Search Results - "Viville, S"

Assisted reproduction treatment and epigenetic inheritance by van Montfoort, A.P.A., Hanssen, L.L.P., de Sutter, P., Viville, S., Geraedts, J.P.M., de Boer, P.

“…BACKGROUND The subject of epigenetic risk of assisted reproduction treatment (ART), initiated by reports on an increase of children with the Beckwith-Wiedemann…”
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Exome sequencing reveals novel causes as well as new candidate genes for human globozoospermia by Oud, M S, Okutman, Ö, Hendricks, L A J, de Vries, P F, Houston, B J, Vissers, L E L M, O’Bryan, M K, Ramos, L, Chemes, H E, Viville, S, Veltman, J A

“…Abstract STUDY QUESTION Can exome sequencing identify new genetic causes of globozoospermia? SUMMARY ANSWER Exome sequencing in 15 cases of unexplained…”
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Recent developments in genetics and medically assisted reproduction: from research to clinical applications by Harper, J C, Aittomäki, K, Borry, P, Cornel, M C, de Wert, G, Dondorp, W, Geraedts, J, Gianaroli, L, Ketterson, K, Liebaers, I, Lundin, K, Mertes, H, Morris, M, Pennings, G, Sermon, K, Spits, C, Soini, S, van Montfoort, A P A, Veiga, A, Vermeesch, J R, Viville, S, Macek, Jr, M

“…Two leading European professional societies, the European Society of Human Genetics and the European Society for Human Reproduction and Embryology, have worked…”
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Assisted oocyte activation overcomes fertilization failure in globozoospermic patients regardless of the DPY19L2 status by Kuentz, P., Vanden Meerschaut, F., ElInati, E., Nasr-Esfahani, M.H., Gurgan, T., Iqbal, N., Carré-Pigeon, F., Brugnon, F., Gitlin, S.A., Velez de la Calle, J., Kilani, Z., De Sutter, P., Viville, S.

“…STUDY QUESTION Does DPY19L2 status influence intracytoplasmic sperm injection (ICSI) outcomes with or without assisted oocyte activation (AOA)? SUMMARY ANSWER…”
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Pathogenic missense variation in PABPC1L/EPAB causes female infertility due to oocyte maturation arrest at the germinal vesicle stage by Okutman, O., Gürbüz, A. S., Büyük, U., Real, E., Leconte, R., Chennen, K., Mayer, C., Muller, J., Le May, N., Viville, S.

“…Women undergoing controlled ovarian hyperstimulation prior to in vitro fertilization (IVF) are treated using various protocols to induce multiple follicular…”
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C10 hESc and IPSc as models for genetic defects by Viville, S

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ESHRE PGD Consortium data collection VI: cycles from January to December 2003 with pregnancy follow-up to October 2004 by Sermon, K.D., Michiels, A., Harton, G., Moutou, C., Repping, S., Scriven, P.N., SenGupta, S., Traeger-Synodinos, J., Vesela, K., Viville, S., Wilton, L., Harper, J.C.

“…The sixth report of the ESHRE PGD Consortium is presented, relating to cycles collected for the calendar year 2003 and follow-up of the pregnancies and babies…”
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ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow-up to October 2005 by Harper, J.C., de Die-Smulders, C., Goossens, V., Harton, G., Moutou, C., Repping, S., Scriven, P.N, SenGupta, S., Traeger-Synodinos, J., Van Rij, M.C., Viville, S., Wilton, L., Sermon, K.D.

“…The seventh report of the ESHRE PGD Consortium is presented documenting cycles collected for the calendar year 2004 and follow-up of the pregnancies and babies…”
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What next for preimplantation genetic screening? More randomized controlled trials needed? by Mastenbroek, S., Scriven, P., Twisk, M., Viville, S., Van der Veen, F., Repping, S.

“…The recent debate on preimplantation genetic screening (PGS) has raised questions about its routine use in clinical practice. It has been suggested that the…”
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Genetic aspects of male infertility: From bench to clinic by Ben Rhouma, M, Okutman, O, Muller, J, Benkhalifa, M, Bahri, H, Ben Rhouma, K, Tebourbi, O, Viville, S

“…The objective of our manuscript is to review the current state of research on the genetics of male infertility, highlighting the genetic abnormalities that can…”
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ESHRE PGD Consortium data collection IV: May–December 2001 by Sermon, K., Moutou, C., Harper, J., Geraedts, J., Scriven, P., Wilton, L., Magli, M.C., Michiels, A., Viville, S., De Die, C.

“…The ESHRE PGD Consortium was formed in 1997 to survey the practice of preimplantation genetic diagnosis (PGD). Since then, three reports have been published…”
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Increased pregnancy rate using standardized coculture on autologous endometrial cells and single blastocyst transfer : a multicentre randomized controlled trial by Ohl, J, de Mouzon, J, Nicollet, B, Benoussaïdh, A, Gouze, J N, Viville, S, Menezo, Y

“…Despite excellent published results, the lack of well-designed, multicentre, randomized clinical trials results in an absence of general consensus on the…”
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Chromosome abnormalities in sperm from infertile men with normal somatic karyotypes: teratozoospermia by Machev, N, Gosset, P, Viville, S

“…Teratozoospermia is characterized by the presence of spermatozoa with abnormal morphology in sperm. This condition is frequently associated with infertility…”
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Creation of a registry for human embryonic stem cells carrying an inherited defect: joint collaboration between ESHRE and hESCreg by Sermon, K.D., Simon, C., Braude, P., Viville, S., Borstlap, J., Veiga, A.

“…Human embryonic stem cells (hESCs), derived from human blastocysts, hold a great promise for regenerative medicine, drug development and basic research in…”
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Strategies and outcomes of PGD of familial adenomatous polyposis by Moutou, C., Gardes, N., Nicod, J.-C., Viville, S.

“…Owing to adult onset of hereditary cancer, prenatal diagnosis (PND) raises numerous ethical issues on the acceptability to terminate an affected pregnancy…”
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Recent developments in genetics and medically-assisted reproduction: from research to clinical applications by Harper, J C, Aittomäki, K, Borry, P, Cornel, M C, de Wert, G, Dondorp, W, Geraedts, J, Gianaroli, L, Ketterson, K, Liebaers, I, Lundin, K, Mertes, H, Morris, M, Pennings, G, Sermon, K, Spits, C, Soini, S, van Montfoort, A P A, Veiga, A, Vermeesch, J R, Viville, S, Macek, Jr, M

“…Two leading European professional societies, the European Society of Human Genetics and the European Society for Human Reproduction and Embryology, have worked…”
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P-714 Clinical utility of FMR1 screening: risk factor or monogenic cause for POI by Okutman, Ö, Van, A, Kelen, Der, Viville, S, Verpoest, W

“…Abstract Study question Is there a risk factor association or a monogenic relationship between FMR1 premutation and developing Fragile X-associated primary…”
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Genomic Structure and Parent-of-Origin-Specific Methylation of Peg1 by Lefebvre, Louis, Viville, Stéphane, Barton, Sheila C., Ishino, Fumitoshi, Surani, M. Azim

“…We previously identified Peg1/Mest as a novel paternay expressed gene in the developing mouse embryo. The human PEG1 gene was recently assigned to 7q32 and…”
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P-522 Custom design gene panel as a diagnostic for human non-syndromic infertility by Okutman, O, Tarabeux, J, Muller, J, Viville, S

“…Abstract Study question What is the relevance to offer panels of infertility genes as a diagnostic tool for infertile patients? Summary answer Our results…”
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A Silencer Element Identified in Drosophila Is Required for Imprinting of H19 Reporter Transgenes in Mice by Brenton, J. D., Drewell, R. A., Viville, S., Hilton, K. J., Barton, S. C., J. F-X. Ainscough, Surani, M. A.

“…The H19 gene is subject to genomic imprinting because it is methylated and repressed after paternal inheritance and is unmethylated and expressed after…”
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