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Author Details

Tushar Bhangale
Genentech Inc.
2004
47
34
PMIDPaper TitleJournal TitlePublished Year
37196676Inhibiting membrane rupture with NINJ1 antibodies limits tissue injury.Nature2023
37652990Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials.Sci Rep2023
37344884Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy.Genome Med2023
36952338Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration.Cell Rep2023
37196676Inhibiting membrane rupture with NINJ1 antibodies limits tissue injury.Nature2023
37291107South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.Nat Commun2023
37652990Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials.Sci Rep2023
36952338Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration.Cell Rep2023
37291107South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.Nat Commun2023
37344884Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy.Genome Med2023
35368043A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk.Sci Rep2022
35368043A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk.Sci Rep2022
34464706Genetic ablation of Gpnmb does not alter synuclein-related pathology.Neurobiol Dis2021
34464706Genetic ablation of Gpnmb does not alter synuclein-related pathology.Neurobiol Dis2021
32430334Polygenic risk for skin autoimmunity impacts immune checkpoint blockade in bladder cancer.Proc Natl Acad Sci U S A2020
32430334Polygenic risk for skin autoimmunity impacts immune checkpoint blockade in bladder cancer.Proc Natl Acad Sci U S A2020
31995762Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration.Cell Rep2020
31995762Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration.Cell Rep2020
29550837Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms.Genes Immun2019
30366082Enabling genome-wide association testing with multiple diseases and no healthy controls.Gene2019
29550837Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms.Genes Immun2019
30948477PTCD1 Is Required for Mitochondrial Oxidative-Phosphorylation: Possible Genetic Association with Alzheimer's Disease.J Neurosci2019
30948477PTCD1 Is Required for Mitochondrial Oxidative-Phosphorylation: Possible Genetic Association with Alzheimer's Disease.J Neurosci2019
30366082Enabling genome-wide association testing with multiple diseases and no healthy controls.Gene2019
29439679Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India.BMC Med Genet2018
29891356Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study.Lancet Respir Med2018
30446528Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of <i>ERAP2</i> transcripts under balancing selection.Genome Res2018
30388101Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease.PLoS Genet2018
30463956Germline genetic polymorphisms influence tumor gene expression and immune cell infiltration.Proc Natl Acad Sci U S A2018
29439679Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India.BMC Med Genet2018
29891356Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study.Lancet Respir Med2018
30463956Germline genetic polymorphisms influence tumor gene expression and immune cell infiltration.Proc Natl Acad Sci U S A2018
30446528Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of <i>ERAP2</i> transcripts under balancing selection.Genome Res2018
30388101Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease.PLoS Genet2018
28035029geneAttribution: trait agnostic identification of candidate genes associated with noncoding variation.Bioinformatics2017
28637922Targeting factor D of the alternative complement pathway reduces geographic atrophy progression secondary to age-related macular degeneration.Sci Transl Med2017
28892059A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.Nat Genet2017
28714988SNP-mediated disruption of CTCF binding at the IFITM3 promoter is associated with risk of severe influenza in humans.Nat Med2017
28714469Transancestral mapping and genetic load in systemic lupus erythematosus.Nat Commun2017
28531322Evaluation of IFITM3 rs12252 Association With Severe Pediatric Influenza Infection.J Infect Dis2017
28738841Identifying and mitigating batch effects in whole genome sequencing data.BMC Bioinformatics2017
28035029geneAttribution: trait agnostic identification of candidate genes associated with noncoding variation.Bioinformatics2017
28106546A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains.J Alzheimers Dis2017
28106546A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains.J Alzheimers Dis2017
28531322Evaluation of IFITM3 rs12252 Association With Severe Pediatric Influenza Infection.J Infect Dis2017
28637922Targeting factor D of the alternative complement pathway reduces geographic atrophy progression secondary to age-related macular degeneration.Sci Transl Med2017
28738841Identifying and mitigating batch effects in whole genome sequencing data.BMC Bioinformatics2017
28714988SNP-mediated disruption of CTCF binding at the IFITM3 promoter is associated with risk of severe influenza in humans.Nat Med2017
28714469Transancestral mapping and genetic load in systemic lupus erythematosus.Nat Commun2017
28892059A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.Nat Genet2017
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Collaborators

Genentech Inc.
Co-authored papers 23
Genentech Inc.
Co-authored papers 22
University of Minnesota School of Medicine
Co-authored papers 10
Genentech Inc.
Co-authored papers 8
Genentech Inc.
Co-authored papers 7
Brigham and Women's Hospital and Harvard Medical School
Co-authored papers 5
Genentech Inc.
Co-authored papers 5
Co-authored papers 5
University of Washington
Co-authored papers 5
Co-authored papers 4
Co-authored papers 4
Co-authored papers 4
Icahn School of Medicine at Mount Sinai
Co-authored papers 4
Co-authored papers 3
Co-authored papers 3
University of Iceland
Co-authored papers 3
Co-authored papers 3
Erasmus University Medical Center
Co-authored papers 3
Co-authored papers 3
Baylor College of Medicine
Co-authored papers 3
Co-authored papers 3
University of Iceland
Co-authored papers 3
University of California davis
Co-authored papers 3
University of Oxford
Co-authored papers 3
Co-authored papers 3
Boston University Chobanian & Avedisian School of Medicine
Co-authored papers 3
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 3
Co-authored papers 3
Co-authored papers 3
Co-authored papers 3