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Year Number of Results
1995 1
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1999 1
2000 3
2001 2
2002 3
2003 6
2004 1
2005 7
2006 4
2007 1
2008 2
2009 8
2010 9
2011 8
2012 5
2013 5
2014 11
2015 9
2016 5
2017 2
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2019 12
2020 12
2021 9
2022 13
2023 8
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141 results

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Page 1
[Autophagy and spermatozoa].
Buschiazzo A, Yefimova M, Bourmeyster N, Fautrel A, Burel A, Neyroud AS, Pimentel C, Jaillard S, Jégou B, Ravel C. Buschiazzo A, et al. Among authors: jaillard s. Med Sci (Paris). 2019 Nov;35(11):852-858. doi: 10.1051/medsci/2019172. Epub 2019 Dec 17. Med Sci (Paris). 2019. PMID: 31845876 Free article. Review. French.
Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency.
Zawerton A, Mignot C, Sigafoos A, Blackburn PR, Haseeb A, McWalter K, Ichikawa S, Nava C, Keren B, Charles P, Marey I, Tabet AC, Levy J, Perrin L, Hartmann A, Lesca G, Schluth-Bolard C, Monin P, Dupuis-Girod S, Guillen Sacoto MJ, Schnur RE, Zhu Z, Poisson A, El Chehadeh S, Alembik Y, Bruel AL, Lehalle D, Nambot S, Moutton S, Odent S, Jaillard S, Dubourg C, Hilhorst-Hofstee Y, Barbaro-Dieber T, Ortega L, Bhoj EJ, Masser-Frye D, Bird LM, Lindstrom K, Ramsey KM, Narayanan V, Fassi E, Willing M, Cole T, Salter CG, Akilapa R, Vandersteen A, Canham N, Rump P, Gerkes EH, Klein Wassink-Ruiter JS, Bijlsma E, Hoffer MJV, Vargas M, Wojcik A, Cherik F, Francannet C, Rosenfeld JA, Machol K, Scott DA, Bacino CA, Wang X, Clark GD, Bertoli M, Zwolinski S, Thomas RH, Akay E, Chang RC, Bressi R, Sanchez Russo R, Srour M, Russell L, Goyette AE, Dupuis L, Mendoza-Londono R, Karimov C, Joseph M, Nizon M, Cogné B, Kuechler A, Piton A; Deciphering Developmental Disorder Study; Klee EW, Lefebvre V, Clark KJ, Depienne C. Zawerton A, et al. Among authors: jaillard s. Genet Med. 2020 Mar;22(3):524-537. doi: 10.1038/s41436-019-0657-0. Epub 2019 Oct 3. Genet Med. 2020. PMID: 31578471 Free PMC article.
[The Sertoli cell].
Ravel C, Jaillard S. Ravel C, et al. Among authors: jaillard s. Morphologie. 2011 Dec;95(311):151-8. doi: 10.1016/j.morpho.2011.07.118. Epub 2011 Nov 16. Morphologie. 2011. PMID: 22094070 Review. French.
Terminal 6q deletions cause brain malformations, a phenotype mimicking heterozygous DLL1 pathogenic variants: A multicenter retrospective case series.
Lesieur-Sebellin M, Till M, Khau Van Kien P, Herve B, Bourgon N, Dupont C, Tabet AC, Barrois M, Coussement A, Loeuillet L, Mousty E, Ea V, El Assal A, Mary L, Jaillard S, Beneteau C, Le Vaillant C, Coutton C, Devillard F, Goumy C, Delabaere A, Redon S, Laurent Y, Lamouroux A, Massardier J, Turleau C, Sanlaville D, Cantagrel V, Sonigo P, Vialard F, Salomon LJ, Malan V. Lesieur-Sebellin M, et al. Among authors: jaillard s. Prenat Diagn. 2022 Jan;42(1):118-135. doi: 10.1002/pd.6074. Epub 2021 Dec 11. Prenat Diagn. 2022. PMID: 34894355
Hypothermic machine perfusion for uterus transplantation.
Dion L, Sousa C, Boudjema K, Val-Laillet D, Jaillard S, Rioux-Leclercq N, Flecher E, Lavoue V. Dion L, et al. Among authors: jaillard s. Fertil Steril. 2023 Dec;120(6):1259-1261. doi: 10.1016/j.fertnstert.2023.08.020. Epub 2023 Sep 1. Fertil Steril. 2023. PMID: 37660880 Free article.
Fetal Presentation of MYRF-Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal Diagnosis.
Favier M, Brischoux-Boucher E, Pyle LC, Mottet N, Auber-Lenoir M, Cattin J, Dahlen E, Cabrol C, Arbez-Gindre F, Attié-Bitach T, Boute O, Devisme L, Trost D, Boughalem A, Chitayat D, Prasov L, Chorin O, Rein-Rothschild A, Kassif E, Weissbach T, Hendon LG, Adam MP, Quelin C, Jaillard S, Mary L, Aukema SM, Heijligers M, de Die-Smulders C, Stegmann S, Badalato L, Ben-Yehuda A, Beneteau C, Forey PL, Kuentz P, Piard J. Favier M, et al. Among authors: jaillard s. Prenat Diagn. 2024 Dec;44(13):1647-1658. doi: 10.1002/pd.6700. Epub 2024 Nov 14. Prenat Diagn. 2024. PMID: 39542847 Free PMC article.
Resolving structural variations missed by short-read sequencing uncovers their pathogenicity.
Schluth-Bolard C, El Khattabi L, Rollat-Farnier PA, Chatron N, Beaumont M, Reynaud N, Uguen K, Diguet F, Labalme A, Bardel C, Mantere T, Bard V, Apetrei A, Afenjar A, Amblard F, Amiel J, Christin-Maître S, Devillard F, Fradin M, Isidor B, Lokchine A, Jaillard S, Olaso R, Rossi M, Valence S, Deleuze JF, Hoischen A, Siffroi JP, Sanlaville D. Schluth-Bolard C, et al. Among authors: jaillard s. J Med Genet. 2025 Nov 21;62(12):750-757. doi: 10.1136/jmg-2025-110838. J Med Genet. 2025. PMID: 40835298
Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes.
Ghieh F, Barbotin AL, Swierkowski-Blanchard N, Leroy C, Fortemps J, Gerault C, Hue C, Mambu Mambueni H, Jaillard S, Albert M, Bailly M, Izard V, Molina-Gomes D, Marcelli F, Prasivoravong J, Serazin V, Dieudonne MN, Delcroix M, Garchon HJ, Louboutin A, Mandon-Pepin B, Ferlicot S, Vialard F. Ghieh F, et al. Among authors: jaillard s. Hum Reprod. 2022 May 30;37(6):1334-1350. doi: 10.1093/humrep/deac057. Hum Reprod. 2022. PMID: 35413094 Free PMC article.
141 results