Browsing by Sponsor/Funder Action on Hearing Loss

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Showing results 1 to 13 of 13
Issue DateTitleAuthor(s)
15-Feb-2015A coherent approach for analysis of the Illumina HumanMethylation450 BeadChip improves data quality and performance in epigenome-wide association studiesLehne, B; Drong, AW; Loh, M; Zhang, W; Scott, WR, et al
15-Feb-2018A large-scale multi-ancestry genome-wide study accounting for smoking bahavior identifies multiple genome-wide significant loci for systolic and diastolic blood pressureSung, YJ; Lehne, B; Scott, WR; Sever, P; Chambers, J, et al
18-Jun-2015Epigenome-wide association of DNA methylation markers in peripheral blood from Indian Asians and Europeans with incident type 2 diabetes: a nested case-control studyChambers, JC; Loh, M; Lehne, B; Drong, A; Kriebel, J, et al
21-Dec-2016Epigenome-wide association study of body mass index, and the adverse outcomes of adiposityWahl, S; Drong, A; Lehne, B; Loh, M; Scott, WR, et al
17-Sep-2018Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traitsEvangelou, E; Warren, HR; Mosen-Ansorena, D; Mifsud, B; Pazoki, R, et al
Jun-2019Multi-ancestry genome-wide association study of lipid levels incorporating gene-alcohol interactionsDe Vries, PS; Brown, MR; Bentley, AR; Sung, YJ; Winkler, TW, et al
1-Apr-2019Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipidsBentley, AR; Sung, YJ; Brown, MR; Winkler, TW; Kraja, AT, et al
-Multi-ancestry genome-wide smoking interaction study of 387,272 individuals identifies novel lipid loci.Bentley, AR; Evangelou, E; Zhang, W; Afaq, S; Lehne, B, et al
18-Jun-2018Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570,000 individuals across multiple ancestriesFeitosa, M; Kraja, A; Zhang, W; Evangelou, E; Gao, H, et al
14-Nov-2018Publisher correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traitsEvangelou, E; Warren, HR; Mosen-Ansorena, D; Mifsud, B; Pazoki, R, et al
1-Feb-2017Rare and low-frequency coding variants alter human adult heightMarouli, E; Graff, M; Medina-Gomez, C; Lo, KS; Wood, AR, et al
19-Dec-2017Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Flannick, J; Froguel, P; Prokopenko, I; Lehne, B; Kooner, JS, et al
12-Sep-2016Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertensionSurendran, P; Drenos, F; Young, R; Warren, H; Cook, JP, et al