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Brain Sciences|January 21, 2022
SCN2A Pathogenic Variants and Epilepsy: Heterogeneous Clinical, Genetic and Diagnostic FeaturesRoberta Epifanio, Roberto Giorda, Maria Carolina Merlano, et al.
American Journal of Medical Genetics. Part A|February 24, 2015
A novel mutation in COL4A1 gene: a possible cause of early postnatal cerebrovascular eventsAlice Decio, Davide Tonduti, Anna Pichiecchio, et al.
European Journal of Human Genetics : EJHG|February 11, 2005
A family-based association study does not support DYX1C1 on 15q21.3 as a candidate gene in developmental dyslexiaCecilia Marino, Roberto Giorda, Maria Luisa Lorusso, et al.
Journal of Neurology|June 11, 2003
The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjectsRoberto Del Bo, Giacomo Pietro Comi, Roberto Giorda, et al.
Infant Mental Health Journal|May 27, 2022
Serotonin transporter gene methylation and emotional regulation in preschool children born preterm: A longitudinal evaluation of the role of negative emotionality in infancyEleonora Mascheroni, Paola Schiavolin, Isabella Lucia Chiara Mariani Wigley, et al.
Epigenomics|July 7, 2016
SLC6A4 promoter region methylation and socio-emotional stress response in very preterm and full-term infantsRosario Montirosso, Livio Provenzi, Roberto Giorda, et al.
Human Mutation|January 31, 2007
Two classes of low-copy repeats comediate a new recurrent rearrangement consisting of duplication at 8p23.1 and triplication at 8p23.2Roberto Giorda, Roberto Ciccone, Giorgio Gimelli, et al.
International Journal of Environmental Research and Public Health|December 10, 2021
Exploring the Contribution of Proximal Family Risk Factors on <i>SLC6A4</i> DNA Methylation in Children with a History of Maltreatment: A Preliminary StudyFrancesco Craig, Eleonora Mascheroni, Roberto Giorda, et al.
Genome Research|August 14, 2003
Neocentromeres in 15q24-26 map to duplicons which flanked an ancestral centromere in 15q25Mario Ventura, Jonathan M Mudge, Valeria Palumbo, et al.
European Journal of Medical Genetics|August 5, 2008
A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrheaElena Rossi, Anna Pia Verri, Maria Grazia Patricelli, et al.
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