G. Másson

发表

A rare IL33 loss-of-function mutation reduces blood eosinophil counts and protects from asthma

D. Gudbjartsson, A. Sigurdsson, A. Jonasdottir, 2017, PLoS genetics.

Large-scale whole-genome sequencing of the Icelandic population

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2015, Nature Genetics.

Common variants conferring risk of schizophrenia

Pall I. Olason, P. Matthews, H. Stefánsson, 2009, Nature.

Parental influence on human germline de novo mutations in 1,548 trios from Iceland

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2017, Nature.

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor–positive breast cancer

D. Gudbjartsson, L. Kiemeney, J. Gulcher, 2007, Nature Genetics.

Common variants on chromosome 5p12 confer susceptibility to estrogen receptor–positive breast cancer

A. Sigurdsson, L. Kiemeney, J. Gulcher, 2008, Nature Genetics.

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

Gerard Tromp, Helena Kuivaniemi, Kari Stefansson, 2010, Nature Genetics.

Fine-scale recombination rate differences between sexes, populations and individuals

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2010, Nature.

A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2007, Science.

Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.

Paolo Vineis, Simonetta Guarrera, Giuseppe Matullo, 2014, Human molecular genetics.

Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche

Andrew D. Johnson, Daniel L. Koller, E. Demerath, 2014, Nature.

Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.

Kari Stefansson, Florian Zink, Gisli Masson, 2017, Blood.

Detection of sharing by descent, long-range phasing and haplotype imputation

Pall I. Olason, H. Stefánsson, A. Ingason, 2008, Nature Genetics.

Determination of active concentrations and association and dissociation rate constants of interacting biomolecules: an analytical solution to the theory for kinetic and mass transport limitations in biosensor technology and its experimental verification.

G. Másson, N. Beauchemin, K. Sigmundsson, 2002, Biochemistry.

Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2015, Nature Communications.

A high-resolution recombination map of the human genome

D. Gudbjartsson, T. Thorgeirsson, J. Gulcher, 2002, Nature Genetics.

A common inversion under selection in Europeans

H. Stefánsson, A. Ingason, A. Gylfason, 2005, Nature Genetics.

Identification of a large set of rare complete human knockouts

H. Stefánsson, D. Gudbjartsson, A. Sigurdsson, 2015, Nature Genetics.

Selection against variants in the genome associated with educational attainment

H. Stefánsson, D. Gudbjartsson, U. Thorsteinsdóttir, 2017, Proceedings of the National Academy of Sciences.

Variants with large effects on blood lipids and the role of cholesterol and triglycerides in coronary disease

D. Gudbjartsson, A. Sigurdsson, Á. Jónasdóttir, 2016, Nature Genetics.

Graphtyper enables population-scale genotyping using pangenome graphs

Kari Stefansson, Hannes P Eggertsson, Bjarni V Halldorsson, 2017, Nature Genetics.

Sequence variants from whole genome sequencing a large group of Icelanders

Kari Stefansson, Bjarni V Halldorsson, Florian Zink, 2015, Scientific Data.

Genetic Architecture of Vitamin B12 and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2013, PLoS genetics.

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

Dan M Roden, Kari Stefansson, Gudmar Thorleifsson, 2011, Nature Genetics.

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

Thomas Meitinger, Pierre Fontanillas, Stefan Johansson, 2014, Nature Genetics.

A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer

Kari Stefansson, Brian T Helfand, Gudmar Thorleifsson, 2012, Nature Genetics.

A common variant on chromosome 9p21 affects the risk of myocardial infarction.

Kari Stefansson, Arshed A Quyyumi, Anna Helgadottir, 2007, Science.

Weighting sequence variants based on their annotation increases power of whole-genome association studies

Anders Albrechtsen, Kari Stefansson, Florian Zink, 2016, Nature Genetics.

GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

A. Uitterlinden, J. V. van Meurs, E. Zeggini, 2019, Nature Communications.

Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2017, Nature Communications.

Sequence variants associating with urinary biomarkers

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2018, Human molecular genetics.

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

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2019, Nature Genetics.

Reconstructing an African haploid genome from the 18th century

Valdis B. Guðmundsdóttir, A. Kong, K. Stefánsson, 2018, Nature Genetics.

A common variant at 8q24.21 is associated with renal cell cancer

D. Gudbjartsson, L. Kiemeney, U. Thorsteinsdóttir, 2013, Nature Communications.

Genetic architecture of band neutrophil fraction in Iceland

D. Gudbjartsson, A. Jonasdottir, Á. Jónasdóttir, 2022, Communications Biology.

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

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2018, Nature Communications.

Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset

Pall I. Olason, H. Stefánsson, D. Gudbjartsson, 2022, Annals of the Rheumatic Diseases.

Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2016, Human molecular genetics.

Rate of de novo mutations and the importance of father’s age to disease risk

S. Steinberg, D. Gudbjartsson, A. Sigurdsson, 2012, Nature.

Severe osteoarthritis of the hand associates with markers within the ALDH1A2 gene and with very rare variants at 1p31

T. Spector, A. Sigurdsson, Á. Jónasdóttir, 2017 .

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2018, Nature Genetics.

HLA alleles, disease severity, and age associate with T-cell responses following infection with SARS-CoV-2

Hannes P. Eggertsson, B. Halldórsson, D. Gudbjartsson, 2022, Communications Biology.

Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

Daniel F. Gudbjartsson, Michael L. Frigge, Kari Stefansson, 2013, Nature.

Multi-nucleotide de novo Mutations in Humans

D. Gudbjartsson, A. Jonasdottir, Á. Jónasdóttir, 2016, PLoS genetics.

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

Bjarni V. Halldórsson, A. Ingason, B. Halldórsson, 2018, Nature Communications.

Physical and neurobehavioral determinants of reproductive onset and success

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2016, Nature Genetics.

The nature of nurture: Effects of parental genotypes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2017, Science.

Large-scale integration of the plasma proteome with genetics and disease

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2021, Nature Genetics.

A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer

Paolo Vineis, Simonetta Guarrera, Giuseppe Matullo, 2010, Nature Genetics.

Sequence variants at the TERT-CLPTM1L locus associate with many cancer types

Paolo Vineis, Giuseppe Matullo, Kari Stefansson, 2009, Nature Genetics.

A direct characterization of human mutation based on microsatellites

Swapan Mallick, Heng Li, Kari Stefansson, 2012, Nature Genetics.

Humoral Immune Response to SARS-CoV-2 in Iceland

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2020, The New England journal of medicine.

Spread of SARS-CoV-2 in the Icelandic Population

Kari Stefansson, Thorolfur Gudnason, Aslaug Jonasdottir, 2020, The New England journal of medicine.

Reconstruction of a large-scale outbreak of SARS-CoV-2 infection in Iceland informs vaccination strategies

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2021, Clinical Microbiology and Infection.

Common Sequence Variants in the LOXL1 Gene Confer Susceptibility to Exfoliation Glaucoma

Kari Stefansson, Gudmar Thorleifsson, Hreinn Stefansson, 2007, Science.

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

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2017, Human molecular genetics.

Loss-of-function variants in ATM confer risk of gastric cancer

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2015, Nature Genetics.

Rate of de novo mutations, father’s age, and disease risk

S. Steinberg, D. Gudbjartsson, A. Sigurdsson, 2012, Nature.

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

Gudmundur A. Thorisson, D. Gudbjartsson, A. Sigurdsson, 2018, Nature Communications.

Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations

H. Stefánsson, A. Ingason, D. Gudbjartsson, 2017, npj Genomic Medicine.

Rare mutations associating with serum creatinine and chronic kidney disease.

Kari Stefansson, Runolfur Palsson, Aslaug Jonasdottir, 2014, Human molecular genetics.

Mutations in BRIP1 confer high risk of ovarian cancer

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2011, Nature Genetics.

Rate of de novo mutations and the importance of father’s age to disease risk

S. Steinberg, D. Gudbjartsson, A. Sigurdsson, 2012, Nature.

Characterizing mutagenic effects of recombination through a sequence-level genetic map

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2019, Science.

Multiple transmissions of de novo mutations in families

Hannes P. Eggertsson, A. Gylfason, B. Halldórsson, 2018, Nature Genetics.

Recurrence of de novo mutations in families

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2017, bioRxiv.

Whole genome characterization of sequence diversity of 15,220 Icelanders

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2017, Scientific Data.

The rate of meiotic gene conversion varies by sex and age

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2016, Nature Genetics.

Identification of low-frequency variants associated with gout and serum uric acid levels

H. Stefánsson, A. Gylfason, D. Gudbjartsson, 2011, Nature Genetics.

Large-scale comparison of immunoassay- and aptamer-based plasma proteomics through genetics and disease

Pall I. Olason, Grimur Hjorleifsson Eldjarn, Bjarni V. Halldórsson, 2022, bioRxiv.

Sequence Variants in the RNF212 Gene Associate with Genome-Wide Recombination Rate

Kari Stefansson, Gudmar Thorleifsson, Hreinn Stefansson, 2008, Science.

The sequences of 150,119 genomes in the UK Biobank

Hannes P. Eggertsson, Brynja D. Sigurpálsdóttir, Pall I. Olason, 2021, Nature.

GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

A. Uitterlinden, J. V. van Meurs, E. Zeggini, 2019, Nature Communications.

Association of BRCA2 K3326* With Small Cell Lung Cancer and Squamous Cell Cancer of the Skin

A. Uitterlinden, D. Gudbjartsson, A. Sigurdsson, 2018, Journal of the National Cancer Institute.

Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31

Kari Stefansson, Evangelos Evangelou, Fernando Rivadeneira, 2014, Nature Genetics.

Common and low-frequency variants associated with genome-wide recombination rate

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2013, Nature Genetics.

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

H. Stefánsson, A. Sigurdsson, A. Jonasdottir, 2010, Nature Genetics.

New basal cell carcinoma susceptibility loci

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2015, Nature Communications.

FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease

D. Gudbjartsson, A. Sigurdsson, U. Thorsteinsdóttir, 2020, Nature.

Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2020, Nature Communications.

Sequence variant at 8 q 24 . 21 associates with sciatica caused by lumbar disc herniation

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2017 .

Comprehensive population-wide analysis of Lynch syndrome in Iceland reveals founder mutations in MSH6 and PMS2

A. Sigurdsson, K. Stefánsson, P. Sulem, 2017, Nature Communications.

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

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2021, Nature Genetics.

Long read sequencing of 1,817 Icelanders provides insight into the role of structural variants in human disease

Guillaume Holley, Daniel F. Gudbjartsson, Kari Stefansson, 2019, bioRxiv.

Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes

Kari Stefansson, Torben Hansen, Niels Grarup, 2014, Nature Genetics.

HLA class II sequence variants influence tuberculosis risk in populations of European ancestry

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2016, Nature Genetics.

Parental origin of sequence variants associated with complex diseases

Daniel F. Gudbjartsson, Michael L. Frigge, Kari Stefansson, 2009, Nature.

Associations of autozygosity with a broad range of human phenotypes

May E. Montasser, Annelot M. Dekker, Blair H. Smith, 2019, Nature Communications.

Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis

D. Gudbjartsson, A. Sigurdsson, U. Thorsteinsdóttir, 2018, Nature Genetics.

A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2017, European heart journal.

Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis

D. Gudbjartsson, T. Thorgeirsson, A. Sigurdsson, 2017, Nature Communications.

Description of the EuroTARGET cohort: A European collaborative project on TArgeted therapy in renal cell cancer-GEnetic- and tumor-related biomarkers for response and toxicity.

L. Kiemeney, K. Stefánsson, G. Másson, 2017, Urologic oncology.

Epigenetic and genetic components of height regulation

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2016, Nature Communications.

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

D. Gudbjartsson, A. Jonasdottir, Á. Jónasdóttir, 2016, Nature Communications.

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

Bjarni V. Halldórsson, A. Ingason, B. Halldórsson, 2018, Nature Communications.

A germline variant in the TP53 polyadenylation signal confers cancer susceptibility

Kari Stefansson, Brian T Helfand, Torben Hansen, 2011, Nature Genetics.

A genome-wide association study yields five novel thyroid cancer risk loci

Sandya Liyanarachchi, Kari Stefansson, Gudmar Thorleifsson, 2017, Nature Communications.

Graphtyper: Population-scale genotyping using pangenome graphs

Daniel F. Gudbjartsson, Kari Stefansson, Florian Zink, 2017, bioRxiv.

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

A Sigurdsson, G Masson, D. Gudbjartsson, 2014, Leukemia.

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

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2018, Communications Biology.

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

Gudmundur A. Thorisson, D. Gudbjartsson, A. Sigurdsson, 2017, BMC Medical Genetics.

Insights into imprinting from parent-of-origin phased methylomes and transcriptomes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2018, Nature Genetics.

Estimating heritability without environmental bias

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2017, bioRxiv.

A rare missense variant in NR1H4 associates with lower cholesterol levels

D. Gudbjartsson, A. Sigurdsson, A. Jonasdottir, 2018, Communications Biology.

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

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2018, Nature Communications.

Parent-of-Origin Specific Allelic Associations Among 106 Genomic Loci for Age at Menarche

Andrew D. Johnson, Daniel L. Koller, E. Demerath, 2014 .

Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood

D. Gudbjartsson, T. Thorgeirsson, U. Thorsteinsdóttir, 2019, Cancer Epidemiology, Biomarkers & Prevention.

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma

D. Gudbjartsson, Á. Jónasdóttir, U. Thorsteinsdóttir, 2014, Human molecular genetics.

New common variants affecting susceptibility to basal cell carcinoma

D. Gudbjartsson, A. Sigurdsson, T. Blondal, 2009, Nature Genetics.

Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2018, Nature Communications.

Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis

D. Gudbjartsson, A. Sigurdsson, U. Thorsteinsdóttir, 2018, Nature Genetics.

GORpipe: a query tool for working with sequence data based on a Genomic Ordered Relational (GOR) architecture

Sigurjón Axel Guðjónsson, Sigmar K. Stefánsson, Hákon Guðbjartsson, 2016, Bioinform..

Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease.

D. Gudbjartsson, A. Sigurdsson, Á. Jónasdóttir, 2016, The New England journal of medicine.

Cohort profile: Copenhagen Hospital Biobank - Cardiovascular Disease Cohort (CHB-CVDC): Construction of a large-scale genetic cohort to facilitate a better understanding of heart diseases

H. Stefánsson, A. Gylfason, D. Gudbjartsson, 2021, BMJ Open.

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

D. Gudbjartsson, A. Jonasdottir, Á. Jónasdóttir, 2020, Communications Biology.

A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2019, Nature Communications.

Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.

H. Stefánsson, D. Gudbjartsson, A. Sigurdsson, 2017, Nature genetics.

Identification of sequence variants influencing immunoglobulin levels

Bjarni V. Halldórsson, A. Gylfason, B. Halldórsson, 2017, Nature Genetics.

Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

H. Stefánsson, D. Gudbjartsson, A. Sigurdsson, 2017, Nature Genetics.

A common variant at 8 q 24 . 21 is associated with renal cell cancer

D. Gudbjartsson, L. Kiemeney, U. Thorsteinsdóttir, 2017 .

Common and rare variants associated with kidney stones and biochemical traits

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2015, Nature Communications.

A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration

Kari Stefansson, Kang Zhang, Gudmar Thorleifsson, 2013, Nature Genetics.

Discovery of common variants associated with low TSH levels and thyroid cancer risk

Kari Stefansson, Gudmar Thorleifsson, Jon Hrafnkelsson, 2012, Nature Genetics.

Rare sequence variants that disrupt ASGR 1 function lower non-HDL cholesterol and protect against coronary artery disease

Nele, A. Sigurdsson, L. Kiemeney, 2016 .

Lifelong Reduction in LDL Cholesterol Due to a Gain-of-Function Mutation in LDLR.

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2020, Circulation. Genomic and precision medicine.

Syddansk Universitet Variant ASGR1 associated with a reduced risk of coronary artery disease

A. Sigurdsson, Á. Jónasdóttir, L. Kiemeney, 2016 .

Genetic Correction of PSA Values Using Sequence Variants Associated with PSA Levels

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2010, Science Translational Medicine.

CDKN2A mutations and melanoma risk in the Icelandic population

U. Thorsteinsdóttir, A. Kong, K. Stefánsson, 2008, Journal of Medical Genetics.

Icelandic population mutations and melanoma risk in the CDKN2A

J. Gulcher, U. Thorsteinsdóttir, P. Sulem, 2008 .

A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences

S. Steinberg, D. Gudbjartsson, T. Thorgeirsson, 2016, Molecular Psychiatry.

Population-level deficit of homozygosity unveils CPSF3 as an intellectual disability syndrome gene

D. Gudbjartsson, A. Jonasdottir, Á. Jónasdóttir, 2022, Nature Communications.

Differences between germline genomes of monozygotic twins

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2021, Nature Genetics.

Differences between germline genomes of monozygotic twins

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2021, Nature Genetics.

Insights into imprinting from parent-of-origin phased methylomes and transcriptomes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2018, Nature Genetics.

Author Correction: The rate of meiotic gene conversion varies by sex and age

A. Gylfason, B. Halldórsson, D. Gudbjartsson, 2018, Nature Genetics.

Multiple transmissions of de novo mutations in families

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2018, Nature Genetics.

Rings of differential operators and étale homomorphisms

G. Másson, 1991 .

BamHash: a checksum program for verifying the integrity of sequence data

Páll Melsted, Gísli Másson, Arna Óskarsdóttir, 2015, bioRxiv.

Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis

A. Gylfason, B. Halldórsson, D. Gudbjartsson, 2020, Nature Communications.

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

Gudmundur A. Thorisson, D. Gudbjartsson, A. Sigurdsson, 2017, BMC Medical Genetics.

Comprehensive population-wide detection of Lynch syndrome in Iceland.

A. Sigurdsson, K. Stefánsson, P. Sulem, 2016 .

Augustine Kong Recombination Rate Gene Associate with Genome-Wide RNF 212 Sequence Variants in the

H. Stefánsson, D. Gudbjartsson, Á. Jónasdóttir, 2022 .

Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study

H. Stefánsson, E. Sigurdsson, D. Gudbjartsson, 2023, Communications medicine.

Molecular benchmarks of a SARS-CoV-2 epidemic

Hannes P. Eggertsson, A. Gylfason, D. Gudbjartsson, 2021, Nature Communications.

Fourteen sequence variants that associate with multiple sclerosis discovered by meta-analysis informed by genetic correlations

H. Stefánsson, A. Ingason, D. Gudbjartsson, 2017, npj Genomic Medicine.

Early Spread of SARS-Cov-2 in the Icelandic Population

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2020, medRxiv.

A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia

G. Másson, C. Goizet, X. Ferrer, 2004, Journal of Medical Genetics.

Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality

R. T. Lie, Bjarni V. Halldórsson, M. Daly, 2023, Nature communications.

the Risk of Myocardial Infarction A Common Variant on Chromosome 9 p 21 Affects

A. Gylfason, D. Gudbjartsson, A. Sigurdsson, 2008 .

Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2018, Nature Communications.

Epigenetic and genetic components of height regulation

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2016, Nature Communications.

Cyclodextrins as permeation enhancers: some theoretical evaluations and in vitro testing.

G. Másson, E. Stefánsson, M. Másson, 1999, Journal of controlled release : official journal of the Controlled Release Society.

Sequence variants affecting the genome-wide rate of germline microsatellite mutations

Hannes P. Eggertsson, Pall I. Olason, Bjarni V. Halldórsson, 2023, Nature communications.

Evaluation of Large-Scale Proteomics for Prediction of Cardiovascular Events.

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2023, JAMA.

Associations of autozygosity with a broad range of human phenotypes

M. P. Concas, May E. Montasser, Cassandra N. Spracklen, 2019, Nature Communications.

A rare missense variant in NR1H4 associates with lower cholesterol levels

D. Gudbjartsson, A. Sigurdsson, A. Jonasdottir, 2018, Communications Biology.

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

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2018, Communications Biology.

Parent-of-origin specific allelic associations among 106 genomic loci for age at menarche

John P. Rice, Daniel L. Koller, D. J. Thompson, 2014, Nature.

A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2019, Nature Communications.

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

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2021, Nature Genetics.

Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura

Jens K. Boldsen, Pall I. Olason, Bjarni V. Halldórsson, 2023, Nature Genetics.

The nature of nurture: Effects of parental genotypes

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2017, Science.

Large-scale plasma proteomics comparisons through genetics and disease associations

Pall I. Olason, Grimur Hjorleifsson Eldjarn, Bjarni V. Halldórsson, 2023, Nature.

Actionable Genotypes and Their Association with Life Span in Iceland.

Gudmundur A. Thorisson, Hannes P. Eggertsson, H. Stefánsson, 2023, The New England journal of medicine.

Physical and neurobehavioral determinants of reproductive onset and success

D. Gudbjartsson, U. Thorsteinsdóttir, A. Kong, 2016, Nature Genetics.

Loss-of-function variants in ATM confer risk of gastric cancer

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