HRS Bibliography

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Fisher GG, Faul JD, Weir DR, Wallace RB. Documentation of Chronic Disease Measures in the Health and Retirement Study. Ann Arbor, Michigan: Institute for Social Research, University of Michigan; 2005.PDF icon Download PDF (460.3 KB)


Nead KT, Li A, Wehner MR, et al. Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals. Human Molecular Genetics. 2015;24(12):3582-94. doi:10.1093/hmg/ddv097.
Joshi PK, Esko T, Mattsson H, et al. Directional dominance on stature and cognition in diverse human populations. Nature. 2015;523(7561):459-62. doi:10.1038/nature14618.
Crimmins EM, Faul JD, Kim JKi, Weir DR. Documentation of Biomarkers in the 2010 and 2012 Health and Retirement Study. Ann Arbor, Michigan: Survey Research Center, University of Michigan; 2015:15.PDF icon Download PDF (198.27 KB)
Locke AE, Kahali B, Berndt SI, et al. Genetic studies of body mass index yield new insights for obesity biology. Nature. 2015;518(7538):197-206. doi:10.1038/nature14177.
Broer L, Aron S. Buchman, Deelen J, Smith JA, et al. GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy. Journals of Gerontology Series A: Biological Sciences and Medical Sciences. 2015;70(1):110-8. doi:10.1093/gerona/glu166.
Day FR, Ruth KS, Thompson DJ, et al. Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Nat Genet. 2015;47(11):1294-303. doi:10.1038/ng.3412.


Faul JD, Mitchell CM, Zhao W. Estimating Telomere Length Heritability in an Unrelated Sample of Adults: Is Heritability of Telomere Length Modified by Life Course Socioeconomic Status?. Biodemography and Social Biology. 2016;62(1):73-86. doi:10.1080/19485565.2015.1120645.
Pattaro C, Teumer A, Gorski M, et al. Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat Commun. 2016;7:10023. doi:10.1038/ncomms10023.
Okbay A, Baselmans BML, De Neve J-E, et al. Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nature Genetics. 2016;48(6):624-33. doi:10.1038/ng.3552.
Barban N, Jansen R, de Vlaming R, et al. Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat Genet. 2016;48(12):1462-1472. doi:10.1038/ng.3698.
Dunn EC, Wiste A, Radmanesh F, et al. Genome-wide association study (GWAS) and genome-wide by environment interaction study (GWEIS) of depressive symptoms in African American and Hispanic/Latina women. Depression & Anxiety. 2016;33(4):265-80. doi:10.1002/da.22484.
Okbay A, Jonathan P. Beauchamp, Fontana MA, Chen G-B, et al. Genome-wide association study identifies 74 loci associated with educational attainment. Nature. 2016;533(7604):539-42. doi:10.1038/nature17671.
Matteini AM, Tanaka T, Karasik D, et al. GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium. Aging Cell. 2016;15(5):792-800. doi:10.1111/acel.12468.
Liu C, Kraja AT, Smith JA, Morrison A, et al. Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Nat Genet. 2016;48(10):1162-70. doi:10.1038/ng.3660.