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Author Details

Brian L Yaspan
Genentech Inc.
2001
66
29
PMIDPaper TitleJournal TitlePublished Year
36343773A genome-wide association study of chronic spontaneous urticaria risk and heterogeneity.J Allergy Clin Immunol2023
37585454Multi-ancestry GWAS analysis identifies two novel loci associated with diabetic eye disease and highlights APOL1 as a high risk locus in patients with diabetic macular edema.PLoS Genet2023
37546732Association study of human leukocyte antigen (HLA) variants and idiopathic pulmonary fibrosis.medRxiv2023
36952338Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration.Cell Rep2023
37388919A systems biology approach uncovers novel disease mechanisms in age-related macular degeneration.Cell Genom2023
37079518Rare CIDEC coding variants enriched in age-related macular degeneration patients with small low-luminance deficit cause lipid droplet and fat storage defects.PLoS One2023
36780644PCSK6 and Survival in Idiopathic Pulmonary Fibrosis.Am J Respir Crit Care Med2023
36603154Identification of a Genetic Susceptibility Locus for Idiopathic Pulmonary Fibrosis in the 16p Subtelomere Using Whole-Genome Sequencing.Am J Respir Crit Care Med2023
34166655Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy.Am J Ophthalmol2022
35368043A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk.Sci Rep2022
35659450Erratum to Gene Set Enrichment Analyses Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy. Am J Ophthalmol 2022;233:111-123.Am J Ophthalmol2022
35487308Genome-wide association study identifies kallikrein 5 in type 2 inflammation-low asthma.J Allergy Clin Immunol2022
35688625Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis.Thorax2022
36516271Dual antibody inhibition of KLK5 and KLK7 for Netherton syndrome and atopic dermatitis.Sci Transl Med2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
31710517Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis.Am J Respir Crit Care Med2020
31995762Integration of eQTL and a Single-Cell Atlas in the Human Eye Identifies Causal Genes for Age-Related Macular Degeneration.Cell Rep2020
31978350An Allosteric Anti-tryptase Antibody for the Treatment of Mast Cell-Mediated Severe Asthma.Cell2020
29550837Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms.Genes Immun2019
31585081An Allosteric Anti-tryptase Antibody for the Treatment of Mast Cell-Mediated Severe Asthma.Cell2019
31268371Rare Protein-Altering Telomere-related Gene Variants in Patients with Chronic Hypersensitivity Pneumonitis.Am J Respir Crit Care Med2019
31021381Imaging, Genetic, and Demographic Factors Associated With Conversion to Neovascular Age-Related Macular Degeneration: Secondary Analysis of a Randomized Clinical Trial.JAMA Ophthalmol2019
30487263Multiethnic Genome-Wide Association Study of Diabetic Retinopathy Using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control.Diabetes2019
30366082Enabling genome-wide association testing with multiple diseases and no healthy controls.Gene2019
30387919Strategies for Pathway Analysis Using GWAS and WGS Data.Curr Protoc Hum Genet2019
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
28637922Targeting factor D of the alternative complement pathway reduces geographic atrophy progression secondary to age-related macular degeneration.Sci Transl Med2017
26752265Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.Nat Genet2016
27153576Pathway analysis by randomization incorporating structure-PARIS: an update.Bioinformatics2016
26774822Regulation of T Cell Receptor Signaling by DENND1B in TH2 Cells and Allergic Disease.Cell2016
26742632Age-related macular degeneration: Complement in action.Immunobiology2016
25483601Functional analysis of protective IL1RL1 variants associated with asthma risk.J Allergy Clin Immunol2015
25934386Stratified medicine in inflammatory disorders: From theory to practice.Clin Immunol2015
24002674Genome-wide association study and meta-analysis of intraocular pressure.Hum Genet2014
25414181DNA copy number variants of known glaucoma genes in relation to primary open-angle glaucoma.Invest Ophthalmol Vis Sci2014
25037249Hypothesis-independent pathway analysis implicates GABA and acetyl-CoA metabolism in primary open-angle glaucoma and normal-pressure glaucoma.Hum Genet2014
24603425Vascular tone pathway polymorphisms in relation to primary open-angle glaucoma.Eye (Lond)2014
24572674Association of CAV1/CAV2 genomic variants with primary open-angle glaucoma overall and by gender and pattern of visual field loss.Ophthalmology2014
24105633Mechanisms of age-related macular degeneration and therapeutic opportunities.J Pathol2014
22828004The NEIGHBOR consortium primary open-angle glaucoma genome-wide association study: rationale, study design, and clinical variables.J Glaucoma2013
23869166Estrogen pathway polymorphisms in relation to primary open angle glaucoma: an analysis accounting for gender from the United States.Mol Vis2013
23953133Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome.Mol Autism2013
23455636Seven new loci associated with age-related macular degeneration.Nat Genet2013
23291589Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.Nat Genet2013
23111177CDKN2B-AS1 genotype-glaucoma feature correlations in primary open-angle glaucoma patients from the United States.Am J Ophthalmol2013
21996756A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder.Hum Genet2012
22661486Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia.Invest Ophthalmol Vis Sci2012
22570617Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.PLoS Genet2012
22301922Measuring alcohol consumption for genomic meta-analyses of alcohol intake: opportunities and challenges.Am J Clin Nutr2012
21279722Genetic analysis of biological pathway data through genomic randomization.Hum Genet2011
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Collaborators

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Kang Zhang
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Augusta University
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Gadi Wollstein
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Terry Gaasterland
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Jamie E Craig
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Peter Kraft
Harvard T. H. Chan School of Public Health
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Allison E Ashley-Koch
Co-authored papers 5
Mark I McCarthy
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William K Scott
John P. Hussman Institute for Human Genomics.
Co-authored papers 5
Daniel H Geschwind
University of California los angeles
Co-authored papers 5
Ching-Yu Cheng
Singapore Eye Research Institute, Singapore Duke-NUS Medical School
Co-authored papers 5
Joseph D Buxbaum
Icahn School of Medicine at Mount Sinai
Co-authored papers 5
Kent D Taylor
Co-authored papers 4
Edwin H Cook
Co-authored papers 4
Mark H Ginsberg
University of California
Co-authored papers 4
Robert R Graham
Genentech Inc.
Co-authored papers 4
Sudha K Iyengar
Co-authored papers 4
Release 1.2