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Journal Abstract Search

653 related items for PubMed ID: 19228405

  • 21. Common variants in the TCF7L2 gene are strongly associated with type 2 diabetes mellitus in the Indian population.
    Chandak GR, Janipalli CS, Bhaskar S, Kulkarni SR, Mohankrishna P, Hattersley AT, Frayling TM, Yajnik CS.
    Diabetologia; 2007 Jan; 50(1):63-7. PubMed ID: 17093941
    [Abstract] [Full Text] [Related]

  • 22. TCF7L2 is reproducibly associated with type 2 diabetes in various ethnic groups: a global meta-analysis.
    Cauchi S, El Achhab Y, Choquet H, Dina C, Krempler F, Weitgasser R, Nejjari C, Patsch W, Chikri M, Meyre D, Froguel P.
    J Mol Med (Berl); 2007 Jul; 85(7):777-82. PubMed ID: 17476472
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  • 23. [Correlation between TCF7L2 gene polymorphism and genetic susceptibility in women with gestational diabetes mellitus].
    Shi X, Cai Q, Zou M, Shen Y.
    Zhonghua Fu Chan Ke Za Zhi; 2014 Aug; 49(8):588-93. PubMed ID: 25354859
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  • 24. TCF7L2 gene variants predispose to the development of type 2 diabetes mellitus among individuals with metabolic syndrome.
    Katsoulis K, Paschou SA, Hatzi E, Tigas S, Georgiou I, Tsatsoulis A.
    Hormones (Athens); 2018 Sep; 17(3):359-365. PubMed ID: 29971604
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  • 25. Association of variants of the TCF7L2 gene with increases in the risk of type 2 diabetes and the proinsulin:insulin ratio in the Spanish population.
    González-Sánchez JL, Martínez-Larrad MT, Zabena C, Pérez-Barba M, Serrano-Ríos M.
    Diabetologia; 2008 Nov; 51(11):1993-7. PubMed ID: 18712344
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  • 26. Association of TCF7L2 Genetic Polymorphisms with Type 2 Diabetes Mellitus in the Uygur Population of China.
    Yao H, Wang Z, Wang T, Ma Y, Su Y, Ma Q, Wang L, Zhu J.
    Int J Environ Res Public Health; 2015 Sep 18; 12(9):11797-814. PubMed ID: 26393635
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  • 27. Loci of TCF7L2, HHEX and IDE on chromosome 10q and the susceptibility of their genetic polymorphisms to type 2 diabetes.
    Nordman S, Ostenson CG, Efendic S, Gu HF.
    Exp Clin Endocrinol Diabetes; 2009 Apr 18; 117(4):186-90. PubMed ID: 19053027
    [Abstract] [Full Text] [Related]

  • 28. Transcription Factor 7-Like 2 (TCF7L2) rs7903146 Polymorphism as a Risk Factor for Gestational Diabetes Mellitus: A Meta-Analysis.
    Lin PC, Lin WT, Yeh YH, Wung SF.
    PLoS One; 2016 Apr 18; 11(4):e0153044. PubMed ID: 27058589
    [Abstract] [Full Text] [Related]

  • 29. Replication study for the association of TCF7L2 with susceptibility to type 2 diabetes in a Japanese population.
    Hayashi T, Iwamoto Y, Kaku K, Hirose H, Maeda S.
    Diabetologia; 2007 May 18; 50(5):980-4. PubMed ID: 17340123
    [Abstract] [Full Text] [Related]

  • 30. TCF7L2 variant genotypes and type 2 diabetes risk in Brazil: significant association, but not a significant tool for risk stratification in the general population.
    Marquezine GF, Pereira AC, Sousa AG, Mill JG, Hueb WA, Krieger JE.
    BMC Med Genet; 2008 Dec 04; 9():106. PubMed ID: 19055834
    [Abstract] [Full Text] [Related]

  • 31. TCF7L2 polymorphisms are associated with amygdalar volume in elderly individuals with Type 2 Diabetes.
    Ganmore I, Livny A, Ravona-Springer R, Cooper I, Alkelai A, Shelly S, Tsarfaty G, Heymann A, Schnaider Beeri M, Greenbaum L.
    Sci Rep; 2019 Nov 01; 9(1):15818. PubMed ID: 31676834
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  • 33. A genetic variation of the transcription factor 7-like 2 gene is associated with risk of type 2 diabetes in the Japanese population.
    Horikoshi M, Hara K, Ito C, Nagai R, Froguel P, Kadowaki T.
    Diabetologia; 2007 Apr 01; 50(4):747-51. PubMed ID: 17245589
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  • 35. TCF7L2 gene polymorphisms and type 2 diabetes: association with diabetic retinopathy and cardiovascular autonomic neuropathy.
    Ciccacci C, Di Fusco D, Cacciotti L, Morganti R, D'Amato C, Novelli G, Sangiuolo F, Spallone V, Borgiani P.
    Acta Diabetol; 2013 Oct 01; 50(5):789-99. PubMed ID: 22843023
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  • 38. Single nucleotide polymorphisms of TCF7L2 are linked to diabetic coronary atherosclerosis.
    Muendlein A, Saely CH, Geller-Rhomberg S, Sonderegger G, Rein P, Winder T, Beer S, Vonbank A, Drexel H.
    PLoS One; 2011 Mar 15; 6(3):e17978. PubMed ID: 21423583
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  • 40. Lack of association between single nucleotide polymorphisms in TCF7L2 and T2DM in the Chinese Yao population: A case-control study.
    Sun SY, Huang RZ, Huang H, Zhang MQ, Sun HL.
    Medicine (Baltimore); 2021 Mar 26; 100(12):e25326. PubMed ID: 33761736
    [Abstract] [Full Text] [Related]

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