HUNTing for genes for myocardial infarction: the impact of rare genetic variants
- Prosjektnummer
- 46060901
- Ansvarlig person
- Kristian Hveem
- Institusjon
- NTNU, ISM
- Prosjektkategori
- Flerårig prosjekt 2011-SO
- Helsekategori
- Cardiovascular, Generic Health Relevance
- Forskningsaktivitet
- 1. Underpinning, 2. Aetiology
Methods for association analysis and meta-analysis of rare variants in families.
Genet Epidemiol 2015 May;39(4):227-38. Epub 2015 mar 4
PMID: 25740221
Impact of sex on the prognostic value of high-sensitivity cardiac troponin I in the general population: the HUNT study.
Clin Chem 2015 Apr;61(4):646-56. Epub 2015 feb 18
PMID: 25695851
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.
Nat Commun 2015;6():10206. Epub 2015 des 22
PMID: 26690388
MDM4 SNP34091 (rs4245739) and its effect on breast-, colon-, lung-, and prostate cancer risk.
Cancer Med 2015 Dec;4(12):1901-7. Epub 2015 okt 16
PMID: 26471763
Genetic Effects on Longitudinal Changes from Healthy to Adverse Weight and Metabolic Status – The HUNT Study.
PLoS One 2015;10(10):e0139632. Epub 2015 okt 7
PMID: 26445370
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk.
Nat Genet 2014 Apr;46(4):345-51. Epub 2014 mar 16
PMID: 24633158
No large-effect low-frequency coding variation found for myocardial infarction.
Hum Mol Genet 2014 Sep 1;23(17):4721-8. Epub 2014 apr 12
PMID: 24728188
Meta-analysis of gene-level tests for rare variant association.
Nat Genet 2014 Feb;46(2):200-4. Epub 2013 des 15
PMID: 24336170
Single nucleotide polymorphisms in G protein signaling pathway genes in preeclampsia.
Hypertension 2013 Mar;61(3):655-61. Epub 2013 jan 21
PMID: 23339167
Trends in overweight and obesity over 22 years in a large adult population: the HUNT Study, Norway.
Clin Obes 2013 Feb;3(1-2):12-20. Epub 2013 mar 19
PMID: 23935708
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explained.
PLoS Genet 2013 Mar;9(3):e1003379. Epub 2013 mar 21
PMID: 23555291
Common variants show predicted polygenic effects on height in the tails of the distribution, except in extremely short individuals.
PLoS Genet 2011 Dec;7(12):e1002439. Epub 2011 des 29
PMID: 22242009
- Inger Njølstad Prosjektdeltaker
- Bendik K S Winsvold Prosjektdeltaker
- John-Anker Zwart Prosjektdeltaker
- Håvard Dalen Prosjektdeltaker
- Lars Øystein Ursin Prosjektdeltaker
- Berge Solberg Prosjektdeltaker
- Maiken Elvestad Gabrielsen Postdoktorstipendiat
- Oddgeir Holmen Doktorgradsstipendiat
- Kristian Hveem Prosjektleder
- Cristen Willer Forskningsgruppeleder
- Arnulf Langhammer Prosjektdeltaker
- Maja-Lisa Løchen Prosjektdeltaker
- Kirsti Kvaløy Prosjektdeltaker
- Frank Skorpen Prosjektdeltaker
- Goncalo Abecasis Prosjektdeltaker
- Lars Johan Vatten Prosjektdeltaker
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