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Volumn 98, Issue 3, 2013, Pages

Common genetic variation contributes significantly to the risk of developing chronic lymphocytic leukemia

Author keywords

Chronic lymphocytic leukemia; Common genetic variation; Heritability; Risk

Indexed keywords

ALLELE; CANCER RISK; CHRONIC LYMPHATIC LEUKEMIA; CONTROLLED STUDY; GENETIC ASSOCIATION; GENETIC VARIABILITY; HERITABILITY; HUMAN; LETTER; MAJOR CLINICAL STUDY; PHENOTYPIC VARIATION; PREVALENCE; RECEIVER OPERATING CHARACTERISTIC; SINGLE NUCLEOTIDE POLYMORPHISM; VARIANCE; BIOLOGICAL MODEL; GENETICS; LEUKEMIA, LYMPHOCYTIC, CHRONIC, B-CELL; RISK;

EID: 84874548735     PISSN: 03906078     EISSN: 15928721     Source Type: Journal    
DOI: 10.3324/haematol.2012.072140     Document Type: Letter
Times cited : (10)

References (10)
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  • 4
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    • Estimating missing heritability for disease from genome-wide association studies
    • Lee SH, Wray NR, Goddard ME, Visscher PM. Estimating missing heritability for disease from genome-wide association studies. Am J Hum Genet. 2011;88(3):294-305.
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    • Lee, S.H.1    Wray, N.R.2    Goddard, M.E.3    Visscher, P.M.4
  • 5
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    • PLINK: A tool set for whole-genome association and population-based linkage analyses
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    • Common SNPs explain a large proportion of the heritability for human height
    • Yang J, Benyamin B, McEvoy BP, Gordon S, Henders AK, Nyholt DR, et al. Common SNPs explain a large proportion of the heritability for human height. Nat Genet. 2010;42(7):565-9.
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    • The genetic interpretation of area under the ROC curve in genomic profiling
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.