Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease

Nature Genetics

Volumn 47, Issue 6, 2015, Pages 577-578

  Gutierrez Achury, Javier ^a   Zhernakova, Alexandra ^a   Pulit, Sara L ^b   Trynka, Gosia ^c   Hunt, Karen A ^d   Romanos, Jihane ^a   Raychaudhuri, Soumya ^e,f,g   Van Heel, David A ^d   Wijmenga, Cisca ^a   De Bakker, Paul I W ^b  

^a UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^b UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^c WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^d QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^e BRIGHAM AND WOMEN S HOSPITAL   (United States)

^f BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^g UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

HLA DQA1 ANTIGEN; HLA DQB1 ANTIGEN; HLA DQ ANTIGEN; HLA-DQA1 ANTIGEN; HLA-DQB1 ANTIGEN;

ALLELE; ARTICLE; CELIAC DISEASE; GENE LOCUS; GENE MAPPING; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; HERITABILITY; MAJOR HISTOCOMPATIBILITY COMPLEX; PRIORITY JOURNAL; CASE CONTROL STUDY; CHROMOSOME MAP; GENETIC PREDISPOSITION; GENETICS; HAPLOTYPE; HUMAN; RISK; RISK FACTOR;

CASE-CONTROL STUDIES; CELIAC DISEASE; CHROMOSOME MAPPING; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HLA-DQ ALPHA-CHAINS; HLA-DQ BETA-CHAINS; HUMANS; RISK; RISK FACTORS;

EID: 84930091570     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.3268     Document Type: Article

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