Alward WL - Search Results

1

Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohort.

Kuehn MH, Wang K, Roos B, Stone EM, Kwon YH, Alward WL, Mullins RF, Fingert JH. Kuehn MH, et al. Among authors: alward wl. Mol Vis. 2011 Feb 8;17:430-5. Mol Vis. 2011. PMID: 21321670 Free PMC article.

2

Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25).

Héon E, Sheth BP, Kalenak JW, Sunden SL, Streb LM, Taylor CM, Alward WL, Sheffield VC, Stone EM. Héon E, et al. Among authors: alward wl. Hum Mol Genet. 1995 Aug;4(8):1435-9. doi: 10.1093/hmg/4.8.1435. Hum Mol Genet. 1995. PMID: 7581385

3

Linkage of posterior polymorphous corneal dystrophy to 20q11.

Héon E, Mathers WD, Alward WL, Weisenthal RW, Sunden SL, Fishbaugh JA, Taylor CM, Krachmer JH, Sheffield VC, Stone EM. Héon E, et al. Among authors: alward wl. Hum Mol Genet. 1995 Mar;4(3):485-8. doi: 10.1093/hmg/4.3.485. Hum Mol Genet. 1995. PMID: 7795607

4

Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma.

Johnson AT, Drack AV, Kwitek AE, Cannon RL, Stone EM, Alward WL. Johnson AT, et al. Among authors: alward wl. Ophthalmology. 1993 Apr;100(4):524-9. doi: 10.1016/s0161-6420(13)31615-7. Ophthalmology. 1993. PMID: 8479711

5

Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31.

Sheffield VC, Stone EM, Alward WL, Drack AV, Johnson AT, Streb LM, Nichols BE. Sheffield VC, et al. Among authors: alward wl. Nat Genet. 1993 May;4(1):47-50. doi: 10.1038/ng0593-47. Nat Genet. 1993. PMID: 8513321

6

Molecular genetics of glaucoma: current status.

Alward WL, Johnson AT, Nishimura DY, Sheffield VC, Stone EM. Alward WL, et al. J Glaucoma. 1996 Aug;5(4):276-84. J Glaucoma. 1996. PMID: 8795774 Review. No abstract available.

7

Fine mapping of the autosomal dominant juvenile open angle glaucoma (GLC1A) region and evaluation of candidate genes.

Sunden SL, Alward WL, Nichols BE, Rokhlina TR, Nystuen A, Stone EM, Sheffield VC. Sunden SL, et al. Among authors: alward wl. Genome Res. 1996 Sep;6(9):862-9. doi: 10.1101/gr.6.9.862. Genome Res. 1996. PMID: 8889553 Free article.

8

Identification of a gene that causes primary open angle glaucoma.

Stone EM, Fingert JH, Alward WL, Nguyen TD, Polansky JR, Sunden SL, Nishimura D, Clark AF, Nystuen A, Nichols BE, Mackey DA, Ritch R, Kalenak JW, Craven ER, Sheffield VC. Stone EM, et al. Among authors: alward wl. Science. 1997 Jan 31;275(5300):668-70. doi: 10.1126/science.275.5300.668. Science. 1997. PMID: 9005853

9

Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene.

Alward WL, Semina EV, Kalenak JW, Héon E, Sheth BP, Stone EM, Murray JC. Alward WL, et al. Am J Ophthalmol. 1998 Jan;125(1):98-100. doi: 10.1016/s0002-9394(99)80242-6. Am J Ophthalmol. 1998. PMID: 9437321

10

Clinical features associated with mutations in the chromosome 1 open-angle glaucoma gene (GLC1A).

Alward WL, Fingert JH, Coote MA, Johnson AT, Lerner SF, Junqua D, Durcan FJ, McCartney PJ, Mackey DA, Sheffield VC, Stone EM. Alward WL, et al. N Engl J Med. 1998 Apr 9;338(15):1022-7. doi: 10.1056/NEJM199804093381503. N Engl J Med. 1998. PMID: 9535666 Free article.

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