Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study - Test2 - elhamkhani - TriplyDB

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

http://www.wikidata.org/entity/Q24622472

about

Behavioral variant frontotemporal lobar degeneration with amyotrophic lateral sclerosis with a chromosome 9p21 hexanucleotide repeat Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study The genetics and neuropathology of frontotemporal lobar degeneration Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD Asparaginase treatment side-effects may be due to genes with homopolymeric Asn codons (Review-Hypothesis)Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis State of play in amyotrophic lateral sclerosis genetics ALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the disease Searching for Grendel: origin and global spread of the C9ORF72 repeat expansion NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases A high-density genome-wide association screen of sporadic ALS in US veterans Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.What causes amyotrophic lateral sclerosis?Global epidemiology of amyotrophic lateral sclerosis: a systematic review of the published literature.XWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X Chromosome A powerful and efficient set test for genetic markers that handles confounders Age-related penetrance of the C9orf72 repeat expansion.C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis Principal component analysis characterizes shared pathogenetics from genome-wide association studies.Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.Gene ontology analysis of pairwise genetic associations in two genome-wide studies of sporadic ALS Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants.Genome wide assessment of young onset Parkinson's disease from Finland Accounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases.Progress in therapy development for amyotrophic lateral sclerosis Genome-wide association studies in neurology.Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population.Understanding the role of TDP-43 and FUS/TLS in ALS and beyond.Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72 Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study.Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p Familial Lund frontotemporal dementia caused by C9ORF72 hexanucleotide expansion.Accurate Non-parametric Estimation of Recent Effective Population Size from Segments of Identity by Descent.Controversies and priorities in amyotrophic lateral sclerosis.

P2860

Q21129431-EED40DB1-36E9-41BF-A61A-93FD67F3307C Q24600803-A483CD36-813C-48C7-9554-E866000B76E7 Q24615201-847054C7-DFD4-40F1-9878-8E51F5FE51C5 Q24633692-6B46B3BF-A0A0-482A-BA95-8E978C6FC561 Q24634583-D332B7E3-DEFE-4E00-A7A0-5D1A2539210D Q26801165-EE51DDA2-0260-4F43-97A0-299E5EFCCAAB Q26863439-32ADF875-26A8-4A3D-A49E-79BEF42F618B Q26864816-1B457B51-ACE4-4825-8189-4DC9A4B70392 Q28392297-F5E68974-C2CB-4D1E-94DA-F845BCC08E2F Q28608607-DF3AA4A6-2994-4924-8945-9610D25A142F Q28650457-437DF2CC-BE80-4A0A-85D7-43C9A1ABC5AE Q28730882-B9EE3592-03F9-4BCC-B543-BD3D4FB21169 Q29417029-863A844F-60AC-4A7B-B31D-E0088009BEF6 Q30234813-74C09D46-0E01-4C83-ACEA-B02F764F215D Q30580165-3FA68290-96EC-4FE6-A17E-9364D5918399 Q30987029-DEBA3155-D342-4B48-8B15-93EADB0D0C6A Q31115587-5C0EA76C-37AC-423B-91D7-B78731859E41 Q33704777-5DBD9F19-07B9-465C-951A-02E8E678ACEC Q34063137-0DFE1EE5-A73E-4E2D-879B-658536673643 Q34165673-BCDE46F4-5679-4DB9-84AA-CC00F8D243AA Q34235637-EC7B2E89-F212-4FEB-9D1F-28EC57221380 Q34290691-9D60D5A0-20E8-4ED8-82A3-08E4BEBFEF4C Q34299422-B1D12BBD-D3B6-439F-9730-918CB035E06B Q34388219-55E3DF2C-E0C2-4D90-8D83-0D006C0DC1BE Q34639949-46921489-DDFC-4E6F-AB8B-ACEE54621B16 Q34640800-D0847C8A-994C-40F2-9F3F-A0838283C674 Q34658391-C98007DF-76E1-4CE2-8B44-35C41B4DE058 Q35086781-B835B134-0E95-4694-A595-88A6031F6E55 Q35587208-9F617A93-DB02-48E7-8224-1BBB12726365 Q35671414-1B0B444D-18BA-4E6D-B3A2-F458E62C2BD2 Q35752001-4A717E08-94DB-429F-B80B-143D6C473710 Q35776895-2999EFAA-2D76-4449-82AA-73BD5A69E3A0 Q35776901-B84AC56B-1E41-4F75-B30F-40CAFAF560E4 Q35776914-537AE9D3-542F-4555-B119-5B4BFCDF3178 Q35776923-76CD49D9-BC8D-485F-A4C7-4555A6F5BF8C Q35859698-BF0BA23F-F906-4C55-A5B9-8D36610188BF Q35878727-FCCB6DAA-E679-4531-A2F6-B300A62439F2 Q36035170-08DBA27B-20AA-40D0-914D-C18453D3F352 Q36045113-B0DC8197-5196-4822-88DC-D75EEB32F815 Q36045826-C1813410-70A6-4479-A993-87000BC3C26A

P2860

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

http://www.wikidata.org/entity/Q24622472

description

2010 nî lūn-bûn

@nan

2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2010年の論文

@ja

2010年学术文章

@wuu

2010年学术文章

@zh-cn

2010年学术文章

@zh-hans

2010年学术文章

@zh-my

2010年学术文章

@zh-sg

2010年學術文章

@yue

name

Chromosome 9p21 in amyotrophic ...... genome-wide association study

@ast

Chromosome 9p21 in amyotrophic ...... genome-wide association study

@en

Chromosome 9p21 in amyotrophic ...... genome-wide association study

@nl

type

label

Chromosome 9p21 in amyotrophic ...... genome-wide association study

@ast

Chromosome 9p21 in amyotrophic ...... genome-wide association study

@en

Chromosome 9p21 in amyotrophic ...... genome-wide association study

@nl

prefLabel

Chromosome 9p21 in amyotrophic ...... genome-wide association study

@ast

Chromosome 9p21 in amyotrophic ...... genome-wide association study

@en

Chromosome 9p21 in amyotrophic ...... genome-wide association study

@nl

P1433

Q24622472-88611727-5D0B-4129-B1CE-3DDE5B358F27

P1476

Q24622472-EF8C7982-FDA2-483D-9168-37B607772DE1

P2093

Q24622472-01A7353E-7241-4CBA-8F2E-6E0C4C87AAE0

Q24622472-0EA55D8D-0451-4E21-AF07-68D156817E30

Q24622472-10D686F6-E298-4CF2-BDC7-6FEB37FD1962

Q24622472-1E06B75F-0D19-40DA-94B8-59B664014BAC

Q24622472-3A55A90E-18D0-4587-9C93-B0BF44D6DDA7

Q24622472-41F05EAC-E0C1-4BB3-A7FD-8895975642CD

Q24622472-49962ED7-CFDE-4FEE-8EFE-1994DCA74513

Q24622472-7FA31020-6D7F-477D-B8D5-33E54DA2A91B

Q24622472-862D3A72-75F3-440D-8452-153479C72E35

Q24622472-99F1F6A5-6471-49D1-9927-1A03FF565B0B

P2860

Q24622472-1289403E-3FF5-40C1-A69E-A85D58D1AFCB

Q24622472-19FFE75D-13A3-4186-B246-D74720EC3278

Q24622472-1CB99F12-74F3-450F-A5A6-554E9D550F9B

Q24622472-222C1754-E9A4-4BB0-BA0D-E9F37CD78353

Q24622472-34184C02-AB91-43B4-9D79-0BC0186280ED

Q24622472-3D6B5353-5E9C-42A3-8FA6-1261131916CD

Q24622472-429C7F77-BCBB-473C-B027-39F112FF7A5A

Q24622472-4332EBF4-79F1-40EC-9CF9-663645C8A8FB

Q24622472-4834C231-90DA-442B-B002-83D2C0CF9704

Q24622472-4A149056-79B7-4261-AA49-383040BB51C7

P304

Q24622472-FBDA7D2E-37D4-406C-8843-78101BDD55DA

P31

Q24622472-C862E5E9-BE1E-4289-B760-834F7C6FC89C

P3181

Q24622472-3B3F0C5E-DD5C-40AA-B10C-3578EC50D3AE

P356

Q24622472-BD17C6BF-9D25-481D-9E1D-7AABD5EA6FFA

P407

Q24622472-6FBFB97C-61B5-4CBC-AA29-2300946EEACF

P433

Q24622472-F9096E1F-79CF-4CAB-AD34-AF96EDA9A2E8

P478

Q24622472-60A6EB24-9B28-4B2B-B6D3-4AD67A21D485

P50

Q24622472-1F319D81-6921-4376-878F-949C10CF01F6

P577

Q24622472-77BE0DD6-833F-4C73-8B17-1E256E52D551

P698

Q24622472-F5549E77-D565-44D6-8A5D-7ABD11960347

P921

Q24622472-5F652C00-A78C-4746-A802-BF13E0C51447

Q24622472-97868B12-E2AA-4DF2-A116-B12CFD461CA8

Q24622472-ABD28F75-B02D-4032-87EC-D50495E7275E

P932

Q24622472-D746BB40-5E8A-457F-9274-0283E2F3CA91

P3181

P356

S1474-4422(10)70184-8

P1433

Lancet Neurology

P1476

Chromosome 9p21 in amyotrophic ...... genome-wide association study

@en

P2093

Bryan J Traynor

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

David Heckerman

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

Dena G Hernandez

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

Hannu Laaksovirta

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

J Raphael Gibbs

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

Jennifer C Schymick

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

Liisa Myllykangas

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

Lilja Jansson

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

Michael A Nalls

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

Pentti J Tienari

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

P2860

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis

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

Haploview: analysis and visualization of LD and haplotype maps

Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

Amyotrophic lateral sclerosis

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

P304

978-85

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

P31

scholarly article

P3181

1706262

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

P356

10.1016/S1474-4422(10)70184-8

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

P407

P433

10

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

P478

9

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

P50

P577

2010-10-01T00:00:00Z

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

P698

20801718

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

P921

genome-wide association study

amyotrophic lateral sclerosis

P932

2965392

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