Work

Genotype phasing in pedigrees using whole-genome sequence data

Year: 2020

Type: article

Source: European Journal of Human Genetics

DOI: 10.1038/s41431-020-0574-3

Authors: August N. Blackburn, Lucy Blondell, Mark Z. Kos, Nicholas B. Blackburn, Juan M. Peralta, Peter T. Stevens, Donna M. Lehman, John Blangero, Harald H. H. Göring

Institutions: St. Mary's University, Texas, The University of Texas Rio Grande Valley, The University of Texas at San Antonio Health Science Center

Language: English

Topic: Genetic Associations and Epidemiology

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

Open Access status: bronze

Funders: U.S. Department of Health and Human Services, National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Diabetes and Digestive and Kidney Diseases, National Center for Research Resources

Awards: Multiethnic Study of Type 2 Diabetes Genes, Identifying T2D Variants by DNA Sequencing in Multiethnic Samples, Identification and Replication of Type 2 Diabetes Genes in Mexican Americans, A Genetic Study of Blood Metabolites and Their Relationship to Diabetes Risk, Discovery of Functional Variants in Type 2 Diabetes Genes in Mexican Americans, G3257426095, G3354169558, Identifying variants causal for Type 2 Diabetes in Major human populations, NIDDM Susceptibility Genes in Mexican Americans, G5079014249, Genetics of Gallbladder Disease in Mexican Americans, G725404114, G7793834193, Type 2 Diabetes Gene Discovery Linked to 3p in Hispanics, Construction of a Biomedical Research Facility at the U*, G9000043073, G9000244037, Whole Genome Sequencing to Identify Causal Genetic Variants Influencing CVD Risk

OpenAlex ID: W3004161192

FWCI: 0.44

Cites: 26

Cited by: 8

Related to: 10