Olivucci, Giulia; Iovino, Emanuela; Innella, Giovanni; Turchetti, Daniela; Pippucci, Tommaso; Magini, Pamela, Long read sequencing on its way to the routine diagnostics of genetic diseases, «FRONTIERS IN GENETICS», 2024, 15, pp. - - - [articolo]
Barbero, Giovanna; Zuntini, Roberta; Magini, Pamela; Desiderio, Laura; Bonaguro, Michela; Perrone, Anna Myriam; Rubino, Daniela; Grippa, Mina; De Leo, Antonio; Ceccarelli, Claudio; Godino, Lea; Miccoli, Sara; Ferrari, Simona; Santini, Donatella; De Iaco, Pierandrea; Zamagni, Claudio; Innella, Giovanni; Turchetti, Daniela, Characterization of BRCA Deficiency in Ovarian Cancer, «CANCERS», 2023, 15, Article number: 1530, pp. 1 - 18 [articolo]Open Access
Giulia Olivucci, Giulia Severi, Paola Visconti, Annio Posar, Maria Cristina Scaduto, Claudio Graziano, Marco seri, Pamela Magini, Clinical interpretation of aCGH results in patients with neurodevelopmental disorders by geneticists: impact on diagnostic yield, «EUROPEAN JOURNAL OF HUMAN GENETICS», 2023, 31, pp. 459 - 459 [abstract]
Marconi, Caterina; Pecci, Alessandro; Palombo, Flavia; Melazzini, Federica; Bottega, Roberta; Nardi, Elena; Bozzi, Valeria; Faleschini, Michela; Barozzi, Serena; Giangregorio, Tania; Magini, Pamela; Balduini, Carlo L; Savoia, Anna; Seri, Marco; Noris, Patrizia; Pippucci, Tommaso, Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup, «HAEMATOLOGICA», 2023, 108, pp. 1909 - 1919 [articolo]Open Access
Gozzelino L.; Kochlamazashvili G.; Baldassari S.; Mackintosh A.I.; Licchetta L.; Iovino E.; Liu Y.-C.; Bennett C.A.; Bennett M.F.; Damiano J.A.; Zsurka G.; Marconi C.; Giangregorio T.; Magini P.; Kuijpers M.; Maritzen T.; Norata G.D.; Baulac S.; Canafoglia L.; Seri M.; Tinuper P.; Scheffer I.E.; Bahlo M.; Berkovic S.F.; Hildebrand M.S.; Kunz W.S.; Giordano L.; Bisulli F.; Martini M.; Haucke V.; Hirsch E.; Pippucci T., Defective lipid signalling caused by mutations in PIK3C2B underlies focal epilepsy, «BRAIN», 2022, 145, pp. 2313 - 2331 [articolo]Open Access
Hirsch, Naama; Dahan, Idit; D'haene, Eva; Avni, Matan; Vergult, Sarah; Vidal-García, Marta; Magini, Pamela; Graziano, Claudio; Severi, Giulia; Bonora, Elena; Nardone, Anna Maria; Brancati, Francesco; Fernández-Jaén, Alberto; Rory, Olson J; Hallgrímsson, Benedikt; Birnbaum, Ramon Y, HDAC9 structural variants disrupting TWIST1 transcriptional regulation lead to craniofacial and limb malformations, «GENOME RESEARCH», 2022, 32, pp. 1242 - 1253 [articolo]Open Access
Pelleri, Maria Chiara; Locatelli, Chiara; Mattina, Teresa; Bonaglia, Maria Clara; Piazza, Francesca; Magini, Pamela; Antonaros, Francesca; Ramacieri, Giuseppe; Vione, Beatrice; Vitale, Lorenza; Seri, Marco; Strippoli, Pierluigi; Cocchi, Guido; Piovesan, Allison; Caracausi, Maria, Partial trisomy 21 with or without highly restricted Down syndrome critical region (HR-DSCR): report of two new cases and reanalysis of the genotype-phenotype association, «BMC MEDICAL GENOMICS», 2022, 15, Article number: 266, pp. 1 - 12 [articolo]Open Access
Cameli C, Viggiano M, Rochat MJ, Maresca A, Caporali L, Fiorini C, Palombo F, Magini P, Duardo RC, Ceroni F, Scaduto MC, Posar A, Seri M, Carelli V, Visconti P, Bacchelli E, Maestrini E., An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder., «JOURNAL OF CELLULAR AND MOLECULAR MEDICINE», 2021, 25, pp. 2459 - 2470 [articolo]Open Access
Zama D.; Muratore E.; Giannetti A.; Neri I.; Conti F.; Magini P.; Ferrari S.; Pession A., Case Report: Hereditary Alpha Tryptasemia in Children: A Pediatric Case Series and a Brief Overview of Literature, «FRONTIERS IN PEDIATRICS», 2021, 9, Article number: 716786, pp. 1 - 9 [articolo]Open Access
Innella G.; Greco D.; Carli D.; Magini P.; Giorgio E.; Galesi O.; Ferrero G.B.; Romano C.; Brusco A.; Graziano C., Clinical spectrum and follow-up in six individuals with Lamb–Shaffer syndrome (SOX5), «AMERICAN JOURNAL OF MEDICAL GENETICS. PART A», 2021, 185, pp. 608 - 613 [articolo]
Dimartino P.; Mariani V.; Marconi C.; Minardi R.; Bramerio M.; Licchetta L.; Menghi V.; Morandi L.; Magini P.; Mongelli P.; Cardinale F.; Seri M.; Tinuper P.; Tassi L.; Pippucci T.; Bisulli F., Accurate Detection of Hot-Spot MTOR Somatic Mutations in Archival Surgical Specimens of Focal Cortical Dysplasia by Molecular Inversion Probes, «MOLECULAR DIAGNOSIS & THERAPY», 2020, 24, pp. 571 - 577 [articolo]
Palombo F.; Graziano C.; Al Wardy N.; Nouri N.; Marconi C.; Magini P.; Severi G.; La Morgia C.; Cantalupo G.; Cordelli D.M.; Gangarossa S.; Al Kindi M.N.; Al Khabouri M.; Salehi M.; Giorgio E.; Brusco A.; Pisani F.; Romeo G.; Carelli V.; Pippucci T.; Seri M., Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East, «HUMAN GENETICS», 2020, 139, pp. 1429 - 1441 [articolo]Open Access
Magini Pamela; Scarano Emanuela; Donati I.; Sensi A.; Mazzanti Laura; Perri Annamaria; Tamburrino Federica; Mongelli P.; Percesepe A.; Visconti Paola; Parmeggiani Antonia; Seri Marco; Graziano Claudio, Corrigendum to “Challenges in the clinical interpretation of small de novo copy number variants in neurodevelopmental disorders” [Gene 706 (2019) 162–171](S037811191930469X)(10.1016/j.gene.2019.05.007), «GENE», 2020, 735, Article number: 144393, pp. 144393 - N/A [articolo]
Bertulli C.; Marzollo A.; Doria M.; Cesare S.D.; La Scola C.; Mencarelli F.; Pasini A.; Affinita M.C.; Vidal E.; Magini P.; Dimartino P.; Masetti R.; Greco L.; Palomba P.; Conti F.; Pession A., Expanding phenotype of schimke immuno-osseous dysplasia: Congenital anomalies of the kidneys and of the urinary tract and alteration of nk cells, «INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES», 2020, 21, Article number: 8604, pp. 1 - 17 [articolo]Open Access
Del Dotto, Valentina; Ullah, Farid; Di Meo, Ivano; Magini, Pamela; Gusic, Mirjana; Maresca, Alessandra; Caporali, Leonardo; Palombo, Flavia; Tagliavini, Francesca; Baugh, Evan Harris; Macao, Bertil; Szilagyi, Zsolt; Peron, Camille; Gustafson, Margaret A; Khan, Kamal; La Morgia, Chiara; Barboni, Piero; Carbonelli, Michele; Valentino, Maria Lucia; Liguori, Rocco; Shashi, Vandana; Sullivan, Jennifer; Nagaraj, Shashi; El-Dairi, Mays; Iannaccone, Alessandro; Cutcutache, Ioana; Bertini, Enrico; Carrozzo, Rosalba; Emma, Francesco; Diomedi-Camassei, Francesca; Zanna, Claudia; Armstrong, Martin; Page, Matthew; Stong, Nicholas; Boesch, Sylvia; Kopajtich, Robert; Wortmann, Saskia; Sperl, Wolfgang; Davis, Erica E; Copeland, William C; Seri, Marco; Falkenberg, Maria; Prokisch, Holger; Katsanis, Nicholas; Tiranti, Valeria; Pippucci, Tommaso; Carelli, Valerio, SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder, «THE JOURNAL OF CLINICAL INVESTIGATION», 2020, 130, pp. 108 - 125 [articolo]
