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Author Details

Matthew Aguirre
Stanford University School of Medicine.
2017
15
9
PMIDPaper TitleJournal TitlePublished Year
37026454Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes.Circ Genom Precis Med2023
37026454Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes.Circ Genom Precis Med2023
37017090Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy.Circ Genom Precis Med2023
37017090Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy.Circ Genom Precis Med2023
35588732Integration of rare expression outlier-associated variants improves polygenic risk prediction.Am J Hum Genet2022
35588732Integration of rare expression outlier-associated variants improves polygenic risk prediction.Am J Hum Genet2022
34608296Author Correction: Genetics of 35 blood and urine biomarkers in the UK Biobank.Nat Genet2021
33558700Polygenic risk modeling with latent trait-related genetic components.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
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
30610202Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide.Mol Psychiatry2020
32275883Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases.Am J Hum Genet2020
33095761A fast and scalable framework for large-scale and ultrahigh-dimensional sparse regression with application to the UK Biobank.PLoS Genet2020
33226994A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population.PLoS Genet2020
30610202Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide.Mol Psychiatry2020
33226994A phenome-wide association study of 26 mendelian genes reveals phenotypic expressivity of common and rare variants within the general population.PLoS Genet2020
33095761A fast and scalable framework for large-scale and ultrahigh-dimensional sparse regression with application to the UK Biobank.PLoS Genet2020
32275883Assessing Digital Phenotyping to Enhance Genetic Studies of Human Diseases.Am J Hum Genet2020
30520965Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics.Bioinformatics2019
30520965Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics.Bioinformatics2019
31492854Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology.Nat Commun2019
31353025Phenome-wide Burden of Copy-Number Variation in the UK Biobank.Am J Hum Genet2019
31353025Phenome-wide Burden of Copy-Number Variation in the UK Biobank.Am J Hum Genet2019
31492854Components of genetic associations across 2,138 phenotypes in the UK Biobank highlight adipocyte biology.Nat Commun2019
29517003Corrigendum: Landscape of X chromosome inactivation across human tissues.Nature2018
29517003Corrigendum: Landscape of X chromosome inactivation across human tissues.Nature2018
29022598Landscape of X chromosome inactivation across human tissues.Nature2017
29022598Landscape of X chromosome inactivation across human tissues.Nature2017
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Collaborators

Manuel A Rivas
Stanford University School of Medicine
Co-authored papers 13
Yosuke Tanigawa
USA Broad Institute of MIT and Harvard
Co-authored papers 9
Christopher DeBoever
Stanford University
Co-authored papers 4
James R Priest
Stanford University School of Medicine
Co-authored papers 3
François Aguet
Co-authored papers 2
Jamie L Marshall
Co-authored papers 2
Themistocles L Assimes
Co-authored papers 2
Johanne M Justesen
Co-authored papers 2
Daniel G MacArthur
Broad Institute of MIT and Harvard
Co-authored papers 2
Aviv Regev
Broad Institute of MIT and Harvard
Co-authored papers 2
Alexandra-Chloé Villani
Co-authored papers 2
Erik Ingelsson
Stanford University School of Medicine
Co-authored papers 2
Laura Gauthier
Co-authored papers 2
Kristin G Ardlie
Co-authored papers 2
Mark J Daly
Massachusetts General Hospital
Co-authored papers 2
Andrea Byrnes
Co-authored papers 2
Mark Fleharty
Broad Institute of Harvard and MIT and Harvard
Co-authored papers 2
Konrad J Karczewski
Broad Institute of MIT and Harvard
Co-authored papers 2
Angela Yen
Co-authored papers 2
Beryl B Cummings
Co-authored papers 2
Rahul Satija
Center for Genomics and Systems Biology, New York University
Co-authored papers 2
Catherine Tcheandjieu
Gladstone Institute of Data Science and Biotechnology, Gladstone Institutes
Co-authored papers 2
Tuuli Lappalainen
Columbia University
Co-authored papers 2
Nir Hacohen
Broad Institute of MIT and Harvard
Co-authored papers 2
Stephane E Castel
Co-authored papers 2
Andrew Kirby
Co-authored papers 2
Taru Tukiainen
Co-authored papers 2
Praneetha Potiny
Stanford Cardiovascular Institute, Stanford University
Co-authored papers 1
Douglas M Ruderfer
Vanderbilt University Medical Center
Co-authored papers 1
Colin G Walsh
Vanderbilt University, Vanderbilt University Medical Center
Co-authored papers 1
Release 1.2