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Author Details

Daniel Shriner
1997
120
43
PMIDPaper TitleJournal TitlePublished Year
36786670Overview of Admixture Mapping.2023
37653728Universal genome-wide association studies: Powerful joint ancestry and association testing.HGG Adv2023
38076833Random forest classifiers trained on simulated data enable accurate short read-based genotyping of structural variants in the alpha globin region at Chr16p13.3.bioRxiv2023
36800387Discovery of a rapidly evolving yeast defense factor, , against the secreted killer toxin K28.2023
35551307Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.Nat Genet2022
35657990Additive genetic effect of GCKR, G6PC2, and SLC30A8 variants on fasting glucose levels and risk of type 2 diabetes.PLoS One2022
34584272Evolutionary genetics and acclimatization in nephrology.Nat Rev Nephrol2021
34117260A UGT1A1 variant is associated with serum total bilirubin levels, which are causal for hypertension in African-ancestry individuals.NPJ Genom Med2021
33846614Author Correction: High-depth African genomes inform human migration and health.Nature2021
33526862Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility.Leukemia2021
33729508Genetic risk scores for cardiometabolic traits in sub-Saharan African populations.Int J Epidemiol2021
34196372GWAS in Africans identifies novel lipids loci and demonstrates heterogenous association within Africa.Hum Mol Genet2021
33603002Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits.Sci Rep2021
33713608Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.Am J Hum Genet2021
33051549Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility.Leukemia2021
32898326Genetic modifiers of long-term survival in sickle cell anemia.Clin Transl Med2020
32315356Admixture mapping identifies genetic regions associated with blood pressure phenotypes in African Americans.PLoS One2020
31841133Refining genome-wide associated loci for serum uric acid in individuals with African ancestry.Hum Mol Genet2020
32001505Whole genome sequence-based haplotypes reveal a single origin of the 1393 bp deletion.Journal of Medical Genetics2020
31871193<i>HLA</i> and autoantibodies define scleroderma subtypes and risk in African and European Americans and suggest a role for molecular mimicry.Proc Natl Acad Sci U S A2020
32601469Ancient familial Mediterranean fever mutations in human pyrin and resistance to Yersinia pestis.Nat Immunol2020
33258447Time-to-event modeling of hypertension reveals the nonexistence of true controls.Elife2020
31832618Type 2 diabetes complications and comorbidity in Sub-Saharan Africans.EClinicalMedicine2019
31792241Genetics of cognitive trajectory in Brazilians: 15 years of follow-up from the Bambuí-Epigen Cohort Study of Aging.Sci Rep2019
29732714Brief Report: Whole-Exome Sequencing to Identify Rare Variants and Gene Networks That Increase Susceptibility to Scleroderma in African Americans.Arthritis Rheumatol2018
30259956Genetic history of Chad.Am J Phys Anthropol2018
30079081Re-analysis of Whole Genome Sequence Data From 279 Ancient Eurasians Reveals Substantial Ancestral Heterogeneity.Frontiers in Genetics2018
29526279Whole-Genome-Sequence-Based Haplotypes Reveal Single Origin of the Sickle Allele during the Holocene Wet Phase.Am J Hum Genet2018
29608727Genetic Ancestry of Hadza and Sandawe Peoples Reveals Ancient Population Structure in Africa.Genome Biol Evol2018
29596498Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia.PLoS One2018
27779243Pharmacogenomic implications of the evolutionary history of infectious diseases in Africa.Pharmacogenomics J2017
28777929Human Germline Genome Editing.Am J Hum Genet2017
28346466Common and rare exonic MUC5B variants associated with type 2 diabetes in Han Chinese.PLoS One2017
28977439The genomic landscape of African populations in health and disease.Hum Mol Genet2017
28484253Human ancestry correlates with language and reveals that race is not an objective genomic classifier.Sci Rep2017
28696560Overview of Admixture Mapping.Current Protocols in Human Genetics2017
27177148Transferability of genome-wide associated loci for asthma in African Americans.J Asthma2017
28296344Genome-wide analysis identifies an african-specific variant in SEMA4D associated with body mass index.Obesity (Silver Spring)2017
27644073The African diaspora: history, adaptation and health.Curr Opin Genet Dev2016
28768256Estimation of FST and the Impact of de novo Mutation.Hum Hered2016
27303364Impact of Type 2 Diabetes on Impaired Kidney Function in Sub-Saharan African Populations.Front Endocrinol (Lausanne)2016
26831199Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.Nat Commun2016
27212471Ancient Human Migration after Out-of-Africa.Sci Rep2016
27313599Migration Route Out of Africa Unresolved by 225 Egyptian and Ethiopian Whole Genome Sequences.Frontiers in Genetics2016
26686224Evolutionary context for the association of γ-globin, serum uric acid, and hypertension in African Americans.BMC Med Genet2015
25644736Addressing population-specific multiple testing burdens in genetic association studies.Ann Hum Genet2015
26317214An Improved F(st) Estimator.PLoS One2015
26131930Directional dominance on stature and cognition in diverse human populations.Nature2015
26507551Genome-wide association study identifies African-ancestry specific variants for metabolic syndrome.Mol Genet Metab2015
26635871Evaluation of Genome Wide Association Study Associated Type 2 Diabetes Susceptibility Loci in Sub Saharan Africans.Front Genet2015
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