Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
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Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseasesA two-stage meta-analysis identifies several new loci for Parkinson's diseaseWeb-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's diseaseGenome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 regionImputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studiesThe genetics and neuropathology of frontotemporal lobar degenerationGenetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosisCoffee, Genetic Variants, and Parkinson's Disease: Gene-Environment InteractionsThe genetics and neuropathology of Parkinson's diseaseLinking the genetic architecture of cytosine modifications with human complex traitsElevated α-synuclein caused by SNCA gene triplication impairs neuronal differentiation and maturation in Parkinson's patient-derived induced pluripotent stem cellsGenetics in Parkinson disease: Mendelian versus non-Mendelian inheritanceFunctional consequences of 17q21.31/WNT3-WNT9B amplification in hPSCs with respect to neural differentiationAlpha-synuclein and tau: teammates in neurodegeneration?Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access databaseGenome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish populationInteraction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.Selegiline Ameliorates Depression-Like Behavior in Mice Lacking the CD157/BST1 Gene, a Risk Factor for Parkinson's Disease.Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.Anxiety- and depression-like behavior in mice lacking the CD157/BST1 gene, a risk factor for Parkinson's disease.Common variation in the LRRK2 gene is a risk factor for Parkinson's disease.A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlations.An immunohistochemical, enzymatic, and behavioral study of CD157/BST-1 as a neuroregulator.FINEMAP: efficient variable selection using summary data from genome-wide association studies.Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data.Rationale for therapeutic silencing of alpha-synuclein in Parkinson's diseaseIntegrated molecular landscape of Parkinson's diseaseGenome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.The genetic contributions of SNCA and LRRK2 genes to Lewy Body pathology in Alzheimer's disease.Evidence for more than one Parkinson's disease-associated variant within the HLA region.Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome.Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.Influence of single nucleotide polymorphisms in COMT, MAO-A and BDNF genes on dyskinesias and levodopa use in Parkinson's disease.Evaluation of Parkinson disease risk variants as expression-QTLs.Association between GRN rs5848 polymorphism and Parkinson's disease in Taiwanese populationGenome-wide association studies in neurology.
P2860
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P2860
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Dissection of the genetics of ...... ssociated haplotypes at 17q21.
@ast
Dissection of the genetics of ...... ssociated haplotypes at 17q21.
@en
type
label
Dissection of the genetics of ...... ssociated haplotypes at 17q21.
@ast
Dissection of the genetics of ...... ssociated haplotypes at 17q21.
@en
prefLabel
Dissection of the genetics of ...... ssociated haplotypes at 17q21.
@ast
Dissection of the genetics of ...... ssociated haplotypes at 17q21.
@en
P2093
P2860
P50
P3181
P356
P1476
Dissection of the genetics of ...... ssociated haplotypes at 17q21.
@en
P2093
Amy Strange
Ananth C Viswanathan
Anna Rautanen
Celine Bellenguez
Chris C A Spencer
Colin N A Palmer
Gavin Band
Gavin Hudson
Hugh S Markus
P2860
P304
P3181
P356
10.1093/HMG/DDQ469
P50
P577
2010-11-02T00:00:00Z