Browsing by Author Smith, Bradley

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Showing results 1 to 6 of 6
Issue DateTitleAuthor(s)Citation
2008Association study on glutathione S-transferase omega 1 and 2 and familial ALS.Gopinath, Sumana; Nicholson, Garth; Ammar, Al Chalabi; Andersen, Peter; Fogh, Isabella; Hu, Xun; Powell, John; Shaw, C.E.; Smith, Bradley; van de Giessen, Elsmarieke; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteAssociation study on glutathione S-transferase omega 1 and 2 and familial ALS., Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, vol.9, 2, 2008,pp 81-84
2016CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementiaCole, Nicholas; Nicholson, Garth; Williams, Kelly; et al, Various; Farrawell, Natalie E.; Fifita, Jennifer A.; Hu, Xun; Smith, Bradley; Topp, Simon; Vance, Caroline; Warraich, Sadaf T.; Yang, Shu; Zhang, Katharine Y; School of Medical Sciences: Anatomy & Histology; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteCCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia, Nature Communications, vol.7, N/A, 2016,pp 1-8
2016CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementiaCole, Nicholas; Nicholson, Garth; Williams, Kelly; et al, Various; Farrawell, Natalie E.; Fifita, Jennifer A.; Hu, Xun; Smith, Bradley; Topp, Simon; Vance, Caroline; Warraich, Sadaf T.; Yang, Shu; Zhang, Katharine Y; School of Medical Sciences: Anatomy & Histology; Concord Clinical School: ANZAC Research Institute; Concord Clinical School: ANZAC Research InstituteCCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia, Nature Communications, vol.7, N/A, 2016,pp 1-8
2014Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALSNicholson, Garth; et al, Various; Fallini, Claudia; Gkazi, Athina Soragia; Keagle, Pamela; Kenna, Kevin; Kost, Jason; Miller, Jack; Scotter, Emma; Smith, Bradley; Ticozzi, Nicola; Topp, Simon; Concord Clinical School: ANZAC Research InstituteExome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS, Neuron, vol.84, 2, 2014,pp 324-331
2009Mutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6Blair, Ian; Nicholson, Garth; De Vos, Kurt; et al, various; Hortobagyi, Tibor; Hu, Xun; Nishimura, Agnes; Rogelj, Boris; Ruddy, Deborah; Smith, Bradley; Sreedharan, Jameen; Vance, Caroline; Wright, Paul; Concord Clinical School: Medicine; Concord Clinical School: ANZAC Research InstituteMutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6, Science, vol.323, 5918,pp 1208-1211
2017Non-nuclear Pool of Splicing Factor SFPQ Regulates Axonal Transcripts Required for Normal Motor DevelopmentNicholson, Garth; Blanc, Eric; et al, Various; Fielding, Triona; Gordon, Patricia; Smith, Bradley; Snowden, Victoria; Taylor, Richard; Thomas-Jinu, Swapna; Topp, Simon; Vance, Caroline; Concord Clinical School: ANZAC Research InstituteNon-nuclear Pool of Splicing Factor SFPQ Regulates Axonal Transcripts Required for Normal Motor Development, Neuron, vol.94, 2, 2017,pp 322-336