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American Journal of Physical Anthropology|September 28, 2018
Genetic history of ChadDaniel Shriner, Charles N RotimiAmerican Journal of Human Genetics|March 13, 2018
Whole-Genome-Sequence-Based Haplotypes Reveal Single Origin of the Sickle Allele during the Holocene Wet PhaseDaniel Shriner, Charles N RotimiNPJ Genomic Medicine|June 12, 2021
A UGT1A1 variant is associated with serum total bilirubin levels, which are causal for hypertension in African-ancestry individualsGuanjie Chen, Adebowale Adeyemo, Jie Zhou, et al.Elife|December 1, 2020
Time-to-event modeling of hypertension reveals the nonexistence of true controlsDaniel Shriner, Amy R Bentley, Jie Zhou, et al.Human Molecular Genetics|December 17, 2019
Refining genome-wide associated loci for serum uric acid in individuals with African ancestryGuanjie Chen, Daniel Shriner, Ayo P Doumatey, et al.Bioinformatics and Biology Insights|August 21, 2012
Simultaneous Analysis of Common and Rare Variants in Complex Traits: Application to SNPs (SCARVAsnp)Guanjie Chen, Ao Yuan, Yanxun Zhou, et al.Plos One|June 3, 2022
Additive genetic effect of GCKR, G6PC2, and SLC30A8 variants on fasting glucose levels and risk of type 2 diabetesGuanjie Chen, Daniel Shriner, Jianhua Zhang, et al.Current Diabetes Reports|September 15, 2019
Genetic Basis of Obesity and Type 2 Diabetes in Africans: Impact on Precision MedicineAyo P Doumatey, Kenneth Ekoru, Adebowale Adeyemo, et al.Clinical and Translational Medicine|September 8, 2020
Genetic modifiers of long-term survival in sickle cell anemiaAmbroise Wonkam, Emile R Chimusa, Khuthala Mnika, et al.Plos One|December 23, 2009
Transferability and fine-mapping of genome-wide associated loci for adult height across human populationsDaniel Shriner, Adebowale Adeyemo, Norman P Gerry, et al.Pageof 33