scholarly article | Q13442814 |
P356 | DOI | 10.1002/MDS.103 |
P932 | PMC publication ID | 6379910 |
P698 | PubMed publication ID | 30302829 |
P4011 | Semantic Scholar paper ID | a61cd941e512ab4e3080b046ebed6d9c18add9ad |
P50 | author | Jose Bras | Q43132633 |
Dena G. Hernandez | Q64856786 | ||
Cornelis Blauwendraat | Q67225140 | ||
P2093 | author name string | Andrew B Singleton | |
Mike A Nalls | |||
Patrick A Lewis | |||
International Parkinson's Disease Genomics Consortium | |||
P2860 | cites work | Multicenter 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 disease | Q28244731 | ||
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases | Q28650457 | ||
Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews | Q34365028 | ||
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 signal | Q38613451 | ||
P433 | issue | 11 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Parkinson's disease | Q11085 |
genome-wide association study | Q1098876 | ||
P304 | page(s) | 1821-1823 | |
P577 | publication date | 2018-10-09 | |
P1433 | published in | Movement Disorders | Q1486418 |
P1476 | title | Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus | |
P478 | volume | 33 |
Q90031839 | Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts |
Q90989706 | Revisiting the non-Gaucher-GBA-E326K carrier state: Is it sufficient to increase Parkinson's disease risk? |
Q91798573 | Ten Years of the International Parkinson Disease Genomics Consortium: Progress and Next Steps |
Q93193246 | The role of monogenic genes in idiopathic Parkinson's disease |
Q92861469 | Vesicular Dysfunction and the Pathogenesis of Parkinson's Disease: Clues From Genetic Studies |
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