I. Olafsson

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.

Discovery and refinement of loci associated with lipid levels

Tanya M. Teslovich, Ross M. Fraser, May E. Montasser, 2013, 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.

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing

Karsten B. Sieber, Benjamin B. Sun, Audrey Y. Chu, 2019 .

Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

Karsten B. Sieber, Nicholette D. Palmer, Benjamin B. Sun, 2019, Nature Communications.

Seventy-five genetic loci influencing the human red blood cell

Christian Gieger, Ian J. Deary, Uwe Völker, 2012, Nature.

Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma

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

Common variants associated with plasma triglycerides and risk for coronary artery disease

Tanya M. Teslovich, Ross M. Fraser, May E. Montasser, 2013, Nature Genetics.

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.

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

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

Isleifur Olafsson, Erna Sif Arnardottir, I. Olafsson, 2010, Journal of sleep research.

Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels

Karsten B. Sieber, M. P. Concas, Cassandra N. Spracklen, 2019, Nature Genetics.

Diversity in non-repetitive human sequences not found in the reference genome

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

C reactive protein levels are increased in non-allergic but not allergic asthma: a multicentre epidemiological study

I. Olafsson, D. Gíslason, T. Gislason, 2005, Thorax.

Hypertension, Systemic Inflammation and Body Weight in Relation to Lung Function Impairment—An Epidemiological Study

A. Buist, I. Olafsson, T. Gislason, 2009, COPD.

Mutation in the cystatin C gene causes hereditary brain hemorrhage.

I. Olafsson, M. Abrahamson, Ó. Jensson, 1989, Progress in clinical and biological research.

The Molecular Pathology of Hereditary Cystatin C Amyloid Angiopathy Causing Brain Hemorrhage

I. Olafsson, Ó. Jensson, L. Thorsteinsson, 1996, Brain pathology.

Prevalence of restless legs syndrome among adults in Iceland and Sweden: Lung function, comorbidity, ferritin, biomarkers and quality of life.

I. Olafsson, T. Gislason, C. Janson, 2010, Sleep medicine.

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.

Persistent Chlamydia Pneumoniae serology is related to decline in lung function in women but not in men. Effect of persistent Chlamydia pneumoniae infection on lung function

I. Olafsson, T. Gislason, C. Janson, 2010, BMC pulmonary medicine.

Structure and expression of the human cystatin C gene.

I. Olafsson, M. Abrahamson, Ó. Jensson, 1990, The Biochemical journal.

MUTATION IN CYSTATIN C GENE CAUSES HEREDITARY BRAIN HAEMORRHAGE

I. Olafsson, M. Abrahamson, Ó. Jensson, 1988, The Lancet.

CRP is associated with lung function decline in men but not women: a prospective study.

V. Gudnason, I. Olafsson, T. Gislason, 2013, Respiratory medicine.

Seroprevalence of Toxoplasma gondii in Sweden, Estonia and Iceland

I. Olafsson, D. Gíslason, T. Gislason, 2006, Scandinavian journal of infectious diseases.

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

Karsten B. Sieber, Laurent F. Thomas, Pashupati P. Mishra, 2022, Kidney international.

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Karsten B. Sieber, M. P. Concas, Nicholette D. Palmer, 2022, Communications Biology.

Infections and obesity: A multinational epidemiological study

I. Olafsson, D. Gíslason, T. Gislason, 2008, Scandinavian journal of infectious diseases.

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.

Bacterial growth blocked by a synthetic peptide based on the structure of a human proteinase inhibitor

I. Olafsson, L. Björck, M. Bohus, 1989, Nature.

Apolipoprotein(a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism.

P. Tsao, D. Gudbjartsson, U. Thorsteinsdóttir, 2012, Journal of the American College of Cardiology.

VHRM_A_204925 143..147

I. Olafsson, S. Gizurarson, K. Andersen, 2019 .

The amino terminal portion of cerebrospinal fluid cystatin C in hereditary cystatin C amyloid angiopathy is not truncated: direct sequence analysis from agarose gel electropherograms.

I. Olafsson, G. Gudmundsson, M. Abrahamson, 1990, Scandinavian journal of clinical and laboratory investigation.

Association of ApoE genotype with clinical features and outcome in idiopathic normal pressure hydrocephalus (iNPH): a preliminary report

I. Olafsson, G. Gudmundsson, G. Kristjansdottir, 2009, Acta Neurochirurgica.

Discovery and Refinement Supplementary

Christian Gieger, Cisca Wijmenga, Inês Barroso, 2015 .

Clinical features and genotype of adenine phosphoribosyltransferase deficiency in iceland.

I. Olafsson, R. Palsson, T. Laxdal, 2001, American journal of kidney diseases : the official journal of the National Kidney Foundation.

Biomarkers for Gastroesophageal Reflux in Respiratory Diseases

I. Olafsson, C. Janson, A. Olin, 2013, Gastroenterology research and practice.

Chronic airflow obstruction and markers of systemic inflammation: results from the BOLD study in Iceland.

A. Buist, I. Olafsson, T. Gislason, 2009, Respiratory medicine.

Systemic inflammation and lung function

V. Gudnason, I. Olafsson, T. Gislason, 2011 .

The effect of infectious burden on the prevalence of atopy and respiratory allergies in Iceland, Estonia, and Sweden.

I. Olafsson, D. Gíslason, T. Gislason, 2007, The Journal of allergy and clinical immunology.

C-reactive protein is elevated in non-allergic but not allergic asthma. : a multicentre epidemiological study.

I. Olafsson, D. Gíslason, T. Gislason, 2005 .

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.

Structure and expression of the gene encoding cystatin D, a novel human cysteine proteinase inhibitor.

I. Olafsson, C. López-Otín, J. Freije, 1991, The Journal of biological chemistry.

Efficient production of native, biologically active human cystatin C by Escherichia coli

I. Olafsson, M. Abrahamson, H. Dalbøge, 1988, FEBS letters.

Defining new reference intervals for serum free light chains in individuals with chronic kidney disease: Results of the iStopMM study

I. Olafsson, P. T. Onundarson, B. Agnarsson, 2022, Blood Cancer Journal.

Genetics and Neuropathology of Hereditary Cystatin C Amyloid Angiopathy (HCCAA)

I. Olafsson, L. Thorsteinsson, 2000 .

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.

The power of genetic diversity in genome-wide association studies of lipids

Christopher D. Brown, Aaron F. McDaid, M. P. Concas, 2021, Nature.

Multiomics study of nonalcoholic fatty liver disease

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2022, Nature Genetics.

The human cystatin C gene promoter: functional analysis and identification of heterogeneous mRNA.

I. Olafsson, 1995, Scandinavian journal of clinical and laboratory investigation.

Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma

Christian Gieger, Yusuke Nakamura, Philippe Froguel, 2011, Nature Genetics.

Synthesis of cysteine proteinase inhibitors structurally based on the proteinase interacting N-terminal region of human cystatin C.

I. Olafsson, M. Abrahamson, F. Kasprzykowski, 1990, Biological chemistry Hoppe-Seyler.

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.

Inactivation of human cystatin C and kininogen by human cathepsin D

Isleifur Olafsson, I. Olafsson, B. Lenarčič, 1991, FEBS letters.

A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis

William J. Astle, Hannes P. Eggertsson, J. Danesh, 2021, Communications Biology.

A catalog of genetic loci associated with kidney function from analyses of a million individuals

Karsten B. Sieber, Nicholette D. Palmer, Cassandra N. Spracklen, 2019, Nature Genetics.

Rare mutations associating with serum creatinine and chronic kidney disease.

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

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

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

Rare SCARB1 mutations associate with high-density lipoprotein cholesterol but not with coronary artery disease

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2018, European heart journal.

Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

Anurag, Cassandra N. Spracklen, I. Ntalla, 2021, medRxiv.

Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease

H. Stefánsson, D. Gudbjartsson, H. Ullum, 2020, European heart journal.

The sequences of 150,119 genomes in the UK Biobank

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

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

A. McRae, T. Spector, H. Stefánsson, 2016, American journal of human genetics.

Genetic variants associated with platelet count are predictive of human disease and physiological markers

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2021, Communications Biology.

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.

Genome-wide analysis yields new loci associating with aortic valve stenosis

G. Abecasis, D. Gudbjartsson, U. Thorsteinsdóttir, 2017, bioRxiv.

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.

Diversity in non-repetitive human sequences not found in the reference genome

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

Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland

Bjarni V. Halldórsson, B. Halldórsson, A. Jonasdottir, 2021, Arteriosclerosis, thrombosis, and vascular biology.

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

Christopher D. Brown, Aaron F. McDaid, Yan V. Sun, 2021, bioRxiv.

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

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

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

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

Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2023, Nature Genetics.

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

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

High-level expression of active human cystatin C in Escherichia coli.

I. Olafsson, M. Abrahamson, H. Dalbøge, 1989, Gene.

Production, characterization and use of monoclonal antibodies against the major extracellular human cysteine proteinase inhibitors cystatin C and kininogen.

I. Olafsson, M. Abrahamson, A. Grubb, 1988, Scandinavian journal of clinical and laboratory investigation.

Hereditary cystatin C amyloid angiopathy: identification of the disease-causing mutation and specific diagnosis by polymerase chain reaction based analysis

I. Olafsson, M. Abrahamson, Ó. Jensson, 1992, Human Genetics.

Molecular cloning and sequence analysis of cDNA coding for the precursor of the human cysteine proteinase inhibitor cystatin C

I. Olafsson, M. Abrahamson, Å. Lundwall, 1987, FEBS letters.

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

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

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

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

A Splice Region Variant in LDLR Lowers Non-high Density Lipoprotein Cholesterol and Protects against Coronary Artery Disease

D. Gudbjartsson, A. Sigurdsson, L. Kiemeney, 2015, PLoS genetics.

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.

Genetic propensities for verbal and spatial ability have opposite effects on body mass index and risk of schizophrenia

H. Stefánsson, E. Sigurdsson, D. Gudbjartsson, 2021 .

Association of Genetically Predicted Lipid Levels With the Extent of Coronary Atherosclerosis in Icelandic Adults

U. Thorsteinsdóttir, K. Stefánsson, G. Eyjolfsson, 2019, JAMA cardiology.

Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood

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

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.

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

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

Screening for Monoclonal Gammopathy of Undetermined Significance: A Population-Based Randomized Clinical Trial. First Results from the Iceland Screens, Treats, or Prevents Multiple Myeloma (iStopMM) Study

I. Olafsson, P. T. Onundarson, B. Agnarsson, 2021, Blood.

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

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

Lipoprotein(a) Concentration and Risks of Cardiovascular Disease and Diabetes.

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2019, Journal of the American College of Cardiology.

University of Groningen Genome-wide analysis yields new loci associating with aortic valve stenosis

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

Identification of sequence variants influencing immunoglobulin levels

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

Common and rare variants associated with kidney stones and biochemical traits

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

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 .

Monoclonal gammopathy of undetermined significance and COVID-19: a population-based cohort study

I. Olafsson, P. T. Onundarson, B. Agnarsson, 2021, Blood Cancer Journal.

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 .

Prevalence of MGUS Is High in the Istopmm Study but the Prevalence of IgA MGUS Does Not Increase with Age in the Way Other Immunoglobulin Subtypes Do

I. Olafsson, P. T. Onundarson, B. Agnarsson, 2022, Blood.

Prevalence of Smoldering Multiple Myeloma: Results from the Iceland Screens, Treats, or Prevents Multiple Myeloma (iStopMM) Study

I. Olafsson, P. T. Onundarson, B. Agnarsson, 2021, Blood.

Estimating Selection Bias in Previous Monoclonal Gammopathy of Undetermined Significance Research - the Importance of Screening: Results from the Population-Based Screening Study Iceland Screens, Treats or Prevents Multiple Myeloma (iStopMM)

I. Olafsson, P. T. Onundarson, B. Agnarsson, 2021, Blood.

Iceland screens, treats, or prevents multiple myeloma (iStopMM): a population-based screening study for monoclonal gammopathy of undetermined significance and randomized controlled trial of follow-up strategies

G. T. Gunnarsson, Andri S. Björnsson, I. Olafsson, 2021, Blood Cancer Journal.

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

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

Monoclonal gammopathy: natural history studied with a retrospective approach.

V. Gudnason, I. Olafsson, H. Ogmundsdottir, 2007, Haematologica.

A catalog of genetic loci associated with kidney function from analyses of a million individuals

Karsten B. Sieber, M. P. Concas, Nicholette D. Palmer, 2019, Nature Genetics.

Prevalence of smoldering multiple myeloma based on nationwide screening

I. Olafsson, B. Agnarsson, T. Aspelund, 2023, Nature Medicine.

Editor’s Choice- Diagnosis of type 2 diabetes and prediabetes among patients with acute coronary syndromes

I. Olafsson, K. Andersen, S. Lund, 2017, European heart journal. Acute cardiovascular care.

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

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

Obstructive sleep apnoea treatment and fasting lipids: a comparative effectiveness study

A. Pack, I. Olafsson, T. Gislason, 2014, European Respiratory Journal.

The interaction of obstructive sleep apnea and obesity on the inflammatory markers C-reactive protein and interleukin-6: the Icelandic Sleep Apnea Cohort.

A. Pack, I. Olafsson, T. Gislason, 2012, Sleep.

Serum ferritin and obstructive sleep apnea—epidemiological study

A. Pack, I. Olafsson, T. Gislason, 2017, Sleep and Breathing.

on the severity of chronic intermittent hypoxia Hyperlipidemia and lipid peroxidation are dependent

A. Pack, I. Olafsson, T. Gislason, 2015 .

Hereditary cystatin C amyloid angiopathy

I. Olafsson, I Olafsson, A. Grubb, 2000, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Promoter-mediated, dexamethasone-induced increase in cystatin C production by HeLa cells.

I. Olafsson, A. Grubb, M. Bjarnadóttir, 1995, Scandinavian journal of clinical and laboratory investigation.

An Isolate of Families with Hereditary Cystatin C Amyloid Angiopathy and Cerebral Haemorrhage in the South of Iceland

I. Olafsson, G. Gudmundsson, M. Abrahamson, 1988 .

The complexity of kidney disease and diagnosing it – cystatin C, selective glomerular hypofiltration syndromes and proteome regulation

I. Olafsson, L. Risch, J. Ärnlöv, 2022, Journal of internal medicine.

Effect of sequence variants on variance in glucose levels predicts type 2 diabetes risk and accounts for heritability

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2017, Nature Genetics.

Alzheimer's disease neuropathology in the hippocampus and brainstem of people with obstructive sleep apnea.

I. Olafsson, T. Gislason, B. Benediktsdóttir, 2020, Sleep.

Gender differences in the association between C-reactive protein, lung function impairment, and COPD

I. Olafsson, D. Gíslason, T. Gislason, 2007, International journal of chronic obstructive pulmonary disease.

Respiratory symptoms, sleep-disordered breathing and biomarkers in nocturnal gastroesophageal reflux

I. Olafsson, T. Gislason, C. Janson, 2016, Respiratory Research.

Stability of thromboxane in blood samples

I. Olafsson, S. Gizurarson, K. Andersen, 2019, Vascular health and risk management.

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.

[Hereditary hearing impairment. Mutation analysis of connexin 26 and POU3F4 genes in Icelanders with nonsyndromic hearing impairment.].

I. Olafsson, G. Eiriksdottir, E. Cook, 2000, Laeknabladid.

Effects of different doses of adrenocorticotrophic hormone on the serum lipoprotein profile in healthy subjects.

I. Olafsson, J. Dallongeville, M. Jóhannsson, 2005, Basic & clinical pharmacology & toxicology.

Defining New Reference Intervals for Serum Free Light Chains in Individuals with Reduced Kidney Function: Results of the Population- Based on Iceland Screens Treats or Prevents Multiple Myeloma (iStopMM) Study

I. Olafsson, P. T. Onundarson, B. Agnarsson, 2021, Blood.

Erratum to: Respiratory symptoms, sleep-disordered breathing and biomarkers in nocturnal gastroesophageal reflux

I. Olafsson, C. Janson, E. Björnsson, 2016, Respiratory Research.

Seroprevalence of Helicobacter pylori and cagA antibodies in Iceland, Estonia and Sweden

I. Olafsson, D. Gíslason, T. Gislason, 2007, Scandinavian journal of infectious diseases.

Definition of nocturnal gastroesophageal reflux for studies on respiratory diseases

I. Olafsson, T. Gislason, C. Janson, 2016, Scandinavian journal of gastroenterology.

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.

Erratum to: Respiratory symptoms, sleep-disordered breathing and biomarkers in nocturnal gastroesophageal reflux

I. Olafsson, C. Janson, E. Björnsson, 2016, Respiratory Research.

Common variants associated with plasma triglycerides and risk for coronary artery disease

Tanya M. Teslovich, Ross M. Fraser, May E. Montasser, 2013, Nature Genetics.

A rare missense variant in NR1H4 associates with lower cholesterol levels

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

Cholesterol not particle concentration mediates the atherogenic risk conferred by apolipoprotein B particles - A Mendelian randomization analysis.

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2022, European journal of preventive cardiology.

Perturbation of processing of cystatin C in monocytes from patients with hereditary cystatin C amyloid angiopathy

I. Olafsson, B. Ásgeirsson, G. Georgsson, 1991 .

MUTATION IN THE CYSTATIN C GENE CAUSES HEREDITARY CYSTATINC AMYLOID ANGIOPATHY WITH CEREBRAL HEMORRHAGE

I. Olafsson, M. Abrahamson, Ó. Jensson, 1988 .

Autoimmune Diseases Are Not Associated with Monoclonal Gammopathy of Undetermined Significance: Results of the Prospective Population-Based Istopmm Study

I. Olafsson, B. Agnarsson, T. Aspelund, 2022, Blood.

Seventy-five genetic loci influencing the human red blood cell

Lorna M. Lopez, P. O’Reilly, P. Elliott, 2012, Nature.

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

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

Complex effects of sequence variants on lipid levels and coronary artery disease

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2023, Cell.

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies LifeLines Cohort

Karsten B. Sieber, Laurent F. Thomas, Pashupati P. Mishra, 2022 .

Diversity in non-repetitive human sequences not found in the reference genome

Bjarni V. Halldórsson, B. Halldórsson, D. Gudbjartsson, 2017, Nature Genetics.

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.

A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.

Christopher D. Brown, Aaron F. McDaid, M. P. Concas, 2022, American journal of human genetics.

Definition of nocturnal gastroesophageal reflux for studies on respiratory diseases

I. Olafsson, T. Gislason, C. Janson, 2016, Scandinavian journal of gastroenterology.

Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

I. Ntalla, M. Kanai, I. Olafsson, 2022, Genome Biology.

Disease associations with monoclonal gammopathy of undetermined significance can only be evaluated using screened cohorts: results from the population-based iStopMM study

I. Olafsson, B. Agnarsson, Sigrún Thorsteinsdóttir, 2023, Haematologica.

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.

Editor’s Choice- Diagnosis of type 2 diabetes and prediabetes among patients with acute coronary syndromes

I. Olafsson, K. Andersen, S. Lund, 2017, European heart journal. Acute cardiovascular care.

The amino terminal portion of cerebrospinal fluid cystatin C in hereditary cystatin C amyloid angiopathy is not truncated: direct sequence analysis from agarose gel electropherograms.

I. Olafsson, Ó. Jensson, Anders Grubb, 1990, Scandinavian journal of clinical and laboratory investigation.

C reactive protein levels are increased in non-allergic but not allergic asthma: a multicentre epidemiological study

I. Olafsson, D. Gíslason, T. Gislason, 2005, Thorax.

Variants at the Interleukin 1 Gene Locus and Pericarditis.

Brynja D. Sigurpálsdóttir, B. Halldórsson, A. Sigurdsson, 2023, JAMA cardiology.

Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity

Jeffrey J. Beck, Zachary F. Gerring, H. Stefánsson, 2023, Human reproduction.