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Author Details
Full Name
Steven Buyske
Affiliation
The State University of New Jersey
ORCID
Career Start Year
1998
Papers
126
H Index
44
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36350676
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.
Nucleic Acids Res
2023
36251081
Common genetic risk factors in ASD and ADHD co-occurring families.
Hum Genet
2023
36308435
Trans-ancestry, Bayesian meta-analysis discovers 20 novel risk loci for inflammatory bowel disease in an African American, East Asian and European cohort.
Hum Mol Genet
2023
36350676
FAVOR: functional annotation of variants online resource and annotator for variation across the human genome.
Nucleic Acids Res
2023
37761888
The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait.
Genes (Basel)
2023
37658231
Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts.
Hum Genet
2023
37686052
Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments.
Int J Mol Sci
2023
37090648
MUSSEL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups.
bioRxiv
2023
36941441
Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.
Nat Genet
2023
37658231
Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts.
Hum Genet
2023
37686052
Structural Variations Contribute to the Genetic Etiology of Autism Spectrum Disorder and Language Impairments.
Int J Mol Sci
2023
37761888
The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive Trait.
Genes (Basel)
2023
37090648
MUSSEL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups.
bioRxiv
2023
36941441
Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals.
Nat Genet
2023
36251081
Common genetic risk factors in ASD and ADHD co-occurring families.
Hum Genet
2023
36308435
Trans-ancestry, Bayesian meta-analysis discovers 20 novel risk loci for inflammatory bowel disease in an African American, East Asian and European cohort.
Hum Mol Genet
2023
34779012
A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.
Genet Epidemiol
2022
35581355
Opportunities and challenges for the use of common controls in sequencing studies.
Nat Rev Genet
2022
35893067
MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders.
Genes (Basel)
2022
36088317
Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.
BMC Med Genomics
2022
35948364
Genome-Wide Epistatic Interaction between <i>DEF1B</i> and <i>APOL1</i> High-Risk Genotypes for Chronic Kidney Disease.
Clin J Am Soc Nephrol
2022
35915156
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.
Nat Med
2022
35468749
Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program.
BMC Infect Dis
2022
34779012
A large-scale transcriptome-wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine-mapping.
Genet Epidemiol
2022
34951656
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.
Diabetologia
2022
35263625
Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits.
Am J Hum Genet
2022
35581355
Opportunities and challenges for the use of common controls in sequencing studies.
Nat Rev Genet
2022
35468749
Identification of SARS-CoV-2 variants using viral sequencing for the Centers for Disease Control and Prevention genomic surveillance program.
BMC Infect Dis
2022
35893067
MicroRNA and MicroRNA-Target Variants Associated with Autism Spectrum Disorder and Related Disorders.
Genes (Basel)
2022
36088317
Genetic pleiotropy underpinning adiposity and inflammation in self-identified Hispanic/Latino populations.
BMC Med Genomics
2022
35948364
Genome-Wide Epistatic Interaction between <i>DEF1B</i> and <i>APOL1</i> High-Risk Genotypes for Chronic Kidney Disease.
Clin J Am Soc Nephrol
2022
35915156
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.
Nat Med
2022
34951656
Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study.
Diabetologia
2022
35263625
Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits.
Am J Hum Genet
2022
33098347
Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome.
Am J Med Genet A
2021
34107879
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
BMC Genomics
2021
34356065
Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations.
Genes (Basel)
2021
33098347
Alternative genomic diagnoses for individuals with a clinical diagnosis of Dubowitz syndrome.
Am J Med Genet A
2021
34517814
Correction 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 Genomics
2021
34604815
Genetic discovery and risk characterization in type 2 diabetes across diverse populations.
HGG Adv
2021
34517814
Correction 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 Genomics
2021
34604815
Genetic discovery and risk characterization in type 2 diabetes across diverse populations.
HGG Adv
2021
34107879
Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study.
BMC Genomics
2021
34356065
Transcriptome-Wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations.
Genes (Basel)
2021
32226016
Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.
PLoS Genet
2020
32171239
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
BMC Genomics
2020
32226016
Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study.
PLoS Genet
2020
32602732
Multi-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 Med
2020
32602732
Multi-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 Med
2020
32171239
Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics.
BMC Genomics
2020
1 - 50 of 252
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Co-authored papers
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Marylyn D Ritchie
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