G. Eyjolfsson

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.

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

D. Postma, I. Hall, H. Stefánsson, 2009, Nature Genetics.

Large-scale whole-genome sequencing of the Icelandic population

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

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.

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.

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

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

Discovery and Refinement Supplementary

Christian Gieger, Cisca Wijmenga, Inês Barroso, 2015 .

Genome-Wide Meta-Analysis for Serum Calcium Identifies Significantly Associated SNPs near the Calcium-Sensing Receptor (CASR) Gene

Luigi Ferrucci, Sven Bergmann, Zoltán Kutalik, 2010, PLoS genetics.

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 First Icelandic Family with X‐Linked Agammaglobulinemia: Studies of Genetic Markers and Immune Function

G. Eyjolfsson, Ó. Jensson, L. Thorsteinsson, 1990, Scandinavian journal of immunology.

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

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

Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

Daniel F. Gudbjartsson, Kari Stefansson, Runolfur Palsson, 2010, PLoS genetics.

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.

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.

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

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

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.

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.

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations

Kari Stefansson, Wei Li, Jon Hrafnkelsson, 2009, Nature Genetics.

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.

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

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

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.

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.

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.

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 .

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.

Correction: Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

D. Gudbjartsson, L. Kiemeney, U. Thorsteinsdóttir, 2010, PLoS Genetics.

Natural killer cell function and malignant cell phenotype in hairy cell leukaemia

G. Eyjolfsson, Ó. Jensson, S. Sveinsdóttir, 1992, APMIS : acta pathologica, microbiologica, et immunologica Scandinavica.

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

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

Epidemiology of hairy cell leukemia in Iceland.

G. Eyjolfsson, P. T. Onundarson, B. Agnarsson, 2002, The hematology journal : the official journal of the European Haematology Association.

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.

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.

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.

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.

Seventy-five genetic loci influencing the human red blood cell

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

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.

Discovery and refinement of loci associated with lipid levels

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

Sequence variants influencing the regulation of serum IgG subclass levels

B. Halldórsson, D. Gudbjartsson, A. Sigurdsson, 2024, Nature communications.