Faisal Fecto, MD, PhD - Publications

Affiliations: 
2000-2006 Biological and Biomedical Sciences Aga Khan University 
 2006-2015 Neurology Northwestern University, Evanston, IL 
 2015-2019 Neurology University of Iowa Hospitals & Clinics, Iowa City, IA, United States 
 2019- Neurology Stanford University, Palo Alto, CA 
Area:
Genetics, Neurodegeneration, ALS, Dementia, Molecular and Cellular Neuroscience, Neuroimaging, Systems Neuroscience, Neurobiology of Disease
Website:
https://profiles.stanford.edu/faisal-fecto

24 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, ... ... Fecto F, et al. Identification of TMEM230 mutations in familial Parkinson's disease. Nature Genetics. PMID 27270108 DOI: 10.1038/Ng.3589  0.713
2015 Ajroud-Driss S, Fecto F, Ajroud K, Lalani I, Calvo SE, Mootha VK, Deng HX, Siddique N, Tahmoush AJ, Heiman-Patterson TD, Siddique T. Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy. Neurogenetics. 16: 1-9. PMID 25193783 DOI: 10.1007/S10048-014-0421-1  0.78
2014 Gorrie GH, Fecto F, Radzicki D, Weiss C, Shi Y, Dong H, Zhai H, Fu R, Liu E, Li S, Arrat H, Bigio EH, Disterhoft JF, Martina M, Mugnaini E, et al. Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2. Proceedings of the National Academy of Sciences of the United States of America. 111: 14524-9. PMID 25246588 DOI: 10.1073/Pnas.1405741111  0.766
2014 Fecto F, Esengul YT, Siddique T. Protein recycling pathways in neurodegenerative diseases. Alzheimer's Research & Therapy. 6: 13. PMID 25031631 DOI: 10.1186/alzrt243  0.661
2012 Fecto F, Siddique T. UBQLN2/P62 cellular recycling pathways in amyotrophic lateral sclerosis and frontotemporal dementia. Muscle & Nerve. 45: 157-62. PMID 22246868 DOI: 10.1002/mus.23278  0.748
2012 Fecto F, Siddique T. What is repeated in ALS and FTLD. The Lancet. Neurology. 11: 25-7. PMID 22154784 DOI: 10.1016/S1474-4422(11)70275-7  0.707
2012 Fecto F, Deng H, Chen W, Hong S, Boycott K, Gorrie G, Siddique N, Yang Y, Shi Y, Zhai H, Jiang H, Hirano M, Rampersaud E, Jansen G, Donkervoort S, et al. UBQLN2 Mutations in ALS and ALS/Dementia: A Genetic, Functional and Histopathological Analysis (S05.006) Neurology. 78: S05.006-S05.006. DOI: 10.1212/Wnl.78.1_Meetingabstracts.S05.006  0.751
2012 Fecto F, Gorrie G, Zhai H, Radzicki D, Fu R, Liu E, Weiss C, Martina M, Disterhoft J, Mugnaini E, Siddique T, Deng H. Mutant UBQLN2 Transgenic Mice Recapitulate Behavioral, Pathological and Neurophysiological Characteristics of Human Ubiqulinopathy (P05.165) Neurology. 78: P05.165-P05.165. DOI: 10.1212/Wnl.78.1_Meetingabstracts.P05.165  0.695
2012 Fecto F, Esengul YT, Deng H, Siddique T. Autophagy Is Impaired by UBQLN2 Mutations Linked to ALS/FTD (P05.164) Neurology. 78: P05.164-P05.164. DOI: 10.1212/wnl.78.1_meetingabstracts.p05.164  0.704
2012 Ajroud-Driss S, Fecto F, Ajroud K, Siddique T. Mutations in the Nuclear Encoded Novel Mitochondrial Protein CHCHD10 Cause an Autosomal Dominant Mitochondrial Myopathy (IN7-2.002) Neurology. 78: IN7-2.002-IN7-2.002. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In7-2.002  0.781
2011 Fecto F, Siddique T. SIGMAR1 mutations, genetic heterogeneity at the chromosome 9p locus, and the expanding etiological diversity of amyotrophic lateral sclerosis. Annals of Neurology. 70: 867-70. PMID 22190360 DOI: 10.1002/ana.22648  0.701
2011 Fecto F, Yan J, Vemula SP, Liu E, Yang Y, Chen W, Zheng JG, Shi Y, Siddique N, Arrat H, Donkervoort S, Ajroud-Driss S, Sufit RL, Heller SL, Deng HX, et al. SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis. Archives of Neurology. 68: 1440-6. PMID 22084127 DOI: 10.1001/Archneurol.2011.250  0.825
2011 Fecto F, Siddique T. Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia. Journal of Molecular Neuroscience : Mn. 45: 663-75. PMID 21901496 DOI: 10.1007/s12031-011-9637-9  0.743
2011 Deng HX, Chen W, Hong ST, Boycott KM, Gorrie GH, Siddique N, Yang Y, Fecto F, Shi Y, Zhai H, Jiang H, Hirano M, Rampersaud E, Jansen GH, Donkervoort S, et al. Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature. 477: 211-5. PMID 21857683 DOI: 10.1038/Nature10353  0.773
2011 Deng HX, Bigio EH, Zhai H, Fecto F, Ajroud K, Shi Y, Yan J, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T. Differential involvement of optineurin in amyotrophic lateral sclerosis with or without SOD1 mutations. Archives of Neurology. 68: 1057-61. PMID 21825243 DOI: 10.1001/Archneurol.2011.178  0.819
2011 Fecto F, Shi Y, Huda R, Martina M, Siddique T, Deng HX. Mutant TRPV4-mediated toxicity is linked to increased constitutive function in axonal neuropathies. The Journal of Biological Chemistry. 286: 17281-91. PMID 21454511 DOI: 10.1074/Jbc.M111.237685  0.634
2011 Klein CJ, Shi Y, Fecto F, Donaghy M, Nicholson G, McEntagart ME, Crosby AH, Wu Y, Lou H, McEvoy KM, Siddique T, Deng HX, Dyck PJ. TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies. Neurology. 76: 887-94. PMID 21288981 DOI: 10.1212/Wnl.0B013E31820F2De3  0.699
2010 Yan J, Deng HX, Siddique N, Fecto F, Chen W, Yang Y, Liu E, Donkervoort S, Zheng JG, Shi Y, Ahmeti KB, Brooks B, Engel WK, Siddique T. Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia. Neurology. 75: 807-14. PMID 20668259 DOI: 10.1212/Wnl.0B013E3181F07E0C  0.747
2010 Yasser S, Fecto F, Siddique T, Sheikh KA, Athar P. An unusual case of familial ALS and cerebellar ataxia. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 11: 568-70. PMID 20540686 DOI: 10.3109/17482961003636874  0.696
2010 Deng HX, Zhai H, Bigio EH, Yan J, Fecto F, Ajroud K, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T. FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis. Annals of Neurology. 67: 739-48. PMID 20517935 DOI: 10.1002/Ana.22051  0.814
2010 Deng HX, Klein CJ, Yan J, Shi Y, Wu Y, Fecto F, Yau HJ, Yang Y, Zhai H, Siddique N, Hedley-Whyte ET, Delong R, Martina M, Dyck PJ, Siddique T. Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4. Nature Genetics. 42: 165-9. PMID 20037587 DOI: 10.1038/Ng.509  0.697
2010 Fecto F, Deng HX, Siddique T. Discovering the connection between familial and sporadic amyotrophic lateral sclerosis: Pathology trumps genetics Future Neurology. 5: 625-628. DOI: 10.2217/fnl.10.47  0.667
2009 Ajroud-Driss S, Fecto F, Ajroud K, Yang Y, Donkervoort S, Siddique N, Siddique T. A novel de novo MFN2 mutation causing CMT2A with upper motor neuron signs. Neurogenetics. 10: 359-61. PMID 19350291 DOI: 10.1007/S10048-009-0188-Y  0.771
2005 Watson R, Jepson JE, Bermudez I, Alexander S, Hart Y, McKnight K, Roubertie A, Fecto F, Valmier J, Sattelle DB, Beeson D, Vincent A, Lang B. Alpha7-acetylcholine receptor antibodies in two patients with Rasmussen encephalitis. Neurology. 65: 1802-4. PMID 16344526 DOI: 10.1212/01.Wnl.0000191566.86977.04  0.528
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