RE-BVS – Piemonte Repository

Sfoglia per AUTORE
BRUSCO A
Collezione ASL Città di Torino

Items : 6

Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus. in American journal of human genetics / Am J Hum Genet. 2025 Jan 2;112(1):154-167. doi: 10.1016/j.ajhg.2024.11.003. Epub 2024 Dec 19.

2025
ASL Città di Torino
AOU Città della Salute di Torino

Scherer SW; Simone L; Zara F; Russell BE; Nelson SF; Graziano C; Schwab M; Corona RI; Mullegama SV; Douine ED; Helbig I; McDonnell PP; Lusk L; Pedro HF; Parisotto S; Keller R; Pullano V; Brusco A; Granger L; Anadiotis G; Charlebois J; Elsabbagh M; MacDonald JR; Ko SY; Frankland PW; Anagnostou E; Reuter MS; Mendes M; Trost B; et alii...

Genetic variants in DDX53 contribute to Autism Spectrum Disorder associated with the Xp22.11 locus. in medRxiv : the preprint server for health sciences / medRxiv [Preprint]. 2023 Dec 27:2023.12.21.23300383. doi: 10.1101/2023.12.21.23300383.

2023
ASL Città di Torino
AOU Città della Salute di Torino

Mullegama SV; Helbig I; McDonnell PP; Lusk L; Pedro HF; Parisotto S; Keller R; Brusco A; Pullano V; Anadiotis G; Granger L; Frankland PW; MacDonald JR; Ko SY; Reuter MS; Shum C; Salazar NB; Trost B; Howe JL; Bradley CA; Scala M; Douine ED; Russell BE; Nelson SF; Zara F; Scherer SW;

A Novel PSEN1 Variant Leading to Posterior Cortical Atrophy: A Case Report. in Journal of Alzheimer's disease reports / J Alzheimers Dis Rep. 2023 May 31;7(1):469-473. doi: 10.3233/ADR230023. eCollection 2023.

2023
ASL Città di Torino
AOU Città della Salute di Torino

Rainero I; Rubino E; Brusco A; Pasini B; Dentelli P; Imperiale D; Gallone S; Atzori C; Boschi S; Cermelli A; Ferrandes F; Grassini A; Marcinnò A; Roveta F;

De novo truncating NOVA2 variants affect alternative splicing and lead to heterogeneous neurodevelopmental phenotypes. in Human mutation / Hum Mutat. 2022 Sep;43(9):1299-1313. doi: 10.1002/humu.24414. Epub 2022 Jun 8.

2022
ASL Città di Torino
AOU Città della Salute di Torino

Striano P; Piton A; Zara F; Charlet-Berguerand N; Saris JJ; Lipska-Zi?tkiewicz BS; Brusco A; Langer T; Schmidts M; Liebelt J; Khan A; Verrotti A; Umair M; Galloni GB; Balagura G; Nobile G; Mancardi MM; Giacomini T; Scudieri P; Uva P; van Slegtenhorst M; Iacomino M; Madia F; de Man SA; Telegrafi A; Pavinato L; Wessels MW; Krygier M; MacLennan SC; et alii...

Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases. in Cell reports / Cell Rep. 2022 Mar 15;38(11):110517. doi: 10.1016/j.celrep.2022.110517.

2022
ASL Città di Torino
AOU Città della Salute di Torino

Pavinato L; Platzer K; Keller R; Rosenhahn E; Strehlow V; Trajkova S; Delanne J; Sukarova-Angelovska E; Leiz S; Mau-Them FT; Brugger M; Roser T; Courtin T; Perrin L; Keren B; Agrawal PB; Madden JA; Brownstein CA; Chatron N; Sabatier I; Lesca G; Barakat TS; van Dooren MF; Wilke M; van Slegtenhorst M; Vetro A; England E; Murali CN; Fehr S; et alii...

Expanding the clinical phenotype of the ultra-rare Skraban-Deardorff syndrome: Two novel individuals with WDR26 loss-of-function variants and a literature review. in American journal of medical genetics. Part A / Am J Med Genet A. 2021 Jun;185(6):1712-1720. doi: 10.1002/ajmg.a.62157. Epub 2021 Mar 6.

2021
ASL Città di Torino
AOU Città della Salute di Torino

Brusco A; Keller R; Buxbaum J; Ferrero GB; De Rubeis S; Tartaglia M; Petlichkovski A; Pippucci T; Dimartino P; Radio FC; Bruselles A; Giorgio E; Grosso E; Trajkova S; Pavinato L;