(Q80599380)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

title

VEGF C-634G polymorphism is associated with protection from isolated ventricular septal defect: case-control and TDT studies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

ventricular septal defect

2 January 2020

main subject

1 reference

1

1 reference

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2 January 2020

author name string

Long Yi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Zheng-Feng Xu

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Xu-Ming Mo

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Ya-Li Hu

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Dong-Jin Wang

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Hao-Zhen Ren

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Bing Han

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Yong Wang

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Chi Yang

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Ye-Lin Zhao

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Dong-Quan Shi

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Yong-Zhong Jiang

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Li Shen

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Di Qiao

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Shi-Lin Chen

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

Bao-Jun Yu

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

publication date

11 July 2007

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

European Journal of Human Genetics

2 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

volume

15

1 reference

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2 January 2020

issue

12

1 reference

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2 January 2020

page(s)

1246-1251

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201890

2 January 2020

exact match

0 references

cites work

The incidence of congenital heart disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

1 reference

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7 January 2021

Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Refined genotype-phenotype correlations in cases of chromosome 6p deletion syndromes.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Ventricular septal defect associated with microdeletions of chromosome 22q11.2.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

The biology of VEGF and its receptors

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Tumor induction of VEGF promoter activity in stromal cells

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Vascular endothelial growth factor in ocular fluid of patients with diabetic retinopathy and other retinal disorders

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Vascular endothelial growth factor gene +405 C/G polymorphism is associated with susceptibility to advanced stage endometriosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

VEGF: a modifier of the del22q11 (DiGeorge) syndrome?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Low expression VEGF haplotype increases the risk for tetralogy of Fallot: a family based association study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Single-nucleotide polymorphisms of VEGF gene are associated with risk of congenital valvuloseptal heart defects

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Novel polymorphisms in the promoter and 5' UTR regions of the human vascular endothelial growth factor gene.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Functional VEGF C-634G polymorphism is associated with development of diabetic macular edema and correlated with macular retinal thickness in type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Neural crest and cardiovascular patterning.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

New tetranucleotide STRP markers for detecting the 22q11.2 deletion.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Vascular endothelial growth factor (VEGF) is released from platelets during blood clotting: implications for measurement of circulating VEGF levels in clinical disease.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Inhibition of genes expression of SARS coronavirus by synthetic small interfering RNAs.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Population stratification and spurious allelic association

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

What's wrong with Bonferroni adjustments

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Heritability for plasma VEGF concentration in the Stanislas family study

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Identification of polymorphisms within the vascular endothelial growth factor (VEGF) gene: correlation with variation in VEGF protein production

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

A common polymorphism in the 5'-untranslated region of the VEGF gene is associated with diabetic retinopathy in type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201890

7 January 2021

SHEsis, a powerful software platform for analyses of linkage disequilibrium, haplotype construction, and genetic association at polymorphism loci

1 reference

20 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/SJ.CR.7290272

Identifiers

DOI

10.1038/SJ.EJHG.5201890

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17625508%20AND%20SRC:MED&resulttype=core&format=json

2 January 2020

1 reference