Stringham HM - Search Results

1

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion.

Huyghe JR, Jackson AU, Fogarty MP, Buchkovich ML, Stančáková A, Stringham HM, Sim X, Yang L, Fuchsberger C, Cederberg H, Chines PS, Teslovich TM, Romm JM, Ling H, McMullen I, Ingersoll R, Pugh EW, Doheny KF, Neale BM, Daly MJ, Kuusisto J, Scott LJ, Kang HM, Collins FS, Abecasis GR, Watanabe RM, Boehnke M, Laakso M, Mohlke KL. Huyghe JR, et al. Among authors: stringham hm. Nat Genet. 2013 Feb;45(2):197-201. doi: 10.1038/ng.2507. Epub 2012 Dec 23. Nat Genet. 2013. PMID: 23263489 Free PMC article.

2

Clinical phenotype of juvenile-onset primary open-angle glaucoma linked to chromosome 1q.

Johnson AT, Richards JE, Boehnke M, Stringham HM, Herman SB, Wong DJ, Lichter PR. Johnson AT, et al. Among authors: stringham hm. Ophthalmology. 1996 May;103(5):808-14. doi: 10.1016/s0161-6420(96)30611-8. Ophthalmology. 1996. PMID: 8637692

3

Identifying marker typing incompatibilities in linkage analysis.

Stringham HM, Boehnke M. Stringham HM, et al. Am J Hum Genet. 1996 Oct;59(4):946-50. Am J Hum Genet. 1996. PMID: 8808612 Free PMC article.

4

Cosegregation of open-angle glaucoma and the nail-patella syndrome.

Lichter PR, Richards JE, Downs CA, Stringham HM, Boehnke M, Farley FA. Lichter PR, et al. Among authors: stringham hm. Am J Ophthalmol. 1997 Oct;124(4):506-15. doi: 10.1016/s0002-9394(14)70866-9. Am J Ophthalmol. 1997. PMID: 9323941

5

Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11.

Othman MI, Sullivan SA, Skuta GL, Cockrell DA, Stringham HM, Downs CA, Fornés A, Mick A, Boehnke M, Vollrath D, Richards JE. Othman MI, et al. Among authors: stringham hm. Am J Hum Genet. 1998 Nov;63(5):1411-8. doi: 10.1086/302113. Am J Hum Genet. 1998. PMID: 9792868 Free PMC article.

6

Point and interval estimates of marker location in radiation hybrid mapping.

Stringham HM, Boehnke M, Lange K. Stringham HM, et al. Am J Hum Genet. 1999 Aug;65(2):545-53. doi: 10.1086/302496. Am J Hum Genet. 1999. PMID: 10417296 Free PMC article.

7

The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.

Watanabe RM, Ghosh S, Langefeld CD, Valle TT, Hauser ER, Magnuson VL, Mohlke KL, Silander K, Ally DS, Chines P, Blaschak-Harvan J, Douglas JA, Duren WL, Epstein MP, Fingerlin TE, Kaleta HS, Lange EM, Li C, McEachin RC, Stringham HM, Trager E, White PP, Balow J Jr, Birznieks G, Chang J, Eldridge W. Watanabe RM, et al. Among authors: stringham hm. Am J Hum Genet. 2000 Nov;67(5):1186-200. Epub 2000 Oct 13. Am J Hum Genet. 2000. PMID: 11032784 Free PMC article.

8

Lod scores for gene mapping in the presence of marker map uncertainty.

Stringham HM, Boehnke M. Stringham HM, et al. Genet Epidemiol. 2001 Jul;21(1):31-9. doi: 10.1002/gepi.1016. Genet Epidemiol. 2001. PMID: 11443732 Free article.

9

Variation in three single nucleotide polymorphisms in the calpain-10 gene not associated with type 2 diabetes in a large Finnish cohort.

Fingerlin TE, Erdos MR, Watanabe RM, Wiles KR, Stringham HM, Mohlke KL, Silander K, Valle TT, Buchanan TA, Tuomilehto J, Bergman RN, Boehnke M, Collins FS. Fingerlin TE, et al. Among authors: stringham hm. Diabetes. 2002 May;51(5):1644-8. doi: 10.2337/diabetes.51.5.1644. Diabetes. 2002. PMID: 11978669

10

X-linked recessive atrophic macular degeneration from RPGR mutation.

Ayyagari R, Demirci FY, Liu J, Bingham EL, Stringham H, Kakuk LE, Boehnke M, Gorin MB, Richards JE, Sieving PA. Ayyagari R, et al. Genomics. 2002 Aug;80(2):166-71. doi: 10.1006/geno.2002.6815. Genomics. 2002. PMID: 12160730

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