Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. - Test2 - elhamkhani - TriplyDB

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

http://www.wikidata.org/entity/Q29417095

about

Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases A two-stage meta-analysis identifies several new loci for Parkinson's disease Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies The genetics and neuropathology of frontotemporal lobar degeneration Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Coffee, Genetic Variants, and Parkinson's Disease: Gene-Environment Interactions The genetics and neuropathology of Parkinson's disease Linking the genetic architecture of cytosine modifications with human complex traits Elevated α-synuclein caused by SNCA gene triplication impairs neuronal differentiation and maturation in Parkinson's patient-derived induced pluripotent stem cells Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance Functional consequences of 17q21.31/WNT3-WNT9B amplification in hPSCs with respect to neural differentiation Alpha-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 database Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population Interaction 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 disease Integrated molecular landscape of Parkinson's disease Genome-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 population Genome-wide association studies in neurology.

P2860

9f82df81f22eee52d6645a3d704c823c9061ce87

P248

Q21144915-CF240583-E234-4C38-8888-09E7D046D1AE Q21144948-1CAA50B8-8846-4E15-AD7E-FA346B26F21A Q21144949-42FBDDEA-A11E-45B9-98B9-009EEAD9E9A8 Q24289047-105903D7-727C-4F93-BD70-794B718FFF73 Q24606055-149F2730-21F5-4550-B6EB-D0E081F88242 Q24615201-5DE9078E-774C-4427-A1B7-CF393E5A5BFD Q24635370-B9D15965-4815-4368-869C-DAA594ECAA18 Q26852456-AC5A38F5-16DF-47CF-B487-ACD03871CAB9 Q26859945-DB5F1C00-5C55-464D-BD66-F747EDC14BE4 Q27301341-73A03EFB-D3D8-416B-BBDF-ADD97928DB97 Q27329722-B16AA2E7-672D-4642-8C41-ACEF3BC00432 Q28077356-C0474D94-6DEC-4CB8-B456-EAD0CA819AA8 Q28119109-9E817125-8B9E-46B4-99FD-05708621C815 Q28250508-CB8E128C-E53F-4504-8BE4-342C716AEDD7 Q28262863-B667FB6A-C5D6-4093-A4A9-17077DE800C8 Q28657400-257EEE68-5C29-460C-939B-9638AFD73562 Q28943392-40F5320C-25C7-4015-95A9-E3A3E6C0D836 Q29417082-E3FC5A82-0996-460B-87EB-AA34716DB91A Q29417106-06AE38E1-EFF8-4AA6-8EC1-A0B03E9E9770 Q29417129-501DED27-30CC-4EAC-A973-DADE795B0620 Q29994860-3403BFA7-73FB-485F-8925-EB200399283A Q30276970-A96C4C38-716C-47D0-BC29-5FD84708AF5E Q30438962-B3BB760A-EAB2-455B-B37C-77AB8C9DA3E9 Q30531323-0D471375-A6EB-403E-9D76-81BFDC8D0825 Q30628518-9966F1AB-7A9C-4801-8648-9FA04AC94788 Q30842879-18E95BCF-EA3B-4FF3-BFD8-07EB9D91A8A8 Q31037165-6EDC887F-97EE-44BF-9BC6-D5AA27C2399B Q31063778-840F475E-416A-41A3-A880-7305BB9853EB Q33636374-CCD9F91A-EE74-41AA-BD89-F42DDDE64E29 Q33767544-BC84D87C-EE25-490F-B8C8-626533071DAE Q33991709-D65E47EA-118B-46CC-BBEC-7C8451F731BA Q34074501-7316D016-C535-4BB3-BA3A-DEA1C7403D16 Q34077754-CFB12AF5-2A8A-4E42-B5F2-2A2A1E0F5774 Q34199600-3EA224AC-9043-4CB8-BE69-03E256AAC9D9 Q34234597-B83B1670-0929-4A91-B78E-373F21848018 Q34298428-0B80D4DB-AA9C-4B10-A585-A9581830F50C Q34326909-69C5E081-29A0-448B-BD3A-542F99249962 Q34446993-02ED7327-CC57-4C39-A3D0-4A74E784210E Q34559477-D98FABC3-063A-4AA5-99F9-8BED87621025 Q34658391-AA62186D-5D85-4F2E-BBDE-5A3F7A5C3719

P2860

Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.

http://www.wikidata.org/entity/Q29417095

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

P1433

Q29417095-98202065-3AC9-41F0-A207-DA4F23A0DB5B

P1476

Q29417095-9996CE3C-1756-4A6F-A8F9-ED16899B7141

P2093

Q29417095-0A29893C-6FC2-414F-8F90-74208B9B9DDC

Q29417095-0FAC4A5D-1673-4C5F-B8BD-612CB5875357

Q29417095-13DD68BC-4B63-4886-A342-8193DE28C650

Q29417095-1A2EC464-408A-45C4-946D-F71667AE263E

Q29417095-1B1B38C6-40E6-4324-A227-05F2D1A224A6

Q29417095-204CFAB8-1BCD-4FEE-8CB9-373AB3B9D337

Q29417095-21CAE6A8-42AA-4611-8800-E5DA837F6651

Q29417095-2F81ABAF-BC40-4114-B8EA-9C1AF7947CB8

Q29417095-32FE45D6-DFC4-47FE-96FC-54ED2C1286B4

Q29417095-3830D928-9B04-41B5-9182-80AEBCC543DC

P2860

Q29417095-0B81068A-2258-4C68-901B-43CA523FBFCB

Q29417095-0C30B2A1-0661-474A-ADDC-9ABD74060BC5

Q29417095-1D229F52-E5F1-42F8-9D5F-96039502B6FD

Q29417095-233F874D-CEDF-4ACF-99C9-E25C27CD6F7A

Q29417095-2976DBA9-FCF8-41D4-BDAD-7B73BB69A9AE

Q29417095-2D27529E-1840-4E5A-9BCD-22804C6C6AAB

Q29417095-3506EECA-7C8D-4961-8B03-3186AA9EF642

Q29417095-4D8470F1-A18D-4E54-BA70-81AE2C537211

Q29417095-613448E4-1A73-45C3-80BD-A2F089C93F92

Q29417095-6A65DA2E-9A2A-4298-A4E6-F9752891186F

P304

Q29417095-79A09E78-1CE9-4C1A-939C-252651FCACB6

P31

Q29417095-E5823127-67E4-4592-91D4-788D17264C8D

P3181

Q29417095-C7D8C6D7-9A97-405D-BE56-B4135F0CB3B4

P356

Q29417095-95A94C67-4013-4A14-A3DD-993C46EAAF1F

P433

Q29417095-0C7A3080-1FA2-4AC8-A56C-676CE7D13805

P478

Q29417095-A51E5178-C788-47B4-A08F-93977D8B2C61

P50

Q29417095-02528F2D-B123-4B89-A50C-0B43EAE24499

Q29417095-19600ACA-CA10-4912-BD56-8F2672812720

Q29417095-2FA28F6B-7412-4435-95FF-E9B821F3F11C

Q29417095-369df040-4521-74a2-b533-9bdec69ae177

Q29417095-38E58457-C970-476A-9A31-3CBB3403CACD

Q29417095-3D30E49B-60C4-477D-8A1D-3D453469E43C

Q29417095-55A5A603-6DA5-483C-BABF-DB1ED07F0E0E

Q29417095-5FACFC66-3C5D-45E5-886F-997A55C30BD8

Q29417095-6262A6BC-58C3-47D2-BE74-B8B9BCFCE616

Q29417095-6ED62F18-6B9F-47DF-B00E-2B750808F622

P577

Q29417095-08550F2B-18A1-4A7F-AD04-814B4E221611

P5875

Q29417095-CC5CB182-7A09-49D8-B0B4-304C068DA63A

P698

Q29417095-FCB94565-1F51-43DD-B261-F4BDF54BF56B

P921

Q29417095-3D30FA79-B948-45B7-8FB0-E54B7D77DEB4

P932

Q29417095-9922B7C6-EF05-4B02-945A-18D8F3F5BDE9

P3181

P356

P1433

Human Molecular Genetics

P1476

Dissection of the genetics of ...... ssociated haplotypes at 17q21.

@en

P2093

Amy Strange

http://www.w3.org/2001/XMLSchema#string

Ananth C Viswanathan

http://www.w3.org/2001/XMLSchema#string

Anna Rautanen

http://www.w3.org/2001/XMLSchema#string

Celine Bellenguez

http://www.w3.org/2001/XMLSchema#string

Chris C A Spencer

http://www.w3.org/2001/XMLSchema#string

Colin N A Palmer

http://www.w3.org/2001/XMLSchema#string

Emma Gray

http://www.w3.org/2001/XMLSchema#string

Gavin Band

http://www.w3.org/2001/XMLSchema#string

Gavin Hudson

http://www.w3.org/2001/XMLSchema#string

Hugh S Markus

http://www.w3.org/2001/XMLSchema#string

P2860

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease

Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls

Genome-wide association study reveals genetic risk underlying Parkinson's disease

Evolutionary toggling of the MAPT 17q21.31 inversion region

PLINK: a tool set for whole-genome association and population-based linkage analyses

alpha-Synuclein locus triplication causes Parkinson's disease

Principal components analysis corrects for stratification in genome-wide association studies

LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1

P304

345-353

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

3630951

http://www.w3.org/2001/XMLSchema#string

P356

10.1093/HMG/DDQ469

http://www.w3.org/2001/XMLSchema#string

P433

2

http://www.w3.org/2001/XMLSchema#string

P478

20

http://www.w3.org/2001/XMLSchema#string

P50

Leena Peltonen-Palotie

Vincent Plagnol

Cordelia Langford

Christopher G. Mathew

Hannah Blackburn

P577

2010-11-02T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

51446252

http://www.w3.org/2001/XMLSchema#string

P698

21044948

http://www.w3.org/2001/XMLSchema#string

P921

Parkinson's disease

P932

3005904

http://www.w3.org/2001/XMLSchema#string