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Items: 1 to 20 of 76

1.

Genetic Association Study of KCNQ5 Polymorphisms with High Myopia.

Liao X, Yap MKH, Leung KH, Kao PYP, Liu LQ, Yip SP.

Biomed Res Int. 2017;2017:3024156. doi: 10.1155/2017/3024156. Epub 2017 Aug 13.

2.

Mutational screening of SLC39A5, LEPREL1 and LRPAP1 in a cohort of 187 high myopia patients.

Feng CY, Huang XQ, Cheng XW, Wu RH, Lu F, Jin ZB.

Sci Rep. 2017 Apr 25;7(1):1120. doi: 10.1038/s41598-017-01285-3.

3.

INVOLVEMENT OF MULTIPLE MOLECULAR PATHWAYS IN THE GENETICS OF OCULAR REFRACTION AND MYOPIA.

Wojciechowski R, Cheng CY.

Retina. 2017 Apr 11. doi: 10.1097/IAE.0000000000001518. [Epub ahead of print]

PMID:
28406858
4.

The investigation on the role of mitochondrial fusion protein 1 in the development of myopia.

Cai YL, Zou YC, Lei JH, Zeng GP, Wang Y.

Indian J Ophthalmol. 2016 Jul;64(7):500-3. doi: 10.4103/0301-4738.190137.

5.

Exploration and detection of potential regulatory variants in refractive error GWAS.

Liao X, Lan C, Liao D, Tian J, Huang X.

Sci Rep. 2016 Sep 8;6:33090. doi: 10.1038/srep33090.

6.

Genetic association of COL1A1 polymorphisms with high myopia in Asian population: a Meta-analysis.

Gong B, Qu C, Huang XF, Ye ZM, Zhang DD, Shi Y, Chen R, Liu YP, Shuai P.

Int J Ophthalmol. 2016 Aug 18;9(8):1187-93. doi: 10.18240/ijo.2016.08.16. eCollection 2016.

7.

G9a and ZNF644 Physically Associate to Suppress Progenitor Gene Expression during Neurogenesis.

Olsen JB, Wong L, Deimling S, Miles A, Guo H, Li Y, Zhang Z, Greenblatt JF, Emili A, Tropepe V.

Stem Cell Reports. 2016 Sep 13;7(3):454-470. doi: 10.1016/j.stemcr.2016.06.012. Epub 2016 Aug 18.

8.

Variation in PTCHD2, CRISP3, NAP1L4, FSCB, and AP3B2 associated with spherical equivalent.

Chen F, Duggal P, Klein BE, Lee KE, Truitt B, Klein R, Iyengar SK, Klein AP.

Mol Vis. 2016 Jul 14;22:783-96. eCollection 2016.

9.

A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping.

Han B, Duong D, Sul JH, de Bakker PI, Eskin E, Raychaudhuri S.

Hum Mol Genet. 2016 May 1;25(9):1857-66. doi: 10.1093/hmg/ddw049. Epub 2016 Feb 21.

10.

The association of TGFB1 genetic polymorphisms with high myopia: a systematic review and meta-analysis.

Meng B, Li SM, Yang Y, Yang ZR, Sun F, Kang MT, Sun YY, Ran AR, Wang JN, Yan R, BaI YW, Wang NL, Zhan SY.

Int J Clin Exp Med. 2015 Nov 15;8(11):20355-67. eCollection 2015.

11.

Polymorphism in the RASGRF1 gene with high myopia: A meta-analysis.

Chen T, Shan G, Ma J, Zhong Y.

Mol Vis. 2015 Nov 14;21:1272-80. eCollection 2015.

12.

APLP2 Regulates Refractive Error and Myopia Development in Mice and Humans.

Tkatchenko AV, Tkatchenko TV, Guggenheim JA, Verhoeven VJ, Hysi PG, Wojciechowski R, Singh PK, Kumar A, Thinakaran G; Consortium for Refractive Error and Myopia (CREAM), Williams C.

PLoS Genet. 2015 Aug 27;11(8):e1005432. doi: 10.1371/journal.pgen.1005432. eCollection 2015 Aug.

13.

RPE and Choroid Mechanisms Underlying Ocular Growth and Myopia.

Zhang Y, Wildsoet CF.

Prog Mol Biol Transl Sci. 2015;134:221-40. doi: 10.1016/bs.pmbts.2015.06.014. Epub 2015 Jul 23. Review.

14.

Transcriptional profiling reveals functional links between RasGrf1 and Pttg1 in pancreatic beta cells.

Manyes L, Arribas M, Gomez C, Calzada N, Fernandez-Medarde A, Santos E.

BMC Genomics. 2014 Nov 25;15:1019. doi: 10.1186/1471-2164-15-1019.

15.

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.

Li Q, Wojciechowski R, Simpson CL, Hysi PG, Verhoeven VJ, Ikram MK, Höhn R, Vitart V, Hewitt AW, Oexle K, Mäkelä KM, MacGregor S, Pirastu M, Fan Q, Cheng CY, St Pourcain B, McMahon G, Kemp JP, Northstone K, Rahi JS, Cumberland PM, Martin NG, Sanfilippo PG, Lu Y, Wang YX, Hayward C, Polašek O, Campbell H, Bencic G, Wright AF, Wedenoja J, Zeller T, Schillert A, Mirshahi A, Lackner K, Yip SP, Yap MK, Ried JS, Gieger C, Murgia F, Wilson JF, Fleck B, Yazar S, Vingerling JR, Hofman A, Uitterlinden A, Rivadeneira F, Amin N, Karssen L, Oostra BA, Zhou X, Teo YY, Tai ES, Vithana E, Barathi V, Zheng Y, Siantar RG, Neelam K, Shin Y, Lam J, Yonova-Doing E, Venturini C, Hosseini SM, Wong HS, Lehtimäki T, Kähönen M, Raitakari O, Timpson NJ, Evans DM, Khor CC, Aung T, Young TL, Mitchell P, Klein B, van Duijn CM, Meitinger T, Jonas JB, Baird PN, Mackey DA, Wong TY, Saw SM, Pärssinen O, Stambolian D, Hammond CJ, Klaver CC, Williams C, Paterson AD, Bailey-Wilson JE, Guggenheim JA; CREAM Consortium.

Hum Genet. 2015 Feb;134(2):131-46. doi: 10.1007/s00439-014-1500-y. Epub 2014 Nov 4.

16.

Genome-wide association studies: applications and insights gained in Ophthalmology.

Chandra A, Mitry D, Wright A, Campbell H, Charteris DG.

Eye (Lond). 2014 Sep;28(9):1066-79. doi: 10.1038/eye.2014.145. Epub 2014 Jun 27. Review.

17.

SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia.

Guo H, Jin X, Zhu T, Wang T, Tong P, Tian L, Peng Y, Sun L, Wan A, Chen J, Liu Y, Li Y, Tian Q, Xia L, Zhang L, Pan Y, Lu L, Liu Q, Shen L, Li Y, Xiong W, Li J, Tang B, Feng Y, Zhang X, Zhang Z, Pan Q, Hu Z, Xia K.

J Med Genet. 2014 Aug;51(8):518-25. doi: 10.1136/jmedgenet-2014-102351. Epub 2014 Jun 2.

18.

Genome-wide association studies of refractive error and myopia, lessons learned, and implications for the future.

Hysi PG, Wojciechowski R, Rahi JS, Hammond CJ.

Invest Ophthalmol Vis Sci. 2014 May 29;55(5):3344-51. doi: 10.1167/iovs.14-14149. Review.

19.

Genetic variation of the RASGRF1 regulatory region affects human hippocampus-dependent memory.

Barman A, Assmann A, Richter S, Soch J, Schütze H, Wüstenberg T, Deibele A, Klein M, Richter A, Behnisch G, Düzel E, Zenker M, Seidenbecher CI, Schott BH.

Front Hum Neurosci. 2014 Apr 29;8:260. doi: 10.3389/fnhum.2014.00260. eCollection 2014.

20.

Association study of 15q14 and 15q25 with high myopia in the Han Chinese population.

Qiang Y, Li W, Wang Q, He K, Li Z, Chen J, Song Z, Qu J, Zhou X, Qin S, Shen J, Wen Z, Ji J, Shi Y.

BMC Genet. 2014 Apr 27;15:51. doi: 10.1186/1471-2156-15-51.

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