Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (Q102075612)

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18 November 2020

title

Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors (English)

1 reference

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genome-wide association study

18 November 2020

main subject

1 reference

Author Correction: Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors

inferred from title

corrigendum / erratum

0 references

author

Mark K. Bakker

1

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18 November 2020

Wouter van Rheenen

3

1 reference

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18 November 2020

Sandrine Morel

4

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18 November 2020

Isabel C Hostettler

6

1 reference

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18 November 2020

Masaru Koido

9

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18 November 2020

Chikashi Terao

11

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18 November 2020

Koichi Matsuda

12

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18 November 2020

Robin G Walters

13

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Zhengming Chen

17

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18 November 2020

Guy A. Rouleau

18

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Kristiina Rannikmäe

20

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18 November 2020

Henry Houlden

22

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18 November 2020

Christian Dina

24

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François Eugène

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18 November 2020

Bendik S. Winsvold

30

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Sigrid Børte

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18 November 2020

Marie Søfteland Sandvei

34

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Gabriel J E Rinkel

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Mikael von Und Zu Fraunberg

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Hubert Desal

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Muralidharan Sargurupremraj

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Bradford B Worrall

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Emília I Gaál-Paavola

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Juha E Jääskeläinen

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18 November 2020

publication date

16 November 2020

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18 November 2020

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describes a project that uses

18 November 2020

genome-wide association study

1 reference

Prevalence of unruptured intracranial aneurysms, with emphasis on sex, age, comorbidity, country, and time period: a systematic review and meta-analysis

inferred from title

cites work

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High risk population isolate reveals low frequency variants predisposing to intracranial aneurysms

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RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population

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Genome-wide association studies of intracranial aneurysms: an update

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Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk

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Genome-wide association study of intracranial aneurysm identifies three new risk loci

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Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies

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Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

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Deficiency of endothelium-specific transcription factor Sox17 induces intracranial aneurysm.

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Chromatin Conformation Links Putative Enhancers in Intracranial Aneurysm-Associated Regions to Potential Candidate Genes

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Trans-ethnic association study of blood pressure determinants in over 750,000 individuals

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Leveraging Polygenic Functional Enrichment to Improve GWAS Power

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Interethnic analyses of blood pressure loci in populations of East Asian and European descent

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Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation

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A missense variant in FGD6 confers increased risk of polypoidal choroidal vasculopathy

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Systems genetics analysis of gene-by-environment interactions in human cells

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THSD1 preserves vascular integrity and protects against intraplaque haemorrhaging in ApoE-/- mice.

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p130Cas/BCAR1 scaffold protein in tissue homeostasis and pathogenesis

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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

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A global overview of pleiotropy and genetic architecture in complex traits

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Genetic identification of brain cell types underlying schizophrenia

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Patient- and Aneurysm-Specific Risk Factors for Intracranial Aneurysm Growth: A Systematic Review and Meta-Analysis

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Risk Factors for Unruptured Intracranial Aneurysms and Subarachnoid Hemorrhage in a Prospective Population-Based Study

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https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Female risk factors for subarachnoid hemorrhage: a systematic review.

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes.

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Genome-wide association study of sporadic brain arteriovenous malformations

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

1 reference

7 January 2021

Epidemiology, Risk Factors, and Clinical Features of Intracerebral Hemorrhage: An Update

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

The neurobiology of antiepileptic drugs

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Sex, Smoking, and Risk for Subarachnoid Hemorrhage

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Risk of rupture of an intracranial aneurysm based on patient characteristics: a case-control study

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Factors affecting formation and growth of intracranial aneurysms: a long-term follow-up study

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Blood pressure, hypertension and the risk of abdominal aortic aneurysms: a systematic review and meta-analysis of cohort studies

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Arterial smooth muscle cell PKD2 (TRPP1) channels regulate systemic blood pressure

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Vascular complications in autosomal dominant polycystic kidney disease

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Colocalization of GWAS and eQTL Signals Detects Target Genes

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Integrative approaches for large-scale transcriptome-wide association studies

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Partitioning heritability by functional annotation using genome-wide association summary statistics

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

GARFIELD classifies disease-relevant genomic features through integration of functional annotations with association signals

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles

1 reference

https://api.crossref.org/works/10.1038%2FS41588-020-00725-7

7 January 2021

10.1038/S41588-020-00725-7

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:33199917%20AND%20SRC:MED&resulttype=core&format=json

18 November 2020

0 references

1 reference