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Volumn 302, Issue 18, 2009, Pages 2028-2029

Genome-wide association studies and human disease: From trickle to flood

Author keywords

[No Author keywords available]

Indexed keywords

FAMILY HISTORY; GENETIC ASSOCIATION; GENETIC DISORDER; GENOTYPE; HERITABILITY; HUMAN; HYPERTENSION; ISCHEMIC HEART DISEASE; NON INSULIN DEPENDENT DIABETES MELLITUS; NOTE; PRIORITY JOURNAL; RETINA MACULA AGE RELATED DEGENERATION; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 70450092426     PISSN: 00987484     EISSN: 15383598     Source Type: Journal    
DOI: 10.1001/jama.2009.1643     Document Type: Note
Times cited : (48)

References (9)
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  • 4
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    • Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels
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    • Benyamin, B.1    McRae, A.F.2    Zhu, G.3
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    • Maher, B.1
  • 7
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    • Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
    • International Schizophrenia Consortium
    • Purcell SM, Wray NR, Stone JL, et al; International Schizophrenia Consortium. Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature. 2009;460(7256):748-752.
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  • 8
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    • Clinical translation of genetic predictors for type 2 diabetes
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.