Kristian Hveem
Researcher Next ID · RN-027449
Researcher · Biochemistry, Genetics and Molecular Biology
Norwegian University of Science and Technology
Trondheim, Norway
- Works count
- 595
- Citation count
- 68,697
- H-index
- 108
- i10-index
- 332
Research interests
Publications
Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder
Nature Genetics · 2024 · https://doi.org/10.1038/s41588-024-01707-9
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
Nature Genetics · 2022 · https://doi.org/10.1038/s41588-021-00990-0
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
Nature Genetics · 2022 · https://doi.org/10.1038/s41588-022-01233-6
Genetic diversity fuels gene discovery for tobacco and alcohol use
Nature · 2022 · https://doi.org/10.1038/s41586-022-05477-4
Cohort Profile Update: The HUNT Study, Norway
International Journal of Epidemiology · 2022 · 10.1093/ije/dyac095
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease
Nature Genetics · 2021 · https://doi.org/10.1038/s41588-021-00921-z
SCORE2 risk prediction algorithms: new models to estimate 10-year risk of cardiovascular disease in Europe
European Heart Journal · 2021 · https://doi.org/10.1093/eurheartj/ehab309
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
Cell · 2021 · https://doi.org/10.1016/j.cell.2021.11.003
Exome sequencing and characterization of 49,960 individuals in the UK Biobank
Nature · 2020 · https://doi.org/10.1038/s41586-020-2853-0
Application of non-HDL cholesterol for population-based cardiovascular risk stratification: results from the Multinational Cardiovascular Risk Consortium
The Lancet · 2019 · https://doi.org/10.1016/s0140-6736(19)32519-x
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
Nature Genetics · 2018 · 10.1038/s41588-018-0171-3
Sodium glucose cotransporter 2 inhibitors and risk of serious adverse events: nationwide register based cohort study
BMJ · 2018 · 10.1136/bmj.k4365
Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies
Nature Genetics · 2018 · https://doi.org/10.1038/s41588-018-0184-y
Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease
Journal of the American College of Cardiology · 2017 · 10.1016/j.jacc.2016.11.056
Exome-wide association study of plasma lipids in >300,000 individuals
Nature Genetics · 2017 · 10.1038/ng.3977
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology
Nature Genetics · 2017 · 10.1038/ng.3985
Development and Validation of a Protein-Based Risk Score for Cardiovascular Outcomes Among Patients With Stable Coronary Heart Disease
JAMA · 2016 · 10.1001/jama.2016.5951
Lifestyle Intervention in Gastroesophageal Reflux Disease
Clinical Gastroenterology and Hepatology · 2015 · 10.1016/j.cgh.2015.04.176
Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk
Nature Genetics · 2014 · 10.1038/ng.2926
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
Nature Genetics · 2014 · https://doi.org/10.1038/ng.2915
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
The American Journal of Human Genetics · 2014 · https://doi.org/10.1016/j.ajhg.2014.01.010
Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis
Nature Genetics · 2013 · https://doi.org/10.1038/ng.2616
Cohort Profile: The HUNT Study, Norway
International Journal of Epidemiology · 2012 · https://doi.org/10.1093/ije/dys095
Several common variants modulate heart rate, PR interval and QRS duration
Nature Genetics · 2010 · 10.1038/ng.511
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
Nature Genetics · 2009 · https://doi.org/10.1038/ng.417
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1)
Nature Genetics · 2009 · 10.1038/ng.353
Identification of a new prostate cancer susceptibility locus on chromosome 8q24
Nature Genetics · 2009 · https://doi.org/10.1038/ng.444
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25
Nature · 2008 · https://doi.org/10.1038/nature06885
Obesity and Estrogen as Risk Factors for Gastroesophageal Reflux Symptoms
JAMA · 2003 · 10.1001/jama.290.1.66
Current projects
No projects listed.