Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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
Text availability
Article attribute
Article type
Publication date

Search Results

90 results
Results by year
Filters applied: . Clear all
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.
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.
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.
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.
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.
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.
[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.
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