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

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

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

http://www.wikidata.org/entity/Q35001476

about

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study The genetics and neuropathology of frontotemporal lobar degeneration Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD Recent advances in amyotrophic lateral sclerosis Toward precision medicine in amyotrophic lateral sclerosis A comprehensive review of amyotrophic lateral sclerosis Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis State of play in amyotrophic lateral sclerosis genetics A high-density genome-wide association screen of sporadic ALS in US veterans PolyQ repeat expansions in ATXN2 associated with ALS are CAA interrupted repeats Age 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 genotypes Modelling amyotrophic lateral sclerosis: progress and possibilities Frontotemporal 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-analysis Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis Mapping 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 ALS Brain 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 cohort Genetic 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 population Genetic 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.

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

http://www.wikidata.org/entity/Q35001476

description

2009 nî lūn-bûn

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2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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Genome-wide association study ...... amyotrophic lateral sclerosis.

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Genome-wide association study ...... amyotrophic lateral sclerosis.

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Genome-wide association study ...... amyotrophic lateral sclerosis.

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Genome-wide association study ...... amyotrophic lateral sclerosis.

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Genome-wide association study ...... amyotrophic lateral sclerosis.

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Anna Birve

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Anneke J van der Kooi

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Barbara Tomik

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Caroline Dahlberg

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Christiaan G J Saris

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Corinna Hendrich

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Eric Strengman

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Ewout J N Groen

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H-Erich Wichmann

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Helenius J Schelhaas

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10.1038/NG.442

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10

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41

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Fernando Rivadeneira

André Uitterlinden

Agnieszka Słowik

Vincent Meininger

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2009-09-06T00:00:00Z

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26793926

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19734901

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genome-wide association study

amyotrophic lateral sclerosis

susceptibility locus