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

Year Number of Results
1993 2
1996 1
2000 1
2002 1
2003 2
2004 2
2005 1
2006 1
2007 2
2008 1
2009 3
2010 1
2011 4
2012 1
2013 5
2014 3
2015 1
2016 3
2017 2
2018 1
2020 1
2021 2
2022 2
2023 2
2024 0

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PubMed for id: 167691

37 results

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Page 1
Involvement of LCA5 in Leber congenital amaurosis and retinitis pigmentosa in the Spanish population.
Corton M, Avila-Fernandez A, Vallespín E, López-Molina MI, Almoguera B, Martín-Garrido E, Tatu SD, Khan MI, Blanco-Kelly F, Riveiro-Alvarez R, Brión M, García-Sandoval B, Cremers FPM, Carracedo A, Ayuso C. Corton M, et al. Ophthalmology. 2014 Jan;121(1):399-407. doi: 10.1016/j.ophtha.2013.08.028. Epub 2013 Oct 18. Ophthalmology. 2014. PMID: 24144451
Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlations.
Mackay DS, Borman AD, Sui R, van den Born LI, Berson EL, Ocaka LA, Davidson AE, Heckenlively JR, Branham K, Ren H, Lopez I, Maria M, Azam M, Henkes A, Blokland E, Qamar R, Webster AR, Cremers FPM, Moore AT, Koenekoop RK; [LCA5 Study Group (see acknowledgements for Universities); Andreasson S, de Baere E, Bennett J, Chader GJ, Berger W, Golovleva I, Greenberg J, den Hollander AI, Klaver CCW, Klevering BJ, Lorenz B, Preising MN, Ramsear R, Roberts L, Roepman R, Rohrschneider K, Wissinger B. Mackay DS, et al. Hum Mutat. 2013 Nov;34(11):1537-1546. doi: 10.1002/humu.22398. Epub 2013 Sep 17. Hum Mutat. 2013. PMID: 23946133 Free PMC article.
Genome-wide association study of hoarding traits.
Perroud N, Guipponi M, Pertusa A, Fullana MA, Iervolino AC, Cherkas L, Spector T, Collier D, Mataix-Cols D. Perroud N, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar;156(2):240-2. doi: 10.1002/ajmg.b.31152. Epub 2010 Dec 28. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21302353 No abstract available.
37 results