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

Year Number of Results
1991 2
1992 1
1993 3
1994 2
1995 2
1996 2
1997 1
1998 2
1999 2
2000 4
2001 2
2002 2
2003 5
2004 4
2005 5
2006 1
2007 4
2008 7
2009 5
2010 5
2011 3
2012 2
2013 3
2014 5
2015 5
2016 4
2017 5
2018 1
2019 3
2020 1
2021 2
2023 0
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Search Results

90 results
Results by year
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Page 1
Nicotine inhibits the VTA-to-amygdala dopamine pathway to promote anxiety.
Nguyen C, Mondoloni S, Le Borgne T, Centeno I, Come M, Jehl J, Solié C, Reynolds LM, Durand-de Cuttoli R, Tolu S, Valverde S, Didienne S, Hannesse B, Fiancette JF, Pons S, Maskos U, Deroche-Gamonet V, Dalkara D, Hardelin JP, Mourot A, Marti F, Faure P. Nguyen C, et al. Among authors: hardelin jp. Neuron. 2021 Aug 18;109(16):2604-2615.e9. doi: 10.1016/j.neuron.2021.06.013. Epub 2021 Jul 8. Neuron. 2021. PMID: 34242565 Free article.
Expert consensus document: European Consensus Statement on congenital hypogonadotropic hypogonadism--pathogenesis, diagnosis and treatment.
Boehm U, Bouloux PM, Dattani MT, de Roux N, Dodé C, Dunkel L, Dwyer AA, Giacobini P, Hardelin JP, Juul A, Maghnie M, Pitteloud N, Prevot V, Raivio T, Tena-Sempere M, Quinton R, Young J. Boehm U, et al. Among authors: hardelin jp. Nat Rev Endocrinol. 2015 Sep;11(9):547-64. doi: 10.1038/nrendo.2015.112. Epub 2015 Jul 21. Nat Rev Endocrinol. 2015. PMID: 26194704 Review.
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: hardelin jp. 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.
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: hardelin jp. 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.
Kallmann syndrome.
Hardelin JP, Soussi-Yanicostas N, Ardouin O, Levilliers J, Petit C. Hardelin JP, et al. Adv Otorhinolaryngol. 2000;56:268-74. doi: 10.1159/000059073. Adv Otorhinolaryngol. 2000. PMID: 10868244 Review. No abstract available.
Kallmann syndrome.
Dodé C, Hardelin JP. Dodé C, et al. Among authors: hardelin jp. Eur J Hum Genet. 2009 Feb;17(2):139-46. doi: 10.1038/ejhg.2008.206. Epub 2008 Nov 5. Eur J Hum Genet. 2009. PMID: 18985070 Free PMC article.
[Hereditary deafness: molecular genetics].
Hardelin JP, Denoyelle F, Levilliers J, Simmler MC, Petit C. Hardelin JP, et al. Med Sci (Paris). 2004 Mar;20(3):311-6. doi: 10.1051/medsci/2004203311. Med Sci (Paris). 2004. PMID: 15067576 Free article. Review. French.
Clinical genetics of Kallmann syndrome.
Dodé C, Hardelin JP. Dodé C, et al. Among authors: hardelin jp. Ann Endocrinol (Paris). 2010 May;71(3):149-57. doi: 10.1016/j.ando.2010.02.005. Epub 2010 Apr 2. Ann Endocrinol (Paris). 2010. PMID: 20362962 Review.
Molecular genetics of hearing loss.
Petit C, Levilliers J, Hardelin JP. Petit C, et al. Among authors: hardelin jp. Annu Rev Genet. 2001;35:589-646. doi: 10.1146/annurev.genet.35.102401.091224. Annu Rev Genet. 2001. PMID: 11700295 Review.
90 results