Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7

Nature Genetics

Volumn 49, Issue 2, 2017, Pages 186-192

  Luo, Yang ^a,b,c   De Lange, Katrina M ^a   Jostins, Luke ^d,e   Moutsianas, Loukas ^a   Randall, Joshua ^a   Kennedy, Nicholas A ^f,g   Lamb, Christopher A ^h   McCarthy, Shane ^a   Ahmad, Tariq ^f,g   Edwards, Cathryn ⁱ   Serra, Eva Goncalves ^a   Hart, Ailsa ^j   Hawkey, Chris ^k   Mansfield, John C ^l   Mowat, Craig ^m   Newman, William G ^n,o   Nichols, Sam ^a   Pollard, Martin ^a   Satsangi, Jack ^p   Simmons, Alison ^q,r   Tremelling, Mark ^s   Uhlig, Holm ^q,t   Wilson, David C ^p,u   Lee, James C ^v   Prescott, Natalie J ^w   Lees, Charlie W ^p   Mathew, Christopher G ^w,x   Parkes, Miles ^v   Barrett, Jeffrey C ^a   Anderson, Carl A ^a   more..

^a WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^b BRIGHAM AND WOMEN S HOSPITAL   (United States)

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

^d UNIVERSITY OF OXFORD   (United Kingdom)

^e CHRIST CHURCH   (United Kingdom)

^f UNIVERSITY OF EXETER   (United Kingdom)

^g ROYAL DEVON AND EXETER NHS FOUNDATION TRUST   (United Kingdom)

^h NEWCASTLE UNIVERSITY   (United Kingdom)

ⁱ TORBAY HOSPITAL   (United Kingdom)

^j ST MARK S HOSPITAL   (United Kingdom)

^k QUEEN S MEDICAL CENTRE   (United Kingdom)

^l NEWCASTLE UNIVERSITY   (United Kingdom)

^m UNIVERSITY OF DUNDEE   (United Kingdom)

ⁿ UNIVERSITY OF MANCHESTER   (United Kingdom)

^o UNIVERSITY OF MANCHESTER   (United Kingdom)

^p UNIVERSITY OF EDINBURGH   (United Kingdom)

^q UNIVERSITY OF OXFORD   (United Kingdom)

^r UNIVERSITY OF OXFORD   (United Kingdom)

^s NORFOLK AND NORWICH UNIVERSITY HOSPITAL   (United Kingdom)

^t UNIVERSITY OF OXFORD   (United Kingdom)

^u ROYAL HOSPITAL FOR SICK CHILDREN   (United Kingdom)

^v ADDENBROOKE S HOSPITAL   (United Kingdom)

^w GUY S HOSPITAL   (United Kingdom)

^x UNIVERSITY OF THE WITWATERSRAND   (South Africa)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ADCY7 GENE; ARTICLE; CONTROLLED STUDY; CROHN DISEASE; DISEASE PREDISPOSITION; GENE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOME-WIDE ASSOCIATION STUDY; HAPLOTYPE; HERITABILITY; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; ULCERATIVE COLITIS; UNITED KINGDOM; WHOLE GENOME SEQUENCING; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; INFLAMMATORY BOWEL DISEASE; PROCEDURES; SINGLE NUCLEOTIDE POLYMORPHISM;

ADENYLATE CYCLASE; ADENYLYL CYCLASE 7;

ADENYLYL CYCLASES; COLITIS, ULCERATIVE; CROHN DISEASE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; INFLAMMATORY BOWEL DISEASES; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 85008626255     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.3761     Document Type: Article

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67. Do, R., et al. Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction. Nature 518, 102-106 (2015).
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