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Kristian Hveem

Researcher Next ID · RN-027449

Researcher · Biochemistry, Genetics and Molecular Biology

Norwegian University of Science and Technology

Trondheim, Norway

Not currently recruitingFunding unknown
Works count
595
Citation count
68,697
H-index
108
i10-index
332

Research interests

Biochemistry, Genetics and Molecular Biology
Medicine
Genetic Associations and Epidemiology
Epigenetics and DNA Methylation
Metabolomics and Mass Spectrometry Studies
Diabetes Treatment and Management
Gastrointestinal motility and disorders

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.