Charles L. Kooperberg
Affiliations: | University of Washington, Seattle, Seattle, WA |
Area:
Statistics, Biostatistics BiologyGoogle:
"Charles Kooperberg"
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Publications
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Huffman JE, Nicholas J, Hahn J, et al. (2024) Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. Blood |
Huffman JE, Nicolas J, Hahn J, et al. (2023) Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles. Medrxiv : the Preprint Server For Health Sciences |
Young KL, Fisher V, Deng X, et al. (2022) Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Hgg Advances. 4: 100163 |
Yengo L, Vedantam S, Marouli E, et al. (2022) A saturated map of common genetic variants associated with human height. Nature |
Taub MA, Conomos MP, Keener R, et al. (2022) Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2 |
Nauffal V, Morrill VN, Jurgens SJ, et al. (2022) Monogenic and Polygenic Contributions to QTc Prolongation in the Population. Circulation |
Tapia AL, Rowland BT, Rosen JD, et al. (2021) Full title: A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping. Genetic Epidemiology |
Choi SH, Jurgens SJ, Haggerty CM, et al. (2021) Rare Coding Variants Associated with Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-ancestry Analysis. Circulation. Genomic and Precision Medicine |
Sarnowski C, Chen H, Biggs ML, et al. (2021) Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. Plos One. 16: e0253611 |
Hu Y, Stilp AM, McHugh CP, et al. (2021) Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. American Journal of Human Genetics |