Sfoglia per AUTORE
HARDY J
Collezione AOU Città della Salute di Torino

  

Items : 13

Genome sequence analyses identify novel risk loci for multiple system atrophy. in Neuron / Neuron. 2024 Jul 3;112(13):2142-2156.e5. doi: 10.1016/j.neuron.2024.04.002. Epub 2024 May 2.
2024
AOU Città della Salute di Torino

Chia R; Ray A; Shah Z; Ding J; Ruffo P; Fujita M; Menon V; Saez-Atienzar S; Reho P; Kaivola K; Walton RL; Reynolds RH; Karra R; Sait S; Akcimen F; Diez-Fairen M; Alvarez I; Fanciulli A; Stefanova N; Seppi K; Duerr S; Leys F; Krismer F; Sidoroff V; Zimprich A; Pirker W; Rascol O; Foubert-Samier A; Meissner WG; et alii...

The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases. in Neurobiology of disease / Neurobiol Dis. 2023 May;180:106082. doi: 10.1016/j.nbd.2023.106082. Epub 2023 Mar 15.
2023
AOU Città della Salute di Torino

Houlden H; Owen MJ; Turner MR; Hardy JA; Silani V; Powell JF; Shaw CE; van den Berg LH; Veldink JH; Shaw PJ; Morrison KE; Corcia P; Chiò A; Robberecht W; Jones AR; Fogh I; Shatunov A; Gustavsson EK; Gagliano Taliun SA; van Rheenen W; Lin K; Pardiñas AF; Reynolds RH; Chen Z; Ryten M; Al-Chalabi A;

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...

New insights into the genetic etiology of Alzheimer's disease and related dementias. in Nature genetics / Nat Genet. 2022 Apr;54(4):412-436. doi: 10.1038/s41588-022-01024-z. Epub 2022 Apr 4.
2022
AOU Città della Salute di Torino

Bellenguez C; Küçükali F; Jansen IE; Kleineidam L; Moreno-Grau S; Amin N; Naj AC; Campos-Martin R; Grenier-Boley B; Andrade V; Holmans PA; Boland A; Damotte V; van der Lee SJ; Costa MR; Kuulasmaa T; Yang Q; de Rojas I; Bis JC; Yaqub A; Prokic I; Chapuis J; Ahmad S; Giedraitis V; Aarsland D; Garcia-Gonzalez P; Abdelnour C; Alarcón-Martín E; Alcolea D; 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...

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. in Nature genetics / Nat Genet. 2021 Mar;53(3):294-303. doi: 10.1038/s41588-021-00785-3. Epub 2021 Feb 15.
2021
AOU Città della Salute di Torino

Morenas-Rodriguez E; Kukull WA; Faber K; Pickering-Brown S; Albani D; Ferrari R; Morris HR; Scherzer CR; Bennett DA; Goate A; Renton AE; Kuzma A; Leverenz JB; Besser LM; Bekris LM; Pastor P; Woltjer R; Kaiser SM; Klein G; Aarsland D; Hodges AK; Al-Sarraj S; Troakes C; Love S; Palmer L; Morris CM; Attems J; Thomas AJ; McKeith IG; et alii...

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis. in Neuron / Neuron. 2021 Feb 3;109(3):448-460.e4. doi: 10.1016/j.neuron.2020.11.005. Epub 2020 Nov 26.
2021
AOU Città della Salute di Torino

Landers JE; Ferrari R; Morris HR; Vonsattel JP; Harms MB; Van Deerlin V; Hardy JA; Kowal N; Brady CB; Pickering-Brown S; Resnick SM; Ferrucci L; Tanaka T; Torkamani A; Ryten M; Ross OA; Singleton AB; Silani V; Glass JD; Viollet C; Jabbari E; Ghidoni R; Binetti G; Benussi L; Nilsson CF; Rowe JB; Johansson PM; Waldo ML; Tagliavini F; et alii...

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...

Complexity of the Genetics and Clinical Presentation of Spinocerebellar Ataxia 17. in Frontiers in cellular neuroscience / Front Cell Neurosci. 2018 Nov 23;12:429. doi: 10.3389/fncel.2018.00429. eCollection 2018.
2018
AOU Città della Salute di Torino

Polke JM; Hardy J; Wood NW; Bhatia KP; Lunn MP; Kennedy A; Limousin P; Rosser E; Houlden H; Cervera C; Labrum R; Sweeney MG; Pemble S; Abeti R; Zeitlberger A; Ging H; Lim WN; Nethisinghe S; Veneziano L; Brusco A; Davis MB; Giunti P; Nethisinghe S; Lim WN; Ging H; Zeitlberger A; Abeti R; Pemble S; Sweeney MG; et alii...

Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia. in Journal of Alzheimer's disease : JAD / J Alzheimers Dis. 2017;56(4):1271-1278. doi: 10.3233/JAD-160949.
2017
AOU Città della Salute di Torino

Ferrari R; Grassi M; Graziano F; Palluzzi F; Archetti S; Bonomi E; Bruni AC; Maletta RG; Bernardi L; Cupidi C; Colao R; Rainero I; Rubino E; Pinessi L; Galimberti D; Scarpini E; Serpente M; Nacmias B; Piaceri I; Bagnoli S; Rossi G; Giaccone G; Tagliavini F; Benussi L; Binetti G; Ghidoni R; Singleton A; Hardy J; Momeni P; 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...

A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia. in Neurobiology of aging / Neurobiol Aging. 2015 Oct;36(10):2904.e13-26. doi: 10.1016/j.neurobiolaging.2015.06.005. Epub 2015 J
2015
AOU Città della Salute di Torino

Ferrari R; Grassi M; Salvi E; Borroni B; Palluzzi F; Pepe D; D'Avila F; Padovani A; Archetti S; Rainero I; Rubino E; Pinessi L; Benussi L; Binetti G; Ghidoni R; Galimberti D; Scarpini E; Serpente M; Rossi G; Giaccone G; Tagliavini F; Nacmias B; Piaceri I; Bagnoli S; Bruni AC; Maletta RG; Bernardi L; Postiglione A; Milan G; et alii...

Frontotemporal dementia and its subtypes: a genome-wide association study. in The Lancet. Neurology / Lancet Neurol. 2014 Jul;13(7):686-99. doi: 10.1016/S1474-4422(14)70065-1.
2014
AOU Città della Salute di Torino

Ferrari R; Hernandez DG; Nalls MA; Rohrer JD; Ramasamy A; Kwok JB; Dobson-Stone C; Brooks WS; Schofield PR; Halliday GM; Hodges JR; Piguet O; Bartley L; Thompson E; Haan E; Hernández I; Ruiz A; Boada M; Borroni B; Padovani A; Cruchaga C; Cairns NJ; Benussi L; Binetti G; Ghidoni R; Forloni G; Galimberti D; Fenoglio C; Serpente M; et alii...