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Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffeeA conserved sorting-associated protein is mutant in chorea-acanthocytosisMolecular markers of early Parkinson's disease based on gene expression in bloodMutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12The deacetylase HDAC6 regulates aggresome formation and cell viability in response to misfolded protein stressIdentification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegia.Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson diseasePGC-1α, a potential therapeutic target for early intervention in Parkinson's diseasemyotilin Mutation found in second pedigree with LGMD1AMutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31Statistical Viewer: a tool to upload and integrate linkage and association data as plots displayed within the Ensembl genome browserPARK10 is a major locus for sporadic neuropathologically confirmed Parkinson diseaseA radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequencesGenomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkageIdentification of MeCP2 mutations in a series of females with autistic disorderGanglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson diseaseLinkage of a gene causing familial membranoproliferative glomerulonephritis type III to chromosome 1Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosisMutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth diseaseThe Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American familyAssociation between the neuron-specific RNA-binding protein ELAVL4 and Parkinson diseaseGenomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigraMeta-analysis of Parkinson's disease: identification of a novel locus, RIT2.Missense mutation in a von Willebrand factor type A domain of the alpha 3(VI) collagen gene (COL6A3) in a family with Bethlem myopathyGenome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease.Comparison of three targeted enrichment strategies on the SOLiD sequencing platformExclusion mapping of chromosomal regions which cross hybridise to FSHD1A associated markers in FSHD1BComprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2APolymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery disease.Combinatorial Mismatch Scan (CMS) for loci associated with dementia in the Amish.GATA2 is associated with familial early-onset coronary artery disease.Pesticide exposure and risk of Parkinson's disease: a family-based case-control studyNeuropeptide Y gene polymorphisms confer risk of early-onset atherosclerosisClinical causes and treatment of the thrombotic storm.SRRM2, a potential blood biomarker revealing high alternative splicing in Parkinson's disease.Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease.
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P50
description
hulumtues
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researcher
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հետազոտող
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Jeffery M Vance
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Jeffery M Vance
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Jeffery M. Vance
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Jeffery M. Vance
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Jeffery Vance
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Jeffery M Vance
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Jeffery M Vance
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Jeffery M. Vance
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Jeffery M. Vance
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Jeffery M Vance
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Jeffery Vance
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Vance JM
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Jeffery M Vance
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Jeffery M Vance
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Jeffery M. Vance
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Jeffery M. Vance
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Jeffery Vance
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P106
P1153
7201366505
P21
P31
P4012
P496
0000-0003-3815-8199