, Langefeld CD, Le Marchand L, Leonard H, Lettre G, Levin AM, Li Y, Li J, Liu Y, Liu Y, Liu S, Lohman K, Lotay V, Lu Y, Maixner W, Manson JE, McKnight B, Meng Y, Monda KL, Monroe K, Moore JH, Mosley TH, Mudgal P, Murphy AB, Nadukuru R, Nalls MA, Nathanson KL, Nayak U, N'Diaye A, Nemesure B, Neslund-Dudas C, Neuhouser ML, Nyante S, Ochs-Balcom H, Ogundiran TO, Ogunniyi A, Ojengbede O, Okut H, Olopade OI, Olshan A, Padhukasahasram B, Palmer J, Palmer CD, Palmer ND, Papanicolaou G, Patel SR, Pettaway CA, Peyser PA, Press MF, Rao DC, Rasmussen-Torvik LJ, Redline S, Reiner AP, Rhie SK, Rodriguez-Gil JL, Rotimi CN, Rotter JI, Ruiz-Narvaez EA, Rybicki BA, Salako B, Sale MM, Sanderson M, Schadt E, Schreiner PJ, Schurmann C, Schwartz AG, Shriner DA, Signorello LB, Singleton AB, Siscovick DS, Smith JA, Smith S, Speliotes E, Spitz M, Stanford JL, Stevens VL, Stram A, Strom SS, Sucheston L, Sun YV, Tajuddin SM, Taylor H, Taylor K, Tayo BO, Thun MJ, Tucker MA, Vaidya D, Van Den Berg DJ, Vedantam S, Vitolins M, Wang Z, Ware EB, Wassertheil-Smoller S, Weir DR, Wiencke JK, Williams SM, Williams LK, Wilson JG, Witte JS, Wrensch M, Wu X, Yao J, Zakai N, Zanetti K, Zemel BS, Zhao W, Zhao JH, Zheng W, Zhi D, Zhou J, Zhu X, Ziegler RG, Zmuda J, Zonderman AB, Psaty BM, Borecki IB, Cupples LA, Liu CT, Haiman CA, Loos R, Ng MCY, North KE. Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. Am J Hum Genet. 2021 04 01; 108(4):564-582.View Related Profiles. PMID: 33713608; PMCID: PMC8059339; DOI: 10.1016/j.ajhg.2021.02.011;
     
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