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Results by year

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

Year Number of Results
1946 1
1961 1
1964 1
1965 1
1966 2
1967 1
1968 1
1969 2
1970 4
1972 1
1973 1
1974 2
1975 1
1976 1
1977 1
1978 1
1981 1
1982 1
1984 2
1985 1
1986 4
1989 4
1990 7
1991 11
1992 10
1993 11
1994 3
1995 10
1996 9
1997 7
1998 8
1999 10
2000 10
2001 6
2002 11
2003 8
2004 9
2005 12
2006 19
2007 17
2008 13
2009 17
2010 22
2011 22
2012 31
2013 35
2014 34
2015 30
2016 40
2017 35
2018 31
2019 41
2020 46
2021 63
2022 50
2023 51

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Search Results

692 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. Among authors: bonnet c. 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.
Reply.
Bonnet C, Chehaibou I, McCannel CA, McCannel TA, Prasad PS, Kreiger AE, Schwartz SD, Aldave A, Hubschman JP. Bonnet C, et al. Retina. 2023 May 1;43(5):e31-e32. doi: 10.1097/IAE.0000000000003757. Retina. 2023. PMID: 36763983 No abstract available.
Brentuximab Vedotin Plus AVD for First-Line Treatment of Early-Stage Unfavorable Hodgkin Lymphoma (BREACH): A Multicenter, Open-Label, Randomized, Phase II Trial.
Fornecker LM, Lazarovici J, Aurer I, Casasnovas RO, Gac AC, Bonnet C, Bouabdallah K, Feugier P, Specht L, Molina L, Touati M, Borel C, Stamatoullas A, Nicolas-Virelizier E, Pascal L, Lugtenburg P, Di Renzo N, Vander Borght T, Traverse-Glehen A, Dartigues P, Hutchings M, Versari A, Meignan M, Federico M, André M; LYSA-FIL-EORTC Intergroup. Fornecker LM, et al. Among authors: bonnet c. J Clin Oncol. 2023 Jan 10;41(2):327-335. doi: 10.1200/JCO.21.01281. Epub 2022 Jul 22. J Clin Oncol. 2023. PMID: 35867960 Free article. Clinical Trial.
Epidemiology of meningiomas.
Baldi I, Engelhardt J, Bonnet C, Bauchet L, Berteaud E, Grüber A, Loiseau H. Baldi I, et al. Among authors: bonnet c. Neurochirurgie. 2018 Mar;64(1):5-14. doi: 10.1016/j.neuchi.2014.05.006. Epub 2014 Sep 22. Neurochirurgie. 2018. PMID: 25249493 Review.
Monomorphic epitheliotropic intestinal T-cell lymphoma comprises morphologic and genomic heterogeneity impacting outcome.
Veloza L, Cavalieri D, Missiaglia E, Ledoux-Pilon A, Bisig B, Pereira B, Bonnet C, Poullot E, Quintanilla-Martinez L, Dubois R, Llamas-Gutierrez F, Bossard C, De Wind R, Drieux F, Fontaine J, Parrens M, Sandrini J, Fataccioli V, Delfau-Larue MH, Daniel A, Lhomme F, Clément-Filliatre L, Lemonnier F, Cairoli A, Morel P, Glaisner S, Joly B, El Yamani A, Laribi K, Bachy E, Siebert R, Vallois D, Gaulard P, Tournilhac O, De Leval L. Veloza L, et al. Among authors: bonnet c. Haematologica. 2023 Jan 1;108(1):181-195. doi: 10.3324/haematol.2022.281226. Haematologica. 2023. PMID: 35708139 Free PMC article.
[Vogt-Koyanagi-Harada disease].
Bonnet C, Daudin JB, Monnet D, Brézin A. Bonnet C, et al. J Fr Ophtalmol. 2017 Jun;40(6):512-519. doi: 10.1016/j.jfo.2017.02.006. Epub 2017 Jun 1. J Fr Ophtalmol. 2017. PMID: 28579215 Review. French.
Limbal stem cell diseases.
Bonnet C, Roberts JS, Deng SX. Bonnet C, et al. Exp Eye Res. 2021 Apr;205:108437. doi: 10.1016/j.exer.2021.108437. Epub 2021 Feb 8. Exp Eye Res. 2021. PMID: 33571530 Free PMC article. Review.
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD.
Granadillo JL, P A Stegmann A, Guo H, Xia K, Angle B, Bontempo K, Ranells JD, Newkirk P, Costin C, Viront J, Stumpel CT, Sinnema M, Panis B, Pfundt R, Krapels IPC, Klaassens M, Nicolai J, Li J, Jiang Y, Marco E, Canton A, Latronico AC, Montenegro L, Leheup B, Bonnet C, M Amudhavalli S, Lawson CE, McWalter K, Telegrafi A, Pearson R, Kvarnung M, Wang X, Bi W, Rosenfeld JA, Shinawi M. Granadillo JL, et al. Among authors: bonnet c. J Med Genet. 2020 Oct;57(10):717-724. doi: 10.1136/jmedgenet-2019-106470. Epub 2020 Mar 9. J Med Genet. 2020. PMID: 32152250
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. 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.
692 results