Sebastian Zollner
Affiliations: | University of Michigan, Ann Arbor, Ann Arbor, MI |
Area:
Biostatistics Biology, GeneticsGoogle:
"Sebastian Zollner"
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Publications
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| Suzuki K, Hatzikotoulas K, Southam L, et al. (2024) Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Nature |
| Jee YH, Thibord F, Dominguez A, et al. (2024) Multi-ancestry polygenic risk scores for venous thromboembolism. Medrxiv : the Preprint Server For Health Sciences |
| Wang A, Shen J, Rodriguez AA, et al. (2023) Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. Nature Genetics |
| Ziyatdinov A, Torres J, Alegre-Díaz J, et al. (2023) Genotyping, sequencing and analysis of 140,000 adults from Mexico City. Nature |
| Zhang X, Brody JA, Graff M, et al. (2023) WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE. Medrxiv : the Preprint Server For Health Sciences |
| Suzuki K, Hatzikotoulas K, Southam L, et al. (2023) Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. Medrxiv : the Preprint Server For Health Sciences |
| 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 |
| Liao K, Carlson J, Zöllner S. (2023) The Effect of Mutation Subtypes on the Allele Frequency Spectrum and Population Genetics Inference. G3 (Bethesda, Md.) |
| Zhou W, Kanai M, Wu KH, et al. (2022) Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. Cell Genomics. 2: 100192 |
| Saunders GRB, Wang X, Chen F, et al. (2022) Genetic diversity fuels gene discovery for tobacco and alcohol use. Nature |