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NEK1 variants confer susceptibility to amyotrophic lateral sclerosisDevelopment of a Smartphone App for a Genetics Website: The Amyotrophic Lateral Sclerosis Online Genetics Database (ALSoD).A comprehensive analysis of rare genetic variation in amyotrophic lateral sclerosis in the UKThe ALSFRS as an outcome measure in therapeutic trials and its relationship to symptom onsetRare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis.Neuroendocrine Merkel cell carcinoma is associated with mutations in key DNA repair, epigenetic and apoptosis pathways: a case-based study using targeted massively parallel sequencingPlasma REST: a novel candidate biomarker of Alzheimer's disease is modified by psychological intervention in an at-risk populationRegionality of disease progression predicts prognosis in amyotrophic lateral sclerosis.Investigation of next-generation sequencing technologies as a diagnostic tool for amyotrophic lateral sclerosis.C9orf72 expansion differentially affects males with spinal onset amyotrophic lateral sclerosis.Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.Meta-analysis of pharmacogenetic interactions in amyotrophic lateral sclerosis clinical trials.Stratified gene expression analysis identifies major amyotrophic lateral sclerosis genes.Intermediate length C9orf72 expansion in an ALS patient without classical C9orf72 neuropathology.Elongator subunit 3 (ELP3) modifies ALS through tRNA modification.Stage at which riluzole treatment prolongs survival in patients with amyotrophic lateral sclerosis: a retrospective analysis of data from a dose-ranging study.Younger age of onset in familial amyotrophic lateral sclerosis is a result of pathogenic gene variants, rather than ascertainment biasJoint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseasesDNAscan: personal computer compatible NGS analysis, annotation and visualisationGenome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsyStage of prolonged survival in ALS - Author's replyTelomere length is greater in ALS than in controls: a whole genome sequencing study
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P50
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Ashley R. Jones
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Ashley R. Jones
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Ashley R. Jones
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