Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease (Q30370974)

14 October 2017

0 references

Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease (English)

1 reference

14 October 2017

Christopher D Anderson

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1 reference

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M. Arfan Ikram

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1 June 2020

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Matthew Traylor

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Lisa J. Martin

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Devin L. Brown

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1 June 2020

Joan Montaner

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1 June 2020

Björn M Hansen

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1 reference

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1 June 2020

Joshua C Bis

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Cathy R Zhang

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1 June 2020

Braxton D. Mitchell

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1 reference

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Christopher Levi

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1 reference

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1 June 2020

Giorgio B Boncoraglio

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1 reference

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Tom Van Agtmael

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1 June 2020

Cathie Sudlow

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1 reference

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1 June 2020

Jessica G Woo

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Agnieszka Słowik

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Agnieszka Slowik

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1 June 2020

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Carl D Langefeld

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25653287%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

18

Chelsea S Kidwell

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25653287%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

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Steven J Kittner

1 reference

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1 June 2020

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Guido J Falcone

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1 June 2020

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James F Meschia

1 reference

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International Stroke Genetics Consortium

1 June 2020

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1 June 2020

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Pippa A Thomson

1 reference

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1 June 2020

42

Bruce M Psaty

1 reference

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1 June 2020

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Myriam Fornage

1 reference

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1 June 2020

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1 June 2020

author name string

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1 June 2020

Gail Davies

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1 June 2020

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1 reference

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1 June 2020

Thomas W K Battey

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1 reference

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1 June 2020

Farid Radmanesh

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1 June 2020

Ranjan Deka

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1 reference

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1 June 2020

Jordi Jimenez-Conde

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1 reference

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1 June 2020

Scott L Silliman

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1 June 2020

Arne G Lindgren

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1 June 2020

Stéphanie Debette

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1 June 2020

Reinhold Schmidt

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1 June 2020

Qiong Yang

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1 June 2020

Pankaj Sharma

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1 reference

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1 June 2020

Elizabeth G Holliday

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1 June 2020

John Attia

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1 June 2020

Deborah L Poole

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Natalia Rost

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1 June 2020

Bradford B Worrall

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1 June 2020

Daniel Woo

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1 June 2020

Hugh S Markus

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1 June 2020

METASTROKE Consortium

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1 reference

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1 June 2020

CHARGE WMH Group

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1 reference

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1 June 2020

ISGC ICH GWAS Study Collaboration

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1 reference

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1 June 2020

WMH in Ischemic Stroke GWAS Study Collaboration

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1 June 2020

Magdy Selim

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1 June 2020

Peter M Rothwell

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1 June 2020

Rainer Malik

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1 June 2020

Martin Dichgans

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1 June 2020

Jonathan Rosand

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1 June 2020

language of work or name

English

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publication date

4 February 2015

1 reference

14 October 2017

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25653287%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

volume

84

1 reference

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1 June 2020

issue

9

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1 June 2020

page(s)

918-926

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25653287%20AND%20SRC:MED&resulttype=core&format=json

Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage

1 June 2020

cites work

1 reference

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3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Stroke Genetics Network (SiGN) study: design and rationale for a genome-wide association study of ischemic stroke subtypes

3 June 2018

1 reference

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Chemical chaperone treatment reduces intracellular accumulation of mutant collagen IV and ameliorates the cellular phenotype of a COL4A2 mutation that causes haemorrhagic stroke

3 June 2018

1 reference

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The Genotype-Tissue Expression (GTEx) project

3 June 2018

1 reference

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17q25 Locus is associated with white matter hyperintensity volume in ischemic stroke, but not with lacunar stroke status

3 June 2018

1 reference

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Burden of blood pressure-related alleles is associated with larger hematoma volume and worse outcome in intracerebral hemorrhage

3 June 2018

1 reference

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Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies

3 June 2018

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Annotation of functional variation in personal genomes using RegulomeDB

3 June 2018

1 reference

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COL4A1 mutations in patients with sporadic late-onset intracerebral hemorrhage

3 June 2018

1 reference

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COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke

3 June 2018

1 reference

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HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Genetic variants of the NOTCH3 gene in the elderly and magnetic resonance imaging correlates of age-related cerebral small vessel disease

3 June 2018

1 reference

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Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium

3 June 2018

1 reference

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Review: molecular genetics and pathology of hereditary small vessel diseases of the brain.

3 June 2018

1 reference

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White matter hyperintensity volume is increased in small vessel stroke subtypes

3 June 2018

1 reference

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A map of human genome variation from population-scale sequencing

3 June 2018

1 reference

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Integrating common and rare genetic variation in diverse human populations

3 June 2018

1 reference

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METAL: fast and efficient meta-analysis of genomewide association scans

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

COL4A1 mutations as a monogenic cause of cerebral small vessel disease: a systematic review

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Genotype imputation for genome-wide association studies

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Targeted capture and massively parallel sequencing of 12 human exomes

3 June 2018

1 reference

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SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

3 June 2018

Mammalian collagen IV

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

A second generation human haplotype map of over 3.1 million SNPs

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Haploview: analysis and visualization of LD and haplotype maps

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

3 June 2018

1 reference

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Measuring inconsistency in meta-analyses

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Genetic and environmental risk factors for intracerebral hemorrhage: preliminary results of a population-based study

3 June 2018

1 reference

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Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351667

Evaluation of Nyholt's procedure for multiple testing correction

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25653287

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12 December 2020

based on heuristic

Evaluation of Nyholt’s Procedure for Multiple Testing Correction – Author’s Reply

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/25653287

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Identifiers

DOI

10.1212/WNL.0000000000001309

1 reference

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1 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25653287%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

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