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Paper Details

Shared genetic variants suggest common pathways in allergy and autoimmune diseases.
J Allergy Clin Immunol
43
2017
290 loci, DNase-hypersensitive site, Encode, SNPs, allergy, autoimmune diseases, autoimmune disorders, chromatin, common loci, gene regulatory regions, genetic loci, genetic variants, immune cells, patients, sensitization, single nucleotide polymorphisms, susceptibility loci, tissue-specific regulatory sites, transcription factor binding sites
Author NameAffiliation
Tune H PersThe Novo Nordisk Foundation Center for Basic Metabolic Research, University of Copenhagen, Denmark Division of Endocrinology and Center for Basic and Translational Obesity Research, Boston Children's Hospital, Broad Institute of MIT and Harvard, Statens Serum Institut
Lude FrankeUniversity of Groningen, University Medical Centre Groningen
Joel N HirschhornDivision of Endocrinology and Center for Basic and Translational Obesity Research, Boston Children's Hospital, Broad Institute of MIT and Harvard, Harvard Medical School
Joel N HirschhornDivision of Endocrinology and Center for Basic and Translational Obesity Research, Boston Children's Hospital, Broad Institute of MIT and Harvard, Harvard Medical School
Alan L JamesBusselton Population Medical Research Foundation, Sir Charles Gairdner Hospital, University of West Australia, West Australian Sleep Disorders Research Institute
Marjo-Riitta JärvelinSchool of Public Health, Imperial College London, United Kingdom Center for Life Course Epidemiology, University of Oulu, Oulu University Hospital, National Institute for Health and Welfare
Nicholas J TimpsonUniversity of Bristol
Manuel A R FerreiraQIMR Berghofer Medical Research Institute
Manuel A R FerreiraQIMR Berghofer Medical Research Institute
David P StrachanPopulation Health Research Institute, University of London
David A Hinds
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