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

Year Number of Results
2000 1
2002 15
2003 15
2004 10
2005 12
2006 5
2007 8
2008 11
2009 10
2010 10
2011 6
2012 6
2013 9
2014 9
2015 9
2016 7
2017 11
2018 9
2019 19
2020 10
2021 8
2022 7
2023 6
2024 2

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199 results

Results by year

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Page 1
Deafness: from genetic architecture to gene therapy.
Petit C, Bonnet C, Safieddine S. Petit C, et al. Nat Rev Genet. 2023 Oct;24(10):665-686. doi: 10.1038/s41576-023-00597-7. Epub 2023 May 12. Nat Rev Genet. 2023. PMID: 37173518 Free article. Review.
Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies.
Jean P, Wong Jun Tai F, Singh-Estivalet A, Lelli A, Scandola C, Megharba S, Schmutz S, Roux S, Mechaussier S, Sudres M, Mouly E, Heritier AV, Bonnet C, Mallet A, Novault S, Libri V, Petit C, Michalski N. Jean P, et al. Among authors: petit c. Proc Natl Acad Sci U S A. 2023 Jun 27;120(26):e2221744120. doi: 10.1073/pnas.2221744120. Epub 2023 Jun 20. Proc Natl Acad Sci U S A. 2023. PMID: 37339214 Free PMC article.
Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model.
Akil O, Dyka F, Calvet C, Emptoz A, Lahlou G, Nouaille S, Boutet de Monvel J, Hardelin JP, Hauswirth WW, Avan P, Petit C, Safieddine S, Lustig LR. Akil O, et al. Among authors: petit c. Proc Natl Acad Sci U S A. 2019 Mar 5;116(10):4496-4501. doi: 10.1073/pnas.1817537116. Epub 2019 Feb 19. Proc Natl Acad Sci U S A. 2019. PMID: 30782832 Free PMC article.
Neurogenetics.
Greenspan R, Petit C. Greenspan R, et al. Among authors: petit c. Curr Opin Neurobiol. 2013 Feb;23(1):1-2. doi: 10.1016/j.conb.2012.12.001. Epub 2012 Dec 22. Curr Opin Neurobiol. 2013. PMID: 23265962 No abstract available.
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.
Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, Gherbi S, Testa F, Simonelli F, Banfi S, Fakin A, Glavač D, Jarc-Vidmar M, Zupan A, Battelino S, Martorell Sampol L, Claveria MA, Catala Mora J, Dad S, Møller LB, Rodriguez Jorge J, Hawlina M, Auricchio A, Sahel JA, Marlin S, Zrenner E, Audo I, Petit C. Bonnet C, et al. Among authors: petit c. Eur J Hum Genet. 2016 Dec;24(12):1730-1738. doi: 10.1038/ejhg.2016.99. Epub 2016 Jul 27. Eur J Hum Genet. 2016. PMID: 27460420 Free PMC article.
[François Gros (1925-2022)].
Petit C, Kourilsky P. Petit C, et al. C R Biol. 2024 Mar 29;346(S2):3-8. doi: 10.5802/crbiol.146. C R Biol. 2024. PMID: 38456447 Free article. French.
DFNA3.
Denoyelle F, Lina-Granade G, Petit C. Denoyelle F, et al. Among authors: petit c. Adv Otorhinolaryngol. 2002;61:47-52. doi: 10.1159/000066803. Adv Otorhinolaryngol. 2002. PMID: 12408062 No abstract available.
Genetics of auditory mechano-electrical transduction.
Michalski N, Petit C. Michalski N, et al. Among authors: petit c. Pflugers Arch. 2015 Jan;467(1):49-72. doi: 10.1007/s00424-014-1552-9. Epub 2014 Jun 25. Pflugers Arch. 2015. PMID: 24957570 Free PMC article. Review.
DFNB21.
Denoyelle F, Mustapha M, Petit C. Denoyelle F, et al. Among authors: petit c. Adv Otorhinolaryngol. 2002;61:153-5. doi: 10.1159/000066827. Adv Otorhinolaryngol. 2002. PMID: 12408078 No abstract available.
Hair-Bundle Links: Genetics as the Gateway to Function.
Richardson GP, Petit C. Richardson GP, et al. Among authors: petit c. Cold Spring Harb Perspect Med. 2019 Dec 2;9(12):a033142. doi: 10.1101/cshperspect.a033142. Cold Spring Harb Perspect Med. 2019. PMID: 30617060 Free PMC article. Review.
199 results