Phenome-wide association study maps new diseases to the human major histocompatibility complex region

Journal of Medical Genetics

Volumn 53, Issue 10, 2016, Pages 681-689

  Liu, Jixia ^a   Ye, Zhan ^a   Mayer, John G ^a   Hoch, Brian A ^a   Green, Clayton ^a   Rolak, Loren ^a   Cold, Christopher ^a   Khor, Seik Soon ^b   Zheng, Xiuwen ^c   Miyagawa, Taku ^b,d   Tokunaga, Katsushi ^b   Brilliant, Murray H ^a   Hebbring, Scott J ^a  

^a MARSHFIELD CLINIC   (United States)

^b UNIVERSITY OF TOKYO   (Japan)

^c UNIVERSITY OF WASHINGTON   (United States)

^d TOKYO METROPOLITAN INSTITUTE OF MEDICAL SCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ANKYLOSING SPONDYLITIS; ARTICLE; CELIAC DISEASE; CONTROLLED STUDY; GENE FREQUENCY; GENETIC ASSOCIATION STUDY; GENETIC VARIABILITY; HUMAN; INSULIN DEPENDENT DIABETES MELLITUS; LICHEN PLANUS; MAJOR CLINICAL STUDY; MAJOR HISTOCOMPATIBILITY COMPLEX; PHENOME WIDE ASSOCIATION STUDY; PHENOTYPE; PLEIOTROPY; PRIORITY JOURNAL; PSORIASIS; SINGLE NUCLEOTIDE POLYMORPHISM; CAUCASIAN; CHROMOSOME 6; FEMALE; GENETIC POLYMORPHISM; GENETICS; IMMUNOPATHOLOGY; INFLAMMATION; MALE; MIDDLE AGED; PROCEDURES;

ADULT; AGED; CHROMOSOMES, HUMAN, PAIR 6; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENETIC ASSOCIATION STUDIES; HUMANS; IMMUNE SYSTEM DISEASES; INFLAMMATION; LICHEN PLANUS; MAJOR HISTOCOMPATIBILITY COMPLEX; MALE; MIDDLE AGED; PHENOTYPE; POLYMORPHISM, GENETIC;

EID: 84979073192     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmedgenet-2016-103867     Document Type: Article

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