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European Journal of Human Genetics : EJHG|January 20, 2005
A 2.3 Mb duplication of chromosome 8q24.3 associated with severe mental retardation and epilepsy detected by standard karyotypeMaria Clara Bonaglia, Roberto Giorda, Romano Tenconi, et al.Frontiers in Psychology|June 3, 2021
Neuroimaging and DNA Methylation: An Innovative Approach to Study the Effects of Early Life Stress on Developmental PlasticityIsabella Lucia Chiara Mariani Wigley, Eleonora Mascheroni, Denis Peruzzo, et al.Molecular Psychiatry|December 13, 2025
How nature nurtures: prenatal exposure to green space buffers the effects of maternal stress on neonatal BDNF methylationSarah Nazzari, Grazia Zulian, Serena Grumi, et al.Journal of Medical Genetics|June 10, 2011
XX males SRY negative: a confirmed cause of infertilityAnnalisa Vetro, Roberto Ciccone, Roberto Giorda, et al.American Journal of Medical Genetics|September 24, 2002
20-Mb duplication of chromosome 9p in a girl with minimal physical findings and normal IQ: narrowing of the 9p duplication critical region to 6 MbMaria Clara Bonaglia, Roberto Giorda, Romeo Carrozzo, et al.Archives of General Psychiatry|January 5, 2005
Influence of the serotonin transporter promoter gene and shyness on children's cerebral responses to facial expressionsMarco Battaglia, Anna Ogliari, Annalisa Zanoni, et al.Biological Psychiatry|August 18, 2004
A case-control and family-based association study of the 5-HTTLPR in pediatric-onset depressive disordersMaria Nobile, Maria Giulia Cataldo, Roberto Giorda, et al.Biochemical and Biophysical Research Communications|August 25, 2004
Over-representation of exonic splicing enhancers in human intronless genes suggests multiple functions in mRNA processingUberto Pozzoli, Laura Riva, Giorgia Menozzi, et al.Psychiatric Genetics|November 27, 2014
GRIN2B mediates susceptibility to intelligence quotient and cognitive impairments in developmental dyslexiaSara Mascheretti, Andrea Facoetti, Roberto Giorda, et al.Journal of Medical Genetics|October 4, 2007
Deletion of a 760 kb region at 4p16 determines the prenatal and postnatal growth retardation characteristic of Wolf-Hirschhorn syndromeDaniela Concolino, Elena Rossi, Pietro Strisciuglio, et al.Pageof 13