Jemma B. Wilk

1998-2002 Epidemiology Boston University School of Medicine, Boston, MA 
"Jemma Wilk"
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Shah S, Henry A, Roselli C, et al. (2020) Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Nature Communications. 11: 163
Hobbs BD, de Jong K, Lamontagne M, et al. (2017) Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. Nature Genetics
Smith JG, Felix JF, Morrison AC, et al. (2016) Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure. Plos Genetics. 12: e1006034
Obeidat M, Hao K, Bossé Y, et al. (2015) Molecular mechanisms underlying variations in lung function: a systems genetics analysis. The Lancet. Respiratory Medicine
London SJ, Gao W, Gharib SA, et al. (2014) ADAM19 and HTR4 variants and pulmonary function: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study. Circulation. Cardiovascular Genetics. 7: 350-8
Loth DW, Artigas MS, Gharib SA, et al. (2014) Genome-wide association analysis identifies six new loci associated with forced vital capacity. Nature Genetics. 46: 669-77
Burkart KM, Manichaikul A, Wilk JB, et al. (2014) APOM and high-density lipoprotein cholesterol are associated with lung function and per cent emphysema. The European Respiratory Journal. 43: 1003-17
Reardon BJ, Hansen JG, Crystal RG, et al. (2013) Vitamin D-responsive SGPP2 variants associated with lung cell expression and lung function. Bmc Medical Genetics. 14: 122
Mukamal KJ, Wilk JB, Biggs ML, et al. (2013) Common FABP4 genetic variants and plasma levels of fatty acid binding protein 4 in older adults. Lipids. 48: 1169-75
Djoussé L, Wilk JB, Hanson NQ, et al. (2013) Association between adiponectin and heart failure risk in the physicians' health study. Obesity (Silver Spring, Md.). 21: 831-4
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