Li Y - Search Results

1

A novel locus for Leber congenital amaurosis maps to chromosome 6q.

Dharmaraj S, Li Y, Robitaille JM, Silva E, Zhu D, Mitchell TN, Maltby LP, Baffoe-Bonnie AB, Maumenee IH. Dharmaraj S, et al. Among authors: li y. Am J Hum Genet. 2000 Jan;66(1):319-26. doi: 10.1086/302719. Am J Hum Genet. 2000. PMID: 10631161 Free PMC article. No abstract available.

2

A CRX null mutation is associated with both Leber congenital amaurosis and a normal ocular phenotype.

Silva E, Yang JM, Li Y, Dharmaraj S, Sundin OH, Maumenee IH. Silva E, et al. Among authors: li y. Invest Ophthalmol Vis Sci. 2000 Jul;41(8):2076-9. Invest Ophthalmol Vis Sci. 2000. PMID: 10892846

3

A G1103R mutation in CRB1 is co-inherited with high hyperopia and Leber congenital amaurosis.

Abouzeid H, Li Y, Maumenee IH, Dharmaraj S, Sundin O. Abouzeid H, et al. Among authors: li y. Ophthalmic Genet. 2006 Mar;27(1):15-20. doi: 10.1080/13816810500481840. Ophthalmic Genet. 2006. PMID: 16543197

4

Genetic basis of total colourblindness among the Pingelapese islanders.

Sundin OH, Yang JM, Li Y, Zhu D, Hurd JN, Mitchell TN, Silva ED, Maumenee IH. Sundin OH, et al. Among authors: li y. Nat Genet. 2000 Jul;25(3):289-93. doi: 10.1038/77162. Nat Genet. 2000. PMID: 10888875

5

Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3.

Kerrison JB, Arnould VJ, Ferraz Sallum JM, Vagefi MR, Barmada MM, Li Y, Zhu D, Maumenee IH. Kerrison JB, et al. Among authors: li y. Arch Ophthalmol. 1999 Jun;117(6):805-10. doi: 10.1001/archopht.117.6.805. Arch Ophthalmol. 1999. PMID: 10369594

6

Dominant inheritance of optic pits.

Stefko ST, Campochiaro P, Wang P, Li Y, Zhu D, Traboulsi EI. Stefko ST, et al. Among authors: li y. Am J Ophthalmol. 1997 Jul;124(1):112-3. doi: 10.1016/s0002-9394(14)71656-3. Am J Ophthalmol. 1997. PMID: 9222245

7

Tibial plateau fractures (AO type B3) combined with tibial tubercle fracture: Case report and review of the literature.

Tan L, Li YH, Li Y, Lin T, Zhu D, Sun DH. Tan L, et al. Among authors: li yh, li y. Medicine (Baltimore). 2018 Sep;97(36):e12015. doi: 10.1097/MD.0000000000012015. Medicine (Baltimore). 2018. PMID: 30200081 Free PMC article. Review.

8

Comparison of internal fixation with Gamma3 Long nails and INTERTAN nails in the treatment of Seinsheimer type V subtrochanteric femoral fractures in elderly patients.

Li YH, Zhu D, Li Y, Zhao T, Cao Z, Tan L. Li YH, et al. Among authors: li y. Medicine (Baltimore). 2019 Jun;98(25):e16140. doi: 10.1097/MD.0000000000016140. Medicine (Baltimore). 2019. PMID: 31232968 Free PMC article.

9

Genotype/Phenotype analysis of a photoreceptor-specific ATP-binding cassette transporter gene, ABCR, in Stargardt disease.

Lewis RA, Shroyer NF, Singh N, Allikmets R, Hutchinson A, Li Y, Lupski JR, Leppert M, Dean M. Lewis RA, et al. Among authors: li y. Am J Hum Genet. 1999 Feb;64(2):422-34. doi: 10.1086/302251. Am J Hum Genet. 1999. PMID: 9973280 Free PMC article.

10

Cloning and characterization of a secreted frizzled-related protein that is expressed by the retinal pigment epithelium.

Chang JT, Esumi N, Moore K, Li Y, Zhang S, Chew C, Goodman B, Rattner A, Moody S, Stetten G, Campochiaro PA, Zack DJ. Chang JT, et al. Among authors: li y. Hum Mol Genet. 1999 Apr;8(4):575-83. doi: 10.1093/hmg/8.4.575. Hum Mol Genet. 1999. PMID: 10072424

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