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 TitleAuthors / EditorsDate
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Triméthylaminurie : un cas pas forcément si rare Pedrazzoli, Damien; Giacobino, Ariane 2020
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Transgenerational effects of the endocrine disruptor vinclozolin on the methylation pattern of imprinted genes in the mouse sperm Stouder, Christelle; Giacobino, Ariane 2010
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The Tutsi genocide and transgenerational transmission of maternal stress: epigenetics and biology of the HPA axis Perroud, Nader Ali; Rutembesa, Eugene; Giacobino, Ariane; Mutabaruka, Jean; ... Karege, Félicien 2014
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The role of DMDs in the maintenance of epigenetic states Giacobino, Ariane; Chaillet, J R 2006
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The association of serotonin receptor 3A methylation with maternal violence exposure, neural activity, and child aggression Schechter, Daniel; Moser, Dominik; Pointet, Virginie; Aue Seil, Tatjana; ... Dayer, Alexandre 2017
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Tests préimplantatoires de l’embryon en médecine de reproduction Benard, Julie Gabrielle Anne; Targa Barrera, Célia; Murisier, Fabien; Giacobino, Ariane; Streuli, Isabelle 2019
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Testicular Dysgenesis Syndrome and Long-Lasting Epigenetic Silencing of Mouse Sperm Genes Involved in the Reproductive System after Prenatal Exposure to DEHP. Stenz, Ludwig; Escoffier Breancon, Jessica; Rahban, Rita; Nef, Serge; Giacobino, Ariane 2017
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Superovulation in mice alters the methylation pattern of imprinted genes in the sperm of the offspring Stouder, Christelle; Deutsch Escalante, Samuel; Giacobino, Ariane 2009
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Stochasticité : la troisième variable Giacobino, Ariane 2013
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Specific transgenerational imprinting effects of the endocrine disruptor methoxychlor on male gametes Stouder, Christelle; Giacobino, Ariane 2011
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Specific language impairment as the prominent feature in a patient with a low-level trisomy 21 mosaicism Giacobino, Ariane; Lemieux, N; Lemyre, E; Lespinasse, J 2007
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Specific differentially methylated domain sequences direct the maintenance of methylation at imprinted genes Reinhart, Bonnie; Giacobino, Ariane; Chaillet, J Richard 2006
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Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing Ratnamala, Uppala; Lyle, Robert; Rawal, Rakesh; Singh, Raminder; ... Radhakrishna, Uppala 2011
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Recipient rs1045642 Polymorphism Is Associated With Office Blood Pressure at 1-Year Post Kidney Transplantation: A Single Center Pharmacogenetic Cohort Pilot Study Bouatou, Yassine; Stenz, Ludwig; Ponte, Belen; Ferrari, Serge Livio; ... Hadaya, Karine 2018
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Prevention of vascular dysfunction and arterial hypertension in mice generated by assisted reproductive technologies by addition of melatonin to culture media Rexhaj, Emrush; Pireva, Agim; Giacobino, Ariane; Allemann, Yves; ... Rimoldi, Stefano F 2015
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Prenatal manifestation in a family affected by nevoid basal cell carcinoma syndrome Le Brun Keris, Yann; Jouk, Pierre-Simon; Saada-Sebag, Géraldine; Roux, Jean-Jacques; ... Lespinasse, James 2008
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Prenatal exposure to ethanol: a specific effect on the H19 gene in sperm Stouder, Christelle; Somm, Emmanuel; Giacobino, Ariane 2011
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Prenatal Exposure to DEHP Affects Spermatogenesis and Sperm DNA Methylation in a Strain-Dependent Manner Prados, Julien; Stenz, Ludwig; Somm, Emmanuel; Stouder, Christelle; ... Giacobino, Ariane 2015
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Preimplantation genetic diagnosis and epigenetics?- continued surveillance Giacobino, Ariane 2006
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Post genomic decade - the epigenome and exposome challenges Giacobino, Ariane 2011
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Patients avec variation du développement sexuel : un exemple de prise en charge interdisciplinaire Phan-Hug, Franziska; Kraus, Cynthia; Giacobino, Ariane; Fellmann, Florence; ... Meyrat, Blaise J 2016
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Parenteral nutrition practices in hospital pharmacies in Switzerland, France, and Belgium Maisonneuve, Nicolas; Raguso, CA; Giacobino, Ariane; Muhlebach, Stefan; ... Pichard, Claude 2004
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Novel NEXMIF pathogenic variant in a boy with severe autistic features, intellectual disability, and epilepsy, and his mildly affected mother Lambert, Nelle; Dauve, Corinne; Ranza, Emmanuelle Nathalie; Makrythanasis, Periklis; ... Giacobino, Ariane 2018
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Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients Laurent, Sacha; Gehrig, Corinne; Nouspikel, Thierry; Amr, Sami S; ... Guipponi, Michel 2021
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Mild intellectual disability associated with a progeny of father-daughter incest: genetic and environmental considerations Ansermet, François; Lespinasse, James; Gimelli, Stefania; Bena, Frédérique; Giacobino, Ariane 2010
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Mice generated by in vitro fertilization exhibit vascular dysfunction and shortened life span Rexhaj, Emrush; Giacobino, Ariane; Rimoldi, Stefano F; Fuster, Daniel G; ... Scherrer, Urs 2013
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Methylation of Serotonin Receptor 3a in ADHD, Borderline Personality, and Bipolar Disorders: Link with Severity of the Disorders and Childhood Maltreatment Perroud, Nader Ali; Zewdie Wondimu, Seblewongel; Stenz, Ludwig; Adouan, Wafae; ... Dayer, Alexandre 2016
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Methylation of NR3C1 is related to maternal PTSD, parenting stress and maternal medial prefrontal cortical activity in response to child separation among mothers with histories of violence exposure Schechter, Daniel; Moser, Dominik; Giacobino, Ariane; Stenz, Ludwig; ... Rusconi Serpa, Sandra 2015
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Maladies trophoblastiques : une prise en charge pluridisciplinaire, un premier centre suisse Rougemont, A-L; Pelte, M-F; Béna, F Sloan; Giacobino, Ariane; ... Finci, Vildana 2011
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Maladies génétiques rénales : perspectives diagnostiques Bouatou, Yassine; Giacobino, Ariane; Parvex, Paloma Maria; De Seigneux Matthey, Sophie 2016
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LARS2-Perrault syndrome: a new case report and literature review Carminho Amaro Rodrigues, Maria Teresa; Klee, Philippe; Laurent, Sacha; Guipponi, Michel; ... Giacobino, Ariane 2020
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La fin du dimorphisme sexuel est-elle programmée ? Giacobino, Ariane; Ansermet, François 2011
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L’instinct aurait-il une base épigénétique ? Giacobino, Ariane 2017
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Intergenerational Transmission of DNA Methylation Signatures Associated with Early Life Stress Stenz, Ludwig; Schechter, Daniel; Rusconi Serpa, Sandra; Giacobino, Ariane 2018
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Increased methylation of glucocorticoid receptor gene (NR3C1) in adults with a history of childhood maltreatment: a link with the severity and type of trauma Perroud, Nader Ali; Giacobino, Ariane; Prada, Paco Boris; Olié, E; ... Malafosse, Alain 2011
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Implications of reproductive technologies for birth and developmental outcomes: imprinting defects and beyond Giacobino, Ariane 2006
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Hormone de croissance et carcinogenèse: le point sur la question Gottraux, Sophie Aline; Giacobino, Ariane; Raguso, Comasia; Genton Graf, Laurence; ... Pichard, Claude 2003
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Handicap intellectuel : apport de la génétique pour le diagnostic étiologique Jouan, Chrystel; Kosel, Markus Mathaus; Abramowicz, Marc; Giacobino, Ariane 2018
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Génétique des troubles auditifs chez l’enfant Giacobino, Ariane; Ranza, Emmanuelle Nathalie; Abramowicz, Marc; Senn, Pascal; Cao Van, Hélène 2019
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Genetics and nutrition Giacobino, Ariane; Grimble, R; Pichard, Claude 2003
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Genetic resistance to DEHP-induced transgenerational endocrine disruption Stenz, Ludwig; Rahban, Rita; Prados, Julien; Nef, Serge; Giacobino, Ariane 2019
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Genetic and epigenetic risks of ART. Giacobino, Ariane 2007
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Frequency of replication/transcription errors in (A)/(T) runs of human genes Giacobino, Ariane; Rossier, Colette; Papasavvas, M.; Antonarakis, Stylianos 2001
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Fire-settng behavior associated with Klinefelter syndrome Eytan, Ariel; Giacobino, Ariane; Thorens, Gabriel; Eugster, Nicole Isabelle; Graf, Isabelle Flora Cécile 2002
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Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders Fokstuen, Siv; Makrythanasis, Periklis; Hammar Bouveret, Eva; Guipponi, Michel; ... Antonarakis, Stylianos 2016
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Evolutionary appearance of mononucleotide repeats in the coding sequences of four genes in primates Giacobino, Ariane; Chaillet, John Richard 2007
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Epigénétique et transmission Giacobino, Ariane 2014
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Epigenetics in reproductive medicine Giacobino, Ariane 2007
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Epigenetic modulations in infertility and reproductive medicine Giacobino, Ariane 2010
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Epigenetic effects of methoxychlor and vinclozolin on male gametes Giacobino, Ariane 2014
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