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Page 1
Autosomal mutations and human spermatogenic failure.
El Inati E, Muller J, Viville S. El Inati E, et al. Among authors: viville s. Biochim Biophys Acta. 2012 Dec;1822(12):1873-9. doi: 10.1016/j.bbadis.2012.07.006. Epub 2012 Jul 27. Biochim Biophys Acta. 2012. PMID: 22841926 Free article. Review.
Search for mutations involved in human globozoospermia.
Pirrello O, Machev N, Schimdt F, Terriou P, Ménézo Y, Viville S. Pirrello O, et al. Among authors: viville s. Hum Reprod. 2005 May;20(5):1314-8. doi: 10.1093/humrep/deh799. Epub 2005 Mar 3. Hum Reprod. 2005. PMID: 15746197
DPY19L2 deletion as a major cause of globozoospermia.
Koscinski I, Elinati E, Fossard C, Redin C, Muller J, Velez de la Calle J, Schmitt F, Ben Khelifa M, Ray PF, Kilani Z, Barratt CL, Viville S. Koscinski I, et al. Among authors: viville s. Am J Hum Genet. 2011 Mar 11;88(3):344-50. doi: 10.1016/j.ajhg.2011.01.018. Am J Hum Genet. 2011. PMID: 21397063 Free PMC article.
Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots.
Elinati E, Kuentz P, Redin C, Jaber S, Vanden Meerschaut F, Makarian J, Koscinski I, Nasr-Esfahani MH, Demirol A, Gurgan T, Louanjli N, Iqbal N, Bisharah M, Pigeon FC, Gourabi H, De Briel D, Brugnon F, Gitlin SA, Grillo JM, Ghaedi K, Deemeh MR, Tanhaei S, Modarres P, Heindryckx B, Benkhalifa M, Nikiforaki D, Oehninger SC, De Sutter P, Muller J, Viville S. Elinati E, et al. Among authors: viville s. Hum Mol Genet. 2012 Aug 15;21(16):3695-702. doi: 10.1093/hmg/dds200. Epub 2012 May 31. Hum Mol Genet. 2012. PMID: 22653751
A new mutation identified in SPATA16 in two globozoospermic patients.
ElInati E, Fossard C, Okutman O, Ghédir H, Ibala-Romdhane S, Ray PF, Saad A, Hennebicq S, Viville S. ElInati E, et al. Among authors: viville s. J Assist Reprod Genet. 2016 Jun;33(6):815-20. doi: 10.1007/s10815-016-0715-3. Epub 2016 Apr 16. J Assist Reprod Genet. 2016. PMID: 27086357 Free PMC article.
A no-stop mutation in MAGEB4 is a possible cause of rare X-linked azoospermia and oligozoospermia in a consanguineous Turkish family.
Okutman O, Muller J, Skory V, Garnier JM, Gaucherot A, Baert Y, Lamour V, Serdarogullari M, Gultomruk M, Röpke A, Kliesch S, Herbepin V, Aknin I, Benkhalifa M, Teletin M, Bakircioglu E, Goossens E, Charlet-Berguerand N, Bahceci M, Tüttelmann F, Viville S. Okutman O, et al. Among authors: viville s. J Assist Reprod Genet. 2017 May;34(5):683-694. doi: 10.1007/s10815-017-0900-z. Epub 2017 Apr 11. J Assist Reprod Genet. 2017. PMID: 28401488 Free PMC article.
Genetic evaluation of patients with non-syndromic male infertility.
Okutman O, Rhouma MB, Benkhalifa M, Muller J, Viville S. Okutman O, et al. Among authors: viville s. J Assist Reprod Genet. 2018 Nov;35(11):1939-1951. doi: 10.1007/s10815-018-1301-7. Epub 2018 Sep 26. J Assist Reprod Genet. 2018. PMID: 30259277 Free PMC article. Review.
[Genetic aspects of male infertility: From bench to clinic].
Ben Rhouma M, Okutman O, Muller J, Benkhalifa M, Bahri H, Ben Rhouma K, Tebourbi O, Viville S. Ben Rhouma M, et al. Among authors: viville s. Gynecol Obstet Fertil Senol. 2019 Jan;47(1):54-62. doi: 10.1016/j.gofs.2018.11.004. Epub 2018 Dec 1. Gynecol Obstet Fertil Senol. 2019. PMID: 30514637 Review. French.
131 results