Genetic approaches in preeclampsia

QR Code

Genetic approaches in preeclampsia

Preeclampsia (PE) is a serious hypertensive disorder that affects up to 8% of all pregnancies annually. An established risk factor for PE is family history, clearly demonstrating an underlying genetic component to the disorder. To date, numerous genetic studies, using both the candidate gene and gen...

Full description

Bibliographic Details
Main Authors:	Yong, H., Murthi, P., Brennecke, S., Moses, Eric
Format:	Book Chapter
Published:	2018
Online Access:	http://hdl.handle.net/20.500.11937/69980

Similar Items

Genetic association of preeclampsia to the inflammatory response gene SEPS1
by: Moses, Eric, et al.
Published: (2008)

Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22
by: Løset, M., et al.
Published: (2014)

The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations
by: Johnson, M., et al.
Published: (2009)

Genetic and molecular functional characterization of variants within TNFSF13B, a positional candidate preeclampsia susceptibility gene on 13q
by: Fenstad, M., et al.
Published: (2010)

Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease
by: Johansson, A., et al.
Published: (2011)

Refined phenotyping identifies links between preeclampsia and related diseases in a Norwegian preeclampsia family cohort
by: Thomsen, L., et al.
Published: (2015)

A transcriptional profile of the decidua in preeclampsia
by: Løset, M., et al.
Published: (2011)

The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia
by: Thomsen, L., et al.
Published: (2016)

Differential Gene Expression at the Maternal-Fetal Interface in Preeclampsia Is Influenced by Gestational Age
by: Lian, I., et al.
Published: (2013)

Molecular genetic studies in pregnancies affected by preeclampsia and intrauterine growth restriction
by: Abd-Rabou, Ayat Abdel-Rahman Sayed
Published: (2011)

Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes
by: Melton, Phillip, et al.
Published: (2019)

Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes
by: Kaartokallio, T., et al.
Published: (2016)

Increased decidual mRNA expression levels of candidate maternal pre-eclampsia susceptibility genes are associated with clinical severity
by: Yong, H., et al.
Published: (2014)

A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2)
by: Roten, L., et al.
Published: (2011)

Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene
by: Johnson, M., et al.
Published: (2012)

Partial correlation network analyses to detect altered gene interactions in human disease: Using preeclampsia as a model
by: Johansson, A., et al.
Published: (2011)

Genome-wide transcriptome directed pathway analysis of maternal pre-eclampsia susceptibility genes
by: Yong, H., et al.
Published: (2015)

Increase in Endothelin-1 expression in umbilical cord arteries in preeclampsia
by: .Algobori, Safa A. K, et al.
Published: (2020)

The severity of preeclampsia and its associated factors in Hospital Universiti Sains Malaysia
by: Mat Tamizi, Nurdiyana Farhana
Published: (2017)

Negative correlation between Placental Growth Factor and Endocan-1 in women with preeclampsia
by: Ribiero Hentchke, Marta, et al.
Published: (2018)

42 Negative correlation between PlGF and Endocan-1 in women with preeclampsia
by: Ribeiro Hentschke, Marta, et al.
Published: (2016)

A web based fuzzy expert system preeclampsia pre-diagnosis / Hafizzah Hamizan
by: Hamizan, Hafizzah
Published: (2006)

Genetic association of the activin A receptor gene (ACVR2A) and pre-eclampsia
by: Fitzpatrick, E., et al.
Published: (2009)

Novel expression and regulation of voltage-dependent potassium (KV7) channels in placentae from women with preeclampsia
by: Mistry, Hiten D., et al.
Published: (2011)

Laboratory and clinical significance of rare antiphospholipid antibodies in preeclampsia patients : a preliminary study by Mimi Azreen Abdullah
by: Abdullah, Mimi Azreen
Published: (2015)

A randomised controlled trial of mgso4 therapy for 24 hours versus early cessation in patients with severe preeclampsia
by: Yunus, Affendi
Published: (2010)

Inherited thrombophilias and adverse pregnancy outcomes: A case-control study in an Australian population
by: Said, J., et al.
Published: (2012)

In reply
by: Said, J., et al.
Published: (2010)

Inherited thrombophilia polymorphisms and pregnancy outcomes in nulliparous women
by: Said, J., et al.
Published: (2010)

Total nucleated cell count and CD34+ cell is reduced in preeclampsia and gestational diabetes mellitus pregnancies: viable affix criteria for cord blood banking
by: Mohd Razif Mohd Idris,, et al.
Published: (2018)

Degradation Of Oxytetracycline From Aquaculture Wastewater Using Sole Ozonation And Catalytic Ozonation In The Presence Of Activated Carbon
by: Murthi, Bohesharvind Naraiyanan
Published: (2022)

A Five Year (2013-2017) Retrospective Study On The Data Of Laboratory Testing For Biocompatibility Of Medical Device Implant Registered With Malaysia Medical Device Authority
by: Anamalai, Sunthara Murthi
Published: (2021)

The PAI-1 4G/5G polymorphism is not associated with an increased risk of adverse pregnancy outcome in asymptomatic nulliparous women
by: Said, J., et al.
Published: (2012)

Molecular markers of preterm labor in the choriodecidua
by: Shankar, R., et al.
Published: (2010)

Longitudinal analytical approaches to genetic data.
by: Chiu, Y., et al.
Published: (2016)

The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population
by: Said, J., et al.
Published: (2008)

Environment Changes Genetic Effects on Respiratory Conditions and Allergic Phenotypes
by: Song, Y., et al.
Published: (2017)

Medical Genetic Conference 2007 Genetic Service: A Team Approach - Abstracts.
by: PPSP, Pusat Pengajian Sains Perubatan
Published: (2007)

The association of host and genetic melanoma risk factors with Breslow thickness in the Western Australian Melanoma Health Study
by: Cadby, G., et al.
Published: (2014)

An Approach to Derive Parametric L-System Using Genetic Algorithm
by: Farooq, H., et al.
Published: (2009)

Cannot write session to /tmp/vufind_sessions/sess_hrbknoks0p38j9k1kpkbvlhr9o