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European Journal of Human Genetics : EJHG|June 4, 2025
Constitutional copy number amplifications: rare or under-evaluated? Revisiting a 25-year-old cold caseEliana Salvo, Romano Tenconi, Roberto Giorda, et al.Biomolecules|August 28, 2025
Internalizing and Externalizing Traits During Adolescence: Using Epigenetics and Perinatal Risks to Differentiate Clusters of SymptomsMaddalena Mauri, Silvia Grazioli, Carolina Bonivento, et al.Journal of Affective Disorders|November 20, 2015
Effect of family structure and TPH2 G-703T on the stability of dysregulation profile throughout adolescenceMaria Nobile, Valentina Bianchi, Dario Monzani, et al.Child Development|January 30, 2016
Serotonin Transporter Gene (SLC6A4) Methylation Associates With Neonatal Intensive Care Unit Stay and 3-Month-Old Temperament in Preterm InfantsRosario Montirosso, Livio Provenzi, Monica Fumagalli, et al.Genes|August 27, 2021
Brain Anatomical Mediators of <i>GRIN2B</i> Gene Association with Attention/Hyperactivity Problems: An Integrated Genetic-Neuroimaging StudyMaria Nobile, Eleonora Maggioni, Maddalena Mauri, et al.Human Genetics|July 13, 2010
Breakpoint determination of 15 large deletions in Peutz-Jeghers subjectsNicoletta Resta, Roberto Giorda, Rosanna Bagnulo, et al.Epigenomics|August 3, 2018
Very preterm birth is associated with PLAGL1 gene hypomethylation at birth and dischargeLivio Provenzi, Pietro De Carli, Monica Fumagalli, et al.Autism Research : Official Journal of the International Society for Autism Research|July 15, 2025
Protein-Altering Variants' Analysis in Autism Subgroups Uncovers Early Brain-Expressed Gene Modules Relevant to Autism PathophysiologyGaia Scaccabarozzi, Luca Fumagalli, Maddalena Mambretti, et al.European Journal of Human Genetics : EJHG|October 16, 2008
Mosaic 22q13 deletions: evidence for concurrent mosaic segmental isodisomy and gene conversionMaria Clara Bonaglia, Roberto Giorda, Silvana Beri, et al.Human Mutation|March 22, 2007
Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocationRenata Bocciardi, Roberto Giorda, Jens Buttgereit, et al.Pageof 13