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Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effects.
Fu M, Kazlauskaite R, Baracho Mde F, Santos MG, Brandão-Neto J, Villares S, Celi FS, Wajchenberg BL, Shuldiner AR. Fu M, et al. Among authors: shuldiner ar. J Clin Endocrinol Metab. 2004 Jun;89(6):2916-22. doi: 10.1210/jc.2003-030485. J Clin Endocrinol Metab. 2004. PMID: 15181077 Free PMC article.
Variants in ARHGEF11, a candidate gene for the linkage to type 2 diabetes on chromosome 1q, are nominally associated with insulin resistance and type 2 diabetes in Pima Indians.
Ma L, Hanson RL, Que LN, Cali AM, Fu M, Mack JL, Infante AM, Kobes S; International Type 2 Diabetes 1q Consortium; Bogardus C, Shuldiner AR, Baier LJ. Ma L, et al. Among authors: shuldiner ar. Diabetes. 2007 May;56(5):1454-9. doi: 10.2337/db06-0640. Epub 2007 Feb 7. Diabetes. 2007. PMID: 17287471
Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations.
Rampersaud E, Damcott CM, Fu M, Shen H, McArdle P, Shi X, Shelton J, Yin J, Chang YP, Ott SH, Zhang L, Zhao Y, Mitchell BD, O'Connell J, Shuldiner AR. Rampersaud E, et al. Among authors: shuldiner ar. Diabetes. 2007 Dec;56(12):3053-62. doi: 10.2337/db07-0457. Epub 2007 Sep 10. Diabetes. 2007. PMID: 17846126
545 results