Wiggs JL - Search Results

1

Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium.

Verma SS, Cooke Bailey JN, Lucas A, Bradford Y, Linneman JG, Hauser MA, Pasquale LR, Peissig PL, Brilliant MH, McCarty CA, Haines JL, Wiggs JL, Vrabec TR, Tromp G, Ritchie MD; eMERGE Network; NEIGHBOR Consortium. Verma SS, et al. Among authors: wiggs jl. PLoS Genet. 2016 Sep 13;12(9):e1006186. doi: 10.1371/journal.pgen.1006186. eCollection 2016 Sep. PLoS Genet. 2016. PMID: 27623284 Free PMC article.

2

Exclusion of chromosome 1q21-q31 from linkage to three pedigrees affected by the pigment-dispersion syndrome.

Paglinauan C, Haines JL, Del Bono EA, Schuman J, Stawski S, Wiggs JL. Paglinauan C, et al. Among authors: wiggs jl. Am J Hum Genet. 1995 May;56(5):1240-3. Am J Hum Genet. 1995. PMID: 7726183 Free PMC article. No abstract available.

3

Genetic linkage of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees.

Wiggs JL, Haines JL, Paglinauan C, Fine A, Sporn C, Lou D. Wiggs JL, et al. Genomics. 1994 May 15;21(2):299-303. doi: 10.1006/geno.1994.1269. Genomics. 1994. PMID: 8088822

4

The distinction between juvenile and adult-onset primary open-angle glaucoma.

Wiggs JL, Damji KF, Haines JL, Pericak-Vance MA, Allingham RR. Wiggs JL, et al. Am J Hum Genet. 1996 Jan;58(1):243-4. Am J Hum Genet. 1996. PMID: 8554064 Free PMC article. No abstract available.

5

A second locus for Rieger syndrome maps to chromosome 13q14.

Phillips JC, del Bono EA, Haines JL, Pralea AM, Cohen JS, Greff LJ, Wiggs JL. Phillips JC, et al. Among authors: wiggs jl. Am J Hum Genet. 1996 Sep;59(3):613-9. Am J Hum Genet. 1996. PMID: 8751862 Free PMC article.

6

A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36.

Andersen JS, Pralea AM, DelBono EA, Haines JL, Gorin MB, Schuman JS, Mattox CG, Wiggs JL. Andersen JS, et al. Among authors: wiggs jl. Arch Ophthalmol. 1997 Mar;115(3):384-8. doi: 10.1001/archopht.1997.01100150386012. Arch Ophthalmol. 1997. PMID: 9076212

7

Adult-onset primary open angle glaucoma does not localize to chromosome 2cen-q13 in North American families.

Allingham RR, Wiggs JL, Damji KF, Herndon L, Youn J, Tallett DA, Jones KH, Del Bono EA, Reardon M, Haines JL, Pericak-Vance MA. Allingham RR, et al. Among authors: wiggs jl. Hum Hered. 1998 Sep-Oct;48(5):251-5. doi: 10.1159/000022812. Hum Hered. 1998. PMID: 9748694

8

Gln368STOP myocilin mutation in families with late-onset primary open-angle glaucoma.

Allingham RR, Wiggs JL, De La Paz MA, Vollrath D, Tallett DA, Broomer B, Jones KH, Del Bono EA, Kern J, Patterson K, Haines JL, Pericak-Vance MA. Allingham RR, et al. Among authors: wiggs jl. Invest Ophthalmol Vis Sci. 1998 Nov;39(12):2288-95. Invest Ophthalmol Vis Sci. 1998. PMID: 9804137

9

Genome-wide scan for adult onset primary open angle glaucoma.

Wiggs JL, Allingham RR, Hossain A, Kern J, Auguste J, DelBono EA, Broomer B, Graham FL, Hauser M, Pericak-Vance M, Haines JL. Wiggs JL, et al. Hum Mol Genet. 2000 Apr 12;9(7):1109-17. doi: 10.1093/hmg/9.7.1109. Hum Mol Genet. 2000. PMID: 10767336

10

DNA sequence variants in the tyrosinase-related protein 1 (TYRP1) gene are not associated with human pigmentary glaucoma.

Lynch S, Yanagi G, DelBono E, Wiggs JL. Lynch S, et al. Among authors: wiggs jl. Mol Vis. 2002 Apr 24;8:127-9. Mol Vis. 2002. PMID: 12011806 Free article.

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