Goncalo Abecasis
Affiliations: | 2001- | University of Michigan, Ann Arbor, Ann Arbor, MI |
Area:
Biostatistics Biology, Genetics, EpidemiologyWebsite:
https://sph.umich.edu/faculty-profiles/abecasis-goncalo.htmlGoogle:
"Goncalo Abecasis"Bio:
https://sph.umich.edu/faculty-profiles/pdf/goncalo.pdf
https://en.wikipedia.org/wiki/Gon%C3%A7alo_Abecasis
Parents
Sign in to add mentorWilliam Cookson | grad student | 2001 | Oxford (GenetiTree) | |
(Methods for fine mapping complex traits in human pedigrees.) |
Children
Sign in to add traineeWei Chen | grad student | University of Michigan | |
Youna Hu | grad student | University of Michigan | |
Mingyao Li | grad student | 2005 | University of Michigan |
Yun Li | grad student | 2009 | University of Michigan (Physics Tree) |
Liming Liang | grad student | 2009 | University of Michigan |
Weihua Guan | grad student | 2010 | University of Michigan |
Jin Zheng | grad student | 2010 | University of Michigan |
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Publications
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Sun X, Bulekova K, Yang J, et al. (2024) Association analysis of mitochondrial DNA heteroplasmic variants: methods and application. Medrxiv : the Preprint Server For Health Sciences |
Kwong A, Zawistowski M, Fritsche LG, et al. (2023) Whole genome sequencing of 4,787 individuals identifies gene-based rare variants in age-related macular degeneration. Human Molecular Genetics |
Ziyatdinov A, Torres J, Alegre-Díaz J, et al. (2023) Genotyping, sequencing and analysis of 140,000 adults from Mexico City. Nature |
Graham SE, Clarke SL, Wu KH, et al. (2023) Author Correction: The power of genetic diversity in genome-wide association studies of lipids. Nature |
Sun KY, Bai X, Chen S, et al. (2023) A deep catalog of protein-coding variation in 985,830 individuals. Biorxiv : the Preprint Server For Biology |
Costanzo MC, von Grotthuss M, Massung J, et al. (2023) The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits. Cell Metabolism |
Zawistowski M, Fritsche LG, Pandit A, et al. (2023) The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients. Cell Genomics. 3: 100257 |
Kessler MD, Damask A, O'Keeffe S, et al. (2023) Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes. Nature. 615: E3 |
Jun G, English A, Metcalf G, et al. (2023) Structural variation across 138,134 samples in the TOPMed consortium. Research Square |
Jun G, English AC, Metcalf GA, et al. (2023) Structural variation across 138,134 samples in the TOPMed consortium. Biorxiv : the Preprint Server For Biology |