Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus

scientific article published on 09 October 2018

Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/MDS.103
P932PMC publication ID6379910
P698PubMed publication ID30302829
P4011Semantic Scholar paper IDa61cd941e512ab4e3080b046ebed6d9c18add9ad

P50authorJose BrasQ43132633
Dena G. HernandezQ64856786
Cornelis BlauwendraatQ67225140
P2093author name stringAndrew B Singleton
Mike A Nalls
Patrick A Lewis
International Parkinson's Disease Genomics Consortium
P2860cites workMulticenter analysis of glucocerebrosidase mutations in Parkinson's disease.Q24634577
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseQ28244731
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseasesQ28650457
Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi JewsQ34365028
Activation of β-Glucocerebrosidase Reduces Pathological α-Synuclein and Restores Lysosomal Function in Parkinson's Patient Midbrain Neurons.Q37110592
The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signalQ38613451
P433issue11
P407language of work or nameEnglishQ1860
P921main subjectParkinson's diseaseQ11085
genome-wide association studyQ1098876
P304page(s)1821-1823
P577publication date2018-10-09
P1433published inMovement DisordersQ1486418
P1476titleCoding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus
P478volume33

Reverse relations

cites work (P2860)
Q90031839Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts
Q90989706Revisiting the non-Gaucher-GBA-E326K carrier state: Is it sufficient to increase Parkinson's disease risk?
Q91798573Ten Years of the International Parkinson Disease Genomics Consortium: Progress and Next Steps
Q93193246The role of monogenic genes in idiopathic Parkinson's disease
Q92861469Vesicular Dysfunction and the Pathogenesis of Parkinson's Disease: Clues From Genetic Studies

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