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Diabetologia
Volumn 58, Issue 8, 2015, Pages 1725-1729
Genomic medicine at the heart of diabetes management
Author keywords

Biomarkers; Genome wide association studies; Genomics; Lifestyle; Prevention; Translation; Treatment; Type 2 diabetes
Indexed keywords

ARTICLE; BIOLOGY; ENVIRONMENTAL EXPOSURE; FUTUROLOGY; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC VARIABILITY; GENOMICS; HUMAN; HUMAN GENETICS; NON INSULIN DEPENDENT DIABETES MELLITUS; PREDICTION; PRIORITY JOURNAL; DIABETES MELLITUS, TYPE 2; GENETICS; GENOTYPE;
EID: 84937500990     PISSN: 0012186X     EISSN: 14320428     Source Type: Journal    
DOI: 10.1007/s00125-015-3588-6     Document Type: Article
Times cited : (18)
References (12)
  • 1
    • 84895868553 scopus 로고    scopus 로고
    • Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
    • COI: 1:CAS:528:DC%2BC2cXitFanuro%3D, PID: 24509480
    • Mahajan A, Go MJ, Zhang W et al (2014) Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet 46:234–244
    • (2014) Nat Genet , vol.46 , pp. 234-244
    • Mahajan, A.1    Go, M.J.2    Zhang, W.3
  • 2
    • 84868337361 scopus 로고    scopus 로고
    • Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
    • COI: 1:CAS:528:DC%2BC38XhtFOgsLfP, PID: 22885922
    • Morris AP, Voight BF, Teslovich TM et al (2012) Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Nat Genet 44:981–990
    • (2012) Nat Genet , vol.44 , pp. 981-990
    • Morris, A.P.1    Voight, B.F.2    Teslovich, T.M.3
  • 3
    • 84901387060 scopus 로고    scopus 로고
    • Gene-lifestyle interaction and type 2 diabetes: the EPIC interact case-cohort study
    • PID: 24845081
    • Langenberg C, Sharp SJ, Franks PW et al (2014) Gene-lifestyle interaction and type 2 diabetes: the EPIC interact case-cohort study. PLoS Med 11:e1001647
    • (2014) PLoS Med , vol.11
    • Langenberg, C.1    Sharp, S.J.2    Franks, P.W.3
  • 4
    • 84881315517 scopus 로고    scopus 로고
    • Validating therapeutic targets through human genetics
    • COI: 1:CAS:528:DC%2BC3sXhtFalsLrI, PID: 23868113
    • Plenge RM, Scolnick EM, Altshuler D (2013) Validating therapeutic targets through human genetics. Nat Rev Drug Discov 12:581–594
    • (2013) Nat Rev Drug Discov , vol.12 , pp. 581-594
    • Plenge, R.M.1    Scolnick, E.M.2    Altshuler, D.3
  • 5
    • 84923206532 scopus 로고    scopus 로고
    • Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility
    • PID: 25631608
    • Wessel J, Chy AY, Willems SW et al (2015) Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Nat Commun 6:5897
    • (2015) Nat Commun , vol.6 , pp. 5897
    • Wessel, J.1    Chy, A.Y.2    Willems, S.W.3
  • 6
    • 33645103550 scopus 로고    scopus 로고
    • Sequence variations in PCSK9, low LDL, and protection against coronary heart disease
    • COI: 1:CAS:528:DC%2BD28Xislequr8%3D, PID: 16554528
    • Cohen JC, Boerwinkle E, Mosley TH Jr, Hobbs HH (2006) Sequence variations in PCSK9, low LDL, and protection against coronary heart disease. N Engl J Med 354:1264–1272
    • (2006) N Engl J Med , vol.354 , pp. 1264-1272
    • Cohen, J.C.1    Boerwinkle, E.2    Mosley, T.H.3    Hobbs, H.H.4
  • 7
    • 84897407583 scopus 로고    scopus 로고
    • Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
    • COI: 1:CAS:528:DC%2BC2cXjtl2jtrY%3D, PID: 24584071
    • Flannick J, Thorleifsson G, Beer NL et al (2014) Loss-of-function mutations in SLC30A8 protect against type 2 diabetes. Nat Genet 46:357–363
    • (2014) Nat Genet , vol.46 , pp. 357-363
    • Flannick, J.1    Thorleifsson, G.2    Beer, N.L.3
  • 8
    • 2342633204 scopus 로고    scopus 로고
    • Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes
    • COI: 1:CAS:528:DC%2BD2cXjsVOhtbk%3D, PID: 15115830
    • Gloyn AL, Pearson ER, Antcliff J et al (2004) Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes. N Engl J Med 350:1838–1849
    • (2004) N Engl J Med , vol.350 , pp. 1838-1849
    • Gloyn, A.L.1    Pearson, E.R.2    Antcliff, J.3
  • 9
    • 56749101779 scopus 로고    scopus 로고
    • Genotype score in addition to common risk factors for prediction of type 2 diabetes
    • COI: 1:CAS:528:DC%2BD1cXhtl2gurnE, PID: 19020323
    • Meigs JB, Shrader P, Sullivan LM et al (2008) Genotype score in addition to common risk factors for prediction of type 2 diabetes. N Engl J Med 359:2208–2219
    • (2008) N Engl J Med , vol.359 , pp. 2208-2219
    • Meigs, J.B.1    Shrader, P.2    Sullivan, L.M.3
  • 10
    • 84920053873 scopus 로고    scopus 로고
    • Age-related clonal hematopoiesis associated with adverse outcomes
    • PID: 25426837
    • Jaiswal S, Fontanillas P, Flannick J et al (2014) Age-related clonal hematopoiesis associated with adverse outcomes. N Engl J Med 371:2488–2498
    • (2014) N Engl J Med , vol.371 , pp. 2488-2498
    • Jaiswal, S.1    Fontanillas, P.2    Flannick, J.3
  • 11
    • 78650197952 scopus 로고    scopus 로고
    • A commentary on ‘common SNPs explain a large proportion of the heritability for human height’ by Yang et al. (2010)
    • PID: 21142928
    • Visscher PM, Yang J, Goddard ME (2010) A commentary on ‘common SNPs explain a large proportion of the heritability for human height’ by Yang et al. (2010). Twin Res Hum Genet 13:517–524
    • (2010) Twin Res Hum Genet , vol.13 , pp. 517-524
    • Visscher, P.M.1    Yang, J.2    Goddard, M.E.3
  • 12
    • 84858433310 scopus 로고    scopus 로고
    • Personal omics profiling reveals dynamic molecular and medical phenotypes
    • COI: 1:CAS:528:DC%2BC38Xkt1GnsbY%3D, PID: 22424236
    • Chen R, Mias GI, Li-Pook-Than J et al (2012) Personal omics profiling reveals dynamic molecular and medical phenotypes. Cell 148:1293–1307
    • (2012) Cell , vol.148 , pp. 1293-1307
    • Chen, R.1    Mias, G.I.2    Li-Pook-Than, J.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.