(Q44691801)

5 December 2017

Susceptibility to pre-eclampsia in Finnish women is associated with R485K polymorphism in the factor V gene, not with Leiden mutation (English)

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5 December 2017

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8

Seppo Heinonen

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5 December 2017

Fareeza Faisel

1

1 reference

5 December 2017

Eeva-Liisa Romppanen

2

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5 December 2017

Mikko Hiltunen

3

1 reference

5 December 2017

Seppo Helisalmi

4

1 reference

5 December 2017

Jaana Laasanen

5

1 reference

5 December 2017

Kari Punnonen

6

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5 December 2017

Jukka T Salonen

7

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5 December 2017

1 March 2004

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European Journal of Human Genetics

5 December 2017

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5 December 2017

12

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5 December 2017

3

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5 December 2017

187-191

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201124

5 December 2017

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cites work

Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

Mutation in blood coagulation factor V associated with resistance to activated protein C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

Activated protein C resistance assay detects thrombotic risk factors other than factor V Leiden.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

Thrombophilic disorders and fetal loss: a meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

The impact of the factor V Leiden mutation on pregnancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

High prevalence of hemostatic abnormalities in women with a history of severe preeclampsia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

Molecular genetics of the Finnish disease heritage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

The factor V Leiden mutation may predispose women to severe preeclampsia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

Maternal and neonatal outcome of preeclamptic pregnancies: the potential roles of factor V Leiden mutation and 5,10 methylenetetrahydrofolate reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

Polymorphism in exon 10 of the human coagulation factor V gene in a population at risk for sickle cell disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

Assignment of gene for coagulation factor V to chromosome 1 in man and to chromosome 13 in rat

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

7 January 2021

Association of the R485K polymorphism of the factor V gene with poor response to activated protein C and increased risk of coronary artery disease in the Chinese population

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

7 January 2021

Association analysis of nine missense polymorphisms in the coagulation factor V gene with severe preeclampsia in pregnant Japanese women

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

7 January 2021

Preeclampsia is associated with a reduced response to activated protein C

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

7 January 2021

Dissecting a population genome for targeted screening of disease mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201124

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201124

1 reference

Dimensions Publication ID

5 December 2017

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1 reference