A. Oddsson

发表

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.

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

Hannes P. Eggertsson, Bjarni V. Halldórsson, B. Halldórsson, 2020, Communications Biology.

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.

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.

Glcci1 deficiency leads to proteinuria.

M. Uhlén, C. Betsholtz, E. Raschperger, 2011, Journal of the American Society of Nephrology : JASN.

Glomerular Filtration Barrier: From Molecular Biology to Regulation Mechanisms

K. Tryggvason, A. Oddsson, J. Patrakka, 2014 .

Characterization of novel genes of importance for renal glomerular function and disease

A. Oddsson, 2013 .

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.

Survival in patients with familial and sporadic myeloproliferative neoplasms.

M. Björkholm, S. Lund, S. Kristinsson, 2015, Blood.

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.

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.

The nature of nurture: Effects of parental genotypes

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

Expression and Subcellular Distribution of Novel Glomerulus-Associated Proteins Dendrin, Ehd3, Sh2d4a, Plekhh2, and 2310066E14Rik

M. Uhlén, C. Szigyarto, Liqun He, 2007 .

Expression and subcellular distribution of novel glomerulus-associated proteins dendrin, ehd3, sh2d4a, plekhh2, and 2310066E14Rik.

M. Uhlén, C. Szigyarto, Liqun He, 2007, Journal of the American Society of Nephrology : JASN.

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

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

Genetics of common complex kidney stone disease: insights from genome-wide association studies

R. Palsson, A. Oddsson, O. Indridason, 2018, Urolithiasis.

Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density

G. M. Zoega, D. Gudbjartsson, U. Thorsteinsdóttir, 2019, Nature Communications.

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.

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

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

A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2022, Nature Communications.

A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy

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

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

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

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.

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

Hannes P. Eggertsson, B. Halldórsson, D. Gudbjartsson, 2020, Communications Biology.

The sequences of 150,119 genomes in the UK Biobank

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

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

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

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.

Glomerulus proteome analysis with two-dimensional gel electrophoresis and mass spectrometry

H. Jörnvall, K. Tryggvason, A. Oddsson, 2007, Cellular and Molecular Life Sciences.

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.

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.

Genetic insight into sick sinus syndrome

D. Gudbjartsson, H. Ullum, U. Thorsteinsdóttir, 2021, European heart journal.

The germline sequence variant rs2736100_C in TERT associates with myeloproliferative neoplasms

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

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

Bjarni V. Halldórsson, H. Stefánsson, B. Halldórsson, 2020, Current Biology.

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.

The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis

Hannes P. Eggertsson, Bjarni V. Halldórsson, A. Gylfason, 2021, Communications biology.

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 variants associated with syncope implicate neural and autonomic processes.

Hannes P. Eggertsson, D. Gudbjartsson, T. Thorgeirsson, 2023, European heart journal.

Loss-of-Function Variants in the Tumor-Suppressor Gene PTPN14 Confer Increased Cancer Risk

Hannes P. Eggertsson, Pall I. Olason, Bjarni V. Halldórsson, 2021, Cancer Research.

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.

Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

Laurent F. Thomas, J. V. van Meurs, R. Mägi, 2022, Nature Communications.

Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology

Laurent F. Thomas, J. V. van Meurs, R. Mägi, 2022, Nature communications.

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.

Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database

A. Jonasdottir, Á. Jónasdóttir, U. Thorsteinsdóttir, 2021, European Journal of Human Genetics.

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

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

Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density

G. M. Zoega, D. Gudbjartsson, U. Thorsteinsdóttir, 2019, Nature Communications.

Rare and Common Variants Conferring Risk of Tooth Agenesis

H. Stefánsson, A. Ingason, S. Steinberg, 2018, Journal of dental research.

Identification of sequence variants influencing immunoglobulin levels

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

Sequence variant at 4q25 near PITX2 associates with appendicitis

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

Common and rare variants associated with kidney stones and biochemical traits

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

Zebrafish: a model system for the study of vertebrate renal development, function, and pathophysiology

C. Betsholtz, K. Tryggvason, K. Hultenby, 2011, Current opinion in nephrology and hypertension.

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

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

Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans

K. Stefánsson, T. Ahluwalia, V. Steinthorsdottir, 2023, Frontiers in Endocrinology.

Knockdown of Tmem234 in zebrafish results in proteinuria.

C. Betsholtz, K. Tryggvason, K. Hultenby, 2015, American journal of physiology. Renal physiology.

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

Grimur Hjorleifsson Eldjarn, Bjarni V. Halldórsson, B. Halldórsson, 2023, Communications biology.

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.

Epigenetic and genetic components of height regulation

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

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

D. Gudbjartsson, K. Stefánsson, P. Sulem, 2023, Journal of the American Heart Association.

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.

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.

An atlas of genetic determinants of forearm fracture

O. Mäkitie, T. Tuomi, S. Movérare-Skrtic, 2023, Nature Genetics.

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.

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

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

Variants at the Interleukin 1 Gene Locus and Pericarditis.

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

Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effect on recombination

B. Halldórsson, D. Gudbjartsson, P. Sulem, 2024, Nature structural & molecular biology.

The correlation between CpG methylation and gene expression is driven by sequence variants

Brynja D. Sigurpálsdóttir, H. Stefánsson, B. Halldórsson, 2024, Nature genetics.

Genetic links between ovarian ageing, cancer risk and de novo mutation rates

M. Hurles, D. Gudbjartsson, M. Weedon, 2024, Nature.

Homozygosity for a stop-gain variant in CCDC201 causes primary ovarian insufficiency

H. Stefánsson, B. Halldórsson, D. Gudbjartsson, 2024, Nature genetics.