Associations between genes methylation, postnatal risk factors and psychiatric symptoms in a clinical sample of children and adolescents: Preliminar results from the remind longitudinal study
Villa, F., Rosi, E., Grazioli, S., Mauri, M., Giorda, R., Brambilla, P., Bonivento, C., Garzitto, M., Molteni, M., Nobile, M.
Published in European psychiatry (01.04.2021)
Published in European psychiatry (01.04.2021)
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An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia
Mascheretti, S., Bureau, A., Trezzi, V., Giorda, R., Marino, C.
Published in Human genetics (01.07.2015)
Published in Human genetics (01.07.2015)
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Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome
Bonaglia, M C, Giorda, R, Mani, E, Aceti, G, Anderlid, B-M, Baroncini, A, Pramparo, T, Zuffardi, O
Published in Journal of medical genetics (01.10.2006)
Published in Journal of medical genetics (01.10.2006)
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Refining the phenotype associated with MEF2C haploinsufficiency
Novara, F, Beri, S, Giorda, R, Ortibus, E, Nageshappa, S, Darra, F, Dalla Bernardina, B, Zuffardi, O, Van Esch, H
Published in Clinical genetics (01.11.2010)
Published in Clinical genetics (01.11.2010)
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An assessment of gene‐by‐environment interactions in developmental dyslexia‐related phenotypes
Mascheretti, S., Bureau, A., Battaglia, M., Simone, D., Quadrelli, E., Croteau, J., Cellino, M. R., Giorda, R., Beri, S., Maziade, M., Marino, C.
Published in Genes, brain and behavior (01.02.2013)
Published in Genes, brain and behavior (01.02.2013)
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Association of short‐term memory with a variant within DYX1C1 in developmental dyslexia
Marino, C., Citterio, A., Giorda, R., Facoetti, A., Menozzi, G., Vanzin, L., Lorusso, M. L., Nobile, M., Molteni, M.
Published in Genes, brain and behavior (01.10.2007)
Published in Genes, brain and behavior (01.10.2007)
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Effect of the serotonin transporter gene and of environment on the continuity of anxiety and depression traits throughout adolescence
Nobile, M., Greco, A., Perna, G., Colombo, P., Bianchi, V., Bellina, M., Giorda, R., Monzani, D., Carlet, O., Griez, E., Molteni, M.
Published in Epidemiology and psychiatric sciences (01.12.2014)
Published in Epidemiology and psychiatric sciences (01.12.2014)
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Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion
Gagliardi, C, Bonaglia, M C, Selicorni, A, Borgatti, R, Giorda, R
Published in Journal of medical genetics (01.07.2003)
Published in Journal of medical genetics (01.07.2003)
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Deletion of a 760 kb region at 4p16 determines the prenatal and postnatal growth retardation characteristic of Wolf-Hirschhorn syndrome
Concolino, Daniela, Rossi, Elena, Strisciuglio, Pietro, Iembo, Maria Antonietta, Giorda, Roberto, Ciccone, Roberto, Tenconi, Romano, Zuffardi, Orsetta
Published in Journal of medical genetics (01.10.2007)
Published in Journal of medical genetics (01.10.2007)
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Olfactory Receptor-Related Duplicons Mediate a Microdeletion at 11q13.2q13.4 Associated with a Syndromic Phenotype
Wischmeijer, A., Magini, P., Giorda, R., Gnoli, M., Ciccone, R., Cecconi, I., Franzoni, E., Mazzanti, L., Romeo, G., Zuffardi, O., Seri, M.
Published in Molecular syndromology (01.01.2011)
Published in Molecular syndromology (01.01.2011)
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Selective disruption of muscle and brain-specific BPAG1 isoforms in a girl with a 6;15 translocation, cognitive and motor delay, and tracheo-oesophageal atresia
Giorda, R, Cerritello, A, Bonaglia, M C, Bova, S, Lanzi, G, Repetti, E, Giglio, S, Baschirotto, C, Pramparo, T, Avolio, L, Bragheri, R, Maraschio, P, Zuffardi, O
Published in Journal of medical genetics (01.06.2004)
Published in Journal of medical genetics (01.06.2004)
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A locus on 15q15-15qter influences dyslexia: further support from a transmission/disequilibrium study in an Italian speaking population
Marino, C, Giorda, R, Vanzin, L, Nobile, M, Lorusso, M L, Baschirotto, C, Riva, L, Molteni, M, Battaglia, M
Published in Journal of medical genetics (01.01.2004)
Published in Journal of medical genetics (01.01.2004)
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Journal Article
The dystrophin gene is alternatively spliced throughout its coding sequence
Sironi, M, Cagliani, R, Pozzoli, U, Bardoni, A, Comi, G.P, Giorda, R, Bresolin, N
Published in FEBS letters (24.04.2002)
Published in FEBS letters (24.04.2002)
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Effect of the catechol-O-methyltransferase val(158)met genotype on children's early phases of facial stimuli processing
Battaglia, M, Zanoni, A, Giorda, R, Pozzoli, U, Citterio, A, Beri, S, Ogliari, A, Nobile, M, Marino, C, Molteni, M
Published in Genes, brain and behavior (01.06.2007)
Published in Genes, brain and behavior (01.06.2007)
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A large analphoid invdup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's lines
Gimelli, G, Giorda, R, Beri, S, Gimelli, S, Zuffardi, O
Published in European journal of medical genetics (01.07.2007)
Published in European journal of medical genetics (01.07.2007)
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Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population
Cagliani, R, Fortunato, F, Giorda, R, Rodolico, C, Bonaglia, M.C, Sironi, M, D'Angelo, M.G, Prelle, A, Locatelli, F, Toscano, A, Bresolin, N, Comi, G.P
Published in Neuromuscular disorders : NMD (01.12.2003)
Published in Neuromuscular disorders : NMD (01.12.2003)
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