(Q30275184)

22 August 2017

Genetic variation at 16q24.2 is associated with small vessel stroke (English)

1 reference

22 August 2017

1 reference

9

0 references

Martin Dichgans

66

0 references

Jonathan Rosand

63

0 references

Gudmar Thorleifsson

6

0 references

Solveig Gretarsdottir

54

0 references

Kári Stefánsson

52

0 references

Unnur Þorsteinsdóttir

53

0 references

Olle Melander

31

0 references

Myriam Fornage

50

0 references

Sudha Seshadri

22

Sudha Seshadri

1 reference

22 August 2017

1

Matthew Traylor

1 reference

22 August 2017

Eilis Hannon

14

0 references

Sara Pulit

Sara L Pulit

41

0 references

Christopher D Anderson

Christopher D Anderson

47

0 references

Robin Lemmens

Robin Lemmens

29

0 references

Vincent N Thijs

Vincent Thijs

60

0 references

Giorgio B Boncoraglio

Giorgio B Boncoraglio

59

0 references

Jordana T. Bell

Jordana T Bell

13

0 references

Cathryn Lewis

Cathryn M Lewis

55

0 references

Jonathan Mill

Jonathan Mill

15

0 references

Jin-Moo Lee

Jin-Moo Lee

40

0 references

Lenore J Launer

21

Lenore J Launer

1 reference

22 August 2017

28

Agnieszka Słowik

1 reference

22 August 2017

33

Ralph L Sacco

1 reference

22 August 2017

34

Tatjana Rundek

1 reference

22 August 2017

2

Rainer Malik

1 reference

22 August 2017

58

Peter M Rothwell

1 reference

22 August 2017

62

James F Meschia

1 reference

22 August 2017

67

Bradford B Worrall

1 reference

22 August 2017

18

Joshua C Bis

1 reference

22 August 2017

36

Donna K Arnett

1 reference

22 August 2017

8

Carl Langefeld

1 reference

22 August 2017

35

Kathryn Rexrode

1 reference

22 August 2017

64

Steven J Kittner

1 reference

22 August 2017

65

Braxton D Mitchell

1 reference

22 August 2017

12

Tim D Spector

1 reference

22 August 2017

Ganesh Chauhan

16

1 reference

ORCID Public Data File 2021

International Stroke Genetics Consortium

69

International Stroke Genetics Consortium

1 reference

22 August 2017

20

M Arfan Ikram

1 reference

22 August 2017

68

Hugh S Markus

1 reference

22 August 2017

3

Mike A Nalls

1 reference

22 August 2017

17

Stephanie Debette

1 reference

22 August 2017

44

Paul I W de Bakker

1 reference

22 August 2017

61

Chris Levi

1 reference

22 August 2017

57

Cathie L M Sudlow

1 reference

22 August 2017

46

Daniel Woo

1 reference

22 August 2017

4

Ioana Cotlarciuc

1 reference

22 August 2017

5

Farid Radmanesh

1 reference

22 August 2017

10

Natalia S Rost

1 reference

22 August 2017

25

Jordi Jimenez-Conde

1 reference

22 August 2017

32

Raji P Grewal

1 reference

22 August 2017

38

Oscar R Benavente

1 reference

Sylvia Wasssertheil-Smoller

22 August 2017

39

Sylvia Wasssertheil-Smoller

1 reference

22 August 2017

45

Patrick F McArdle

1 reference

22 August 2017

49

Laura Heitsch

1 reference

22 August 2017

51

Christina Jern

1 reference

22 August 2017

43

Stephen S Rich

1 reference

22 August 2017

William T. Longstreth

19

W T Longstreth

1 reference

22 August 2017

Ken B Hanscombe

7

1 reference

22 August 2017

Idil Yet

11

1 reference

22 August 2017

METASTROKE, UK Young Lacunar DNA Study, NINDS Stroke Genetics Network, Neurology Working Group of the CHARGE Consortium

23

1 reference

22 August 2017

Monica Anne Hamilton-Bruce

24

1 reference

22 August 2017

John W Cole

26

1 reference

22 August 2017

Reinhold Schmidt

27

1 reference

22 August 2017

Arne Lindgren

30

1 reference

22 August 2017

Julie A Johnson

37

1 reference

22 August 2017

Quenna Wong

42

1 reference

22 August 2017

Huichun Xu

48

1 reference

22 August 2017

Pankaj Sharma

56

1 reference

22 August 2017

20 December 2016

1 reference

22 August 2017

1 reference

22 August 2017

81

1 reference

22 August 2017

3

1 reference

22 August 2017

383-394

1 reference

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

22 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of 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=5366092

Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Methylation QTLs in the developing brain and their enrichment in schizophrenia risk loci

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Genetic Architecture of Lacunar Stroke

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Monogenic causes of stroke: now and the future

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Polygenic risk of Parkinson disease is correlated with disease age at onset

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Integrative analysis of 111 reference human epigenomes

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Genetic architecture of white matter hyperintensities differs in hypertensive and nonhypertensive ischemic stroke.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Methylation QTLs are associated with coordinated changes in transcription factor binding, histone modifications, and gene expression levels

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

A novel MMP12 locus is associated with large artery atherosclerotic stroke using a genome-wide age-at-onset informed approach

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Bayesian test for colocalisation between pairs of genetic association studies using summary statistics

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

The effect of genotype and in utero environment on interindividual variation in neonate DNA methylomes

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

GeMes, clusters of DNA methylation under genetic control, can inform genetic and epigenetic analysis of disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

DNA methylation age of human tissues and cell types

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Systematic identification of trans eQTLs as putative drivers of known disease associations

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Neuroimaging standards for research into small vessel disease and its contribution to ageing and neurodegeneration

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Informed conditioning on clinical covariates increases power in case-control 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=5366092

An integrated map of genetic variation from 1,092 human genomes

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of 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=5366092

An integrated encyclopedia of DNA elements in the human genome

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Matrix eQTL: ultra fast eQTL analysis via large matrix operations

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Cohort Profile: TwinsUK and healthy ageing twin study

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Five years of GWAS discovery

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

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=5366092

DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

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=5366092

Practical aspects of imputation-driven meta-analysis of 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=5366092

Lifetime risk of stroke and dementia: current concepts, and estimates from the Framingham Study

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Differences in stroke subtypes between black and white patients with stroke: the South London Ethnicity and Stroke Study.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Principal components analysis corrects for stratification in 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=5366092

Early risk of recurrence by subtype of ischemic stroke in population-based incidence 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=5366092

Fox's in development and disease

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5366092

Genomic control for 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=5366092

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=5366092

Evaluating the genetic component of ischemic stroke subtypes: a family history study.

3 June 2018

1 reference

Heritability of leukoaraiosis in hypertensive sibships

21 January 2018

1 reference

Improved whole-chromosome phasing for disease and population genetic studies

21 January 2018

1 reference

A computerized algorithm for etiologic classification of ischemic stroke: the Causative Classification of Stroke System.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.24840

1 reference

release_4f7monhrznbbtoqgkmsudohuai

22 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/4f7monhrznbbtoqgkmsudohuai

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

22 August 2017

1 reference