Jemma B. Wilk

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1998-2002 Epidemiology Boston University School of Medicine, Boston, MA 
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Sun BB, Kurki MI, Foley CN, et al. (2022) Genetic associations of protein-coding variants in human disease. Nature. 603: 95-102
Lumbers RT, Shah S, Lin H, et al. (2021) The genomics of heart failure: design and rationale of the HERMES consortium. Esc Heart Failure
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
Winslow AR, Hyde CL, Wilk JB, et al. (2018) Self-report data as a tool for subtype identification in genetically-defined Parkinson's Disease. Scientific Reports. 8: 12992
Howson JMM, Zhao W, Barnes DR, et al. (2017) Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms. Nature Genetics
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
Aschard H, Tobin MD, Hancock DB, et al. (2017) Evidence for large-scale gene-by-smoking interaction effects on pulmonary function. International Journal of Epidemiology
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
Gharib SA, Loth DW, Soler Artigas M, et al. (2015) Integrative Pathway Genomics of Lung Function and Airflow Obstruction. Human Molecular Genetics
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