Faisal Fecto
Stanford University(US)
Publications by Year
Research Areas
Amyotrophic Lateral Sclerosis Research, Parkinson's Disease Mechanisms and Treatments, Ubiquitin and proteasome pathways, Neurogenetic and Muscular Disorders Research, Neurological diseases and metabolism
Most-Cited Works
- → Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia(2011)1,161 cited
- → <emph type="ital">SQSTM1</emph> Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis(2011)637 cited
- → FUS‐immunoreactive inclusions are a common feature in sporadic and non‐SOD1 familial amyotrophic lateral sclerosis(2010)349 cited
- → Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4(2009)271 cited
- → Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia(2010)208 cited
- → Identification of TMEM230 mutations in familial Parkinson's disease(2016)174 cited
- → Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy(2014)126 cited
- → TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies(2011)88 cited
- → Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2(2014)77 cited
- → α7-Acetylcholine receptor antibodies in two patients with Rasmussen encephalitis(2005)72 cited