A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis - Wikidata - awgldk - TriplyDB

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

http://www.wikidata.org/entity/Q24648667

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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study Toward precision medicine in amyotrophic lateral sclerosis State of play in amyotrophic lateral sclerosis genetics NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases A high-density genome-wide association screen of sporadic ALS in US veterans 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.Molecular Identification of d-Ribulokinase in Budding Yeast and Mammals.Design of association studies with pooled or un-pooled next-generation sequencing data.Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.Selective pattern of motor system damage in gamma-synuclein transgenic mice mirrors the respective pathology in amyotrophic lateral sclerosis.Genome-wide association studies in neurology.Risk genotypes at TMEM106B are associated with cognitive impairment in amyotrophic lateral sclerosis.Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus.Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.Chromosome 9 ALS and FTD locus is probably derived from a single founder Controversies and priorities in amyotrophic lateral sclerosis.Genome-wide analysis of the heritability of amyotrophic lateral sclerosis.A Pilot Trial of Pioglitazone HCl and Tretinoin in ALS: Cerebrospinal Fluid Biomarkers to Monitor Drug Efficacy and Predict Rate of Disease Progression.Moving toward a predictive and personalized clinical approach in amyotrophic lateral sclerosis: novel developments and future directions in diagnosis, genetics, pathogenesis and therapies Expanding the genetics of amyotrophic lateral sclerosis and frontotemporal dementia.Single-nucleotide Polymorphism rs2275294 in ZNF512B is not Associated with Susceptibility to Amyotrophic Lateral Sclerosis in a Large Chinese Cohort Screening for novel hexanucleotide repeat expansions at ALS- and FTD-associated loci.Variants within the SP110 nuclear body protein modify risk of canine degenerative myelopathy.Diverse evolutionary histories for beta-adrenoreceptor genes in humans Clinical neurogenetics: amyotrophic lateral sclerosis.Homozygosity analysis in amyotrophic lateral sclerosis.A genome-wide association study in multiple system atrophy.Population genomics in a disease targeted primary cell model.Genetic ablation of IP3 receptor 2 increases cytokines and decreases survival of SOD1G93A mice.Genetic risk and age in Parkinson's disease: Continuum not stratum.No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.Modulatory mechanisms and multiple functions of somatodendritic A-type K (+) channel auxiliary subunits Effect of genetic background on phenotype variability in transgenic mouse models of amyotrophic lateral sclerosis: a window of opportunity in the search for genetic modifiers.Keeping up with genetic discoveries in amyotrophic lateral sclerosis: the ALSoD and ALSGene databases.Unfolded proteins and endoplasmic reticulum stress in neurodegenerative disorders Genetic and epigenetic studies of amyotrophic lateral sclerosis.The role of FUS gene variants in neurodegenerative diseases.Genetic causes of amyotrophic lateral sclerosis: new genetic analysis methodologies entailing new opportunities and challenges.

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A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

http://www.wikidata.org/entity/Q24648667

description

2009 nî lūn-bûn

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2009 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2009 թվականի ապրիլին հրատարակված գիտական հոդված

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2009年の論文

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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年論文

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2009年論文

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2009年论文

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name

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

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A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

@en

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

@nl

type

label

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

@ast

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

@en

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

@nl

prefLabel

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

@ast

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

@en

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

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Human Molecular Genetics

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Amelia Conte

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Angela Britton

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Bryan J Traynor

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Cecilia Carlesi

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Dena Hernandez

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Eugene Z Oddone

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Fabio Giannini

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P2860

A genome-wide association study identifies protein quantitative trait loci (pQTLs)

The missing (L) UNC?

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

A second generation human haplotype map of over 3.1 million SNPs

PLINK: a tool set for whole-genome association and population-based linkage analyses

Haploview: analysis and visualization of LD and haplotype maps

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

Multiple loci identified in a genome-wide association study of prostate cancer

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1524-32

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1706278

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10.1093/HMG/DDP059

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18

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Heinz Erich Wichmann

David J. Hunter

Stephen Chanock

Christian Gieger

Stefania Bandinelli

Dalia Kasperaviciute

Gabriella Restagno

Sampath Arepalli

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2009-04-15T00:00:00Z

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23980109

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19193627

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genome-wide association study

amyotrophic lateral sclerosis

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2664150

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