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Collezione AOU Città della Salute di Torino

Items : 9

Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration. in Nature communications / Nat Commun. 2024 Jul 2;15(1):5560. doi: 10.1038/s41467-024-49938-y.

2024
AOU Città della Salute di Torino

Fogh I; Shatunov A; Mehta PR; Mayl K; Abel O; Topp SD; Iacoangeli A; Opie-Martin S; Bowles H; Limbachiya N; Spargo TP; Al-Khleifat A; Williams KL; Jockel-Balsarotti J; Bali T; Self W; Henden L; Nicholson GA; Ticozzi N; McKenna-Yasek D; Tang L; Shaw PJ; Chio A; Ludolph A; Weishaupt JH; Landers JE; Glass JD; Mora JS; Robberecht W; et alii...

The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration. in Nature communications / Nat Commun. 2022 Nov 12;13(1):6901. doi: 10.1038/s41467-022-34620-y.

2022
AOU Città della Salute di Torino

Opie-Martin S; Iacoangeli A; Topp SD; Abel O; Mayl K; Mehta PR; Shatunov A; Fogh I; Bowles H; Limbachiya N; Spargo TP; Al-Khleifat A; Williams KL; Jockel-Balsarotti J; Bali T; Self W; Henden L; Nicholson GA; Ticozzi N; McKenna-Yasek D; Tang L; Shaw PJ; Chio A; Ludolph A; Weishaupt JH; Landers JE; Glass JD; Mora JS; Robberecht W; et alii...

Author Correction: Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. in Nature genetics / Nat Genet. 2022 Mar;54(3):361. doi: 10.1038/s41588-022-01020-3.

2022
AOU Città della Salute di Torino
AOU Novara
ASL Torino 4
ASL Asti
ASL Biella
ASL Vercelli

Silani V; Weber M; Rouleau GA; Pinto S; de Carvalho M; Petri S; Wallace L; Henders AK; Curtis CJ; Breen G; Sachdev PS; Mather KA; Williams KL; Steyn FJ; Rowe DB; Pamphlett R; Nicholson GA; Ngo ST; Needham M; McCombe PA; Mathers S; Furlong S; Henderson RD; Benyamin B; Kiernan MC; Blair IP; Povedano M; Stevi? Z; Drory V; et alii...

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis. in NPJ genomic medicine / NPJ Genom Med. 2022 Jan 28;7(1):8. doi: 10.1038/s41525-021-00267-9.

2022
AOU Città della Salute di Torino

Al Khleifat A; Iacoangeli A; van Vugt JJFA; Bowles H; Moisse M; Zwamborn RAJ; van der Spek RAA; Shatunov A; Cooper-Knock J; Topp S; Byrne R; Gellera C; López V; Jones AR; Opie-Martin S; Vural A; Campos Y; van Rheenen W; Kenna B; Van Eijk KR; Kenna K; Weber M; Smith B; Fogh I; Silani V; Morrison KE; Dobson R; van Es MA; McLaughlin RL; et alii...

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data. in Frontiers in cellular neuroscience / Front Cell Neurosci. 2022 Dec 15;16:1050596. doi: 10.3389/fncel.2022.1050596. eCollection 2022.

2022
AOU Città della Salute di Torino

Landers JE; Glass JD; Shaw PJ; Mora JS; Panades MP; Gotkine M; de Carvalho M; Corcia P; Chio A; Vourc'h P; McLaughlin RL; van Es MA; Dobson R; Morrison KE; Silani V; Fogh I; Smith B; Weber M; Campos Y; Vural A; Opie-Martin S; López V; Byrne R; Kenna K; Van Eijk KR; Kenna B; van Rheenen W; Topp S; Cooper-Knock J; et alii...

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis. in JAMA neurology / JAMA Neurol. 2021 Oct 1;78(10):1236-1248. doi: 10.1001/jamaneurol.2021.2598.

2021
AOU Città della Salute di Torino
AOU Novara

Tremolizzo L; Trojsi F; Torriello A; Tranquilli S; Tedeschi G; Ticca A; Tanel R; Simonini C; Spataro R; Simone I; Sbaiz L; Sideri R; Santarelli M; Salivetto M; Salvi F; Sabatelli M; Salamone P; Riolo G; Riva N; Russo M; Ricci C; Pugliatti M; Quattrini A; Pozzi S; Petrelli C; Petrucci A; Passaniti C; Origone P; Murru MR; et alii...

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. in Nature genetics / Nat Genet. 2021 Dec;53(12):1636-1648. doi: 10.1038/s41588-021-00973-1. Epub 2021 Dec 6.

2021
AOU Città della Salute di Torino
AOU Novara
ASL Torino 4
ASL Asti
ASL Biella
ASL Vercelli

Sachdev PS; Mather KA; Williams KL; Steyn FJ; Rowe DB; Pamphlett R; Nicholson GA; Ngo ST; Needham M; McCombe PA; Mathers S; Furlong S; Henderson RD; Benyamin B; Kiernan MC; Blair IP; Povedano M; Stevi? Z; Drory V; Glava? D; Ravnik-Glava? M; Zidar J; Koritnik B; Rogelj B; Ataulina A; Demeshonok V; Fominykh V; Brylev L; Hübner CA; et alii...

Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. in Nature genetics / Nat Genet. 2016 Sep;48(9):1043-8. doi: 10.1038/ng.3622. Epub 2016 Jul 25.

2016
AOU Città della Salute di Torino
AOU Novara

Casale F; Leigh PN; Hübner CA; Kurth I; Stubendorff B; Prell T; Ringer T; Witte OW; Grosskreutz J; Kiernan MC; Pamphlett R; Rowe DB; Nicholson GA; Fifita JA; McCann EP; Zhang K; Stuit RJ; Blair I; Muller B; Filosto M; Padovani A; Riva N; Penco S; Lunetta C; Zecca C; Capozzo R; Brunetti M; Arcuti S; Moglia C; et alii...

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis. in JAMA neurology / JAMA Neurol. 2016 Jul 1;73(7):812-20. doi: 10.1001/jamaneurol.2016.1114.

2016
AOU Città della Salute di Torino
AOU Novara

Shaw CE; van den Berg LH; Lewis CM; Hardiman O; Landers JE; Brown RH; Robberecht W; Van Damme P; D'Alfonso S; Traynor BJ; Mazzini L; Ticozzi N; Comi GP; Andersen PM; Leigh PN; Shaw PJ; Morrison KE; Melki J; Meininger V; van Rheenen W; Topp S; Smith BN; Dobson R; Glass JD; Newhouse S; Castellotti B; Cereda C; Del Bo R; Stahl D; et alii...