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 TitleAuthors / EditorsDate
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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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Case report: a 58 -year -old man with small kidneys and elevated liver enzymes Dash, Jonathan; Saudan, Patrick; Giacobino, Ariane; Moll, Solange; De Seigneux Matthey, Sophie 2020
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Triméthylaminurie : un cas pas forcément si rare Pedrazzoli, Damien; Giacobino, Ariane 2020
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Altered BDNF methylation in patients with chronic musculoskeletal pain and high biopsychosocial complexity Giacobino, Ariane; Luthi, François; Stenz, Ludwig; Le Carré, Joane; ... Léger, Bertrand 2020
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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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Génétique des troubles auditifs chez l’enfant Giacobino, Ariane; Ranza, Emmanuelle Nathalie; Abramowicz, Marc; Senn, Pascal; Cao Van, Hélène 2019
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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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Entre gènes et sexe : quelle détermination ? Giacobino, Ariane 2019
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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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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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Handicap intellectuel : apport de la génétique pour le diagnostic étiologique Jouan, Chrystel; Kosel, Markus Mathaus; Abramowicz, Marc; Giacobino, Ariane 2018
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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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L’instinct aurait-il une base épigénétique ? Giacobino, Ariane 2017
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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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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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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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Maladies génétiques rénales : perspectives diagnostiques Bouatou, Yassine; Giacobino, Ariane; Parvex, Paloma Maria; De Seigneux Matthey, Sophie 2016
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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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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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BDNF promoter I methylation correlates between post-mortem human peripheral and brain tissues Stenz, Ludwig; Zewdie Wondimu, Seblewongel; Laforge-Escarra, Térèse; Prados, Julien; ... Aubry, Jean-Michel 2015
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