Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Acta Neuropathologica Communications|July 19, 2019
C9orf72 intermediate expansions of 24-30 repeats are associated with ALSAlfredo Iacoangeli, Ahmad Al Khleifat, Ashley R Jones, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 2, 2018
Younger age of onset in familial amyotrophic lateral sclerosis is a result of pathogenic gene variants, rather than ascertainment biasPuja R Mehta, Ashley R Jones, Sarah Opie-Martin, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|April 2, 2019
Telomere length is greater in ALS than in controls: a whole genome sequencing studyAhmad Al Khleifat, Alfredo Iacoangeli, Aleksey Shatunov, et al.
Brain : a Journal of Neurology|April 22, 2017
A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UKSarah Morgan, Aleksey Shatunov, William Sproviero, et al.
Neurobiology of Aging|March 25, 2015
Stratified gene expression analysis identifies major amyotrophic lateral sclerosis genesAshley R Jones, Claire Troakes, Andrew King, et al.
Neurobiology of Disease|August 24, 2013
Genetic ablation of phospholipase C delta 1 increases survival in SOD1(G93A) miceKim A Staats, Lawrence Van Helleputte, Ashley R Jones, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|September 2, 2016
Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosisBenjamin Gaastra, Aleksey Shatunov, Sara Pulit, et al.
Neurobiology of Aging|April 17, 2013
Residual association at C9orf72 suggests an alternative amyotrophic lateral sclerosis-causing hexanucleotide repeatAshley R Jones, Ione Woollacott, Aleksey Shatunov, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 7, 2019
Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsyZhongbo Chen, Jason A Chen, Aleksey Shatunov, et al.
Molecular Neurodegeneration|August 10, 2018
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseasesJason A Chen, Zhongbo Chen, Hyejung Won, et al.
Pageof 4