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Author Details
Full Name
Tushar Bhangale
Affiliation
Genentech Inc.
ORCID
Career Start Year
2004
Papers
47
H Index
34
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37196676
Inhibiting membrane rupture with NINJ1 antibodies limits tissue injury.
Nature
2023
37652990
Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials.
Sci Rep
2023
37344884
Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy.
Genome Med
2023
36952338
Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration.
Cell Rep
2023
37196676
Inhibiting membrane rupture with NINJ1 antibodies limits tissue injury.
Nature
2023
37291107
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.
Nat Commun
2023
37652990
Genome-wide study of longitudinal brain imaging measures of multiple sclerosis progression across six clinical trials.
Sci Rep
2023
36952338
Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration.
Cell Rep
2023
37291107
South Asian medical cohorts reveal strong founder effects and high rates of homozygosity.
Nat Commun
2023
37344884
Whole genome sequencing across clinical trials identifies rare coding variants in GPR68 associated with chemotherapy-induced peripheral neuropathy.
Genome Med
2023
35368043
A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk.
Sci Rep
2022
35368043
A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk.
Sci Rep
2022
34464706
Genetic ablation of Gpnmb does not alter synuclein-related pathology.
Neurobiol Dis
2021
34464706
Genetic ablation of Gpnmb does not alter synuclein-related pathology.
Neurobiol Dis
2021
32430334
Polygenic risk for skin autoimmunity impacts immune checkpoint blockade in bladder cancer.
Proc Natl Acad Sci U S A
2020
32430334
Polygenic risk for skin autoimmunity impacts immune checkpoint blockade in bladder cancer.
Proc Natl Acad Sci U S A
2020
31995762
Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration.
Cell Rep
2020
31995762
Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration.
Cell Rep
2020
29550837
Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms.
Genes Immun
2019
30366082
Enabling genome-wide association testing with multiple diseases and no healthy controls.
Gene
2019
29550837
Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms.
Genes Immun
2019
30948477
PTCD1 Is Required for Mitochondrial Oxidative-Phosphorylation: Possible Genetic Association with Alzheimer's Disease.
J Neurosci
2019
30948477
PTCD1 Is Required for Mitochondrial Oxidative-Phosphorylation: Possible Genetic Association with Alzheimer's Disease.
J Neurosci
2019
30366082
Enabling genome-wide association testing with multiple diseases and no healthy controls.
Gene
2019
29439679
Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India.
BMC Med Genet
2018
29891356
Analysis 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 Med
2018
30446528
Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of <i>ERAP2</i> transcripts under balancing selection.
Genome Res
2018
30388101
Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease.
PLoS Genet
2018
30463956
Germline genetic polymorphisms influence tumor gene expression and immune cell infiltration.
Proc Natl Acad Sci U S A
2018
29439679
Comprehensive genomic analysis identifies pathogenic variants in maturity-onset diabetes of the young (MODY) patients in South India.
BMC Med Genet
2018
29891356
Analysis 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 Med
2018
30463956
Germline genetic polymorphisms influence tumor gene expression and immune cell infiltration.
Proc Natl Acad Sci U S A
2018
30446528
Genetic analysis of isoform usage in the human anti-viral response reveals influenza-specific regulation of <i>ERAP2</i> transcripts under balancing selection.
Genome Res
2018
30388101
Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease.
PLoS Genet
2018
28035029
geneAttribution: trait agnostic identification of candidate genes associated with noncoding variation.
Bioinformatics
2017
28637922
Targeting factor D of the alternative complement pathway reduces geographic atrophy progression secondary to age-related macular degeneration.
Sci Transl Med
2017
28892059
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.
Nat Genet
2017
28714988
SNP-mediated disruption of CTCF binding at the IFITM3 promoter is associated with risk of severe influenza in humans.
Nat Med
2017
28714469
Transancestral mapping and genetic load in systemic lupus erythematosus.
Nat Commun
2017
28531322
Evaluation of IFITM3 rs12252 Association With Severe Pediatric Influenza Infection.
J Infect Dis
2017
28738841
Identifying and mitigating batch effects in whole genome sequencing data.
BMC Bioinformatics
2017
28035029
geneAttribution: trait agnostic identification of candidate genes associated with noncoding variation.
Bioinformatics
2017
28106546
A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains.
J Alzheimers Dis
2017
28106546
A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains.
J Alzheimers Dis
2017
28531322
Evaluation of IFITM3 rs12252 Association With Severe Pediatric Influenza Infection.
J Infect Dis
2017
28637922
Targeting factor D of the alternative complement pathway reduces geographic atrophy progression secondary to age-related macular degeneration.
Sci Transl Med
2017
28738841
Identifying and mitigating batch effects in whole genome sequencing data.
BMC Bioinformatics
2017
28714988
SNP-mediated disruption of CTCF binding at the IFITM3 promoter is associated with risk of severe influenza in humans.
Nat Med
2017
28714469
Transancestral mapping and genetic load in systemic lupus erythematosus.
Nat Commun
2017
28892059
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.
Nat Genet
2017
1 - 50 of 94
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row(s) 1 - 30 of 30
Collaborators
Timothy W Behrens
Genentech Inc.
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Robert R Graham
Genentech Inc.
Co-authored papers
22
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University of Minnesota School of Medicine
Co-authored papers
10
Julie Hunkapiller
Genentech Inc.
Co-authored papers
8
Brian L Yaspan
Genentech Inc.
Co-authored papers
7
Soumya Raychaudhuri
Brigham and Women's Hospital and Harvard Medical School
Co-authored papers
5
Arthur Wuster
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Co-authored papers
5
Lindsey A Criswell
Co-authored papers
5
Deborah A Nickerson
University of Washington
Co-authored papers
5
Sekar Kathiresan
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4
Javier MartÃn
Co-authored papers
4
Mark I McCarthy
Co-authored papers
4
Alison M Goate
Icahn School of Medicine at Mount Sinai
Co-authored papers
4
Mark J Rieder
Co-authored papers
3
Deborah S Cunninghame Graham
Co-authored papers
3
Kari Stefansson
University of Iceland
Co-authored papers
3
Alistair S Hall
Co-authored papers
3
Andr?? G Uitterlinden
Erasmus University Medical Center
Co-authored papers
3
Peter K Gregersen
Co-authored papers
3
Eric Boerwinkle
Baylor College of Medicine
Co-authored papers
3
Nilesh J Samani
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3
Unnur Thorsteinsdottir
University of Iceland
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3
Michael F Seldin
University of California davis
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3
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3
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