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Author Details

Manuel A Rivas
Stanford University School of Medicine
2008
99
42
PMIDPaper TitleJournal TitlePublished Year
36696485SGLT2 inhibitor ameliorates endothelial dysfunction associated with the common <i>ALDH2</i> alcohol flushing variant.Sci Transl Med2023
36696485SGLT2 inhibitor ameliorates endothelial dysfunction associated with the common <i>ALDH2</i> alcohol flushing variant.Sci Transl Med2023
37188663Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy.Nat Commun2023
37188663Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy.Nat Commun2023
32989444Fast Lasso method for large-scale and ultrahigh-dimensional Cox model with applications to UK Biobank.Biostatistics2022
35588732Integration of rare expression outlier-associated variants improves polygenic risk prediction.Am J Hum Genet2022
36038634Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.Nat Genet2022
35581355Opportunities and challenges for the use of common controls in sequencing studies.Nat Rev Genet2022
36091495LARGE-SCALE MULTIVARIATE SPARSE REGRESSION WITH APPLICATIONS TO UK BIOBANK.Ann Appl Stat2022
34269393Corrigendum to: Fast Lasso method for large-scale and ultrahigh-dimensional Cox model with applications to UK Biobank.Biostatistics2022
32989444Fast Lasso method for large-scale and ultrahigh-dimensional Cox model with applications to UK Biobank.Biostatistics2022
35324888Significant sparse polygenic risk scores across 813 traits in UK Biobank.PLoS Genet2022
35581355Opportunities and challenges for the use of common controls in sequencing studies.Nat Rev Genet2022
35588732Integration of rare expression outlier-associated variants improves polygenic risk prediction.Am J Hum Genet2022
36038634Large-scale sequencing identifies multiple genes and rare variants associated with Crohn's disease susceptibility.Nat Genet2022
36091495LARGE-SCALE MULTIVARIATE SPARSE REGRESSION WITH APPLICATIONS TO UK BIOBANK.Ann Appl Stat2022
35324888Significant sparse polygenic risk scores across 813 traits in UK Biobank.PLoS Genet2022
34269393Corrigendum to: Fast Lasso method for large-scale and ultrahigh-dimensional Cox model with applications to UK Biobank.Biostatistics2022
32873964Sex-specific genetic effects across biomarkers.Eur J Hum Genet2021
33590606Exome sequencing in patient-parent trios suggests new candidate genes for early-onset primary sclerosing cholangitis.Liver Int2021
33587031GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background.Elife2021
34216550Nonsense-mediated decay is highly stable across individuals and tissues.Am J Hum Genet2021
34108459Time trajectories in the transcriptomic response to exercise - a meta-analysis.Nat Commun2021
33513366A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density.Cell Metab2021
34146108Fast numerical optimization for genome sequencing data in population biobanks.Bioinformatics2021
33560296Survival analysis on rare events using group-regularized multi-response Cox regression.Bioinformatics2021
33558700Polygenic risk modeling with latent trait-related genetic components.Eur J Hum Genet2021
33441555Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks.Nat Commun2021
34029116Combining Clinical and Polygenic Risk Improves Stroke Prediction Among Individuals With Atrial Fibrillation.Circ Genom Precis Med2021
32651235Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBD.Gut2021
32873964Sex-specific genetic effects across biomarkers.Eur J Hum Genet2021
34608296Author Correction: Genetics of 35 blood and urine biomarkers in the UK Biobank.Nat Genet2021
34822764Bayesian model comparison for rare-variant association studies.Am J Hum Genet2021
34594039A cross-population atlas of genetic associations for 220 human phenotypes.Nat Genet2021
34637446Association of accelerometer-derived sleep measures with lifetime psychiatric diagnoses: A cross-sectional study of 89,205 participants from the UK Biobank.PLoS Med2021
33513366A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density.Cell Metab2021
33590606Exome sequencing in patient-parent trios suggests new candidate genes for early-onset primary sclerosing cholangitis.Liver Int2021
33587031GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background.Elife2021
33560296Survival analysis on rare events using group-regularized multi-response Cox regression.Bioinformatics2021
33558700Polygenic risk modeling with latent trait-related genetic components.Eur J Hum Genet2021
34822764Bayesian model comparison for rare-variant association studies.Am J Hum Genet2021
34637446Association of accelerometer-derived sleep measures with lifetime psychiatric diagnoses: A cross-sectional study of 89,205 participants from the UK Biobank.PLoS Med2021
34608296Author Correction: Genetics of 35 blood and urine biomarkers in the UK Biobank.Nat Genet2021
34594039A cross-population atlas of genetic associations for 220 human phenotypes.Nat Genet2021
34216550Nonsense-mediated decay is highly stable across individuals and tissues.Am J Hum Genet2021
34146108Fast numerical optimization for genome sequencing data in population biobanks.Bioinformatics2021
34029116Combining Clinical and Polygenic Risk Improves Stroke Prediction Among Individuals With Atrial Fibrillation.Circ Genom Precis Med2021
34108459Time trajectories in the transcriptomic response to exercise - a meta-analysis.Nat Commun2021
33441555Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks.Nat Commun2021
32651235Whole exome sequencing analyses reveal gene-microbiota interactions in the context of IBD.Gut2021
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Collaborators

Mark J Daly
Massachusetts General Hospital
Co-authored papers 34
Mark I McCarthy
Co-authored papers 22
Yosuke Tanigawa
USA Broad Institute of MIT and Harvard
Co-authored papers 20
David Altshuler
Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)
Co-authored papers 16
Erik Ingelsson
Stanford University School of Medicine
Co-authored papers 15
Michael Boehnke
Co-authored papers 15
Benjamin M Neale
Massachusetts General Hospital
Co-authored papers 14
Cecilia M Lindgren
Co-authored papers 14
John D Rioux
Co-authored papers 14
Andre Franke
Institute of Clinical Molecular Biology, Kiel University
Co-authored papers 13
Johanne M Justesen
Co-authored papers 13
Adam E Locke
Co-authored papers 13
Matthew Aguirre
Stanford University School of Medicine.
Co-authored papers 13
Daniel G MacArthur
Broad Institute of MIT and Harvard
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Gon??alo R Abecasis
Regeneron Pharmaceuticals Inc.
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Alisa K Manning
Co-authored papers 13
James G Wilson
Beth Israel Deaconess Medical Center
Co-authored papers 12
Jose C Florez
Co-authored papers 12
Xueling Sim
Co-authored papers 12
Andrew P Morris
The University of Manchester
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Markku Laakso
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Stacey Gabriel
Broad Institute of MIT and Harvard
Co-authored papers 12
Jason Flannick
Co-authored papers 11
Robert A Scott
Co-authored papers 11
Ramnik J Xavier
Broad Institute of MIT and Harvard
Co-authored papers 11
Peter Donnelly
University of Oxford
Co-authored papers 11
Karen L Mohlke
Co-authored papers 11
Tim D Spector
King's College London
Co-authored papers 11
Veikko Salomaa
Co-authored papers 11
Allan Linneberg
Co-authored papers 11
Release 1.2