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Author Details

Albert V Smith
University of Michigan School of Public Health ann arbor
1987
315
109
PMIDPaper TitleJournal TitlePublished Year
36255742FGF20 and PGM2 variants are associated with childhood asthma in family-based whole-genome sequencing studies.Hum Mol Genet2023
36255742FGF20 and PGM2 variants are associated with childhood asthma in family-based whole-genome sequencing studies.Hum Mol Genet2023
37749248Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.Nat Genet2023
38028628Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.Front Genet2023
37802043Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.Am J Hum Genet2023
37709864Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease.Nat Genet2023
37770635Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.Nat Genet2023
37348055Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.Genetics2023
36778406Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.bioRxiv2023
36778386Structural variation across 138,134 samples in the TOPMed consortium.Res Sq2023
37466697Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential.Cancer Epidemiol Biomarkers Prev2023
36810122FixItFelix: improving genomic analysis by fixing reference errors.Genome Biol2023
37126548The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.Sci Adv2023
36747810Structural variation across 138,134 samples in the TOPMed consortium.bioRxiv2023
37046083Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.Nature2023
36602845Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants.Am J Respir Crit Care Med2023
37425772Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.medRxiv2023
37503126Understanding the genetic complexity of puberty timing across the allele frequency spectrum.medRxiv2023
37495751Tutorial: a statistical genetics guide to identifying HLA alleles driving complex disease.Nat Protoc2023
38028628Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.Front Genet2023
37802043Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study.Am J Hum Genet2023
37709864Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease.Nat Genet2023
37749248Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk.Nat Genet2023
37503126Understanding the genetic complexity of puberty timing across the allele frequency spectrum.medRxiv2023
37770635Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification.Nat Genet2023
37495751Tutorial: a statistical genetics guide to identifying HLA alleles driving complex disease.Nat Protoc2023
37425772Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study.medRxiv2023
37348055Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.Genetics2023
37046083Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.Nature2023
37466697Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential.Cancer Epidemiol Biomarkers Prev2023
37126548The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.Sci Adv2023
36747810Structural variation across 138,134 samples in the TOPMed consortium.bioRxiv2023
36810122FixItFelix: improving genomic analysis by fixing reference errors.Genome Biol2023
36778406Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.bioRxiv2023
36778386Structural variation across 138,134 samples in the TOPMed consortium.Res Sq2023
36602845Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants.Am J Respir Crit Care Med2023
34166655Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy.Am J Ophthalmol2022
35974141Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning.Mol Psychiatry2022
35647563Accounting for population structure in genetic studies of cystic fibrosis.HGG Adv2022
35953715GAWMerge expands GWAS sample size and diversity by combining array-based genotyping and whole-genome sequencing.Commun Biol2022
35508176Meta-imputation: An efficient method to combine genotype data after imputation with multiple reference panels.Am J Hum Genet2022
35385311Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.Sci Adv2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
35504290TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data.Am J Hum Genet2022
35927319Rare genetic variants explain missing heritability in smoking.Nat Hum Behav2022
35981533Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing.Am J Hum Genet2022
35659450Erratum to Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy. Am J Ophthalmol 2022;233:111-123.Am J Ophthalmol2022
36568030Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants.HGG Adv2022
36481753Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program.Nat Commun2022
34166655Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy.Am J Ophthalmol2022
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Collaborators

Vilmundur Gudnason
Co-authored papers 236
Tamara B Harris
National Institute on Aging
Co-authored papers 196
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers 189
Lenore J Launer
Co-authored papers 179
Bruce M Psaty
Co-authored papers 172
Albert Hofman
Harvard T.H. Chan School of Public Health
Co-authored papers 158
Jerome I Rotter
Co-authored papers 157
Cornelia M van Duijn
University of Oxford
Co-authored papers 156
Eric Boerwinkle
Baylor College of Medicine
Co-authored papers 148
Caroline Hayward
Co-authored papers 111
Fernando Rivadeneira
University Medical Center Rotterdam
Co-authored papers 103
Joshua C Bis
Co-authored papers 103
Ruth J F Loos
Co-authored papers 95
Yongmei Liu
Co-authored papers 95
Igor Rudan
Co-authored papers 93
Ozren Polasek
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Gudny Eiriksdottir
Co-authored papers 87
Terho Lehtim??ki
Finnish Cardiovascular Research Center-Tampere - FCRCT, Tampere University
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Daniel I Chasman
Harvard Medical School, Harvard University
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Kent D Taylor
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Paul M Ridker
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Myriam Fornage
Co-authored papers 82
Tim D Spector
King's College London
Co-authored papers 79
Alexander Teumer
University Medicine Greifswald
Co-authored papers 78
Olli T Raitakari
Co-authored papers 75
Najaf Amin
Co-authored papers 74
Mika K??h??nen
Tampere University
Co-authored papers 74
Laura Adrienne Cupples
Co-authored papers 74
James F Wilson
Co-authored papers 74
Sharon L R Kardia
School of Public Health, University of Michigan ann arbor
Co-authored papers 73
Release 1.2