Zhang K - Search Results

1

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.

Fritsche LG, Igl W, Bailey JN, Grassmann F, Sengupta S, Bragg-Gresham JL, Burdon KP, Hebbring SJ, Wen C, Gorski M, Kim IK, Cho D, Zack D, Souied E, Scholl HP, Bala E, Lee KE, Hunter DJ, Sardell RJ, Mitchell P, Merriam JE, Cipriani V, Hoffman JD, Schick T, Lechanteur YT, Guymer RH, Johnson MP, Jiang Y, Stanton CM, Buitendijk GH, Zhan X, Kwong AM, Boleda A, Brooks M, Gieser L, Ratnapriya R, Branham KE, Foerster JR, Heckenlively JR, Othman MI, Vote BJ, Liang HH, Souzeau E, McAllister IL, Isaacs T, Hall J, Lake S, Mackey DA, Constable IJ, Craig JE, Kitchner TE, Yang Z, Su Z, Luo H, Chen D, Ouyang H, Flagg K, Lin D, Mao G, Ferreyra H, Stark K, von Strachwitz CN, Wolf A, Brandl C, Rudolph G, Olden M, Morrison MA, Morgan DJ, Schu M, Ahn J, Silvestri G, Tsironi EE, Park KH, Farrer LA, Orlin A, Brucker A, Li M, Curcio CA, Mohand-Saïd S, Sahel JA, Audo I, Benchaboune M, Cree AJ, Rennie CA, Goverdhan SV, Grunin M, Hagbi-Levi S, Campochiaro P, Katsanis N, Holz FG, Blond F, Blanché H, Deleuze JF, Igo RP Jr, Truitt B, Peachey NS, Meuer SM, Myers CE, Moore EL, Klein R, Hauser MA, Postel EA, Courtenay MD, Schwartz SG, Kovach JL, Scott WK, Liew G, Tan AG, Gopinath B, Merriam JC, Smith RT, Khan JC,… See abstract for full author list ➔ Fritsche LG, et al. Among authors: zhang k. Nat Genet. 2016 Feb;48(2):134-43. doi: 10.1038/ng.3448. Epub 2015 Dec 21. Nat Genet. 2016. PMID: 26691988 Free PMC article.

2

A new locus for autosomal dominant stargardt-like disease maps to chromosome 4.

Kniazeva M, Chiang MF, Morgan B, Anduze AL, Zack DJ, Han M, Zhang K. Kniazeva M, et al. Among authors: zhang k. Am J Hum Genet. 1999 May;64(5):1394-9. doi: 10.1086/302377. Am J Hum Genet. 1999. PMID: 10205271 Free PMC article.

3

Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease.

Kniazeva MF, Chiang MF, Cutting GR, Zack DJ, Han M, Zhang K. Kniazeva MF, et al. Among authors: zhang k. Ophthalmic Genet. 1999 Jun;20(2):71-81. doi: 10.1076/opge.20.2.71.2287. Ophthalmic Genet. 1999. PMID: 10420191

4

The ABCR gene in recessive and dominant Stargardt diseases: a genetic pathway in macular degeneration.

Zhang K, Kniazeva M, Hutchinson A, Han M, Dean M, Allikmets R. Zhang K, et al. Genomics. 1999 Sep 1;60(2):234-7. doi: 10.1006/geno.1999.5896. Genomics. 1999. PMID: 10486215 Free article.

5

Clinical spectrum of chromosome 6-linked autosomal dominant drusen and macular degeneration.

Stefko ST, Zhang K, Gorin MB, Traboulsi EI. Stefko ST, et al. Among authors: zhang k. Am J Ophthalmol. 2000 Aug;130(2):203-8. doi: 10.1016/s0002-9394(00)00562-6. Am J Ophthalmol. 2000. PMID: 11004295

6

A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy.

Zhang K, Kniazeva M, Han M, Li W, Yu Z, Yang Z, Li Y, Metzker ML, Allikmets R, Zack DJ, Kakuk LE, Lagali PS, Wong PW, MacDonald IM, Sieving PA, Figueroa DJ, Austin CP, Gould RJ, Ayyagari R, Petrukhin K. Zhang K, et al. Nat Genet. 2001 Jan;27(1):89-93. doi: 10.1038/83817. Nat Genet. 2001. PMID: 11138005

7

Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy.

Wilkie SE, Li Y, Deery EC, Newbold RJ, Garibaldi D, Bateman JB, Zhang H, Lin W, Zack DJ, Bhattacharya SS, Warren MJ, Hunt DM, Zhang K. Wilkie SE, et al. Among authors: zhang k, zhang h. Am J Hum Genet. 2001 Sep;69(3):471-80. doi: 10.1086/323265. Epub 2001 Jul 31. Am J Hum Genet. 2001. PMID: 11484154 Free PMC article.

8

Diverse macular dystrophy phenotype caused by a novel complex mutation in the ELOVL4 gene.

Bernstein PS, Tammur J, Singh N, Hutchinson A, Dixon M, Pappas CM, Zabriskie NA, Zhang K, Petrukhin K, Leppert M, Allikmets R. Bernstein PS, et al. Among authors: zhang k. Invest Ophthalmol Vis Sci. 2001 Dec;42(13):3331-6. Invest Ophthalmol Vis Sci. 2001. PMID: 11726641

9

Evaluation of the ELOVL4 gene in patients with age-related macular degeneration.

Ayyagari R, Zhang K, Hutchinson A, Yu Z, Swaroop A, Kakuk LE, Seddon JM, Bernstein PS, Lewis RA, Tammur J, Yang Z, Li Y, Zhang H, Yashar BM, Liu J, Petrukhin K, Sieving PA, Allikmets R. Ayyagari R, et al. Among authors: zhang k, zhang h. Ophthalmic Genet. 2001 Dec;22(4):233-9. doi: 10.1076/opge.22.4.233.2219. Ophthalmic Genet. 2001. PMID: 11803489

10

Mutations in the RPGR gene cause X-linked cone dystrophy.

Yang Z, Peachey NS, Moshfeghi DM, Thirumalaichary S, Chorich L, Shugart YY, Fan K, Zhang K. Yang Z, et al. Among authors: zhang k. Hum Mol Genet. 2002 Mar 1;11(5):605-11. doi: 10.1093/hmg/11.5.605. Hum Mol Genet. 2002. PMID: 11875055

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