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Author Details

Sebastian Z??llner
University of Michigan ann arbor
1998
76
34
PMIDPaper TitleJournal TitlePublished Year
36759699The effect of mutation subtypes on the allele frequency spectrum and population genetics inference.G3 (Bethesda)2023
37601974Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries.Cell Genom2023
37662265WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.medRxiv2023
37268629Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.Nat Commun2023
36759699The effect of mutation subtypes on the allele frequency spectrum and population genetics inference.G3 (Bethesda)2023
37248299Polygenic prediction of preeclampsia and gestational hypertension.Nat Med2023
37541830Cohort Profile Update: The Heinz C. Prechter Longitudinal Study of Bipolar Disorder.Int J Epidemiol2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37662265WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.medRxiv2023
37541830Cohort Profile Update: The Heinz C. Prechter Longitudinal Study of Bipolar Disorder.Int J Epidemiol2023
37601974Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries.Cell Genom2023
37248299Polygenic prediction of preeclampsia and gestational hypertension.Nat Med2023
37034649Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.medRxiv2023
37268629Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups.Nat Commun2023
34378841A survey of functional dyspepsia in 361,360 individuals: Phenotypic and genetic cross-disease analyses.Neurogastroenterol Motil2022
36055210Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience.Am J Hum Genet2022
36477530Genetic diversity fuels gene discovery for tobacco and alcohol use.Nature2022
34378841A survey of functional dyspepsia in 361,360 individuals: Phenotypic and genetic cross-disease analyses.Neurogastroenterol Motil2022
36477530Genetic diversity fuels gene discovery for tobacco and alcohol use.Nature2022
36055210Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience.Am J Hum Genet2022
33503551Stability of personality traits in bipolar disorder: Findings from a longitudinal cohort.J Affect Disord2021
33674754Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.Mol Psychiatry2021
33730541A powerful subset-based method identifies gene set associations and improves interpretation in UK Biobank.Am J Hum Genet2021
33503551Stability of personality traits in bipolar disorder: Findings from a longitudinal cohort.J Affect Disord2021
33674754Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder.Mol Psychiatry2021
33730541A powerful subset-based method identifies gene set associations and improves interpretation in UK Biobank.Am J Hum Genet2021
33339817Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.Nat Commun2020
31964835De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.Proc Natl Acad Sci U S A2020
33339817Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.Nat Commun2020
31964835De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population.Proc Natl Acad Sci U S A2020
30503783Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.Eur Neuropsychopharmacol2019
31869403Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.PLoS Genet2019
30503783Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder.Eur Neuropsychopharmacol2019
31385397Analysis of somatic mutations identifies signs of selection during in vitro aging of primary dermal fibroblasts.Aging Cell2019
31869403Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.PLoS Genet2019
31385397Analysis of somatic mutations identifies signs of selection during in vitro aging of primary dermal fibroblasts.Aging Cell2019
28709926An efficient algorithm for generating the internal branches of a Kingman coalescent.Theor Popul Biol2018
28709926An efficient algorithm for generating the internal branches of a Kingman coalescent.Theor Popul Biol2018
30218074Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans.Nat Commun2018
30486787Helmsman: fast and efficient mutation signature analysis for massive sequencing datasets.BMC Genomics2018
30415424Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.Int J Bipolar Disord2018
29279374Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.Proc Natl Acad Sci U S A2018
29414032Functional TSPO polymorphism predicts variance in the diurnal cortisol rhythm in bipolar disorder.Psychoneuroendocrinology2018
30218074Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans.Nat Commun2018
30486787Helmsman: fast and efficient mutation signature analysis for massive sequencing datasets.BMC Genomics2018
30415424Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics.Int J Bipolar Disord2018
29414032Functional TSPO polymorphism predicts variance in the diurnal cortisol rhythm in bipolar disorder.Psychoneuroendocrinology2018
29279374Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.Proc Natl Acad Sci U S A2018
26916109Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck.Genome Res2016
27329760Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.Hum Mol Genet2016
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Collaborators

Melvin G McInnis
University of Michigan ann arbor
Co-authored papers 18
Peng Zhang
University of Michigan ann arbor
Co-authored papers 11
Peter P Zandi
Johns Hopkins University School of Medicine
Co-authored papers 11
James B Potash
University Hospital Frankfurt
Co-authored papers 11
Matthew Zawistowski
Co-authored papers 11
John P Rice
Washington University School of Medicine
Co-authored papers 10
Michael Boehnke
Co-authored papers 10
Elliot S Gershon
University of Chicago
Co-authored papers 10
Chunyu Liu
Boston University School of Public Health
Co-authored papers 10
Evaristus Nwulia
Howard University Hospital
Co-authored papers 9
Thomas G Schulze
SUNY Upstate Medical University
Co-authored papers 9
Tatiana Foroud
Indiana University School of Medicine
Co-authored papers 9
David W Craig
University of Southern California
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Tiffany A Greenwood
University of California San Diego
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John I Nurnberger
Stark Neurosciences Research Institute, Indiana University School of Medicine
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Caroline M Nievergelt
VA San Diego Healthcare System (VASDHS)
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William Coryell
University of Iowa
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University of Pennsylvania
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Gon??alo R Abecasis
Regeneron Pharmaceuticals Inc.
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William A Scheftner
Rush Medical College
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William B Lawson
Howard University
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William Byerley
University of California san francisco
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Cinnamon Bloss
University of California
Co-authored papers 9
Erin N Smith
Department of Pediatrics and Rady's Children's Hospital, University of California
Co-authored papers 9
John R Kelsoe
University of California
Co-authored papers 9
Pamela B Mahon
Brigham & Women's Hospital, Harvard Medical School
Co-authored papers 9
Nicholas J Schork
University of California San Diego
Co-authored papers 9
Daniel L Koller
Indiana University School of Medicine
Co-authored papers 9
Howard J Edenberg
Indiana University School of Medicine
Co-authored papers 9
Maria Hipolito
Howard University Hospital
Co-authored papers 9
Release 1.2