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William Cookson grad student 2001 Oxford (GenetiTree)
 (Methods for fine mapping complex traits in human pedigrees.)
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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
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