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Author Details

Hua Tang
Stanford University School of Medicine
1999
115
48
PMIDPaper TitleJournal TitlePublished Year
37749212A computational framework for the inference of protein complex remodeling from whole-proteome measurements.Nat Methods2023
37749212A computational framework for the inference of protein complex remodeling from whole-proteome measurements.Nat Methods2023
34553764Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.Hum Mol Genet2022
36302058A Prism Vote method for individualized risk prediction of traits in genotype data of Multi-population.PLoS Genet2022
35861404Sex-biased admixture and assortative mating shape genetic variation and influence demographic inference in admixed Cabo Verdeans.G3 (Bethesda)2022
35922509Transcriptome variation in human tissues revealed by long-read sequencing.Nature2022
35915156Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.Nat Med2022
34553764Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative.Hum Mol Genet2022
35157715Expanding human variation at PLOS Genetics.PLoS Genet2022
35102136Rare transmission of commensal and pathogenic bacteria in the gut microbiome of hospitalized adults.Nat Commun2022
35861404Sex-biased admixture and assortative mating shape genetic variation and influence demographic inference in admixed Cabo Verdeans.G3 (Bethesda)2022
36302058A Prism Vote method for individualized risk prediction of traits in genotype data of Multi-population.PLoS Genet2022
35922509Transcriptome variation in human tissues revealed by long-read sequencing.Nature2022
35915156Large-scale genome-wide association study of coronary artery disease in genetically diverse populations.Nat Med2022
35102136Rare transmission of commensal and pathogenic bacteria in the gut microbiome of hospitalized adults.Nat Commun2022
35157715Expanding human variation at PLOS Genetics.PLoS Genet2022
33098413RobNorm: model-based robust normalization method for labeled quantitative mass spectrometry proteomics data.Bioinformatics2021
35492964Advances and challenges in quantitative delineation of the genetic architecture of complex traits.Quant Biol2021
33887194Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.Am J Hum Genet2021
34035245Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.Nat Commun2021
34087167Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.Am J Hum Genet2021
33821006Functional and structural basis of extreme conservation in vertebrate 5' untranslated regions.Nat Genet2021
33098413RobNorm: model-based robust normalization method for labeled quantitative mass spectrometry proteomics data.Bioinformatics2021
34582791Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.Am J Hum Genet2021
35492964Advances and challenges in quantitative delineation of the genetic architecture of complex traits.Quant Biol2021
33821006Functional and structural basis of extreme conservation in vertebrate 5' untranslated regions.Nat Genet2021
33887194Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.Am J Hum Genet2021
34582791Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program.Am J Hum Genet2021
34035245Identification of putative causal loci in whole-genome sequencing data via knockoff statistics.Nat Commun2021
34087167Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program.Am J Hum Genet2021
31489982Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017.Hum Mutat2020
31940240κ Opioid Receptor 1 Single Nucleotide Polymorphisms were Associated with the Methadone Dosage.Genet Test Mol Biomarkers2020
32652930Detecting fitness epistasis in recently admixed populations with genome-wide data.BMC Genomics2020
32888494The Polygenic and Monogenic Basis of Blood Traits and Diseases.Cell2020
31489982Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017.Hum Mutat2020
31940240κ Opioid Receptor 1 Single Nucleotide Polymorphisms were Associated with the Methadone Dosage.Genet Test Mol Biomarkers2020
32888494The Polygenic and Monogenic Basis of Blood Traits and Diseases.Cell2020
32652930Detecting fitness epistasis in recently admixed populations with genome-wide data.BMC Genomics2020
31127295A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.Hum Mol Genet2019
31603891Evaluating the strength of genetic results: Risks and responsibilities.PLoS Genet2019
31127295A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.Hum Mol Genet2019
31337231Association of <i>APOL1</i> Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran Program.Circulation2019
31603891Evaluating the strength of genetic results: Risks and responsibilities.PLoS Genet2019
31337231Association of <i>APOL1</i> Risk Alleles With Cardiovascular Disease in Blacks in the Million Veteran Program.Circulation2019
29455858A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.Am J Hum Genet2018
29912962Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.PLoS One2018
30571773Doubling down on forensic twin studies.PLoS Genet2018
30275531Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program.Nat Genet2018
29750786Correction: Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations.PLoS Genet2018
29455858A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.Am J Hum Genet2018
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Collaborators

Charles Kooperberg
Co-authored papers 22
Alexander P Reiner
Co-authored papers 20
Xiaofeng Zhu
Co-authored papers 19
Eric Boerwinkle
Baylor College of Medicine
Co-authored papers 19
Lisa R Yanek
Co-authored papers 15
Richard S Cooper
Loyola University Chicago
Co-authored papers 14
Ruth J F Loos
Co-authored papers 14
Bruce M Psaty
Co-authored papers 14
Alanna C Morrison
Co-authored papers 13
Jerome I Rotter
Co-authored papers 13
Sharon L R Kardia
School of Public Health, University of Michigan ann arbor
Co-authored papers 13
Myriam Fornage
Co-authored papers 13
Gregory S Barsh
HudsonAlpha Institute for Biotechnology, Stanford University
Co-authored papers 12
Dabeeru C Rao
Co-authored papers 11
Themistocles L Assimes
Co-authored papers 11
Mike A Nalls
Center for Alzheimer's and Related Dementias, National Institutes of Health
Co-authored papers 11
Bamidele O Tayo
Loyola University Medical Center.
Co-authored papers 11
Alan B Zonderman
National Institute on Aging
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Michele K Evans
National Institute on Aging
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Leslie A Lange
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Diane M Becker
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Albert V Smith
University of Michigan School of Public Health ann arbor
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Guillaume Lettre
Co-authored papers 10
Nora Franceschini
University of North Carolina
Co-authored papers 10
Kent D Taylor
Co-authored papers 9
Erwin P Bottinger
Hasso Plattner Institute for Digital Health at Mount Sinai
Co-authored papers 9
Elad Ziv
Institute for Human Genetics, University of California San Francisco (UCSF)
Co-authored papers 9
Paul L Auer
Co-authored papers 9
Andrew D Johnson
and Blood Institute
Co-authored papers 9
Christopher J O'Donnell
Brigham and Women's Hospital, Harvard Medical School
Co-authored papers 9
Release 1.2