Exome Sequencing and Rare Variant Analysis Reveals Multiple Filaggrin Mutations in Bangladeshi Families with Atopic Eczema and Additional Risk Genes
Year: 2018
Type: article
Study design: Observational Study
Authors: Manuela Pigors, John E.A. Common, Xuan Fei Colin C. Wong, Sajid Malik, Claire A. Scott, Niloofar Tabarra, Herty Liany, Jianjun Liu, Vachiranee Limviphuvadh, Sebastian Maurer-Stroh, Mark B.Y. Tang, Nicholas Lench, David J. Margolis, David A. van Heel, Charles A. Mein, Natalija Novak, Hansjörg Baurecht, Stephan Weidinger, W.H. Irwin McLean, Alan D. Irvine, Edel A. O’Toole, Michael A. Simpson, David P. Kelsell
Institutions: Queen Mary University of London, Blizard Institute, Agency for Science, Technology and Research, Institute of Medical Biology, Quaid-i-Azam University, Genome Institute of Singapore, Bioinformatics Institute, National Skin Centre, Congenica Ltd. (United Kingdom), University of Pennsylvania, University Hospital Bonn, University Hospital Schleswig-Holstein, University of Dundee, Trinity College Dublin, Children's Health Ireland at Crumlin, National Children’s Research Centre, Guy's Hospital, King's College London
Language: English
Subfield: Dermatology
Field: Medicine
Domain: Health Sciences
Open Access status: bronze
Awards: G1009429141, G122132715, Filaggrin Mutations and the Prognosis of Atopic Dermatitis, G2022026185, East London Genes & Health: human knockouts in a population genomic medicine cohort of British-South Asians, G4267133268, Verbundprojekt sysINFLAME: Netzwerk für Systemmedizin chronisch-entzündlicher Erkrankungen, CP1a, 2, 3, 4 , 5, 7, 8, 9b, 10b, AP, G7197510632, G778448485, G8442778785
OpenAlex ID: W2883963591