Lee W - Search Results

1

Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations.

Cremers FPM, Lee W, Collin RWJ, Allikmets R. Cremers FPM, et al. Among authors: lee w. Prog Retin Eye Res. 2020 Nov;79:100861. doi: 10.1016/j.preteyeres.2020.100861. Epub 2020 Apr 9. Prog Retin Eye Res. 2020. PMID: 32278709 Free PMC article. Review.

2

Disruption of the human cone photoreceptor mosaic from a defect in NR2E3 transcription factor function in young adults.

Park SP, Hong IH, Tsang SH, Lee W, Horowitz J, Yzer S, Allikmets R, Chang S. Park SP, et al. Among authors: lee w. Graefes Arch Clin Exp Ophthalmol. 2013 Oct;251(10):2299-309. doi: 10.1007/s00417-013-2296-5. Epub 2013 Apr 19. Graefes Arch Clin Exp Ophthalmol. 2013. PMID: 23604511 Free PMC article.

3

Distinct characteristics of inferonasal fundus autofluorescence patterns in stargardt disease and retinitis pigmentosa.

Duncker T, Lee W, Tsang SH, Greenberg JP, Zernant J, Allikmets R, Sparrow JR. Duncker T, et al. Among authors: lee w. Invest Ophthalmol Vis Sci. 2013 Oct 17;54(10):6820-6. doi: 10.1167/iovs.13-12895. Invest Ophthalmol Vis Sci. 2013. PMID: 24071957 Free PMC article.

4

Disease progression in autosomal dominant cone-rod dystrophy caused by a novel mutation (D100G) in the GUCA1A gene.

Nong E, Lee W, Merriam JE, Allikmets R, Tsang SH. Nong E, et al. Among authors: lee w. Doc Ophthalmol. 2014 Feb;128(1):59-67. doi: 10.1007/s10633-013-9420-z. Epub 2013 Dec 19. Doc Ophthalmol. 2014. PMID: 24352742 Free PMC article.

5

Whole exome sequencing identifies CRB1 defect in an unusual maculopathy phenotype.

Tsang SH, Burke T, Oll M, Yzer S, Lee W, Xie YA, Allikmets R. Tsang SH, et al. Among authors: lee w. Ophthalmology. 2014 Sep;121(9):1773-82. doi: 10.1016/j.ophtha.2014.03.010. Epub 2014 May 6. Ophthalmology. 2014. PMID: 24811962 Free PMC article.

6

New syndrome with retinitis pigmentosa is caused by nonsense mutations in retinol dehydrogenase RDH11.

Xie YA, Lee W, Cai C, Gambin T, Nõupuu K, Sujirakul T, Ayuso C, Jhangiani S, Muzny D, Boerwinkle E, Gibbs R, Greenstein VC, Lupski JR, Tsang SH, Allikmets R. Xie YA, et al. Among authors: lee w. Hum Mol Genet. 2014 Nov 1;23(21):5774-80. doi: 10.1093/hmg/ddu291. Epub 2014 Jun 10. Hum Mol Genet. 2014. PMID: 24916380 Free PMC article.

7

Genetic and clinical analysis of ABCA4-associated disease in African American patients.

Zernant J, Collison FT, Lee W, Fishman GA, Noupuu K, Yuan B, Cai C, Lupski JR, Yannuzzi LA, Tsang SH, Allikmets R. Zernant J, et al. Among authors: lee w. Hum Mutat. 2014 Oct;35(10):1187-94. doi: 10.1002/humu.22626. Hum Mutat. 2014. PMID: 25066811 Free PMC article.

8

Choroidal and retinal thickening in severe preeclampsia.

Garg A, Wapner RJ, Ananth CV, Dale E, Tsang SH, Lee W, Allikmets R, Bearelly S. Garg A, et al. Among authors: lee w. Invest Ophthalmol Vis Sci. 2014 Jul 29;55(9):5723-9. doi: 10.1167/iovs.14-14143. Invest Ophthalmol Vis Sci. 2014. PMID: 25074772 Free PMC article.

9

The external limiting membrane in early-onset Stargardt disease.

Lee W, Nõupuu K, Oll M, Duncker T, Burke T, Zernant J, Bearelly S, Tsang SH, Sparrow JR, Allikmets R. Lee W, et al. Invest Ophthalmol Vis Sci. 2014 Aug 19;55(10):6139-49. doi: 10.1167/iovs.14-15126. Invest Ophthalmol Vis Sci. 2014. PMID: 25139735 Free PMC article.

10

Quantitative fundus autofluorescence distinguishes ABCA4-associated and non-ABCA4-associated bull's-eye maculopathy.

Duncker T, Tsang SH, Lee W, Zernant J, Allikmets R, Delori FC, Sparrow JR. Duncker T, et al. Among authors: lee w. Ophthalmology. 2015 Feb;122(2):345-55. doi: 10.1016/j.ophtha.2014.08.017. Epub 2014 Oct 3. Ophthalmology. 2015. PMID: 25283059 Free PMC article.

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