Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia HX Deng, W Chen, ST Hong, KM Boycott, GH Gorrie, N Siddique, Y Yang, ... Nature 477 (7363), 211-215, 2011 | 1377 | 2011 |
SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis F Fecto, J Yan, SP Vemula, E Liu, Y Yang, W Chen, JG Zheng, Y Shi, ... Archives of neurology 68 (11), 1440-1446, 2011 | 765 | 2011 |
FUS‐immunoreactive inclusions are a common feature in sporadic and non‐SOD1 familial amyotrophic lateral sclerosis HX Deng, H Zhai, EH Bigio, J Yan, F Fecto, K Ajroud, M Mishra, ... Annals of neurology 67 (6), 739-748, 2010 | 432 | 2010 |
Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4 HX Deng, CJ Klein, J Yan, Y Shi, Y Wu, F Fecto, HJ Yau, Y Yang, H Zhai, ... Nature genetics 42 (2), 165-169, 2010 | 290 | 2010 |
Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia J Yan, HX Deng, N Siddique, F Fecto, W Chen, Y Yang, E Liu, ... Neurology 75 (9), 807-814, 2010 | 237 | 2010 |
Identification of TMEM230 mutations in familial Parkinson's disease HX Deng, Y Shi, Y Yang, KB Ahmeti, N Miller, C Huang, L Cheng, H Zhai, ... Nature genetics 48 (7), 733-739, 2016 | 194 | 2016 |
Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy S Ajroud-Driss, F Fecto, K Ajroud, I Lalani, SE Calvo, VK Mootha, ... Neurogenetics 16, 1-9, 2015 | 108 | 2015 |
Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia F Fecto, T Siddique Journal of Molecular Neuroscience 45, 663-675, 2011 | 89 | 2011 |
TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies CJ Klein, Y Shi, F Fecto, M Donaghy, G Nicholson, ME McEntagart, ... Neurology 76 (10), 887-894, 2011 | 85 | 2011 |
Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2 GH Gorrie, F Fecto, D Radzicki, C Weiss, Y Shi, H Dong, H Zhai, R Fu, ... Proceedings of the National Academy of Sciences 111 (40), 14524-14529, 2014 | 79 | 2014 |
Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations HX Deng, EH Bigio, H Zhai, F Fecto, K Ajroud, Y Shi, J Yan, M Mishra, ... Archives of neurology 68 (8), 1057-1061, 2011 | 79 | 2011 |
α7-acetylcholine receptor antibodies in two patients with Rasmussen encephalitis R Watson, JEC Jepson, I Bermudez, S Alexander, Y Hart, K McKnight, ... Neurology 65 (11), 1802-1804, 2005 | 79 | 2005 |
UBQLN2/P62 cellular recycling pathways in amyotrophic lateral sclerosis and frontotemporal dementia F Fecto, T Siddique Muscle & nerve 45 (2), 157-162, 2012 | 61 | 2012 |
Mutant TRPV4-mediated toxicity is linked to increased constitutive function in axonal neuropathies F Fecto, Y Shi, R Huda, M Martina, T Siddique, HX Deng Journal of Biological Chemistry 286 (19), 17281-17291, 2011 | 56 | 2011 |
Protein recycling pathways in neurodegenerative diseases F Fecto, YT Esengul, T Siddique Alzheimer's research & therapy 6, 1-9, 2014 | 30 | 2014 |
Signaling mechanisms mediated by G-protein coupled receptors in human platelets SA Saeed, H Rasheed, FAW Fecto, MI Achakzai, R Ali, JD Connor, ... Acta Pharmacologica Sinica 25, 887-892, 2004 | 20 | 2004 |
A novel de novo MFN2 mutation causing CMT2A with upper motor neuron signs S Ajroud-Driss, F Fecto, K Ajroud, Y Yang, S Donkervoort, N Siddique, ... Neurogenetics 10, 359-361, 2009 | 17 | 2009 |
An unusual case of familial ALS and cerebellar ataxia S Yasser, F Fecto, T Siddique, KA Sheikh, P Athar Amyotrophic Lateral Sclerosis 11 (6), 568-570, 2010 | 16 | 2010 |
SIGMAR1 mutations, genetic heterogeneity at the chromosome 9p locus, and the expanding etiological diversity of amyotrophic lateral sclerosis. F Fecto, T Siddique Annals of neurology 70 (6), 867-870, 2011 | 9 | 2011 |
Patterns of tuberculosis in the central nervous system S Raza, A Sadaf, F Fecto, RP Ali, ME Bari, A Enam Infectious Diseases Journal of Pakistan, 99, 2004 | 8 | 2004 |