(Q30417040)

18 August 2017

NOTCH3 variants and risk of ischemic stroke (English)

1 reference

18 August 2017

Sruti Rayaprolu

6

0 references

Zbigniew K Wszolek

12

object named as

Zbigniew K Wszolek

1 reference

18 August 2017

10

Rita Guerreiro

1 reference

18 August 2017

1

Owen A Ross

1 reference

18 August 2017

9

Andrew Singleton

1 reference

18 August 2017

13

Thomas G Brott

1 reference

18 August 2017

16

James F Meschia

1 reference

18 August 2017

3

Michael G Heckman

1 reference

18 August 2017

15

Bradford B Worrall

1 reference

18 August 2017

Alexandra I Soto-Ortolaza

2

1 reference

18 August 2017

Christophe Verbeeck

4

1 reference

18 August 2017

Daniel J Serie

5

1 reference

18 August 2017

Stephen S Rich

7

1 reference

18 August 2017

Michael A Nalls

8

1 reference

18 August 2017

Emma Kinsella

11

1 reference

18 August 2017

Robert D Brown

14

1 reference

18 August 2017

language of work or name

English

0 references

publication date

23 September 2013

1 reference

18 August 2017

1 reference

18 August 2017

8

1 reference

18 August 2017

9

1 reference

18 August 2017

e75035

1 reference

Creative Commons CC0 License

18 August 2017

start time

23 September 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted, dedicated to the public domain by copyright holder

0 references

cites work

Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

Genetic susceptibility to ischemic stroke

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

Haploview: Visualization and analysis of SNP genotype data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

Linking Notch signaling to ischemic stroke

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

Activating NOTCH3 mutation in a patient with small-vessel-disease of the brain

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

The multifaceted role of Notch in cardiac development and disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

Advancing stroke therapeutics through genetic understanding

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

The spectrum of mutations for CADASIL diagnosis

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

Human non-synonymous SNPs: server and survey

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in an octogenarian paucisymptomatic patient

20 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0075035

A novel CADASIL-causing mutation in a stroke patient

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

Multiple testing. Part I. Single-step procedures for control of general type I error rates

26 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3781028

The World Health Organization MONICA Project (monitoring trends and determinants in cardiovascular disease): a major international collaboration. WHO MONICA Project Principal Investigators

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24086431

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0075035

1 reference

18 August 2017

0 references

1 reference

18 August 2017

PubMed publication ID

24086431

1 reference