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Volumn 27, Issue 3, 2016, Pages 429-434

Implications of polygenic risk for personalised colorectal cancer screening

Author keywords

Colorectal cancer; Personalised screening European Union 258236; Polygenic risk

Indexed keywords

ADULT; AGE; AGED; ARTICLE; CANCER INCIDENCE; CANCER MORTALITY; CANCER RISK; CANCER SCREENING; CANCER SUSCEPTIBILITY; COLORECTAL CANCER; CONTROLLED STUDY; FEMALE; GENETIC ASSOCIATION; GENETIC RISK; GENETIC TRAIT; GENETIC VARIABILITY; GENOME WIDE COMPLEX TRAIT ANALYSIS; HEALTH PROGRAM; HERITABILITY; HIGH RISK PATIENT; HUMAN; MAJOR CLINICAL STUDY; MALE; MATHEMATICAL ANALYSIS; NATIONAL BOWEL SCREENING PROGRAM; NATIONAL HEALTH SERVICE; PERSONALISED SCREENING; POLYGENIC RISK SCORE; PREDICTIVE VALUE; PRIORITY JOURNAL; RECEIVER OPERATING CHARACTERISTIC; SEX DIFFERENCE; SINGLE NUCLEOTIDE POLYMORPHISM; UNITED KINGDOM; COLORECTAL NEOPLASMS; EARLY CANCER DIAGNOSIS; ENGLAND; MASS SCREENING; MIDDLE AGED; PERSONALIZED MEDICINE; PROCEDURES; RISK; RISK FACTOR;

EID: 84959893914     PISSN: 09237534     EISSN: 15698041     Source Type: Journal    
DOI: 10.1093/annonc/mdv540     Document Type: Article
Times cited : (69)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.