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	Title	Authors / Editors	Date
unige:137333	LARS2-Perrault syndrome: a new case report and literature review	Carminho Amaro Rodrigues, Maria Teresa; Klee, Philippe; Laurent, Sacha; Guipponi, Michel; ... Giacobino, Ariane	2020
unige:137335	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
unige:137971	Triméthylaminurie : un cas pas forcément si rare	Pedrazzoli, Damien; Giacobino, Ariane	2020
unige:138350	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
unige:119650	Genetic resistance to DEHP-induced transgenerational endocrine disruption	Stenz, Ludwig; Rahban, Rita; Prados, Julien; Nef, Serge; Giacobino, Ariane	2019
unige:137972	Génétique des troubles auditifs chez l’enfant	Giacobino, Ariane; Ranza, Emmanuelle Nathalie; Abramowicz, Marc; Senn, Pascal; Cao Van, Hélène	2019
unige:137980	Tests préimplantatoires de l’embryon en médecine de reproduction	Benard, Julie Gabrielle Anne; Targa Barrera, Célia; Murisier, Fabien; Giacobino, Ariane; Streuli, Isabelle	2019
unige:137981	Entre gènes et sexe : quelle détermination ?	Giacobino, Ariane	2019
unige:103516	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
unige:104800	Intergenerational Transmission of DNA Methylation Signatures Associated with Early Life Stress	Stenz, Ludwig; Schechter, Daniel; Rusconi Serpa, Sandra; Giacobino, Ariane	2018
unige:126802	Handicap intellectuel : apport de la génétique pour le diagnostic étiologique	Jouan, Chrystel; Kosel, Markus Mathaus; Abramowicz, Marc; Giacobino, Ariane	2018
unige:123733	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
unige:112491	L’instinct aurait-il une base épigénétique ?	Giacobino, Ariane	2017
unige:92437	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
unige:92432	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
unige:88998	Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders	Fokstuen, Siv; Makrythanasis, Periklis; Hammar Bouveret, Eva; Guipponi, Michel; ... Antonarakis, Stylianos	2016
unige:92439	Maladies génétiques rénales : perspectives diagnostiques	Bouatou, Yassine; Giacobino, Ariane; Parvex, Paloma Maria; De Seigneux Matthey, Sophie	2016
unige:78757	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
unige:92438	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
unige:47608	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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