Transmission distortion in Crohn's disease risk gene ATG16L1 leads to sex difference in disease association

Inflammatory Bowel Diseases

Volumn 18, Issue 2, 2012, Pages 312-322

  Liu, Linda Y ^a,b   Schaub, Marc A ^c   Sirota, Marina ^a,b   Butte, Atul J ^a,b  

^a STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b LUCILE PACKARD CHILDREN S HOSPITAL   (United States)

^c Stanford University   (United States)

Author keywords

ATG16L1; inflammatory bowel disease; sexual dimorphism; transmission distortion

Indexed keywords

ALLELE; ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; CROHN DISEASE; DISEASE ASSOCIATION; FEMALE; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE MAP; HUMAN; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PRIORITY JOURNAL; RISK FACTOR; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE; TRANSMISSION DISTORTION;

ADULT; CARRIER PROTEINS; COHORT STUDIES; CROHN DISEASE; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; HAPMAP PROJECT; HUMANS; MALE; NERVE TISSUE PROTEINS; NOD2 SIGNALING ADAPTOR PROTEIN; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, INTERLEUKIN; RISK; SEX FACTORS;

EID: 84855713869     PISSN: 10780998     EISSN: 15364844     Source Type: Journal    
DOI: 10.1002/ibd.21781     Document Type: Article

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