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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1995 1
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1997 3
2001 1
2003 1
2004 1
2006 4
2007 3
2008 3
2009 3
2011 1
2013 2
2014 3
2015 2
2016 1
2017 2
2018 2
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2025 3

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43 results

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Page 1
Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndrome.
Alvino FG, Gini S, Minetti A, Pagani M, Sastre-Yagüe D, Barsotti N, De Guzman E, Schleifer C, Stuefer A, Kushan L, Montani C, Galbusera A, Papaleo F, Kates WR, Murphy D, Lombardo MV, Pasqualetti M, Bearden CE, Gozzi A. Alvino FG, et al. Among authors: montani c. Sci Adv. 2025 Mar 14;11(11):eadq2807. doi: 10.1126/sciadv.adq2807. Epub 2025 Mar 12. Sci Adv. 2025. PMID: 40073125 Free PMC article.
Sex-biasing influence of autism-associated Ube3a gene overdosage at connectomic, behavioral, and transcriptomic levels.
Montani C, Balasco L, Pagani M, Alvino FG, Barsotti N, de Guzman AE, Galbusera A, de Felice A, Nickl-Jockschat TK, Migliarini S, Casarosa S, Lau P, Mattioni L, Pasqualetti M, Provenzano G, Bozzi Y, Lombardo MV, Gozzi A. Montani C, et al. Sci Adv. 2024 Jul 12;10(28):eadg1421. doi: 10.1126/sciadv.adg1421. Epub 2024 Jul 12. Sci Adv. 2024. PMID: 38996019 Free PMC article.
Biological subtyping of autism via cross-species fMRI.
Pagani M, Zerbi V, Gini S, Alvino F, Banerjee A, Barberis A, Basson MA, Bozzi Y, Galbusera A, Ellegood J, Fagiolini M, Lerch J, Matteoli M, Montani C, Pozzi D, Provenzano G, Scattoni ML, Wenderoth N, Xu T, Lombardo M, Milham MP, Martino AD, Gozzi A. Pagani M, et al. Among authors: montani c. bioRxiv [Preprint]. 2025 Mar 5:2025.03.04.641400. doi: 10.1101/2025.03.04.641400. bioRxiv. 2025. PMID: 40093106 Free PMC article. Preprint.
Connectomic and behavioural alterations in creatine transporter deficiency are partially normalized by gene therapy.
Montani C, Iovino L, Di Vetta F, Pasquin Mariani JR, De Guzman AE, Gini S, Galbusera A, D'Epifanio B, Ghirardini E, Cornuti S, Dadà L, Putignano E, Alessandrì MG, Vasirani G, Mandrup Bertozzi S, Armirotti A, Baroncelli L, Gozzi A. Montani C, et al. Brain. 2025 Jul 29:awaf275. doi: 10.1093/brain/awaf275. Online ahead of print. Brain. 2025. PMID: 40729420
Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndrome.
Alvino FG, Gini S, Minetti A, Pagani M, Sastre-Yagüe D, Barsotti N, De Guzman E, Schleifer C, Stuefer A, Kushan L, Montani C, Galbusera A, Papaleo F, Lombardo MV, Pasqualetti M, Bearden CE, Gozzi A. Alvino FG, et al. Among authors: montani c. bioRxiv [Preprint]. 2024 Apr 3:2024.03.29.587339. doi: 10.1101/2024.03.29.587339. bioRxiv. 2024. Update in: Sci Adv. 2025 Mar 14;11(11):eadq2807. doi: 10.1126/sciadv.adq2807. PMID: 38585897 Free PMC article. Updated. Preprint.
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis.
Ramos-Brossier M, Montani C, Lebrun N, Gritti L, Martin C, Seminatore-Nole C, Toussaint A, Moreno S, Poirier K, Dorseuil O, Chelly J, Hackett A, Gecz J, Bieth E, Faudet A, Heron D, Frank Kooy R, Loeys B, Humeau Y, Sala C, Billuart P. Ramos-Brossier M, et al. Among authors: montani c. Hum Mol Genet. 2015 Feb 15;24(4):1106-18. doi: 10.1093/hmg/ddu523. Epub 2014 Oct 9. Hum Mol Genet. 2015. PMID: 25305082 Free PMC article.
The X-Linked Intellectual Disability Protein IL1RAPL1 Regulates Dendrite Complexity.
Montani C, Ramos-Brossier M, Ponzoni L, Gritti L, Cwetsch AW, Braida D, Saillour Y, Terragni B, Mantegazza M, Sala M, Verpelli C, Billuart P, Sala C. Montani C, et al. J Neurosci. 2017 Jul 12;37(28):6606-6627. doi: 10.1523/JNEUROSCI.3775-16.2017. Epub 2017 Jun 2. J Neurosci. 2017. PMID: 28576939 Free PMC article.
43 results