| Title | Authors / Editors | Date |
unige:155120 |
Genome-wide epigenomic analyses in patients with nociceptive and neuropathic chronic pain subtypes reveals alterations in methylation of genes involved in the neuro-musculoskeletal system |
Stenz, Ludwig; Carré, Joane Le; Luthi, François; Vuistiner, Philippe; ... Léger, Bertrand |
2021 |
unige:154577 |
Benefits of exome sequencing in children with suspected isolated hearing loss |
Van Heurck, Roxane; Carminho Amaro Rodrigues, Maria Teresa; Ranza, Emmanuelle Nathalie; Stafuzza, Caterina; ... Giacobino, Ariane |
2021 |
unige:159359 |
Epigenomic changes after acupuncture treatment in patients suffering from burnout |
Petitpierre, Marc; Stenz, Ludwig; Giacobino, Ariane |
2021 |
unige:148701 |
Molecular characterization of pathogenic OTOA gene conversions in hearing loss patients |
Laurent, Sacha; Gehrig, Corinne; Nouspikel, Thierry; Amr, Sami S; ... Guipponi, Michel |
2021 |
unige:156292 |
Epigenomic analyses in sub-populations of spermatozoa from infertile men with short anogenital distance |
Stenz, Ludwig; Beyens, Matthias; Gill, Mark; De Geyter, Christian; Giacobino, Ariane |
2021 |
unige:152622 |
Gestational trophoblastic disease in Switzerland: retrospective study of the impact of a regional reference centre |
Fehlmann, Aurore; Benkortbi, Khadidja; Rosseel, Ginette; Meyer-Hamme, Ulrike; ... Undurraga Malinverno, Manuela Stefania |
2021 |
unige:137971 |
Triméthylaminurie : un cas pas forcément si rare |
Pedrazzoli, Damien; Giacobino, Ariane |
2020 |
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: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:137981 |
Entre gènes et sexe : quelle détermination ? |
Giacobino, Ariane |
2019 |
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:104800 |
Intergenerational Transmission of DNA Methylation Signatures Associated with Early Life Stress |
Stenz, Ludwig; Schechter, Daniel; Rusconi Serpa, Sandra; Giacobino, Ariane |
2018 |
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: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:126802 |
Handicap intellectuel : apport de la génétique pour le diagnostic étiologique |
Jouan, Chrystel; Kosel, Markus Mathaus; Abramowicz, Marc; Giacobino, Ariane |
2018 |
unige:112491 |
L'instinct aurait-il une base épigénétique ? |
Giacobino, Ariane |
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 |