HRS Bibliography

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Fuentes Lde Las, Sung YJu, Noordam R, et al. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Mol Psychiatry. 2021;26(6):2111-2125. doi:10.1038/s41380-020-0719-3.
Fuentes Lde Las, Sung YJu, Noordam R, et al. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Mol Psychiatry. 2021;26(6):2111-2125. doi:10.1038/s41380-020-0719-3.
Fuentes Lde Las, Sung YJu, Noordam R, et al. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Mol Psychiatry. 2021;26(6):2111-2125. doi:10.1038/s41380-020-0719-3.
Fuentes Lde Las, Sung YJu, Noordam R, et al. Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Mol Psychiatry. 2021;26(6):2111-2125. doi:10.1038/s41380-020-0719-3.
M. Islam A, Alzaid AA, Chowdhury RI, Sultan KS. A generalized bivariate Bernoulli model with covariate dependence. Journal of Applied Statistics. 2013;40:1064-1075. doi:10.1080/02664763.2013.780156.
Ejima K, Pavela G, Li P, Allison DB. Generalized lambda distribution for flexibly testing differences beyond the mean in the distribution of a dependent variable such as body mass index. International Journal of Obesity. 2018;42(4):930-933. doi:10.1038/ijo.2017.262.
Kulminski AM, Shu L, Loika Y, et al. Genetic and regulatory architecture of Alzheimer's disease in the APOE region. Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring. 2020;12:e12008. doi:https://doi.org/10.1002/dad2.12008.
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.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
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.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
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.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
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.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
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.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
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.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
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.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
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.
http://www.ncbi.nlm.nih.gov/pubmed/26831199?dopt=Abstract
Bae H, Lunetta KL, Murabito JM, et al. Genetic associations with age of menopause in familial longevity. Menopause. 2019. doi:10.1097/GME.0000000000001367.
http://www.ncbi.nlm.nih.gov/pubmed/31188284?dopt=Abstract
Wertz J, Moffitt TE, Arseneault L, et al. Genetic associations with parental investment from conception to wealth inheritance in six cohorts. Nat Hum Behav. 2023. doi:10.1038/s41562-023-01618-5.