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438 related items for PubMed ID: 24269186

  • 1. An obesity genetic risk score is associated with metabolic syndrome in Chinese children.
    Zhao X, Xi B, Shen Y, Wu L, Hou D, Cheng H, Mi J.
    Gene; 2014 Feb 10; 535(2):299-302. PubMed ID: 24269186
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  • 10. [Association between rs10938397 polymorphism in GNPDA2 and obesity in children at different stages of development].
    Gao LW, Zhang MX, Wu LJ, Fu LW, Zhao XY, Mi J.
    Zhonghua Liu Xing Bing Xue Za Zhi; 2018 Jan 10; 39(1):75-80. PubMed ID: 29374901
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  • 11. Association of BDNF rs6265 and MC4R rs17782313 with metabolic syndrome in Pakistanis.
    Rana S, Sultana A, Bhatti AA.
    J Biosci; 2019 Sep 10; 44(4):. PubMed ID: 31502573
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  • 15. An obesity genetic risk score predicts risk of insulin resistance among Chinese children.
    Xi B, Zhao X, Shen Y, Wu L, Hou D, Cheng H, Mi J.
    Endocrine; 2014 Dec 10; 47(3):825-32. PubMed ID: 24619288
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  • 16. Study of eight GWAS-identified common variants for association with obesity-related indices in Chinese children at puberty.
    Wang J, Mei H, Chen W, Jiang Y, Sun W, Li F, Fu Q, Jiang F.
    Int J Obes (Lond); 2012 Apr 10; 36(4):542-7. PubMed ID: 22083549
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  • 17. Obesity susceptibility genetic variants identified from recent genome-wide association studies: implications in a chinese population.
    Cheung CY, Tso AW, Cheung BM, Xu A, Ong KL, Fong CH, Wat NM, Janus ED, Sham PC, Lam KS.
    J Clin Endocrinol Metab; 2010 Mar 10; 95(3):1395-403. PubMed ID: 20061430
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  • 18. Sexual Dimorphism of a Genetic Risk Score for Obesity and Related Traits among Chinese Patients with Type 2 Diabetes.
    Kong X, Xing X, Zhang X, Hong J, Yang W.
    Obes Facts; 2019 Mar 10; 12(3):328-343. PubMed ID: 31167208
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  • 19. Studies of metabolic phenotypic correlates of 15 obesity associated gene variants.
    Sandholt CH, Vestmar MA, Bille DS, Borglykke A, Almind K, Hansen L, Sandbæk A, Lauritzen T, Witte D, Jørgensen T, Pedersen O, Hansen T.
    PLoS One; 2011 Mar 10; 6(9):e23531. PubMed ID: 21912638
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  • 20. Association between obesity and polymorphisms in SEC16B, TMEM18, GNPDA2, BDNF, FAIM2 and MC4R in a Japanese population.
    Hotta K, Nakamura M, Nakamura T, Matsuo T, Nakata Y, Kamohara S, Miyatake N, Kotani K, Komatsu R, Itoh N, Mineo I, Wada J, Masuzaki H, Yoneda M, Nakajima A, Funahashi T, Miyazaki S, Tokunaga K, Kawamoto M, Ueno T, Hamaguchi K, Tanaka K, Yamada K, Hanafusa T, Oikawa S, Yoshimatsu H, Nakao K, Sakata T, Matsuzawa Y, Kamatani N, Nakamura Y.
    J Hum Genet; 2009 Dec 10; 54(12):727-31. PubMed ID: 19851340
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