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Author Details

Steven Buyske
The State University of New Jersey
1998
126
44
PMIDPaper TitleJournal TitlePublished Year
36350676FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.Nucleic Acids Res2023
36251081Common genetic risk factors in ASD and ADHD co-occurring families.Hum Genet2023
36308435Trans-ancestry, Bayesian meta-analysis discovers 20 novel risk loci for inflammatory bowel disease in an African American, East Asian and European cohort.Hum Mol Genet2023
36350676FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.Nucleic Acids Res2023
37761888The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait.Genes (Basel)2023
37658231Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts.Hum Genet2023
37686052Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments.Int J Mol Sci2023
37090648MUSSEL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups.bioRxiv2023
36941441Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.Nat Genet2023
37658231Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts.Hum Genet2023
37686052Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments.Int J Mol Sci2023
37761888The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait.Genes (Basel)2023
37090648MUSSEL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups.bioRxiv2023
36941441Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.Nat Genet2023
36251081Common genetic risk factors in ASD and ADHD co-occurring families.Hum Genet2023
36308435Trans-ancestry, Bayesian meta-analysis discovers 20 novel risk loci for inflammatory bowel disease in an African American, East Asian and European cohort.Hum Mol Genet2023
34779012A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.Genet Epidemiol2022
35581355Opportunities and challenges for the use of common controls in sequencing studies.Nat Rev Genet2022
35893067MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders.Genes (Basel)2022
36088317Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.BMC Med Genomics2022
35948364Genome-Wide Epistatic Interaction between <i>DEF1B</i> and <i>APOL1</i> High-Risk Genotypes for Chronic Kidney Disease.Clin J Am Soc Nephrol2022
35915156Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.Nat Med2022
35468749Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program.BMC Infect Dis2022
34779012A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.Genet Epidemiol2022
34951656Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.Diabetologia2022
35263625Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits.Am J Hum Genet2022
35581355Opportunities and challenges for the use of common controls in sequencing studies.Nat Rev Genet2022
35468749Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program.BMC Infect Dis2022
35893067MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders.Genes (Basel)2022
36088317Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.BMC Med Genomics2022
35948364Genome-Wide Epistatic Interaction between <i>DEF1B</i> and <i>APOL1</i> High-Risk Genotypes for Chronic Kidney Disease.Clin J Am Soc Nephrol2022
35915156Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.Nat Med2022
34951656Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.Diabetologia2022
35263625Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits.Am J Hum Genet2022
33098347Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome.Am J Med Genet A2021
34107879Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.BMC Genomics2021
34356065Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations.Genes (Basel)2021
33098347Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome.Am J Med Genet A2021
34517814Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.BMC Genomics2021
34604815Genetic discovery and risk characterization in type 2 diabetes across diverse populations.HGG Adv2021
34517814Correction to: Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) Study.BMC Genomics2021
34604815Genetic discovery and risk characterization in type 2 diabetes across diverse populations.HGG Adv2021
34107879Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.BMC Genomics2021
34356065Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations.Genes (Basel)2021
32226016Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.PLoS Genet2020
32171239Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.BMC Genomics2020
32226016Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.PLoS Genet2020
32602732Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits.Circ Genom Precis Med2020
32602732Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits.Circ Genom Precis Med2020
32171239Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.BMC Genomics2020
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Center for Systems Genomics, Pennsylvania State University, University Park
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The State University of New Jersey
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