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Faisal Fecto, MD, PhD

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
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Parents

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Daniel Hoch research assistant 2002-2002 Harvard
Bethan Lang research assistant 2003-2003 Oxford
Angela Vincent research assistant 2003-2003 Oxford
Syed Ather Enam research assistant 2003-2005 Aga Khan University
William Klein research assistant 2006-2006 Northwestern
Teepu Siddique grad student 2006-2012 Northwestern
 (Protein Degradation Pathways in Amyotrophic Lateral Sclerosis and Frontotemporal Lobe Dementia.)
Teepu Siddique post-doc 2012- Northwestern
Peggy C. Nopoulos research scientist 2016- University of Iowa
Manish Saggar research scientist 2020- Stanford
Senda Ajroud-Driss research scientist 2007-2012 Northwestern

Children

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Y. Taylan Esengul research assistant 2010- Northwestern

Collaborators

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John Disterhoft collaborator Northwestern
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Publications

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Deng HX, Shi Y, Yang Y, et al. (2016) Identification of TMEM230 mutations in familial Parkinson's disease. Nature Genetics
Ajroud-Driss S, Fecto F, Ajroud K, et al. (2015) Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy. Neurogenetics. 16: 1-9
Gorrie GH, Fecto F, Radzicki D, et al. (2014) 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
Fecto F, Esengul YT, Siddique T. (2014) Protein recycling pathways in neurodegenerative diseases. Alzheimer's Research & Therapy. 6: 13
Fecto F, Siddique T. (2012) UBQLN2/P62 cellular recycling pathways in amyotrophic lateral sclerosis and frontotemporal dementia. Muscle & Nerve. 45: 157-62
Fecto F, Siddique T. (2012) What is repeated in ALS and FTLD. The Lancet. Neurology. 11: 25-7
Fecto F, Siddique T. (2011) SIGMAR1 mutations, genetic heterogeneity at the chromosome 9p locus, and the expanding etiological diversity of amyotrophic lateral sclerosis. Annals of Neurology. 70: 867-70
Fecto F, Yan J, Vemula SP, et al. (2011) SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis. Archives of Neurology. 68: 1440-6
Fecto F, Siddique T. (2011) Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia. Journal of Molecular Neuroscience : Mn. 45: 663-75
Deng HX, Chen W, Hong ST, et al. (2011) Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. Nature. 477: 211-5
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