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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
2000 2
2001 4
2002 5
2003 3
2004 4
2005 5
2006 3
2007 7
2008 3
2009 1
2010 2
2012 3
2013 1
2015 1
2016 1
2023 0
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39 results
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Page 1
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: ebenezer nd. Mol Vis. 2007 Oct 4;13:1887-91. Mol Vis. 2007. PMID: 17960127 Free PMC article.
Identification of the gene for Nance-Horan syndrome (NHS).
Brooks SP, Ebenezer ND, Poopalasundaram S, Lehmann OJ, Moore AT, Hardcastle AJ. Brooks SP, et al. Among authors: ebenezer nd. J Med Genet. 2004 Oct;41(10):768-71. doi: 10.1136/jmg.2004.022517. J Med Genet. 2004. PMID: 15466011 Free PMC article.
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).
Vithana EN, Morgan P, Sundaresan P, Ebenezer ND, Tan DT, Mohamed MD, Anand S, Khine KO, Venkataraman D, Yong VH, Salto-Tellez M, Venkatraman A, Guo K, Hemadevi B, Srinivasan M, Prajna V, Khine M, Casey JR, Inglehearn CF, Aung T. Vithana EN, et al. Among authors: ebenezer nd. Nat Genet. 2006 Jul;38(7):755-7. doi: 10.1038/ng1824. Epub 2006 Jun 11. Nat Genet. 2006. PMID: 16767101
A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5).
Gardner JC, Webb TR, Kanuga N, Robson AG, Holder GE, Stockman A, Ripamonti C, Ebenezer ND, Ogun O, Devery S, Wright GA, Maher ER, Cheetham ME, Moore AT, Michaelides M, Hardcastle AJ. Gardner JC, et al. Among authors: ebenezer nd. Adv Exp Med Biol. 2012;723:595-601. doi: 10.1007/978-1-4614-0631-0_76. Adv Exp Med Biol. 2012. PMID: 22183383 No abstract available.
X-linked cone dystrophy caused by mutation of the red and green cone opsins.
Gardner JC, Webb TR, Kanuga N, Robson AG, Holder GE, Stockman A, Ripamonti C, Ebenezer ND, Ogun O, Devery S, Wright GA, Maher ER, Cheetham ME, Moore AT, Michaelides M, Hardcastle AJ. Gardner JC, et al. Among authors: ebenezer nd. Am J Hum Genet. 2010 Jul 9;87(1):26-39. doi: 10.1016/j.ajhg.2010.05.019. Epub 2010 Jun 24. Am J Hum Genet. 2010. PMID: 20579627 Free PMC article.
A novel keratocan mutation causing autosomal recessive cornea plana.
Lehmann OJ, El-ashry MF, Ebenezer ND, Ocaka L, Francis PJ, Wilkie SE, Patel RJ, Ficker L, Jordan T, Khaw PT, Bhattacharya SS. Lehmann OJ, et al. Among authors: ebenezer nd. Invest Ophthalmol Vis Sci. 2001 Dec;42(13):3118-22. Invest Ophthalmol Vis Sci. 2001. PMID: 11726611
39 results