Matthew S. Zawistowski, Ph.D.
Affiliations: | 2011 | University of Michigan, Ann Arbor, Ann Arbor, MI |
Area:
Biostatistics Biology, GeneticsGoogle:
"Matthew Zawistowski"Parents
Sign in to add mentor| Sebastian Zollner | grad student | 2011 | University of Michigan | |
| (Statistical Methods and Models for Modern Genetic Analysis.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Suzuki K, Hatzikotoulas K, Southam L, et al. (2024) Genetic drivers of heterogeneity in type 2 diabetes pathophysiology. Nature |
| 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 |
| 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 |
| Bastarache L, Delozier S, Pandit A, et al. (2023) The phenotype-genotype reference map: Improving biobank data science through replication. American Journal of Human Genetics |
| 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 |
| Zhou W, Kanai M, Wu KH, et al. (2022) Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. Cell Genomics. 2: 100192 |
| Georges A, Yang ML, Berrandou TE, et al. (2022) Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nature Communications. 13: 2251 |
| Eijsbouts C, Zheng T, Kennedy NA, et al. (2021) Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders. Nature Genetics. 53: 1543-1552 |
| Georges A, Yang ML, Berrandou TE, et al. (2021) Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Nature Communications. 12: 6031 |