Glaser B - Search Results

1

Common variants in WFS1 confer risk of type 2 diabetes.

Sandhu MS, Weedon MN, Fawcett KA, Wasson J, Debenham SL, Daly A, Lango H, Frayling TM, Neumann RJ, Sherva R, Blech I, Pharoah PD, Palmer CN, Kimber C, Tavendale R, Morris AD, McCarthy MI, Walker M, Hitman G, Glaser B, Permutt MA, Hattersley AT, Wareham NJ, Barroso I. Sandhu MS, et al. Among authors: glaser b. Nat Genet. 2007 Aug;39(8):951-3. doi: 10.1038/ng2067. Epub 2007 Jul 1. Nat Genet. 2007. PMID: 17603484 Free PMC article.

2

Dinucleotide repeat polymorphism at the human CCKBR locus.

Glaser B, Anker R, Chiu KC, Donis-Keller H, Permutt MA. Glaser B, et al. Hum Mol Genet. 1994 Nov;3(11):2081. Hum Mol Genet. 1994. PMID: 7874137 No abstract available.

3

Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

Nestorowicz A, Wilson BA, Schoor KP, Inoue H, Glaser B, Landau H, Stanley CA, Thornton PS, Clement JP 4th, Bryan J, Aguilar-Bryan L, Permutt MA. Nestorowicz A, et al. Among authors: glaser b. Hum Mol Genet. 1996 Nov;5(11):1813-22. doi: 10.1093/hmg/5.11.1813. Hum Mol Genet. 1996. PMID: 8923011

4

Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews.

Behn PS, Wasson J, Chayen S, Smolovitch I, Thomas J, Glaser B, Permutt MA. Behn PS, et al. Among authors: glaser b. Diabetes. 1998 Jun;47(6):967-9. doi: 10.2337/diabetes.47.6.967. Diabetes. 1998. PMID: 9604876 No abstract available.

5

Genetic heterogeneity in familial hyperinsulinism.

Nestorowicz A, Glaser B, Wilson BA, Shyng SL, Nichols CG, Stanley CA, Thornton PS, Permutt MA. Nestorowicz A, et al. Among authors: glaser b. Hum Mol Genet. 1998 Jul;7(7):1119-28. doi: 10.1093/hmg/7.7.1119. Hum Mol Genet. 1998. PMID: 9618169

6

Genetics of type II diabetes.

Permutt MA, Chiu K, Ferrer J, Glaser B, Inoue H, Nestorowicz A, Stanley CA, Tanizawa Y. Permutt MA, et al. Among authors: glaser b. Recent Prog Horm Res. 1998;53:201-16. Recent Prog Horm Res. 1998. PMID: 9769709 Review.

7

Mapping of the human insulin receptor substrate-2 gene, identification of a linked polymorphic marker and linkage analysis in families with Type II diabetes: no evidence for a major susceptibility role.

Kalidas K, Wasson J, Glaser B, Meyer JM, Duprat LJ, White MF, Permutt MA. Kalidas K, et al. Among authors: glaser b. Diabetologia. 1998 Nov;41(11):1389-91. doi: 10.1007/s001250051081. Diabetologia. 1998. PMID: 9833949

8

Neonatal Hyperinsulinism.

Glaser B, Landau H, Permutt MA. Glaser B, et al. Trends Endocrinol Metab. 1999 Mar;10(2):55-61. doi: 10.1016/s1043-2760(98)00102-7. Trends Endocrinol Metab. 1999. PMID: 10322395

9

Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism.

Glaser B, Furth J, Stanley CA, Baker L, Thornton PS, Landau H, Permutt MA. Glaser B, et al. Hum Mutat. 1999;14(1):23-9. doi: 10.1002/(SICI)1098-1004(1999)14:1<23::AID-HUMU3>3.0.CO;2-#. Hum Mutat. 1999. PMID: 10447255

10

A genome scan for type 2 diabetes susceptibility loci in a genetically isolated population.

Permutt MA, Wasson JC, Suarez BK, Lin J, Thomas J, Meyer J, Lewitzky S, Rennich JS, Parker A, DuPrat L, Maruti S, Chayen S, Glaser B. Permutt MA, et al. Among authors: glaser b. Diabetes. 2001 Mar;50(3):681-5. doi: 10.2337/diabetes.50.3.681. Diabetes. 2001. PMID: 11246891

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