Genetic diagnosis of embryos: Clear explanation, not rhetoric, is needed

Por Bouffard, Chantal, Viville, Stéphane, Knoppers, Bartha Maria
Publicado em 2009

A Quantitative and Morphological Analysis of Oocytes Collected During 438 IVF Cycles

Por Wittemer, Christiane, Ohl, Jeanine, Bettahar-Lebugle, Karima, Viville, Stéphane, Nisand, Israel
Publicado em 2000

Genetic evaluation of patients with non-syndromic male infertility

Por Okutman, Ozlem, Rhouma, Maroua Ben, Benkhalifa, Moncef, Muller, Jean, Viville, Stéphane
Publicado no J Assist Reprod Genet (2018)

Autism, imprinting and epigenetic disorders: a metabolic syndrome linked to anomalies in homocysteine recycling starting in early life??

Por Ménézo, Yves, Mares, Pierre, Cohen, Marc, Brack, Michel, Viville, Stephane, Elder, Kay
Publicado em 2011

Tex19 and Sectm1 concordant molecular phylogenies support co-evolution of both eutherian-specific genes

Por Bianchetti, Laurent, Tarabay, Yara, Lecompte, Odile, Stote, Roland, Poch, Olivier, Dejaegere, Annick, Viville, Stéphane
Publicado no BMC Evol Biol (2015)

The Pluripotency-Associated Gene Dppa4 Is Dispensable for Embryonic Stem Cell Identity and Germ Cell Development but Essential for Embryogenesis

Por Madan, Babita, Madan, Vikas, Weber, Odile, Tropel, Philippe, Blum, Carmen, Kieffer, Emmanuelle, Viville, Stéphane, Fehling, Hans Jörg
Publicado em 2009

Extended passaging increases the efficiency of neural differentiation from induced pluripotent stem cells

Por Koehler, Karl R, Tropel, Philippe, Theile, Jonathan W, Kondo, Takako, Cummins, Theodore R, Viville, Stéphane, Hashino, Eri
Publicado em 2011

Homozygous Splice Site Mutation in ZP1 Causes Familial Oocyte Maturation Defect

Por Okutman, Özlem, Demirel, Cem, Tülek, Firat, Pfister, Veronique, Büyük, Umut, Muller, Jean, Charlet-Berguerand, Nicolas, Viville, Stéphane
Publicado no Genes (Basel) (2020)

Highly Dynamic and Sex-Specific Expression of microRNAs During Early ES Cell Differentiation

Por Ciaudo, Constance, Servant, Nicolas, Cognat, Valérie, Sarazin, Alexis, Kieffer, Emmanuelle, Viville, Stéphane, Colot, Vincent, Barillot, Emmanuel, Heard, Edith, Voinnet, Olivier
Publicado em 2009

A new mutation identified in SPATA16 in two globozoospermic patients

Por ElInati, Elias, Fossard, Camille, Okutman, Ozlem, Ghédir, Houda, Ibala-Romdhane, Samira, Ray, Pierre F., Saad, Ali, Hennebicq, Sylvianne, Viville, Stéphane
Publicado no J Assist Reprod Genet (2016)

TRIM28 repression of retrotransposon-based enhancers is necessary to preserve transcriptional dynamics in embryonic stem cells

Por Rowe, Helen M., Kapopoulou, Adamandia, Corsinotti, Andrea, Fasching, Liana, Macfarlan, Todd S., Tarabay, Yara, Viville, Stéphane, Jakobsson, Johan, Pfaff, Samuel L., Trono, Didier
Publicado em 2013

Toxoplasma gondii ROP16 kinase silences the cyclin B1 gene promoter by hijacking host cell UHRF1-dependent epigenetic pathways

Por Sabou, Marcela, Doderer-Lang, Cécile, Leyer, Caroline, Konjic, Ana, Kubina, Sophie, Lennon, Sarah, Rohr, Olivier, Viville, Stéphane, Cianférani, Sarah, Candolfi, Ermanno, Pfaff, Alexander W., Brunet, Julie
Publicado no Cell Mol Life Sci (2019)

Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres

Por Van Rij, Maartje C, De Rademaeker, Marjan, Moutou, Céline, Dreesen, Jos CFM, De Rycke, Martine, Liebaers, Inge, Geraedts, Joep PM, De Die-Smulders, Christine EM, Viville, Stéphane
Publicado em 2012

A dual role of linker histone H1.4 Lys 34 acetylation in transcriptional activation

Por Kamieniarz, Kinga, Izzo, Annalisa, Dundr, Miroslav, Tropberger, Philipp, Ozretić, Luka, Kirfel, Jutta, Scheer, Elisabeth, Tropel, Philippe, Wiśniewski, Jacek R., Tora, Laszlo, Viville, Stephane, Buettner, Reinhard, Schneider, Robert
Publicado em 2012

Random Mutagenesis, Clonal Events, and Embryonic or Somatic Origin Determine the mtDNA Variant Type and Load in Human Pluripotent Stem Cells

Por Zambelli, Filippo, Mertens, Joke, Dziedzicka, Dominika, Sterckx, Johan, Markouli, Christina, Keller, Alexander, Tropel, Philippe, Jung, Laura, Viville, Stephane, Van de Velde, Hilde, Geens, Mieke, Seneca, Sara, Sermon, Karen, Spits, Claudia
Publicado no Stem Cell Reports (2018)

Homozygous Mutation in SPATA16 Is Associated with Male Infertility in Human Globozoospermia

Por Dam, Anika H. D. M. , Koscinski, Isabelle , Kremer, Jan A. M. , Moutou, Céline , Jaeger, Anne-Sophie , Oudakker, Astrid R. , Tournaye, Herman , Charlet, Nicolas , Lagier-Tourenne, Clotilde , van Bokhoven, Hans , Viville, Stéphane 
Publicado em 2007

Red blood cell generation from human induced pluripotent stem cells: perspectives for transfusion medicine

Por Lapillonne, Hélène, Kobari, Ladan, Mazurier, Christelle, Tropel, Philippe, Giarratana, Marie-Catherine, Zanella-Cleon, Isabelle, Kiger, Laurent, Wattenhofer-Donzé, Marie, Puccio, Hélène, Hebert, Nicolas, Francina, Alain, Andreu, Georges, Viville, Stéphane, Douay, Luc
Publicado em 2010

DPY19L2 Deletion as a Major Cause of Globozoospermia

Por Koscinski, Isabelle, ElInati, Elias, Fossard, Camille, Redin, Claire, Muller, Jean, Velez de la Calle, Juan, Schmitt, Françoise, Ben Khelifa, Mariem, Ray, Pierre, Kilani, Zaid, Barratt, Christopher L.R., Viville, Stéphane
Publicado em 2011

Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres

Por Van Rij, Maartje C, De Rademaeker, Marjan, Moutou, Céline, Dreesen, Jos C F M, De Rycke, Martine, Liebaers, Inge, Geraedts, Joep P M, De Die-Smulders, Christine E M, Viville, Stéphane
Publicado em 2012

DPY19L2 Deletion as a Major Cause of Globozoospermia

Por Koscinski, Isabelle, ElInati, Elias, Fossard, Camille, Redin, Claire, Muller, Jean, Velez de la Calle, Juan, Schmitt, Françoise, Ben Khelifa, Mariem, Ray, Pierre F., Kilani, Zaid, Barratt, Christopher L.R., Viville, Stéphane
Publicado em 2011