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William Cookson grad student 2001 Oxford (GenetiTree)
 (Methods for fine mapping complex traits in human pedigrees.)
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Kessler MD, Damask A, O'Keeffe S, et al. (2025) Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes. Nature
Li R, Gagliano Taliun SA, Liao K, et al. (2024) Whole genome sequence-based association analysis of African American individuals with bipolar disorder and schizophrenia. Medrxiv : the Preprint Server For Health Sciences
Borda V, Loesch DP, Guo B, et al. (2024) Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas. Cell Genomics. 100692
Gaynor SM, Joseph T, Bai X, et al. (2024) Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. Nature Genetics
Sun X, Bulekova K, Yang J, et al. (2024) Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application. Mitochondrion. 101954
Sun KY, Bai X, Chen S, et al. (2024) A deep catalogue of protein-coding variation in 983,578 individuals. Nature
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
Willems SM, Ng NHJ, Fernandez J, et al. (2023) Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization. Wellcome Open Research. 8: 483
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
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