Lenker
Postadresse
Det medisinske fakultet Institutt for samfunnsmedisin Helseundersøkelsen i Nord-Trøndelag
Norges teknisk-naturvitenskapelige universitet
7489 Trondheim
Elin Pettersen Sørgjerd
Rådgiver
Kort biografi Maks 160 tegn [0/160]
Lang biografi
Vitenskaplig, faglig og kunstnerisk arbeid
Et utvalg av nyere tidsskriftspublikasjoner, kunstneriske produksjoner, bok, inklusiv bokdeler og rapport-del.
Tidsskriftspublikasjoner
- (2013) Prevalence of ZnT8 antibody in relation to phenotype and SLC30A8 polymorphism in adult autoimmune diabetes. Results from the HUNT study, Norway. Autoimmunity. 2013; volum 46 (1).
- (2012) Time dynamics of autoantibodies are coupled to phenotypes and add to the heterogeneity of autoimmune diabetes in adults: the HUNT study, Norway. Diabetologia. 2012; volum 55 (5).
- (2011) No effect by the common gene variant rs10830963 of the melatonin receptor 1B on the association between sleep disturbances and type 2 diabetes: results from the Nord-Trondelag Health Study. Diabetologia. 2011; volum 54 (6).
- (2011) Pattern as well as pre-diabetic abscence or presence of antibodies reveal phenotypic difference among LADA patients: Results from the HUNT Study. Abstract, European Association for the Study of Diabetes , Lisbon 2011. Diabetologia. 2011; volum 54.
- (2010) Common variant of MTNR1B is associated with difficulties maintaining sleep but fails to influence the association between sleep disturbances and type 2 diabetes: the HUNT study. Diabetologia. 2010; volum 53.
- (2010) Genetic heterogeneity in latent autoimmune diabetes (LADA) is linked to a varying degree of autoimmune activity. Results from the Nord-Trondelag Health Study. Diabetes. 2010; volum 59 (1).
- (2008) COMT genotypes and use of antipsychotic medication: linking population-based prescription database to the HUNT study. Pharmacoepidemiology and Drug Safety. 2008; volum 17 (4).
- (2008) COMT genotypes and use of antipsychotic medication: linking population-based prescription database to the HUNT study. Pharmacoepidemiology and Drug Safety. 2008; volum 17 (4).
- (2008) Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Nature Genetics. 2008; volum 40 (5).
- (2007) High Systolic Blood Pressure Is Associated With Val/Val Genotype in the Catechol-O-Methyltransferase Gene The Nord-Trondelag Health Study (HUNT). American Journal of Hypertension. 2007; volum 20 (1).
- (2007) The impact of the Catechol-O-methyltransferase Val158Met polymorhism on survival in the general population -The HUNT study. BMC Medical Genetics. 2007; volum 8 (1).
- (2006) No association between chronic musculoskeletal complaints and Val158Met polymorphism in the Catechol-O-methyltransferase gene. Hhe HUNT Study. BMC Musculoskeletal Disorders. 2006; volum 4.
- (2006) No association between chronic musculoskeletal complaints and Val158Met polymorphism in the Catechol-O-methyltransferase gene. The HUNT study. BMC Musculoskeletal Disorders. 2006; volum 7.
- (2006) The association between headache and Val/Met polymorphism in the Catechol-O-methyltransferase gene. The HUNT Study. Journal of Headache and Pain. 2006; volum 7.
