Hauser MA - Search Results

1

Mitochondrial polymorphism A10398G and Haplogroup I are associated with Fuchs' endothelial corneal dystrophy.

Li YJ, Minear MA, Qin X, Rimmler J, Hauser MA, Allingham RR, Igo RP, Lass JH, Iyengar SK, Klintworth GK, Afshari NA, Gregory SG; FECD Genetics Consortium. Li YJ, et al. Among authors: hauser ma. Invest Ophthalmol Vis Sci. 2014 Jun 10;55(7):4577-84. doi: 10.1167/iovs.13-13517. Invest Ophthalmol Vis Sci. 2014. PMID: 24917144 Free PMC article.

2

Prevalence of myocilin mutations in adults with primary open-angle glaucoma in Ghana, West Africa.

Challa P, Herndon LW, Hauser MA, Broomer BW, Pericak-Vance MA, Ababio-Danso B, Allingham RR. Challa P, et al. Among authors: hauser ma. J Glaucoma. 2002 Oct;11(5):416-20. doi: 10.1097/00061198-200210000-00008. J Glaucoma. 2002. PMID: 12362081

3

Association between the neuron-specific RNA-binding protein ELAVL4 and Parkinson disease.

Noureddine MA, Qin XJ, Oliveira SA, Skelly TJ, van der Walt J, Hauser MA, Pericak-Vance MA, Vance JM, Li YJ. Noureddine MA, et al. Among authors: hauser ma. Hum Genet. 2005 Jun;117(1):27-33. doi: 10.1007/s00439-005-1259-2. Epub 2005 Apr 13. Hum Genet. 2005. PMID: 15827745

4

Early adult-onset POAG linked to 15q11-13 using ordered subset analysis.

Allingham RR, Wiggs JL, Hauser ER, Larocque-Abramson KR, Santiago-Turla C, Broomer B, Del Bono EA, Graham FL, Haines JL, Pericak-Vance MA, Hauser MA. Allingham RR, et al. Among authors: hauser er, hauser ma. Invest Ophthalmol Vis Sci. 2005 Jun;46(6):2002-5. doi: 10.1167/iovs.04-1477. Invest Ophthalmol Vis Sci. 2005. PMID: 15914615 Free PMC article.

5

Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra.

Noureddine MA, Li YJ, van der Walt JM, Walters R, Jewett RM, Xu H, Wang T, Walter JW, Scott BL, Hulette C, Schmechel D, Stenger JE, Dietrich F, Vance JM, Hauser MA. Noureddine MA, et al. Among authors: hauser ma. Mov Disord. 2005 Oct;20(10):1299-309. doi: 10.1002/mds.20573. Mov Disord. 2005. PMID: 15966006

6

SNPselector: a web tool for selecting SNPs for genetic association studies.

Xu H, Gregory SG, Hauser ER, Stenger JE, Pericak-Vance MA, Vance JM, Züchner S, Hauser MA. Xu H, et al. Among authors: hauser er, hauser ma. Bioinformatics. 2005 Nov 15;21(22):4181-6. doi: 10.1093/bioinformatics/bti682. Epub 2005 Sep 22. Bioinformatics. 2005. PMID: 16179360 Free PMC article.

7

Distribution of WDR36 DNA sequence variants in patients with primary open-angle glaucoma.

Hauser MA, Allingham RR, Linkroum K, Wang J, LaRocque-Abramson K, Figueiredo D, Santiago-Turla C, del Bono EA, Haines JL, Pericak-Vance MA, Wiggs JL. Hauser MA, et al. Invest Ophthalmol Vis Sci. 2006 Jun;47(6):2542-6. doi: 10.1167/iovs.05-1476. Invest Ophthalmol Vis Sci. 2006. PMID: 16723468

8

NOS2A and the modulating effect of cigarette smoking in Parkinson's disease.

Hancock DB, Martin ER, Fujiwara K, Stacy MA, Scott BL, Stajich JM, Jewett R, Li YJ, Hauser MA, Vance JM, Scott WK. Hancock DB, et al. Among authors: hauser ma. Ann Neurol. 2006 Sep;60(3):366-73. doi: 10.1002/ana.20915. Ann Neurol. 2006. PMID: 16823855

9

Complement factor H increases risk for atrophic age-related macular degeneration.

Postel EA, Agarwal A, Caldwell J, Gallins P, Toth C, Schmidt S, Scott WK, Hauser MA, Haines JL, Pericak-Vance MA. Postel EA, et al. Among authors: hauser ma. Ophthalmology. 2006 Sep;113(9):1504-7. doi: 10.1016/j.ophtha.2006.02.049. Epub 2006 Jul 7. Ophthalmology. 2006. PMID: 16828512

10

Juvenile bilateral lens dislocation and glaucoma associated with a novel mutation in the fibrillin 1 gene.

Challa P, Hauser MA, Luna CC, Freedman SF, Pericak-Vance M, Yang J, McDonald MT, Allingham RR. Challa P, et al. Among authors: hauser ma. Mol Vis. 2006 Aug 28;12:1009-15. Mol Vis. 2006. PMID: 16971892 Free article.

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