1. Appropriateness of array‐CGH in the ADHD clinics: A comparative study. (12th April 2020) Authors: Baccarin, Marco; Picinelli, Chiara; Tomaiuolo, Pasquale; Castronovo, Paola; Costa, Anna; Verdecchia, Magda; Cannizzaro, Chiara; Barbieri, Giusi; Sacco, Roberto; Persico, Antonio M.; Lintas, Carla Journal: Genes, brain, and behavior Issue: Volume 19:Number 6(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. FARP‐1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family. Issue 9 (25th June 2020) Authors: Cucinotta, Francesca; Ricciardello, Arianna; Turriziani, Laura; Calabrese, Giorgia; Briguglio, Marilena; Boncoddo, Maria; Bellomo, Fabiana; Tomaiuolo, Pasquale; Martines, Silvia; Bruschetta, Marianna; La Fauci Belponer, Francesca; Di Bella, Tiziana; Colombi, Costanza; Baccarin, Marco; Picinelli, ... Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 9(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Huntingtin gene CAG repeat size affects autism risk: Family‐based and case–control association study. Issue 6 (11th July 2020) Authors: Piras, Ignazio Stefano; Picinelli, Chiara; Iennaco, Raffaele; Baccarin, Marco; Castronovo, Paola; Tomaiuolo, Pasquale; Cucinotta, Francesca; Ricciardello, Arianna; Turriziani, Laura; Nanetti, Lorenzo; Mariotti, Caterina; Gellera, Cinzia; Lintas, Carla; Sacco, Roberto; Zuccato, Chiara; Cattaneo, E... Journal: American journal of medical genetics Issue: Volume 183:Issue 6(2020) Page Start: 341 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Impaired Angiogenic Potential of Human Placental Mesenchymal Stromal Cells in Intrauterine Growth Restriction. (8th March 2016) Authors: Mandò, Chiara; Razini, Paola; Novielli, Chiara; Anelli, Gaia Maria; Belicchi, Marzia; Erratico, Silvia; Banfi, Stefania; Meregalli, Mirella; Tavelli, Alessandro; Baccarin, Marco; Rolfo, Alessandro; Motta, Silvia; Torrente, Yvan; Cetin, Irene Journal: Stem cells translational medicine Issue: Volume 5:Number 4(2016) Page Start: 451 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Insights into 6q21‐q22: Refinement of the critical region for acro‐cardio‐facial syndrome. (2nd July 2016) Authors: Milani, Donatella; Cagnoli, Giulia Anna; Baccarin, Marco; Alfei, Enrico; Guerneri, Silvana; Esposito, Susanna Journal: Congenital anomalies Issue: Volume 56:Number 4(2016) Page Start: 187 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Interstitial 6q25 microdeletion syndrome: ARID1B is the key gene. Issue 5 (11th January 2016) Authors: Ronzoni, Luisa; Tagliaferri, Francesco; Tucci, Arianna; Baccarin, Marco; Esposito, Susanna; Milani, Donatella Journal: American journal of medical genetics Issue: Volume 170:Issue 5(2016) Page Start: 1257 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Molecular cytogenetic characterization of a 2q35‐q37 duplication and a 4q35.1‐q35.2 deletion in two cousins: A genotype–phenotype analysis. (6th April 2015) Authors: Ronzoni, Luisa; Peron, Angela; Bianchi, Vera; Baccarin, Marco; Guerneri, Silvana; Silipigni, Rosamaria; Lalatta, Faustina; Bedeschi, Maria Francesca Journal: American journal of medical genetics Issue: Volume 167:Number 7(2015:Jul.) Page Start: 1551 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review. Issue 1 (7th May 2019) Authors: Castronovo, Paola; Baccarin, Marco; Ricciardello, Arianna; Picinelli, Chiara; Tomaiuolo, Pasquale; Cucinotta, Francesca; Frittoli, Myriam; Lintas, Carla; Sacco, Roberto; Persico, Antonio M. Journal: Clinical genetics Issue: Volume 97:Issue 1(2020) Page Start: 125 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Prenatal diagnosis of Simpson–Golabi–Behmel syndrome. Issue 12 (9th September 2016) Authors: Magini, Pamela; Palombo, Flavia; Boito, Simona; Lanzoni, Giulia; Mongelli, Patrizia; Rizzuti, Tommaso; Baccarin, Marco; Pippucci, Tommaso; Seri, Marco; Lalatta, Faustina Journal: American journal of medical genetics Issue: Volume 170:Issue 12(2016) Page Start: 3258 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Prenatal upper-limb mesomelia and 2q31.1 microdeletions affecting the regulatory genome. (November 2018) Authors: Peron, Angela; Boito, Simona; Rizzuti, Tommaso; Borzani, Irene; Baccarin, Marco; Bedeschi, Maria; Lalatta, Faustina Journal: Genetics in medicine Issue: Volume 20:Number 11(2018) Page Start: 1483 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗