Hysi PG - Search Results

1

Sequencing of the CHST6 gene in Czech macular corneal dystrophy patients supports the evidence of a founder mutation.

Liskova P, Veraitch B, Jirsova K, Filipec M, Neuwirth A, Ebenezer ND, Hysi PG, Hardcastle AJ, Tuft SJ, Bhattacharya SS. Liskova P, et al. Among authors: hysi pg. Br J Ophthalmol. 2008 Feb;92(2):265-7. doi: 10.1136/bjo.2007.125252. Epub 2007 Oct 25. Br J Ophthalmol. 2008. PMID: 17962390

2

Study of p.N247S KERA mutation in a British family with cornea plana.

Liskova P, Hysi PG, Williams D, Ainsworth JR, Shah S, de la Chapelle A, Tuft SJ, Bhattacharya SS. Liskova P, et al. Among authors: hysi pg. Mol Vis. 2007 Jul 27;13:1339-47. Mol Vis. 2007. PMID: 17679937

3

The Roles of PAX6 and SOX2 in Myopia: lessons from the 1958 British Birth Cohort.

Simpson CL, Hysi P, Bhattacharya SS, Hammond CJ, Webster A, Peckham CS, Sham PC, Rahi JS. Simpson CL, et al. Invest Ophthalmol Vis Sci. 2007 Oct;48(10):4421-5. doi: 10.1167/iovs.07-0231. Invest Ophthalmol Vis Sci. 2007. PMID: 17898260

4

Molecular analysis of the VSX1 gene in familial keratoconus.

Liskova P, Ebenezer ND, Hysi PG, Gwilliam R, El-Ashry MF, Moodaley LC, Hau S, Twa M, Tuft SJ, Bhatacharya SS. Liskova P, et al. Among authors: hysi pg. Mol Vis. 2007 Oct 4;13:1887-91. Mol Vis. 2007. PMID: 17960127 Free PMC article.

5

Evidence for keratoconus susceptibility locus on chromosome 14: a genome-wide linkage screen using single-nucleotide polymorphism markers.

Liskova P, Hysi PG, Waseem N, Ebenezer ND, Bhattacharya SS, Tuft SJ. Liskova P, et al. Among authors: hysi pg. Arch Ophthalmol. 2010 Sep;128(9):1191-5. doi: 10.1001/archophthalmol.2010.200. Arch Ophthalmol. 2010. PMID: 20837804

6

Common polymorphisms in the SERPINI2 gene are associated with refractive error in the 1958 British Birth Cohort.

Hysi PG, Simpson CL, Fok YK, Gerrelli D, Webster AR, Bhattacharya SS, Hammond CJ, Sham PC, Rahi JS. Hysi PG, et al. Invest Ophthalmol Vis Sci. 2012 Jan 25;53(1):440-7. doi: 10.1167/iovs.10-5640. Invest Ophthalmol Vis Sci. 2012. PMID: 22110064

7

Macular displacement following rhegmatogenous retinal detachment repair.

Lee E, Williamson TH, Hysi P, Shunmugam M, Dogramaci M, Wong R, Laidlaw DA. Lee E, et al. Br J Ophthalmol. 2013 Oct;97(10):1297-302. doi: 10.1136/bjophthalmol-2013-303637. Epub 2013 Jul 18. Br J Ophthalmol. 2013. PMID: 23868959

8

Clarifying the role of ATOH7 in glaucoma endophenotypes.

Venturini C, Nag A, Hysi PG, Wang JJ, Wong TY, Healey PR, Mitchell P, Hammond CJ, Viswanathan AC; Wellcome Trust Case Control Consortium 2, BMES GWAS Group. Venturini C, et al. Among authors: hysi pg. Br J Ophthalmol. 2014 Apr;98(4):562-6. doi: 10.1136/bjophthalmol-2013-304080. Epub 2014 Jan 23. Br J Ophthalmol. 2014. PMID: 24457358

9

Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness.

Davidson AE, Cheong SS, Hysi PG, Venturini C, Plagnol V, Ruddle JB, Ali H, Carnt N, Gardner JC, Hassan H, Gade E, Kearns L, Jelsig AM, Restori M, Webb TR, Laws D, Cosgrove M, Hertz JM, Russell-Eggitt I, Pilz DT, Hammond CJ, Tuft SJ, Hardcastle AJ. Davidson AE, et al. Among authors: hysi pg. PLoS One. 2014 Aug 5;9(8):e104163. doi: 10.1371/journal.pone.0104163. eCollection 2014. PLoS One. 2014. PMID: 25093588 Free PMC article.

10

Validation of rs2956540:G>C and rs3735520:G>A association with keratoconus in a population of European descent.

Dudakova L, Palos M, Jirsova K, Stranecky V, Krepelova A, Hysi PG, Liskova P. Dudakova L, et al. Among authors: hysi pg. Eur J Hum Genet. 2015 Nov;23(11):1581-3. doi: 10.1038/ejhg.2015.28. Epub 2015 Mar 4. Eur J Hum Genet. 2015. PMID: 25735481 Free PMC article.

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