NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

scientific article

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/J.NEUROBIOLAGING.2014.07.028
P8608Fatcat IDrelease_lrc53eyndnc6biyhbzvg6e5r3a
P3181OpenCitations bibliographic resource ID2226842
P932PMC publication ID4317375
P698PubMed publication ID25444595
P4011Semantic Scholar paper ID9a40792fd2d16355b2c7234e3b9481564c7cdf3d

P50authorJohn Anthony HardyQ6237755
Andrew SingletonQ4758591
Rita GuerreiroQ20049176
Christina M LillQ47817873
Maria MartinezQ56827527
Francis WalkerQ61152996
Thomas GasserQ64856147
Dena G. HernandezQ64856786
Michele T M HuQ64857486
Margaux F KellerQ64860204
Elisa MajounieQ64860206
Peter HeutinkQ66718007
Lars BertramQ91179371
J Raphael GibbsQ114270383
Connor EdsallQ125293550
Vincent PlagnolQ28320554
Bryan TraynorQ28777952
Sampath ArepalliQ30089854
Daniela BergQ30500724
Claudia SchulteQ38323121
Nathan PankratzQ42577075
Jose BrasQ43132633
Alan RentonQ44478769
Anita L DeStefanoQ47502953
Hannah PlinerQ47817868
P2093author name stringJoyce Y Tung
Mohamad Saad
Nick Wood
Margaret Sutherland
Mike A Nalls
Nicholas Eriksson
Janet Brooks
Steven Lubbe
Noah Nichols
Iris Jansen
Chris Letson
Tatiana Faroud
P2860cites workA two-stage meta-analysis identifies several new loci for Parkinson's diseaseQ21144948
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's diseaseQ21144949
Potential etiologic and functional implications of genome-wide association loci for human diseases and traitsQ22066284
An integrated map of genetic variation from 1,092 human genomesQ22122153
A large study reveals no association between APOE and Parkinson's diseaseQ24598836
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studiesQ24606055
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyQ24622472
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosisQ24648667
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseQ28244731
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's diseaseQ28292932
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsyQ29417026
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.Q29417029
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene databaseQ29417106
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing dataQ29547161
Integrating common and rare genetic variation in diverse human populationsQ29547220
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's diseaseQ29614879
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's diseaseQ29614881
Fast and accurate genotype imputation in genome-wide association studies through pre-phasingQ29614942
Best practices and joint calling of the HumanExome BeadChip: the CHARGE ConsortiumQ30418185
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical geneticsQ30440042
Chromosome 9 ALS and FTD locus is probably derived from a single founderQ35853974
Locus-specific mutation databases for neurodegenerative brain diseasesQ36302037
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectdata sharingQ5227350
neurodegenerationQ1755122
P304page(s)1605.e7-12
P577publication date2015-03-01
P1433published inNeurobiology of AgingQ7002141
P1476titleNeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
P478volume36

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cites work (P2860)
Q92534876A Targeted Gene Panel That Covers Coding, Non-coding and Short Tandem Repeat Regions Improves the Diagnosis of Patients With Neurodegenerative Diseases
Q57177625A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease
Q36311348A data-driven approach links microglia to pathology and prognosis in amyotrophic lateral sclerosis
Q47823702A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.
Q33640996Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
Q28602162Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI)
Q33614811C9ORF72 hexanucleotide repeat exerts toxicity in a stable, inducible motor neuronal cell model, which is rescued by partial depletion of Pten
Q42145966Circulating Cholesterol Levels May Link to the Factors Influencing Parkinson's Risk
Q39852415Clinical-genetic model predicts incident impulse control disorders in Parkinson's disease
Q57291461Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus
Q37572904Common variant rs356182 near SNCA defines a Parkinson's disease endophenotype
Q37615837Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Q38379396Epigenetic mechanisms in neurological and neurodegenerative diseases
Q36396085Evaluating pathogenic dementia variants in posterior cortical atrophy
Q50424585Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease
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