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Journal Abstract Search

728 related items for PubMed ID: 18443202

  • 1. Association analysis in african americans of European-derived type 2 diabetes single nucleotide polymorphisms from whole-genome association studies.
    Lewis JP, Palmer ND, Hicks PJ, Sale MM, Langefeld CD, Freedman BI, Divers J, Bowden DW.
    Diabetes; 2008 Aug; 57(8):2220-5. PubMed ID: 18443202
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  • 2. Impact of common variants of PPARG, KCNJ11, TCF7L2, SLC30A8, HHEX, CDKN2A, IGF2BP2, and CDKAL1 on the risk of type 2 diabetes in 5,164 Indians.
    Chauhan G, Spurgeon CJ, Tabassum R, Bhaskar S, Kulkarni SR, Mahajan A, Chavali S, Kumar MV, Prakash S, Dwivedi OP, Ghosh S, Yajnik CS, Tandon N, Bharadwaj D, Chandak GR.
    Diabetes; 2010 Aug; 59(8):2068-74. PubMed ID: 20424228
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  • 3. Replication study of candidate genes associated with type 2 diabetes based on genome-wide screening.
    Tabara Y, Osawa H, Kawamoto R, Onuma H, Shimizu I, Miki T, Kohara K, Makino H.
    Diabetes; 2009 Feb; 58(2):493-8. PubMed ID: 19033397
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  • 4. Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians.
    Ng MC, Park KS, Oh B, Tam CH, Cho YM, Shin HD, Lam VK, Ma RC, So WY, Cho YS, Kim HL, Lee HK, Chan JC, Cho NH.
    Diabetes; 2008 Aug; 57(8):2226-33. PubMed ID: 18469204
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  • 5. Common variants in CDKAL1, CDKN2A/B, IGF2BP2, SLC30A8, and HHEX/IDE genes are associated with type 2 diabetes and impaired fasting glucose in a Chinese Han population.
    Wu Y, Li H, Loos RJ, Yu Z, Ye X, Chen L, Pan A, Hu FB, Lin X.
    Diabetes; 2008 Oct; 57(10):2834-42. PubMed ID: 18633108
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  • 6. Genetic risk assessment of type 2 diabetes-associated polymorphisms in African Americans.
    Cooke JN, Ng MC, Palmer ND, An SS, Hester JM, Freedman BI, Langefeld CD, Bowden DW.
    Diabetes Care; 2012 Feb; 35(2):287-92. PubMed ID: 22275441
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  • 7. Contribution of common genetic variation to the risk of type 2 diabetes in the Mexican Mestizo population.
    Gamboa-Meléndez MA, Huerta-Chagoya A, Moreno-Macías H, Vázquez-Cárdenas P, Ordóñez-Sánchez ML, Rodríguez-Guillén R, Riba L, Rodríguez-Torres M, Guerra-García MT, Guillén-Pineda LE, Choudhry S, Del Bosque-Plata L, Canizales-Quinteros S, Pérez-Ortiz G, Escobedo-Aguirre F, Parra A, Lerman-Garber I, Aguilar-Salinas CA, Tusié-Luna MT.
    Diabetes; 2012 Dec; 61(12):3314-21. PubMed ID: 22923468
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  • 12. Resequencing and analysis of variation in the TCF7L2 gene in African Americans suggests that SNP rs7903146 is the causal diabetes susceptibility variant.
    Palmer ND, Hester JM, An SS, Adeyemo A, Rotimi C, Langefeld CD, Freedman BI, Ng MC, Bowden DW.
    Diabetes; 2011 Feb; 60(2):662-8. PubMed ID: 20980453
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  • 13. Extension of type 2 diabetes genome-wide association scan results in the diabetes prevention program.
    Moore AF, Jablonski KA, McAteer JB, Saxena R, Pollin TI, Franks PW, Hanson RL, Shuldiner AR, Knowler WC, Altshuler D, Florez JC, Diabetes Prevention Program Research Group.
    Diabetes; 2008 Sep; 57(9):2503-10. PubMed ID: 18544707
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  • 14. Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based study.
    van Hoek M, Dehghan A, Witteman JC, van Duijn CM, Uitterlinden AG, Oostra BA, Hofman A, Sijbrands EJ, Janssens AC.
    Diabetes; 2008 Nov; 57(11):3122-8. PubMed ID: 18694974
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  • 17. [Association analysis of genetic polymorphisms of TCF7L2, CDKAL1, SLC30A8, HHEX genes and microvascular complications of type 2 diabetes mellitus].
    Fu LL, Lin Y, Yang ZL, Yin YB.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Apr; 29(2):194-9. PubMed ID: 22487833
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  • 18. A comparison of type 2 diabetes risk allele load between African Americans and European Americans.
    Keaton JM, Cooke Bailey JN, Palmer ND, Freedman BI, Langefeld CD, Ng MC, Bowden DW.
    Hum Genet; 2014 Dec; 133(12):1487-95. PubMed ID: 25273842
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