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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.
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.
Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome.
Sellier C, Buijsen RAM, He F, Natla S, Jung L, Tropel P, Gaucherot A, Jacobs H, Meziane H, Vincent A, Champy MF, Sorg T, Pavlovic G, Wattenhofer-Donze M, Birling MC, Oulad-Abdelghani M, Eberling P, Ruffenach F, Joint M, Anheim M, Martinez-Cerdeno V, Tassone F, Willemsen R, Hukema RK, Viville S, Martinat C, Todd PK, Charlet-Berguerand N. Sellier C, et al. Among authors: viville s. Neuron. 2017 Jan 18;93(2):331-347. doi: 10.1016/j.neuron.2016.12.016. Epub 2017 Jan 5. Neuron. 2017. PMID: 28065649 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.
Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia.
Oud MS, Ramos L, O'Bryan MK, McLachlan RI, Okutman Ö, Viville S, de Vries PF, Smeets DFCM, Lugtenberg D, Hehir-Kwa JY, Gilissen C, van de Vorst M, Vissers LELM, Hoischen A, Meijerink AM, Fleischer K, Veltman JA, Noordam MJ. Oud MS, et al. Among authors: viville s. Hum Mutat. 2017 Nov;38(11):1592-1605. doi: 10.1002/humu.23312. Epub 2017 Sep 6. Hum Mutat. 2017. PMID: 28801929
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.
130 results