Jemma B. Wilk
Affiliations: | 1998-2002 | Epidemiology | Boston University School of Medicine, Boston, MA |
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Parents
Sign in to add mentorRichard H. Myers | grad student | 1998-2002 | Boston University School of Public Health and School of Medicine |
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Publications
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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 |