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Chromosomal instability in the prediction of pituitary neuroendocrine tumors prognosis.
Lasolle H, Elsensohn MH, Wierinckx A, Alix E, Bonnefille C, Vasiljevic A, Cortet C, Decoudier B, Sturm N, Gaillard S, Ferrière A, Roy P, Jouanneau E, Bertolino P, Bardel C, Sanlaville D, Raverot G. Lasolle H, et al. Among authors: sanlaville d. Acta Neuropathol Commun. 2020 Nov 10;8(1):190. doi: 10.1186/s40478-020-01067-5. Acta Neuropathol Commun. 2020. PMID: 33168091 Free PMC article.
Neuropathological features in a female fetus with OPHN1 deletion and cerebellar hypoplasia.
Rocas D, Alix E, Michel J, Cordier MP, Labalme A, Guilbert H, Till M, Schluth-Bolard C, de Haas P, Massardier J, Portes Vd, Edery P, Touraine R, Guibaud L, Vasiljevic A, Sanlaville D. Rocas D, et al. Among authors: sanlaville d. Eur J Med Genet. 2013 May;56(5):270-3. doi: 10.1016/j.ejmg.2013.01.014. Epub 2013 Feb 14. Eur J Med Genet. 2013. PMID: 23416624
Refining the phenotypical and mutational spectrum of Taybi-Linder syndrome.
Putoux A, Alqahtani A, Pinson L, Paulussen AD, Michel J, Besson A, Mazoyer S, Borg I, Nampoothiri S, Vasiljevic A, Uwineza A, Boggio D, Champion F, de Die-Smulders CE, Gardeitchik T, van Putten WK, Perez MJ, Musizzano Y, Razavi F, Drunat S, Verloes A, Hennekam R, Guibaud L, Alix E, Sanlaville D, Lesca G, Edery P. Putoux A, et al. Among authors: sanlaville d. Clin Genet. 2016 Dec;90(6):550-555. doi: 10.1111/cge.12781. Epub 2016 Jun 2. Clin Genet. 2016. PMID: 27040866 Free article.
Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA.
Dimassi S, Simonet T, Labalme A, Boutry-Kryza N, Campan-Fournier A, Lamy R, Bardel C, Elsensohn MH, Roucher-Boulez F, Chatron N, Putoux A, de Bellescize J, Ville D, Schaeffer L, Roy P, Mougou-Zerelli S, Saad A, Calender A, Sanlaville D, Lesca G. Dimassi S, et al. Among authors: sanlaville d. Appl Transl Genom. 2015 Oct 17;7:19-25. doi: 10.1016/j.atg.2015.10.001. eCollection 2015 Dec. Appl Transl Genom. 2015. PMID: 27054081 Free PMC article.
Statistical method to compare massive parallel sequencing pipelines.
Elsensohn MH, Leblay N, Dimassi S, Campan-Fournier A, Labalme A, Roucher-Boulez F, Sanlaville D, Lesca G, Bardel C, Roy P. Elsensohn MH, et al. Among authors: sanlaville d. BMC Bioinformatics. 2017 Mar 1;18(1):139. doi: 10.1186/s12859-017-1552-9. BMC Bioinformatics. 2017. PMID: 28249565 Free PMC article.
Comment on "Trisomy 21 noninvasive prenatal testing for twin pregnancies".
Chatron N, Raymond L, Schluth-Bolard C, Bardel C, Huissoud C, Nouchy M, Sanlaville D, Massoud M. Chatron N, et al. Among authors: sanlaville d. Prenat Diagn. 2019 Jun;39(7):571-572. doi: 10.1002/pd.5456. Epub 2019 May 20. Prenat Diagn. 2019. PMID: 31106873 No abstract available.
294 results