Susceptibility loci for intracranial aneurysm in European and Japanese populations (Q24643743)

6

0 references

Cisca Wijmenga

25

0 references

Aarno Palotie

30

0 references

Kaya Bilguvar

1

0 references

Mika Niemelä

3

Mika Niemelä

0 references

Juha Hernesniemi

28

Mikael von und zu Fraunberg

Juha Hernesniemi

0 references

5

Mikael von Und Zu Fraunberg

0 references

Katsuhito Yasuno

Katsuhito Yasuno

2

0 references

Juha Ohman

Juha Ohman

23

0 references

Atsushi Tajima

Atsushi Tajima

17

0 references

Akira Hata

19

Akira Hata

0 references

Aki Laakso

Aki Laakso

18

0 references

Leonard H van den Berg

7

Leonard H van den Berg

0 references

Gabriël Rinkel

27

Gabriel J E Rinkel

0 references

Ynte Ruigrok

4

Ynte M Ruigrok

0 references

Christopher E. Mason

9

Christopher E Mason

0 references

Monique Breteler

24

Monique M B Breteler

0 references

author name string

Shrikant Mane

8

0 references

Murim Choi

10

0 references

Emília Gaál

11

0 references

Yasar Bayri

12

0 references

Luis Kolb

13

0 references

Zulfikar Arlier

14

0 references

Sudhakar Ravuri

15

0 references

Antti Ronkainen

16

0 references

Hidetoshi Kasuya

20

0 references

Timo Koivisto

21

0 references

Jaakko Rinne

22

0 references

Matthew W State

26

0 references

Juha E Jääskeläinen

29

0 references

Ituro Inoue

31

0 references

Richard P Lifton

32

0 references

Murat Günel

33

0 references

language of work or name

English

0 references

publication date

December 2008

0 references

published in

Nature Genetics

0 references

volume

40

0 references

issue

12

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

9

0 references

page(s)

1472-7

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

A second generation human haplotype map of over 3.1 million SNPs

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

A common allele on chromosome 9 associated with coronary heart disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Mapping a Mendelian form of intracranial aneurysm to 1p34.3-p36.13

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Assessing the impact of population stratification on genetic association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Bone marrow-derived circulating endothelial precursors do not contribute to vascular endothelium and are not needed for tumor growth

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Sox17 dependence distinguishes the transcriptional regulation of fetal from adult hematopoietic stem cells

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Redundant roles of Sox17 and Sox18 in early cardiovascular development of mouse embryos

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Isolation of putative progenitor endothelial cells for angiogenesis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Redundant roles of Sox17 and Sox18 in postnatal angiogenesis in mice

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

A common variant on chromosome 9p21 affects the risk of myocardial infarction

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Population structure, differential bias and genomic control in a large-scale, case-control association study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Variants conferring risk of atrial fibrillation on chromosome 4q25.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Differential roles of vascular endothelial growth factor receptor-1 and receptor-2 in angiogenesis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

KDR receptor: a key marker defining hematopoietic stem cells

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Genomewide Linkage in a Large Dutch Family With Intracranial Aneurysms

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Stem-cell ageing modified by the cyclin-dependent kinase inhibitor p16INK4a

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682433

Recommendations for the management of patients with unruptured intracranial aneurysms: A Statement for healthcare professionals from the Stroke Council of the American Heart Association

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18997786

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial aneurysmal subarachnoid hemorrhage: a community-based study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18997786

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Molecular genetic analysis of two large kindreds with intracranial aneurysms demonstrates linkage to 11q24-25 and 14q23-31

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18997786

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.240

1 reference

Dimensions Publication ID

4549020

1008937050

0 references

4549020

1 reference

1 reference

1 reference