Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment

Human Molecular Genetics

Volumn 22, Issue 15, 2013, Pages 3174-3185

  Kirin, Mirna ^a   Chandra, Aman ^b,c   Charteris, David G ^b   Hayward, Caroline ^d   Campbell, Susan ^d   Celap, Ivana ^e   Bencic, Goran ^f   Vatavuk, Zoran ^f   Kirac, Iva ^e   Richards, Allan J ^g,h   Tenesa, Albert ^d,i   Snead, Martin P ^g   Fleck, Brian W ^j   Singh, Jaswinder ^j   Harsum, Steven ^b   MacLaren, Robert E ^b   den Hollander, Anneke I ^k   Dunlop, Malcolm G ^d   Hoyng, Carel B ^k   Wright, Alan F ^d   Campbell, Harry ^a   Vitart, Veronique ^d   Mitry, Danny ^a   more..

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b MOORFIELDS EYE HOSPITAL   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d UNIVERSITY OF EDINBURGH   (United Kingdom)

^e SESTRE MILOSRDNICE UNIVERSITY HOSPITAL   (Croatia)

^f UNIVERSITY OF ZAGREB   (Croatia)

^g CAMBRIDGE UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

^h UNIVERSITY OF CAMBRIDGE   (United Kingdom)

ⁱ UNIVERSITY OF EDINBURGH   (United Kingdom)

^j PRINCESS ALEXANDRA EYE PAVILION   (United Kingdom)

^k RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

more..

Author keywords

[No Author keywords available]

Indexed keywords

CERAMIDE SYNTHASE 2; SYNTHETASE; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; CELL ADHESION; CELL MIGRATION; CHILD; CONTROLLED STUDY; GENE; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SCREENING; GENOTYPE; HUMAN; INTRON; LDB2 GENE; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; RETINA DETACHMENT; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SS18 GENE; TIAM1 GENE; TSTA3 GENE; UNITED KINGDOM;

ALLELES; CASE-CONTROL STUDIES; EYE DISEASES, HEREDITARY; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; META-ANALYSIS AS TOPIC; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE; RETINAL DETACHMENT;

EID: 84880291076     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddt169     Document Type: Article

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