A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2)
The etiology of preeclampsia is complex, with susceptibility being attributable to multiple environmental factors and a large genetic component. Although many candidate genes for preeclampsia have been suggested and studied, the specific causative genes still remain to be identified. Catechol-O-meth...
| Main Authors: | Roten, L., Fenstad, M., Forsmo, S., Johnson, M., Moses, Eric, Austgulen, R., Skorpen, F. |
|---|---|
| Format: | Journal Article |
| Published: |
2011
|
| Online Access: | http://hdl.handle.net/20.500.11937/17090 |
Similar Items
The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations
by: Johnson, M., et al.
Published: (2009)
by: Johnson, M., et al.
Published: (2009)
Refined phenotyping identifies links between preeclampsia and related diseases in a Norwegian preeclampsia family cohort
by: Thomsen, L., et al.
Published: (2015)
by: Thomsen, L., et al.
Published: (2015)
Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study)
by: Roten, L., et al.
Published: (2009)
by: Roten, L., 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)
by: Fenstad, M., et al.
Published: (2010)
A transcriptional profile of the decidua in preeclampsia
by: Løset, M., et al.
Published: (2011)
by: Løset, M., et al.
Published: (2011)
Genetic association of preeclampsia to the inflammatory response gene SEPS1
by: Moses, Eric, et al.
Published: (2008)
by: Moses, Eric, et al.
Published: (2008)
Partial correlation network analyses to detect altered gene interactions in human disease: Using preeclampsia as a model
by: Johansson, A., et al.
Published: (2011)
by: Johansson, A., et al.
Published: (2011)
Identification of ACOX2 as a shared genetic risk factor for preeclampsia and cardiovascular disease
by: Johansson, A., et al.
Published: (2011)
by: Johansson, A., et al.
Published: (2011)
Genetic approaches in preeclampsia
by: Yong, H., et al.
Published: (2018)
by: Yong, H., et al.
Published: (2018)
Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22
by: Løset, M., et al.
Published: (2014)
by: Løset, M., et al.
Published: (2014)
The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia
by: Thomsen, L., et al.
Published: (2016)
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)
by: Lian, I., et al.
Published: (2013)
COMT methylation as a potential peripheral biomarker of schizophrenia
by: Abd. Rahim, Nour El Huda, et al.
Published: (2017)
by: Abd. Rahim, Nour El Huda, et al.
Published: (2017)
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)
by: Johnson, M., et al.
Published: (2012)
STOX2 but not STOX1 is differentially expressed in decidua from preeclamptic women: Data from the Second Nord-Trøndelag Health Study
by: Fenstad, M., et al.
Published: (2010)
by: Fenstad, M., et al.
Published: (2010)
Dietary Intake Contributed the Most to Chlorinated Paraffin Body Burden in a Norwegian Cohort
by: Yuan, Bo, et al.
Published: (2022)
by: Yuan, Bo, et al.
Published: (2022)
Prediction of clinical symptoms of schizophrenia based on COMT methylation marker
by: Abd. Rahim, Nour El Huda, et al.
Published: (2017)
by: Abd. Rahim, Nour El Huda, et al.
Published: (2017)
SD1000 Collaboration: Hunting down the Subdwarf Populations
by: Nemeth, P., et al.
Published: (2014)
by: Nemeth, P., et al.
Published: (2014)
Genetic Predisposition Of M2 Annexin A5 Haplotype In Recurrent Pregnancy Loss Among The Malays In Malaysia
by: Ang, Kai Cheen
Published: (2018)
by: Ang, Kai Cheen
Published: (2018)
Eating disorders, pregnancy, and the postpartum period: Findings from the Norwegian Mother and Child Cohort Study (MoBa)
by: Watson, Hunna, et al.
Published: (2014)
by: Watson, Hunna, et al.
Published: (2014)
Serum concentrations of legacy and emerging halogenated flame retardants in a Norwegian cohort: Relationship to external exposure
by: Tay, Joo Hui, et al.
Published: (2019)
by: Tay, Joo Hui, et al.
Published: (2019)
The evolution and diversity of TNF block haplotypes in European, Asian and Australian aboriginal populations
by: Valente, F., et al.
Published: (2009)
by: Valente, F., et al.
Published: (2009)
The hunt for mutations
by: Chung, Clarissa
Published: (2021)
by: Chung, Clarissa
Published: (2021)
TNF block haplotypes associated with conserved MHC haplotypes in European, Asian and Australian Aboriginal donors
by: Valente, F., et al.
Published: (2009)
by: Valente, F., et al.
Published: (2009)
Haplotype analyses of Orang Asli population in Taman Negara Pahang using Y-STR markers
by: Sofia S. M. Y.,, et al.
Published: (2015)
by: Sofia S. M. Y.,, et al.
Published: (2015)
Pelajar UPM Tingkat Kemahiran Bahasa Perancis di Université de Franche-Comté
by: Universiti Putra Malaysia, Bahagian Komunikasi Korporat
Published: (2010)
by: Universiti Putra Malaysia, Bahagian Komunikasi Korporat
Published: (2010)
TNF haplotypes in a Southern African population resemble those seen in Caucasians and Asians
by: Chew, C., et al.
Published: (2013)
by: Chew, C., et al.
Published: (2013)
Replay: for Matthew Hunt
by: Costantino, Thea
Published: (2011)
by: Costantino, Thea
Published: (2011)
Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes
by: Melton, Phillip, et al.
Published: (2019)
by: Melton, Phillip, et al.
Published: (2019)
Quantification of DNA methylation for COMT, RELN and HTR2C in schizophrenia using methylight assay
by: Abd. Rahim, Nour El Huda, et al.
Published: (2015)
by: Abd. Rahim, Nour El Huda, et al.
Published: (2015)
Role of caffeic acid O-methyltransferase (COMT) in the interaction between oil palm and Ganoderma boninense
by: Tan, Wee Pheng
Published: (2016)
by: Tan, Wee Pheng
Published: (2016)
An Investigation of the Factors Leading to Underpricing in the Norwegian IPO Market.
by: Barfod, Jonathan Andreas
Published: (2009)
by: Barfod, Jonathan Andreas
Published: (2009)
Wiggle your hips and drive like a Norwegian
Published: (2008)
Published: (2008)
Increase in Endothelin-1 expression in umbilical cord arteries in preeclampsia
by: .Algobori, Safa A. K, et al.
Published: (2020)
by: .Algobori, Safa A. K, et al.
Published: (2020)
Hunting patterns of the Iban community of Kampung Sebandi and the status of wildlife populations in Sebandi Forest
by: Nafisah, Bt. Tahir
Published: (2004)
by: Nafisah, Bt. Tahir
Published: (2004)
Hunting the Mammoth, Pleistocene to Postmodern
by: Chrulew, Matthew
Published: (2011)
by: Chrulew, Matthew
Published: (2011)
Hunting down the agents of illness
by: New Sunday, Times
Published: (1998)
by: New Sunday, Times
Published: (1998)
No more the hunted in land of the hornbills
by: The Borneo, Post
Published: (2016)
by: The Borneo, Post
Published: (2016)
On A Hunt For More Men
by: The Star, Ng Wei Loon
Published: (2008)
by: The Star, Ng Wei Loon
Published: (2008)
Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes
by: Kaartokallio, T., et al.
Published: (2016)
by: Kaartokallio, T., et al.
Published: (2016)
Similar Items
-
The ERAP2 gene is associated with preeclampsia in Australian and Norwegian populations
by: Johnson, M., et al.
Published: (2009) -
Refined phenotyping identifies links between preeclampsia and related diseases in a Norwegian preeclampsia family cohort
by: Thomsen, L., et al.
Published: (2015) -
Association between the candidate susceptibility gene ACVR2A on chromosome 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study)
by: Roten, L., 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) -
A transcriptional profile of the decidua in preeclampsia
by: Løset, M., et al.
Published: (2011)