Related references
Note: Only part of the references are listed.Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variant
Yu-Shuen Tsai et al.
ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY (2020)
Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS
Hiroya Naruse et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2019)
Novel genes associated with amyotrophic lateral sclerosis: diagnostic and clinical implications
Ruth Chia et al.
LANCET NEUROLOGY (2018)
NEK1 genetic variability in a Belgian cohort of ALS and ALS-FTD patients
Hung Phuoc Nguyen et al.
NEUROBIOLOGY OF AGING (2018)
Molecular epidemiological study of familial amyotrophic lateral sclerosis in Japanese population by whole-exome sequencing and identification of novel HNRNPA1 mutation
Hiroya Naruse et al.
NEUROBIOLOGY OF AGING (2018)
Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese
Jacob Gratten et al.
GENOME MEDICINE (2017)
NEK1 mutations in familial amyotrophic lateral sclerosis
David Brenner et al.
BRAIN (2016)
Amyotrophic lateral sclerosis: recent genetic highlights
Matthew A. White et al.
CURRENT OPINION IN NEUROLOGY (2016)
Decoding ALS: from genes to mechanism
J. Paul Taylor et al.
NATURE (2016)
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Kevin P. Kenna et al.
NATURE GENETICS (2016)
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Elizabeth T. Cirulli et al.
SCIENCE (2015)
Dissection of genetic factors associated with amyotrophic lateral sclerosis
Claire S. Leblond et al.
EXPERIMENTAL NEUROLOGY (2014)
State of play in amyotrophic lateral sclerosis genetics
Alan E. Renton et al.
NATURE NEUROSCIENCE (2014)
ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19
Yuji Takahashi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
Investigation of the freely available easy-to-use software 'EZR' for medical statistics
Y. Kanda
BONE MARROW TRANSPLANTATION (2013)
C9ORF72 Repeat Expansion in Amyotrophic Lateral Sclerosis in the Kii Peninsula of Japan
Hiroyuki Ishiura et al.
ARCHIVES OF NEUROLOGY (2012)
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
Alan E. Renton et al.
NEURON (2011)
Development of a high-throughput microarray-based resequencing system for neurological disorders and its application to molecular genetics of amyotrophic lateral sclerosis
Yuji Takahashi et al.
ARCHIVES OF NEUROLOGY (2008)
El Escorial revisited: Revised criteria for the diagnosis of amyotrophic lateral sclerosis
BR Brooks et al.
AMYOTROPHIC LATERAL SCLEROSIS AND OTHER MOTOR NEURON DISORDERS (2000)