Genetikk og svangerskapsforgiftning
- Prosjektnummer
- 46036400
- Ansvarlig person
- Linda Tømmerdal Roten
- Institusjon
- NTNU, IKM
- Prosjektkategori
- Postdoc-stipend 2010
- Helsekategori
- Cancer, Cardiovascular, Reproductive Health and Childbirth
- Forskningsaktivitet
- 2. Aetiology
Validity of the diagnosis of pre-eclampsia in the Medical Birth Registry of Norway.
Acta Obstet Gynecol Scand 2013 Aug;92(8):943-50. Epub 2013 mai 29
PMID: 23621424
Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease.
Mol Hum Reprod 2013 Jul;19(7):423-37. Epub 2013 feb 18
PMID: 23420841
Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene.
PLoS One 2012;7(3):e33666. Epub 2012 mar 14
PMID: 22432041
A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2).
Mol Hum Reprod 2011 Jul;17(7):439-46. Epub 2011 feb 25
PMID: 21355050
STOX2 but not STOX1 is differentially expressed in decidua from pre-eclamptic women: data from the Second Nord-Trondelag Health Study.
Mol Hum Reprod 2010 Dec;16(12):960-8. Epub 2010 jul 19
PMID: 20643876
Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22
Pregnancy Hypertension, 2014
Heritability of cardiovascular diseases in a preeclampsia family cohort
63rd Annual Meeting of The American Society of Human Genetics, October, 2013 in Boston, MA, USA
A PREECLAMPSIA GENOME-WIDE LINKAGE SCAN IN NORWEGIAN FAMILIES
Pregnancy hypertension, 2013; vol 3(2) OP006 pp. 64.
ARVELIGHET AV KARDIOVASKULÆR SYKDOM I EN FAMILIEKOHORT MED OPPHOPNING AV PREEKLAMPSI
Norsk Gynekologisk Forenings årsmøte 2013
Er det en link mellom svangerskapsforgiftning og brystkreft?
Blog.medisin.ntnu.no, 2013
Shared genetic risk factors for preeclampsia and cardiovascular disease
Hypertension Pregnancy 2012; vol 2 (issue 3)
Genome-wide association scans identify novel maternal lsusceptibility loci for preeclampsia.
Hypertens Pregnancy 2012; vol 2 (issue 3) OS046 pp. 202
Shared genetic risk factors for preeclampsia and cardiovascular disease.
Hypertens Pregnancy 2012; vol 2 (issue 3) OS070 pp. 214
The chromosome 2q22 preeclampsia susceptibility locus reveals shared novel risk factors for CVD
Hypertens Pregnancy 2012; vol 2 (issue 3) OS077 pp. 219-220.
Investigating genetic predisposition and occurrence of preeclampsia and cardiovascular disease through a family-based design.
Placenta 33 (2012) A82.
Kartlegging av den genetiske arkitekturen for preeklampsi. En familie-basert studie.
Regional forskningskonferanse HMN, Trondheim, Norway 2012.
ESTABLISHMENT OF A NORWEGIAN PREECLAMPSIA FAMILY BIOBANK
Placenta 2011; 32: A85
Classification of pre-eclamptic pregnancies in health registries.
. Hypertens Pregnancy 2010;1 (supplement 1) S56
Classification of pre-eclamptic pregnancies in health registries.
17th ISSHP World Congress, Melbourne, Australia 2010
Genetic Predisposition to Preeclampsia
- Disputert:
- februar 2014
- Hovedveileder:
- Rigmor Austgulen
- Tom Grotmol Prosjektdeltaker
- Rebecca Troisi Prosjektdeltaker
- Anne Cathrine Staff Prosjektdeltaker
- Linda Tømmerdal Roten Prosjektleder
eRapport er utarbeidet av Sølvi Lerfald og Reidar Thorstensen, Regionalt kompetansesenter for klinisk forskning, Helse Vest RHF, og videreutvikles av de fire RHF-ene i fellesskap, med støtte fra Helse Vest IKT
Alle henvendelser rettes til Helse Midt-Norge RHF - Samarbeidsorganet og FFU