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Author/Creator Traynor, Bryan J.

2. A genome-wide association study in multiple system atrophy. (11th October 2016)

Authors:
Sailer, Anna; Scholz, Sonja W.; Nalls, Michael A.; Schulte, Claudia; Federoff, Monica; Price, T. Ryan; Lees, Andrew; Ross, Owen A.; Dickson, Dennis W.; Mok, Kin; Mencacci, Niccolo E.; Schottlaender, Lucia; Chelban, Viorica; Ling, Helen; O'Sullivan, Sean S.; Wood, Nicholas W.; Traynor, Bryan J.; F...
Journal:
Neurology
Issue:
Volume 87:Number 15(2016)
Page Start:
Record Type:
Journal Article
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4. Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+). (February 2018)

Authors:
Mäkelä, Mira; Kaivola, Karri; Valori, Miko; Paetau, Anders; Polvikoski, Tuomo; Singleton, Andrew B.; Traynor, Bryan J.; Stone, David J.; Peuralinna, Terhi; Tienari, Pentti J.; Tanskanen, Maarit; Myllykangas, Liisa
Journal:
Neurology
Issue:
Volume 4:Number 1(2018)
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Record Type:
Journal Article
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5. C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: A genome‐wide meta‐analysis. Issue 1 (27th June 2014)

Authors:
Diekstra, Frank P.; Van Deerlin, Vivianna M.; van Swieten, John C.; Al‐Chalabi, Ammar; Ludolph, Albert C.; Weishaupt, Jochen H.; Hardiman, Orla; Landers, John E.; Brown, Robert H.; van Es, Michael A.; Pasterkamp, R. Jeroen; Koppers, Max; Andersen, Peter M.; Estrada, Karol; Rivadeneira, Fernando; ...
Journal:
Annals of neurology
Issue:
Volume 76:Issue 1(2014:Jul.)
Page Start:
120
Record Type:
Journal Article
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6. C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten. (1st February 2017)

Authors:
Stopford, Matthew J.; Higginbottom, Adrian; Hautbergue, Guillaume M.; Cooper-Knock, Johnathan; Mulcahy, Padraig J.; De Vos, Kurt J.; Renton, Alan E.; Pliner, Hannah; Calvo, Andrea; Chio, Adriano; Traynor, Bryan J.; Azzouz, Mimoun; Heath, Paul R.; Kirby, Janine; Shaw, Pamela J.
Journal:
Human molecular genetics
Issue:
Volume 26:Number 6(2017:Mar. 15)
Page Start:
1133
Record Type:
Journal Article
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7. CAG Somatic Instability in a Huntington Disease Expansion Carrier Presenting with a Progressive Supranuclear Palsy‐like Phenotype. Issue 7 (5th May 2022)

Authors:
Dewan, Ramita; Jaunmuktane, Zane; Garcia‐Segura, Monica Emili; Strand, Catherine; Wild, Edward; Villar, Joaquin; Dalgard, Clifton L.; Tabrizi, Sarah J.; Traynor, Bryan J.; Proukakis, Christos
Journal:
Movement disorders
Issue:
Volume 37:Issue 7(2022)
Page Start:
1555
Record Type:
Journal Article
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8. Clinical and Metabolic Signature of UNC13A rs12608932 Variant in Amyotrophic Lateral Sclerosis. (26th December 2022)

Authors:
Calvo, Andrea; Canosa, Antonio; Moglia, Cristina; Manera, Umberto; Grassano, Maurizio; Vasta, Rosario; Palumbo, Francesca; Cugnasco, Paolo; Gallone, Salvatore; Brunetti, Maura; De Marchi, Fabiola; Arena, Vincenzo; Pagani, Marco; Dalgard, Clifton; Scholz, Sonja W.; Chia, Ruth; Corrado, Lucia; Dalf...
Journal:
Neurology
Issue:
Volume 8:Number 6(2022)
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Record Type:
Journal Article
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9. Common polymorphisms of chemokine (C‐X3‐C motif) receptor 1 gene modify amyotrophic lateral sclerosis outcome: A population‐based study. Issue 2 (25th April 2017)

Authors:
Calvo, Andrea; Moglia, Cristina; Canosa, Antonio; Cammarosano, Stefania; Ilardi, Antonio; Bertuzzo, Davide; Traynor, Bryan J.; Brunetti, Maura; Barberis, Marco; Mora, Gabriele; Casale, Federico; Chiò, Adriano
Journal:
Muscle & nerve
Issue:
Volume 57:Issue 2(2018)
Page Start:
212
Record Type:
Journal Article
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