Shuldiner AR - Search Results

1

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.

2

Association between a novel variant of the human type 2 deiodinase gene Thr92Ala and insulin resistance: evidence of interaction with the Trp64Arg variant of the beta-3-adrenergic receptor.

Mentuccia D, Proietti-Pannunzi L, Tanner K, Bacci V, Pollin TI, Poehlman ET, Shuldiner AR, Celi FS. Mentuccia D, et al. Among authors: shuldiner ar. Diabetes. 2002 Mar;51(3):880-3. doi: 10.2337/diabetes.51.3.880. Diabetes. 2002. PMID: 11872697

3

A genome-wide scan for autoimmune thyroiditis in the Old Order Amish: replication of genetic linkage on chromosome 5q11.2-q14.3.

Allen EM, Hsueh WC, Sabra MM, Pollin TI, Ladenson PW, Silver KD, Mitchell BD, Shuldiner AR. Allen EM, et al. Among authors: shuldiner ar. J Clin Endocrinol Metab. 2003 Mar;88(3):1292-6. doi: 10.1210/jc.2002-020634. J Clin Endocrinol Metab. 2003. PMID: 12629121

4

The role of peroxisome proliferator-activated receptor gamma in diabetes and obesity.

Celi FS, Shuldiner AR. Celi FS, et al. Among authors: shuldiner ar. Curr Diab Rep. 2002 Apr;2(2):179-85. doi: 10.1007/s11892-002-0078-2. Curr Diab Rep. 2002. PMID: 12643137 Review.

5

Variation in the lamin A/C gene: associations with metabolic syndrome.

Steinle NI, Kazlauskaite R, Imumorin IG, Hsueh WC, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR. Steinle NI, et al. Among authors: shuldiner ar. Arterioscler Thromb Vasc Biol. 2004 Sep;24(9):1708-13. doi: 10.1161/01.ATV.0000136384.53705.c9. Epub 2004 Jun 17. Arterioscler Thromb Vasc Biol. 2004. PMID: 15205219

6

Polymorphism in the calsequestrin 1 (CASQ1) gene on chromosome 1q21 is associated with type 2 diabetes in the old order Amish.

Fu M, Damcott CM, Sabra M, Pollin TI, Ott SH, Wang J, Garant MJ, O'Connell JR, Mitchell BD, Shuldiner AR. Fu M, et al. Among authors: shuldiner ar. Diabetes. 2004 Dec;53(12):3292-9. doi: 10.2337/diabetes.53.12.3292. Diabetes. 2004. PMID: 15561962

7

Vesicle-associated membrane protein 4, a positional candidate gene on 1q24-q25, is not associated with type 2 diabetes in the Old Order Amish.

Sabra MM, Damcott C, Fu M, Ott S, O'Connell JR, Mitchell BD, Shuldiner AR. Sabra MM, et al. Among authors: shuldiner ar. Mol Genet Metab. 2005 Jun;85(2):133-9. doi: 10.1016/j.ymgme.2004.09.012. Mol Genet Metab. 2005. PMID: 15896658

8

The relationship between parity and bone mineral density in women characterized by a homogeneous lifestyle and high parity.

Streeten EA, Ryan KA, McBride DJ, Pollin TI, Shuldiner AR, Mitchell BD. Streeten EA, et al. Among authors: shuldiner ar. J Clin Endocrinol Metab. 2005 Aug;90(8):4536-41. doi: 10.1210/jc.2004-1924. Epub 2005 May 17. J Clin Endocrinol Metab. 2005. PMID: 15899951

9

Variants in the ghrelin gene are associated with metabolic syndrome in the Old Order Amish.

Steinle NI, Pollin TI, O'Connell JR, Mitchell BD, Shuldiner AR. Steinle NI, et al. Among authors: shuldiner ar. J Clin Endocrinol Metab. 2005 Dec;90(12):6672-7. doi: 10.1210/jc.2005-0549. Epub 2005 Oct 4. J Clin Endocrinol Metab. 2005. PMID: 16204371

10

The Thr92Ala deiodinase type 2 (DIO2) variant is not associated with type 2 diabetes or indices of insulin resistance in the old order of Amish.

Mentuccia D, Thomas MJ, Coppotelli G, Reinhart LJ, Mitchell BD, Shuldiner AR, Celi FS. Mentuccia D, et al. Among authors: shuldiner ar. Thyroid. 2005 Nov;15(11):1223-7. doi: 10.1089/thy.2005.15.1223. Thyroid. 2005. PMID: 16356084

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