Nailah Siddique

FUS‐immunoreactive inclusions are a common feature in sporadic and non‐SOD1 familial amyotrophic lateral sclerosis

Han‐Xiang Deng, Hong Zhai, Eileen H. Bigio et al. · Annals of Neurology · 2010 · 346 citations · Full text

Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4

Han‐Xiang Deng, Christopher J. Klein, Jianhua Yan et al. · Nature Genetics · 2009 · 271 citations · Full text

Rare Diseases, Allelic Disorders, Medicine +5

Identification of TMEM230 mutations in familial Parkinson's disease

Han‐Xiang Deng, Yi Yang, Kreshnik Ahmeti et al. · Nature Genetics · 2016 · 171 citations · Full text

Neurodegenerative Diseases, Genetic Disorder, Medicine +5

Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy

Senda Ajroud‐Driss, Faisal Fecto, Kaouther Ajroud et al. · Neurogenetics · 2014 · 126 citations · Full text

Mitochondrial Myopathy, Mendelian Disorder, Mitochondrial Function +6

Marked accumulation of 27-hydroxycholesterol in SPG5 patients with hereditary spastic paresis

Rebecca Schüle, Teepu Siddique, Han‐Xiang Deng et al. · Journal of Lipid Research · 2009 · 114 citations · Full text