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

Year Number of Results
2001 2
2002 2
2003 4
2005 1
2006 5
2007 2
2008 4
2009 3
2010 2
2011 2
2012 4
2013 2
2014 3
2015 4
2016 2
2017 5
2018 3
2019 2
2020 1
2021 2
2022 1
2023 1
2024 2

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54 results

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Page 1
Small Supernumerary Marker Chromosomes in Human Infertility.
Armanet N, Tosca L, Brisset S, Liehr T, Tachdjian G. Armanet N, et al. Among authors: brisset s. Cytogenet Genome Res. 2015;146(2):100-108. doi: 10.1159/000438718. Epub 2015 Aug 14. Cytogenet Genome Res. 2015. PMID: 26398339 Free article. Review.
Prenatal Diagnosis of Primrose Syndrome.
Abdallah W, Spaggiari E, Brisset S, Dard R, Attié Bitach T, Bault JP, Quibel T. Abdallah W, et al. Among authors: brisset s. J Ultrasound Med. 2024 Feb;43(2):411-414. doi: 10.1002/jum.16354. Epub 2023 Nov 6. J Ultrasound Med. 2024. PMID: 37929614
Comment garantir des données médicales de qualité dans les études cliniques, pharmaco-épidémiologiques et en pharmacovigilance ?
Alla F, Rosilio M, Funck-Brentano C; les participants à la table ronde N° 2 de Giens XXVIII :; Barthélémy P, Brisset S, Cellier D, Chassany O, Demarez JP, Diebolt V, Francillon A, Gambotti L, Hannachi H, Lechat P, Lemaire F, Lièvre M, Misse C, Nguon M, Pariente A, Rosenheim M, Weisslinger-Darmon N. Alla F, et al. Among authors: brisset s. Therapie. 2013 Jul-Aug;68(4):209-16. doi: 10.2515/therapie/2013035. Therapie. 2013. PMID: 27392724 French. No abstract available.
Terminal 14q32.33 deletion: genotype-phenotype correlation.
Maurin ML, Brisset S, Le Lorc'h M, Poncet V, Trioche P, Aboura A, Labrune P, Tachdjian G. Maurin ML, et al. Among authors: brisset s. Am J Med Genet A. 2006 Nov 1;140(21):2324-9. doi: 10.1002/ajmg.a.31438. Am J Med Genet A. 2006. PMID: 17022077 Review.
iPSCs derived from infertile men carrying complex genetic abnormalities can generate primordial germ-like cells.
Mouka A, Arkoun B, Moison P, Drévillon L, Jarray R, Brisset S, Mayeur A, Bouligand J, Boland-Auge A, Deleuze JF, Yates F, Lemonnier T, Callier P, Duffourd Y, Nitschke P, Ollivier E, Bourdin A, De Vos J, Livera G, Tachdjian G, Maouche-Chrétien L, Tosca L. Mouka A, et al. Among authors: brisset s. Sci Rep. 2022 Aug 22;12(1):14302. doi: 10.1038/s41598-022-17337-2. Sci Rep. 2022. PMID: 35995809 Free PMC article.
How can the quality of medical data in pharmacovigilance, pharmacoepidemiology and clinical studies be guaranteed?
Alla F, Rosilio M, Funck-Brentano C; Participants of round table N° 2 of Giens Workshops XXVIII (th); Barthélémy P, Brisset S, Cellier D, Chassany O, Demarez JP, Diebolt V, Francillon A, Gambotti L, Hannachi H, Lechat P, Lemaire F, Lièvre M, Misse C, Nguon M, Pariente A, Rosenheim M, Weisslinger-Darmon N. Alla F, et al. Among authors: brisset s. Therapie. 2013 Jul-Aug;68(4):209-23. doi: 10.2515/therapie/2013040. Epub 2013 Aug 28. Therapie. 2013. PMID: 23981258 Free article. English, French.
Genotype-phenotype correlation in 13q13.3-q21.3 deletion.
Tosca L, Brisset S, Petit FM, Metay C, Latour S, Lautier B, Lebas A, Druart L, Picone O, Mas AE, Prévot S, Tardieu M, Goossens M, Tachdjian G. Tosca L, et al. Among authors: brisset s. Eur J Med Genet. 2011 Sep-Oct;54(5):e489-94. doi: 10.1016/j.ejmg.2011.06.004. Epub 2011 Jun 21. Eur J Med Genet. 2011. PMID: 21741501
Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2C.
Tosca L, Drévillon L, Mouka A, Lecerf L, Briand A, Ortonne V, Benoit V, Brisset S, Van Maldergem L, Laudouar Q, Heide S, Goossens M, Giurgea I, Tachdjian G, Métay C. Tosca L, et al. Among authors: brisset s. Mol Genet Genomic Med. 2021 Nov;9(11):e1645. doi: 10.1002/mgg3.1645. Epub 2021 Sep 28. Mol Genet Genomic Med. 2021. PMID: 34582124 Free PMC article.
54 results