Linda Tømmerdal Roten
Linda Tømmerdal Roten
Rådgiver REK
MH fakultetsadministrasjon Fakultet for medisin og helsevitenskapBakgrunn og aktiviteter
Ansettelsesforhold
Ansatt rådgiver hos Regional komité for medisinsk og helsefaglig forskningsetikk (REK) Midt-Norge.
Curriculum Vitae
- Rådgiver hos REK midt, NTNU 2014-nå
- Forsker ved Institutt for laboratoriemedisin, barne- og kvinnesykdommer, NTNU 2014-2017
- Førsteamanuensis ved Institutt for laboratoriemedisin, barne- og kvinnesykdommer, NTNU 2013 (januar-august)
- Post doktor ved Institutt for kreftforskning og molekylær medisin, NTNU 2010-2013
- Ph.d. i molekylær medisin ved Institutt for kreftforskning og molekylær medisin, NTNU 2004-2009
- Forskningsopphold ved Department of Genetics, Texas Biomedical Research Institute, San Antonio, Texas, USA, 2005
- Avdelingsingeniør, Institutt for kreftforskning og molekylær medisin, NTNU 2003-2004
- Sivilingeniør i bioteknologi ved NTNU, 2003
- Studentassistent in SIK4035 Biopolymer kjemi, Institutt for bioteknologi, Fakultet for naturvitenskap og teknologi, NTNU, 2002
Vitenskapelig, faglig og kunstnerisk arbeid
Et utvalg av nyere tidsskriftspublikasjoner, kunstneriske produksjoner, bok, inklusiv bokdeler og rapport-del. Se alle publikasjoner i databasen
Tidsskriftspublikasjoner
- (2022) Research based on existing clinical data and biospecimens: a systematic study of patients’ opinions. BMC Medical Ethics. vol. 23 (60).
- (2015) The Norwegian preeclampsia family cohort study: a new resource for investigating genetic aspects and heritability of preeclampsia and related phenotypes. BMC Pregnancy and Childbirth. vol. 15:319.
- (2015) A genetic connection between preeclampsia and chronic hypertension in Norwegian families. Pregnancy Hypertension. vol. 5.
- (2015) Refined phenotyping identifies links between preeclampsia and related diseases in a Norwegian preeclampsia family cohort. Journal of Hypertension. vol. 33 (11).
- (2015) ADAMTS13 gene variants and function in women with preeclampsia: A population- based nested case- control study from the HUNT Study. Thrombosis Research. vol. 136 (2).
- (2014) Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22. Pregnancy Hypertension. vol. 4 (2).
- (2013) Genetic dissection of the pre-eclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease. Molecular human reproduction. vol. 19 (7).
- (2013) A SNP associated with susceptibility to preeclampsia near the Inhibin, beta B gene, is also associated with cardiovascular disease risk traits. Pregnancy Hypertension. vol. 3 (2).
- (2013) A preeclampsia genome-wide linkage scan in Norwegian families. Pregnancy Hypertension. vol. 3 (2).
- (2013) Arvelighet av kardiovaskulær sykdom i en familiekohort med økt forekomst av preeklampsi. Gynekologen. vol. 26 (3).
- (2013) Validity of the diagnosis of pre-eclampsia in the Medical Birth Registry of Norway. Acta Obstetricia et Gynecologica Scandinavica. vol. 92 (8).
- (2013) Validity of pre-eclampsia diagnosis in Medical Birth Registry of Norway. Acta Obstetricia et Gynecologica Scandinavica.
- (2012) Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. PLOS ONE. vol. 7 (3).
- (2012) Genome-wide association scans identify novel maternal susceptibility loci for preeclampsia. Pregnancy Hypertension. vol. 2 (3).
- (2012) Shared genetic risk factors for preeclampsia and cardiovascular disease. Pregnancy Hypertension. vol. 2 (3).
- (2012) The chromosome 2q22 preeclampsia susceptibility locus reveals shared novel risk factors for CVD. Pregnancy Hypertension. vol. 2 (3).
- (2012) A population and family based study design to investigate genetic predisposition to preeclampsia and cardiovascular disease. The Norwegian Preeclampsia Family Study. Acta Obstetricia et Gynecologica Scandinavica. vol. 91.
- (2012) INVESTIGATING GENETIC PREDISPOSITION AND CLINICAL OCCURRENCE OF PREECLAMPSIA AND CARDIOVASCULAR DISEASE THROUGH A FAMILY-BASED DESIGN. Placenta. vol. 33 (9).
- (2011) A low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2). Molecular human reproduction. vol. 17 (7).
- (2011) Establishment of a Norwegian Preeclampsia Family Biobank. Placenta. vol. 32 (9).