Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
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Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyThe genetics and neuropathology of frontotemporal lobar degenerationChromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyExpanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALSA hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDRecent advances in amyotrophic lateral sclerosisToward precision medicine in amyotrophic lateral sclerosisA comprehensive review of amyotrophic lateral sclerosisConverging mechanisms in ALS and FTD: disrupted RNA and protein homeostasisState of play in amyotrophic lateral sclerosis geneticsA high-density genome-wide association screen of sporadic ALS in US veteransPolyQ repeat expansions in ATXN2 associated with ALS are CAA interrupted repeatsAge of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.What causes amyotrophic lateral sclerosis?Global epidemiology of amyotrophic lateral sclerosis: a systematic review of the published literature.The role of copy number variation in susceptibility to amyotrophic lateral sclerosis: genome-wide association study and comparison with published loci.Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor.Copy number variations play important roles in heredity of common diseases: a novel method to calculate heritability of a polymorphism.Chromogranin B P413L variant as risk factor and modifier of disease onset for amyotrophic lateral sclerosis.The Analysis of Two BDNF Polymorphisms G196A/C270T in Chinese Sporadic Amyotrophic Lateral Sclerosis.An estimate of amyotrophic lateral sclerosis heritability using twin data.Association of ALS with head injury, cigarette smoking and APOE genotypesModelling amyotrophic lateral sclerosis: progress and possibilitiesFrontotemporal dementia and its subtypes: a genome-wide association study.Microarray analysis of peripheral blood lymphocytes from ALS patients and the SAFE detection of the KEGG ALS pathway.C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisPolymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosisMapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.A de novo missense mutation of the FUS gene in a "true" sporadic ALS case.Gene ontology analysis of pairwise genetic associations in two genome-wide studies of sporadic ALSBrain expression genome-wide association study (eGWAS) identifies human disease-associated variants.Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohortGenetic modifiers in carriers of repeat expansions in the C9ORF72 gene.Selective pattern of motor system damage in gamma-synuclein transgenic mice mirrors the respective pathology in amyotrophic lateral sclerosis.ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish populationGenetic variability in the regulation of gene expression in ten regions of the human brain.Genetic heterogeneity of amyotrophic lateral sclerosis: implications for clinical practice and research.Role of genomics in cardiovascular medicine.Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family.
P2860
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P2860
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Genome-wide association study ...... amyotrophic lateral sclerosis.
@ast
Genome-wide association study ...... amyotrophic lateral sclerosis.
@en
type
label
Genome-wide association study ...... amyotrophic lateral sclerosis.
@ast
Genome-wide association study ...... amyotrophic lateral sclerosis.
@en
prefLabel
Genome-wide association study ...... amyotrophic lateral sclerosis.
@ast
Genome-wide association study ...... amyotrophic lateral sclerosis.
@en
P2093
P50
P921
P356
P1433
P1476
Genome-wide association study ...... amyotrophic lateral sclerosis.
@en
P2093
Anna Birve
Anneke J van der Kooi
Barbara Tomik
Caroline Dahlberg
Christiaan G J Saris
Corinna Hendrich
Eric Strengman
Ewout J N Groen
H-Erich Wichmann
Helenius J Schelhaas
P2888
P304
P356
10.1038/NG.442
P407
P50
P577
2009-09-06T00:00:00Z