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Track record
Selected work.
Peer-reviewed research from our team, and client engagements where we led the statistics. The record spans randomised trials, nationwide registry epidemiology, human genetics and clinical machine learning, and is heaviest in haematology and cancer, with a long line of work in migraine and headache.
Epidemiological and genetic evidence for shared mechanisms between migraine and pre-eclampsia: a nationwide cohort and genetic risk study in Denmark
View Article →The Danish Lymphoid Cancer Research (DALY-CARE): Genetic Cohort Profile
View Article →Mosaic chromosomal alterations and relation to haematological cancer in two large Danish cohorts
View Article →Hierarchical vision transformers for Epstein-Barr virus status and histological subtype prediction in Hodgkin lymphoma whole-slide images
View Article →Intent to Treat Analysis of the Primary and Secondary Outcomes for the ODINN Intact Fish Skin Graft for Deep Diabetic Foot Wounds Trial
View Article →Rituximab maintenance after first-line rituximab-bendamustine
View Article →Severe toxicity-free survival following acute lymphoblastic leukemia in patients aged 1-45 years: a Danish cohort study
View Article →Post-treatment infection prediction in CLL using domain adaptation of lymphoma electronic health records
View Article →Resistant Hypertension Variants Link to Hyperaldosteronism and Potassium Levels
View Article →Sex differences in cancer incidence and survival: a Danish nationwide population-based study assessing 35 cancer sites
View Article →Disentangling shifting demographic and treatment effects on years of life lost to cancer in Denmark
View Article →Hypertension affects survival and treatment in chronic lymphocytic leukemia
View Article →CD20 negativity at the start of second-line therapy predicts a shorter overall survival in B-cell lymphomas
View Article →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
View Article →Machine learning enhances risk stratification and treatment failure prediction in diffuse large B-cell lymphoma
View Article →Prediagnostic opioid use and survival in multiple myeloma: a nationwide register-based study
View Article →Risk of infectious mononucleosis is not associated with prior infection morbidity
View Article →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
View Article →Trigeminal neuralgia and its comorbidities: a nationwide disease trajectory study
View Article →Machine Learning for Prediction of High-Risk Hospitalizations in Lymphoma Patients: A Danish Population-Based Study
View Article →Associations between past infectious mononucleosis diagnosis and 47 inflammatory and vascular stress biomarkers
View Article →The Danish Lymphoid Cancer Research (DALY-CARE) Data Resource: The Basis for Developing Data-Driven Hematology
View Article →Polypharmacy independently predicts survival, hospitalization, and infections in patients with lymphoid cancer
View Article →Blood donation and migraine relief: A national population cohort study in Denmark
View Article →Genome-wide association study reveals a locus in ADARB2 for complete freedom from headache in Danish Blood Donors
View Article →Infections and their prognostic significance before diagnosis of chronic lymphocytic leukemia, non-Hodgkin lymphoma, or multiple myeloma
View Article →Exclusive Breastfeeding Duration and Risk of Childhood Cancers
View Article →Intact Fish Skin Graft to Treat Deep Diabetic Foot Ulcers
View Article →Sex differences in clinical characteristics of migraine and its burden: a population-based study
View Article →Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland
View Article →Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria
View Article →Childhood cancer confers increased risk of migraine - A Danish nationwide register study
View Article →Genetic architecture of band neutrophil fraction in Iceland
View Article →Genetic insight into sick sinus syndrome
View Article →Twenty-five years of triptans - a nationwide population study
View Article →Long-read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traits
View Article →Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis
View Article →Fish skin grafts compared to human amnion/chorion membrane allografts: A double-blind, prospective, randomized clinical trial of acute wound healing
View Article →Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming
View Article →Familial analysis reveals rare risk variants for migraine in regulatory regions
View Article →Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank
View Article →Genetic predisposition to mosaic Y chromosome loss in blood
View Article →A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
View Article →Sequence variants with large effects on cardiac electrophysiology and disease
View Article →Sequence variants associating with urinary biomarkers
View Article →Migraine polygenic risk score associates with efficacy of migraine-specific drugs
View Article →A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease
View Article →Genome-wide association meta-analysis yields 20 loci associated with gallstone disease
View Article →A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin
View Article →A rare missense variant in NR1H4 associates with lower cholesterol levels
View Article →Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation
View Article →Variants in NKX2-5 and FLNC Cause Dilated Cardiomyopathy and Sudden Cardiac Death
View Article →Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits
View Article →Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters
View Article →A Missense Variant in PLEC Increases Risk of Atrial Fibrillation
View Article →A rare splice donor mutation in the haptoglobin gene associates with blood lipid levels and coronary artery disease
View Article →Sequence variant at 4q25 near PITX2 associates with appendicitis
View Article →COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA
View Article →Epigenetic and genetic components of height regulation
View Article →Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility
View Article →Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase
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