Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population

Controversies and priorities in amyotrophic lateral sclerosis

(2013) Martin R Turner et al.   LANCET NEUROLOGY

Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis

(2013) Min Deng et al.   NATURE GENETICS

Current pathways for epidemiological research in amyotrophic lateral sclerosis

(2013) Pam Factor-Litvak et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1

(2012)   NEUROBIOLOGY OF AGING

UNC13A influences survival in Italian amyotrophic lateral sclerosis patients: a population-based study

(2012) Adriano Chiò et al.   NEUROBIOLOGY OF AGING

Genetic counseling for FTD/ALS caused by the C9ORF72 hexanucleotide expansion

(2012) Jamie C Fong et al.   Alzheimers Research & Therapy

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

(2011) Ilse Gijselinck et al.   LANCET NEUROLOGY

Replication analysis of SNPs on 9p21.2 and 19p13.3 with amyotrophic lateral sclerosis in East Asians

(2011) Aritoshi Iida et al.   NEUROBIOLOGY OF AGING

UNC13A is a modifier of survival in amyotrophic lateral sclerosis

(2011) Frank P. Diekstra et al.   NEUROBIOLOGY OF AGING

Clinical feature and DYT1 mutation screening in primary dystonia patients from South-West China

(2010) S.-S. Zhang et al.   EUROPEAN JOURNAL OF NEUROLOGY

Pharmacogenetic association of hypertension candidate genes with fasting glucose in the GenHAT Study

(2010) Marguerite R Irvin et al.   JOURNAL OF HYPERTENSION

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

(2010) Hannu Laaksovirta et al.   LANCET NEUROLOGY

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

(2010) Aleksey Shatunov et al.   LANCET NEUROLOGY

Energy metabolism in amyotrophic lateral sclerosis

(2010) Luc Dupuis et al.   LANCET NEUROLOGY

Clinical and genetic features of patients with sporadic amyotrophic lateral sclerosis in south-west China

(2009) Deng-Fu Fang et al.   Amyotrophic Lateral Sclerosis

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

(2009) Michael A van Es et al.   NATURE GENETICS

New application of intelligent agents in sporadic Amyotrophic Lateral Sclerosis identifies unexpected specific genetic background

(2008) Silvana Penco et al.   BMC BIOINFORMATICS

Diagnostic criteria for amyotrophic lateral sclerosis (ALS)

(2008) Anders Fuglsang-Frederiksen   CLINICAL NEUROPHYSIOLOGY

Vesicle Priming and Recruitment by ubMunc13-2 Are Differentially Regulated by Calcium and Calmodulin

(2008) D. Zikich et al.   JOURNAL OF NEUROSCIENCE

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

(2008) Vivianna M Van Deerlin et al.   LANCET NEUROLOGY

Genetics of familial amyotrophic lateral sclerosis

(2008) P. N. Valdmanis et al.   NEUROLOGY

Prevalence of SOD1 mutations in the Italian ALS population

(2008) A. Chio et al.   NEUROLOGY