Search for intracranial aneurysm susceptibility gene(s) using Finnish families (Q24799061)

4 July 2017

Search for intracranial aneurysm susceptibility gene(s) using Finnish families (English)

1 reference

4 July 2017

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5

Juha Hernesniemi

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Helena Kuivaniemi

object named as

Helena Kuivaniemi

3

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Gerard Tromp

object named as

Gerard Tromp

8

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Sompong Vongpunsawad

2

object named as

Sompong Vongpunsawad

1 reference

4 July 2017

Jane M Olson

1

1 reference

4 July 2017

Antti Ronkainen

4

1 reference

4 July 2017

Markku Ryynänen

6

1 reference

4 July 2017

Lee-Lian Kim

7

1 reference

4 July 2017

language of work or name

English

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publication date

1 August 2002

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4 July 2017

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4 July 2017

3

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4 July 2017

1

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page(s)

7

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https://scigraph.springernature.com/pub.10.1186/1471-2350-3-7

4 July 2017

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cites work

Molecular cloning, expression, and chromosomal localization of a human brain-specific Na(+)-dependent inorganic phosphate cotransporter

1 reference

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Disease gene mapping in isolated human populations: the example of Finland

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

The structure of the urokinase-type plasminogen activator receptor gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Episodic ataxia type 2 (EA2) and spinocerebellar ataxia type 6 (SCA6) due to CAG repeat expansion in the CACNA1A gene on chromosome 19p

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Isolation and characterization of the human cardiac troponin I gene (TNNI3)

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Complete multipoint sib-pair analysis of qualitative and quantitative traits

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Genomewide-linkage and haplotype-association studies map intracranial aneurysm to chromosome 7q11

7 April 2017

1 reference

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One-stage versus two-stage strategies for genome scans

28 September 2017

1 reference

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Cost-effectiveness analysis of screening for asymptomatic, unruptured intracranial aneurysms. A mathematical model

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Relationship estimation by Markov-process models in a sib-pair linkage study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Should we screen for familial intracranial aneurysm?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Unruptured intracranial aneurysms--risk of rupture and risks of surgical intervention

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Linkage disequilibrium mapping in isolated populations: the example of Finland revisited

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Prevalence of cerebral aneurysms in patients with fibromuscular dysplasia: a reassessment

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Is Marfan syndrome associated with symptomatic intracranial aneurysms?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Familial subarachnoid hemorrhage in east Finland, 1977-1990.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Impact of early surgery on outcome after aneurysmal subarachnoid hemorrhage. A population-based study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

On the inheritance of intracranial aneurysms

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

A ten percent prevalence of asymptomatic familial intracranial aneurysms: preliminary report on 110 magnetic resonance angiography studies in members of 21 Finnish familial intracranial aneurysm families

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Origin, growth, and rupture of saccular aneurysms: a review

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Linkage strategies for genetically complex traits. I. Multilocus models

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Whole genome amplification from a single cell: implications for genetic analysis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Messages from an isolate: lessons from the Finnish gene pool

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Which unruptured cerebral aneurysms should be treated? A cost-utility analysis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Improved set of short-tandem-repeat polymorphisms for screening the human genome.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Morbidity and mortality from elective surgery for asymptomatic, unruptured, intracranial aneurysms: a meta-analysis.

30 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-7

Elective surgery for asymptomatic, unruptured, intracranial aneurysms: a cost-effectiveness analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-7

Special features of familial intracranial aneurysms: report of 215 familial aneurysms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-7

Risk of harboring an unruptured intracranial aneurysm.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-7

Positional cloning of disease genes: advantages of genetic isolates

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-7

Intracranial aneurysms: MR angiographic screening in 400 asymptomatic individuals with increased familial risk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-7

Gene for progressive familial heart block type I maps to chromosome 19q13.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-7

Familial intracranial aneurysms

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-3-7

Subarachnoid Haemorrhage in Identical Twins.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Primer-extension preamplified DNA is a reliable template for genotyping

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Two-stage global search designs for linkage analysis II: including discordant relative pairs in the study.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Efficient strategies for genome scanning using maximum-likelihood affected-sib-pair analysis.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119849

Magnetic resonance angiographic screening for asymptomatic intracranial aneurysms: the problem of false negatives: technical case report

28 November 2018

1 reference

12 December 2020

Mapping TNNC1, the gene that encodes cardiac troponin I in the human and the mouse

1 reference

12 December 2020

Intracranial aneurysms

1 reference

12 December 2020

Two-stage global search designs for linkage analysis using pairs of affected relatives

1 reference

12 December 2020

Two-stage global search designs for linkage analysis I: use of the mean statistic for affected sib pairs

1 reference

12 December 2020

Risks of surgery for unruptured intracranial aneurysms

1 reference

12 December 2020

Intracranial aneurysms and heredity

1 reference

12 December 2020

Cigarette smoking and alcohol consumption as risk factors for aneurysmal subarachnoid hemorrhage

1 reference

12 December 2020

Exclusion of mutations in the gene for type III collagen (COL3A1) as a common cause of intracranial aneurysms or cervical artery dissections: results from sequence analysis of the coding sequences of type III collagen from 55 unrelated patients

1 reference

12 December 2020

Type III collagen deficiency in saccular intracranial aneurysms. Defect in gene regulation?

1 reference

12 December 2020

An isolated cardiac conduction disease maps to chromosome 19q

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-3-7

1 reference

Dimensions Publication ID

4 July 2017

0 references

1 reference

4 July 2017

1 reference