Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.
about
A genomic pathway approach to a complex disease: axon guidance and Parkinson diseaseThe power of meta-analysis in genome-wide association studiesVisualizing disease associations: graphic analysis of frequency distributions as a function of age using moving average plots (MAP) with application to Alzheimer's and Parkinson's diseaseAssociation analysis of MAPT H1 haplotype and subhaplotypes in Parkinson's disease.Pure and Confounded Effects of Causal SNPs on Longevity: Insights for Proper Interpretation of Research Findings in GWAS of Populations with Different Genetic Structures.Meta-analysis in genome-wide association datasets: strategies and application in Parkinson disease.Genetic variability of histamine receptors in patients with Parkinson's disease.Neither replication nor simulation supports a role for the axon guidance pathway in the genetics of Parkinson's diseaseWhole genome survey of coding SNPs reveals a reproducible pathway determinant of Parkinson diseaseGlucocerebrosidase gene mutations: a risk factor for Lewy body disorders.A novel locus for dementia with Lewy bodies: a clinically and genetically heterogeneous disorder.Convergence of miRNA expression profiling, α-synuclein interacton and GWAS in Parkinson's disease.Analysis of GWAS-linked loci in Parkinson disease reaffirms PARK16 as a susceptibility locus.Fine-mapping and candidate gene investigation within the PARK10 locus.Replication of GWAS associations for GAK and MAPT in Parkinson's disease.Using the BITOLA system to identify candidate genes for Parkinson's disease.Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study.A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease.Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles.The etiopathogenesis of Parkinson disease and suggestions for future research. Part II.Identity by descent: variation in meiosis, across genomes, and in populationsSusceptibility genes in movement disorders.Calibration of credibility of agnostic genome-wide associations.Phactr2 and Parkinson's disease.Methods for analysis in pharmacogenomics: lessons from the Pharmacogenetics Research Network Analysis Group.Association between the ubiquitin carboxyl-terminal esterase L1 gene (UCHL1) S18Y variant and Parkinson's Disease: a HuGE review and meta-analysis.Whole-genome analysis in Korean patients with autoimmune myasthenia gravis.Exploiting the potential of molecular profiling in Parkinson's disease: current practice and future probabilities.Genetics of Parkinson's disease and parkinsonism.Behavior genetics and postgenomics.A likelihood-ratio test of twin zygosity using molecular genetic markers.
P2860
Q24288779-EDA8C54D-355E-4F0E-9264-E14DC4301766Q28658972-28E6C20B-F54C-454D-A970-EBB607D356ACQ30492462-68DA0B81-62F6-4149-B644-3C98921B050CQ30493604-8DE606FE-A81F-4F48-B9C5-67EA4D5EDDB6Q30827855-32ADD3C2-F845-443C-AA42-7A65831A4917Q33276409-C35F1C0C-2A85-424B-BBC2-EECDFBAD936AQ33325644-C9B0B697-C382-4C0A-8389-799F10F9E192Q33352050-DED432C1-2EE7-42AE-85A6-A11362934651Q33375794-F9DCB256-5E56-463E-9E3B-31FF92AD2637Q33677320-04DE1583-B077-4C0F-BBF3-42E87019EDC1Q34005558-4D518E35-B105-46A2-88D3-DF8533CC3107Q34049272-BF31CC59-2853-47E6-980C-F2549558DA31Q34053286-94351807-F81D-4238-B44B-8BA9EBCF9933Q34325867-2EB4F68D-EA40-4C44-8C36-527C65D93453Q34781481-0F995783-F72F-4900-93B3-6D266D91BCAEQ35184668-658E82A5-E0C8-4A5C-95D3-DD893210160CQ36426250-473F0224-6FF4-4E26-8AF4-7E030E358168Q36494703-BA7D27F8-415C-4AE4-B3E9-7A8835ADFC19Q36718902-AC8D298D-93B6-42C1-90E9-FEFBB1D8B1E9Q36812817-5AA621D2-9AF2-44C9-B152-83B258D3F85CQ36878562-237755DD-24DD-47A0-9AA4-FE25D7050861Q37098892-033718B6-F118-49BE-B5CA-AC497A1037C4Q37117080-E8E6C4A0-9E41-41AF-9F40-CE1C7E5AB4CFQ37198961-5916F059-1A85-485F-887E-AB123F7B3241Q37331268-D4EF2CE9-C395-4DBC-B717-8F1FDC0BC0A2Q37424589-8F027552-5546-4511-86E8-D4A5780FC99FQ37708262-01F2074B-3523-46F4-912A-3CD508267907Q37809870-DF73884A-AF16-4405-9B3F-816508E85C8BQ40204484-DBE9A3CE-BDA8-41B6-8A88-4E5735C99B3CQ48323081-EB146E6D-FFDD-4E57-91CC-DEF4F1DE40D7Q51894312-F0BDCCDB-8B65-4842-9339-D9995F6D383A
P2860
Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study.
description
2006 nî lūn-bûn
@nan
2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Lack of replication of thirtee ...... rge-scale international study.
@ast
Lack of replication of thirtee ...... rge-scale international study.
@en
type
label
Lack of replication of thirtee ...... rge-scale international study.
@ast
Lack of replication of thirtee ...... rge-scale international study.
@en
prefLabel
Lack of replication of thirtee ...... rge-scale international study.
@ast
Lack of replication of thirtee ...... rge-scale international study.
@en
P2093
P2860
P50
P1433
P1476
Lack of replication of thirtee ...... rge-scale international study.
@en
P2093
Alexis Elbaz
Audrey Southwick
Brian K Fiske
Carlo Ferrarese
Donald S Higgins
Georgios M Hadjigeorgiou
Haydeh Payami
Hideshi Kawakami
Jennifer S Montimurro
P2860
P304
P356
10.1016/S1474-4422(06)70579-8
P50
P577
2006-11-01T00:00:00Z