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

Year Number of Results
2001 1
2002 12
2003 5
2004 7
2005 8
2006 7
2007 9
2008 4
2009 8
2010 13
2011 14
2012 18
2013 12
2014 10
2015 4
2016 10
2017 3
2018 1
2019 1
2020 2
2021 1
2023 2
2024 0

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136 results

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Page 1
Gene of the month: PRPF31.
Rose AM, Luo R, Radia UK, Bhattacharya SS. Rose AM, et al. Among authors: bhattacharya ss. J Clin Pathol. 2017 Sep;70(9):729-732. doi: 10.1136/jclinpath-2016-203971. Epub 2017 Jun 29. J Clin Pathol. 2017. PMID: 28663330 Review.
CRB1 mutations in inherited retinal dystrophies.
Bujakowska K, Audo I, Mohand-Saïd S, Lancelot ME, Antonio A, Germain A, Léveillard T, Letexier M, Saraiva JP, Lonjou C, Carpentier W, Sahel JA, Bhattacharya SS, Zeitz C. Bujakowska K, et al. Among authors: bhattacharya ss. Hum Mutat. 2012 Feb;33(2):306-15. doi: 10.1002/humu.21653. Epub 2011 Dec 27. Hum Mutat. 2012. PMID: 22065545 Free PMC article. Review.
Fox's in development and disease.
Lehmann OJ, Sowden JC, Carlsson P, Jordan T, Bhattacharya SS. Lehmann OJ, et al. Among authors: bhattacharya ss. Trends Genet. 2003 Jun;19(6):339-44. doi: 10.1016/S0168-9525(03)00111-2. Trends Genet. 2003. PMID: 12801727 Review.
WDR34, a candidate gene for non-syndromic rod-cone dystrophy.
Solaguren-Beascoa M, Bujakowska KM, Méjécase C, Emmenegger L, Orhan E, Neuillé M, Mohand-Saïd S, Condroyer C, Lancelot ME, Michiels C, Demontant V, Antonio A, Letexier M, Saraiva JP, Lonjou C, Carpentier W, Léveillard T, Pierce EA, Dollfus H, Sahel JA, Bhattacharya SS, Audo I, Zeitz C. Solaguren-Beascoa M, et al. Among authors: bhattacharya ss. Clin Genet. 2021 Feb;99(2):298-302. doi: 10.1111/cge.13872. Epub 2020 Nov 9. Clin Genet. 2021. PMID: 33124039 Free PMC article.
136 results