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Selected work.

Peer-reviewed research from our team, and client engagements where we led the statistics.

55 publications
Blood Advances2026

Rituximab maintenance after first-line rituximab-bendamustine

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Leukemia2026

Severe toxicity-free survival following acute lymphoblastic leukemia in patients aged 1-45 years: a Danish cohort study

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Acta Oncologica2026

Post-treatment infection prediction in CLL using domain adaptation of lymphoma electronic health records

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Hypertension2026

Resistant Hypertension Variants Link to Hyperaldosteronism and Potassium Levels

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British Journal of Cancer2026

Sex differences in cancer incidence and survival: a Danish nationwide population-based study assessing 35 cancer sites

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npj Aging2026

Disentangling shifting demographic and treatment effects on years of life lost to cancer in Denmark

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Blood Advances2026

Hypertension affects survival and treatment in chronic lymphocytic leukemia

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Blood Neoplasia2026

CD20 negativity at the start of second-line therapy predicts a shorter overall survival in B-cell lymphomas

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British Journal of Haematology2026

Effects of chronic lymphocytic leukaemia (CLL)-directed therapy on diffuse large B-cell lymphoma (DLBCL) type Richter transformation compared to de novo DLBCL in a nationwide cohort

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HemaSphere2026

Machine learning enhances risk stratification and treatment failure prediction in diffuse large B-cell lymphoma

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Scientific Reports2026

Prediagnostic opioid use and survival in multiple myeloma: a nationwide register-based study

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Cancer Causes & Control2025

Use of healthcare services and prescription medication prior to sarcoma diagnosis in children, adolescents, and young adults in 1997-2020: a population-based cohort study

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Pain2025

Trigeminal neuralgia and its comorbidities: a nationwide disease trajectory study

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European Journal of Haematology2025

Machine Learning for Prediction of High-Risk Hospitalizations in Lymphoma Patients: A Danish Population-Based Study

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Scientific Reports2025

Associations between past infectious mononucleosis diagnosis and 47 inflammatory and vascular stress biomarkers

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Clinical Epidemiology2025

The Danish Lymphoid Cancer Research (DALY-CARE) Data Resource: The Basis for Developing Data-Driven Hematology

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HemaSphere2025

Polypharmacy independently predicts survival, hospitalization, and infections in patients with lymphoid cancer

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Transfusion2024

Blood donation and migraine relief: A national population cohort study in Denmark

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Communications Biology2024

Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood Donors

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British Journal of Cancer2024

Infections and their prognostic significance before diagnosis of chronic lymphocytic leukemia, non-Hodgkin lymphoma, or multiple myeloma

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JAMA Network Open2024

Exclusive Breastfeeding Duration and Risk of Childhood Cancers

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European Journal of Neurology2023

Sex differences in clinical characteristics of migraine and its burden: a population-based study

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Journal of the American Heart Association2023

Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland

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Communications Biology2023

Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria

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Cancer Epidemiology2022

Childhood cancer confers increased risk of migraine - A Danish nationwide register study

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Communications Biology2022

Genetic architecture of band neutrophil fraction in Iceland

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European Heart Journal2021

Genetic insight into sick sinus syndrome

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Cephalalgia2021

Twenty-five years of triptans - a nationwide population study

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Nature Genetics2021

Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits

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Communications Biology2020

Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis

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Current Biology2020

Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming

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Neurogenetics2020

Familial analysis reveals rare risk variants for migraine in regulatory regions

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Communications Biology2020

Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank

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Nature2019

Genetic predisposition to mosaic Y chromosome loss in blood

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Nature Genetics2019

A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis

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Nature Communications2019

Sequence variants with large effects on cardiac electrophysiology and disease

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Human Molecular Genetics2019

Sequence variants associating with urinary biomarkers

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Neurology: Genetics2019

Migraine polygenic risk score associates with efficacy of migraine-specific drugs

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Nature Communications2018

A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease

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Nature Communications2018

Genome-wide association meta-analysis yields 20 loci associated with gallstone disease

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Communications Biology2018

A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin

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Communications Biology2018

A rare missense variant in NR1H4 associates with lower cholesterol levels

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Communications Biology2018

Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation

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Circulation: Genomic and Precision Medicine2018

Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death

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Nature Communications2018

Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits

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BMC Medical Genetics2017

Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters

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Journal of the American College of Cardiology2017

A Missense Variant in PLEC Increases Risk of Atrial Fibrillation

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Human Molecular Genetics2017

A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease

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Scientific Reports2017

Sequence variant at 4q25 near PITX2 associates with appendicitis

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BMC Medical Genetics2017

COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

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Nature Communications2016

Epigenetic and genetic components of height regulation

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American Journal of Human Genetics2016

Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility

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Nature Communications2016

Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase

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