Christopher S. Carlson
Affiliations: | Genome Sciences | University of Washington, Seattle, Seattle, WA |
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"Christopher Carlson"Parents
Sign in to add mentor| David R. Cox | grad student | 2000 | Stanford (Cell Biology Tree) | |
| (Analysis of linkage disequilibrium and haplotype at the single -minded homology 2 locus in four populations, as a model for analysis of candidate loci in complex genetic disease.) | ||||
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Publications
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| 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 |
| Rajabli F, Benchek P, Tosto G, et al. (2023) Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences |
| Hu Y, Graff M, Haessler J, et al. (2020) Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. Plos Genetics. 16: e1008684 |
| Bien SA, Su YR, Conti DV, et al. (2019) Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. Human Genetics |
| Wojcik GL, Graff M, Nishimura KK, et al. (2019) Genetic analyses of diverse populations improves discovery for complex traits. Nature |
| Bien SA, Su YR, Conti DV, et al. (2019) Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer. Human Genetics |
| Mayer SE, Weiss NS, Chubak J, et al. (2018) CYP2D6-inhibiting medication use and inherited CYP2D6 variation in relation to adverse breast cancer outcomes after tamoxifen therapy. Cancer Causes & Control : Ccc |
| Wojcik GL, Fuchsberger C, Taliun D, et al. (2018) Imputation-Aware Tag SNP Selection To Improve Power for Large-Scale, Multi-ethnic Association Studies. G3 (Bethesda, Md.) |
| Schmit SL, Edlund CK, Schumacher FR, et al. (2018) Novel Common Genetic Susceptibility Loci for Colorectal Cancer. Journal of the National Cancer Institute |
| Kocarnik JM, Richard M, Graff M, et al. (2018) Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study. Human Molecular Genetics |