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Author Details

Robert R Graham
Genentech Inc.
2001
88
52
PMIDPaper TitleJournal TitlePublished Year
36829046Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36653562FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36829046Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36653562FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
35487308Genome-wide association study identifies kallikrein 5 in type 2 inflammation-low asthma.J Allergy Clin Immunol2022
35487308Genome-wide association study identifies kallikrein 5 in type 2 inflammation-low asthma.J Allergy Clin Immunol2022
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
29550837Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms.Genes Immun2019
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
30997344Influence of genetic copy number variants of the human GLUT3 glucose transporter gene <i>SLC2A3</i> on protein expression, glycolysis and rheumatoid arthritis risk: A genetic replication study.Mol Genet Metab Rep2019
30948477PTCD1 Is Required for Mitochondrial Oxidative-Phosphorylation: Possible Genetic Association with Alzheimer's Disease.J Neurosci2019
30997344Influence of genetic copy number variants of the human GLUT3 glucose transporter gene <i>SLC2A3</i> on protein expression, glycolysis and rheumatoid arthritis risk: A genetic replication study.Mol Genet Metab Rep2019
30388101Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease.PLoS Genet2018
30388101Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease.PLoS Genet2018
28892059A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.Nat Genet2017
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
28714976Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.Nat Genet2017
28714469Transancestral mapping and genetic load in systemic lupus erythematosus.Nat Commun2017
28738841Identifying and mitigating batch effects in whole genome sequencing data.BMC 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
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
28714976Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.Nat Genet2017
28714469Transancestral mapping and genetic load in systemic lupus erythematosus.Nat Commun2017
27723758Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.Nat Genet2016
27723758Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.Nat Genet2016
25531812Rarity of the Alzheimer disease-protective APP A673T variant in the United States.JAMA Neurol2015
25531812Rarity of the Alzheimer disease-protective APP A673T variant in the United States.JAMA Neurol2015
25849893TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits.PLoS One2015
25512081RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency.J Allergy Clin Immunol2015
26214276Genetic Modifiers of Age at Onset in Carriers of the G206A Mutation in PSEN1 With Familial Alzheimer Disease Among Caribbean Hispanics.JAMA Neurol2015
26502338Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus.Nat Genet2015
26382853The Ro60 autoantigen binds endogenous retroelements and regulates inflammatory gene expression.Science2015
26382853The Ro60 autoantigen binds endogenous retroelements and regulates inflammatory gene expression.Science2015
26502338Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus.Nat Genet2015
26214276Genetic Modifiers of Age at Onset in Carriers of the G206A Mutation in PSEN1 With Familial Alzheimer Disease Among Caribbean Hispanics.JAMA Neurol2015
25849893TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits.PLoS One2015
25512081RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency.J Allergy Clin Immunol2015
24439484Missense variant in TREML2 protects against Alzheimer's disease.Neurobiol Aging2014
25419706A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death.Nat Med2014
24439484Missense variant in TREML2 protects against Alzheimer's disease.Neurobiol Aging2014
24390342Genetics of rheumatoid arthritis contributes to biology and drug discovery.Nature2014
24702955Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription.Am J Hum Genet2014
25096029Using gene expression to improve the power of genome-wide association analysis.Hum Hered2014
24925725Lupus nephritis susceptibility loci in women with systemic lupus erythematosus.J Am Soc Nephrol2014
24598797MHC associations with clinical and autoantibody manifestations in European SLE.Genes Immun2014
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Collaborators

Genentech Inc.
Co-authored papers 68
University of Minnesota School of Medicine
Co-authored papers 30
Co-authored papers 28
Co-authored papers 24
Co-authored papers 24
Genentech Inc.
Co-authored papers 22
Co-authored papers 21
Wake Forest University School of Medicine
Co-authored papers 17
Co-authored papers 17
Co-authored papers 16
Co-authored papers 13
Massachusetts General Hospital
Co-authored papers 12
Co-authored papers 12
University of California davis
Co-authored papers 12
Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)
Co-authored papers 11
Co-authored papers 11
US Department of Veterans Affairs Medical Center
Co-authored papers 11
Co-authored papers 10
Co-authored papers 9
Co-authored papers 8
Co-authored papers 8
Co-authored papers 8
Genentech Inc.
Co-authored papers 8
Co-authored papers 8
Co-authored papers 7
Co-authored papers 7
Vertex Pharmaceuticals
Co-authored papers 7
Co-authored papers 6
Icahn School of Medicine at Mount Sinai
Co-authored papers 6
Co-authored papers 6