G. Bjornsdottir

发表

Large-scale whole-genome sequencing of the Icelandic population

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

Genetics of gene expression and its effect on disease

H. Stefánsson, R. Fossdal, D. Gudbjartsson, 2008, Nature.

Polygenic risk scores for schizophrenia and bipolar disorder predict creativity

A. Hofman, H. Stefánsson, A. Ingason, 2015, Nature Neuroscience.

A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline

Ole A. Andreassen, Daniel F. Gudbjartsson, Erik G. Jönsson, 2012, Nature.

Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses

Jonathan P. Beauchamp, Joseph K. Pickrell, Sara M. Willems, 2016, Nature Genetics.

An Internet‐Based Survey of Icelandic Nurses on Their Use of and Attitudes Toward NANDA, NIC, and NOC

Gyda Bjornsdottir, Ingibjorg Thorhallsdottir, G. Bjornsdottir, 2003 .

Genome-wide association study identifies 74 loci associated with educational attainment

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2016, Nature.

HeartCare: an Internet-based information and support system for patient home recovery after coronary artery bypass graft (CABG) surgery.

P. Brennan, G. Bjornsdottir, S. Moore, 2001, Journal of advanced nursing.

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Dajiang J. Liu, A. Reiner, R. Mägi, 2018, Nature Genetics.

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

N. Eriksson, M. Nalls, C. Gieger, 2016 .

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2019, 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.

Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders

Chi-Hua Chen, Kari Stefansson, Dominic Holland, 2016, Nature Genetics.

The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2021, Arthritis & rheumatology.

Brain age prediction using deep learning uncovers associated sequence variants

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

CNVs conferring risk of autism or schizophrenia affect cognition in controls

Adam J. Schwarz, Orla M. Doyle, Kari Stefansson, 2013, Nature.

A variant associated with nicotine dependence, lung cancer and peripheral arterial disease

Daniel F. Gudbjartsson, Kari Stefansson, Gudmar Thorleifsson, 2008, Nature.

Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles

Laurent F. Thomas, M. Pirinen, T. Lehtimäki, 2021, Nature Genetics.

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

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

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

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

The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals

Xiaofeng Zhu, Vladan Mijatovic, Inês Barroso, 2016, Nature Genetics.

The Nursing Specialist Group

Josette F. Jones, P. Brennan, G. Bjornsdottir, 2008 .

Prevalence and clinical characteristics of ankylosing spondylitis in Iceland - a nationwide study.

K. Kristjánsson, G. Bjornsdottir, B. Gudbjornsson, 2010, Clinical and experimental rheumatology.

Variant in the sequence of the LINGO1 gene confers risk of essential tremor

H. Stefánsson, S. Steinberg, J. Gulcher, 2009, Nature Genetics.

Human Centred Design Considerations for Multidisciplinary Chronic Heart Failure Disease Management Technology

G. Bjornsdottir, 2000 .

Tailoring health information on the web: The role of knowledge representation and formal vocabularies

Josette F. Jones, Patricia Flatley Brennan, Gyda Bjornsdottir, 2011 .

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

The nature of nurture: Effects of parental genotypes

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

Thirty novel sequence variants impacting human intracranial volume

H. Stefánsson, E. Sigurdsson, D. Gudbjartsson, 2022, Brain communications.

Genetic diversity fuels gene discovery for tobacco and alcohol use

John P. Rice, Dajiang J. Liu, Yoonjung Yoonie Joo, 2022, Nature.

Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor

H. Stefánsson, S. Steinberg, J. Gulcher, 2009, Nature Genetics.

Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits

D. Gudbjartsson, A. Sigurdsson, Á. Jónasdóttir, 2008, Nature Genetics.

A. Reiner, R. Mägi, E. Rimm, 2019 .

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

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

A genome-wide meta-analysis identi es 53 sequence variants associating with carpal tunnel syndrome

H. Stefánsson, K. Stefánsson, I. Jónsdóttir, 2022 .

A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo

H. Stefánsson, D. Rujescu, D. Gudbjartsson, 2021, Communications Biology.

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.

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

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

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2022, Nature Genetics.

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

John P. Rice, Dajiang J. Liu, A. Reiner, 2018, Nature Genetics.

Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

Tom R. Gaunt, Alexander E. Lopez, Laurent F. Thomas, 2021, Cell.

Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Jonathan P. Beauchamp, Joseph K. Pickrell, Sara M. Willems, 2016, Nature Genetics.

Deep learning based brain age prediction uncovers associated sequence variants

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2019, bioRxiv.

CONTRIBUTOR LIST FOR THE SOCIAL SCIENCE GENETIC ASSOCIATION CONSORTIUM RESEARCH TEAM:

Jonathan P. Beauchamp, Katja, Joseph K. Pickrell, 2019 .

Causal relationships between migraine and microstructural white matter: a Mendelian randomization study

M. Pirinen, T. Lehtimäki, H. Stefánsson, 2023, The Journal of Headache and Pain.

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

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

Model-based assessment of replicability for genome-wide association meta-analysis

John P. Rice, Dajiang J. Liu, A. Reiner, 2021, 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.

Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction

H. Stefánsson, A. Ingason, S. Steinberg, 2017, Addiction biology.

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

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

Estimating heritability without environmental bias

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

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 .

15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia

D Brandeis, M Brammer, H. Stefánsson, 2017, Translational Psychiatry.

The Adult Reading History Questionnaire (ARHQ) in Icelandic

H. Stefánsson, S. Steinberg, K. Stefánsson, 2014, Journal of learning disabilities.

Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood

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

New common variants affecting susceptibility to basal cell carcinoma

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

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.

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.

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.

Rare and Common Variants Conferring Risk of Tooth Agenesis

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

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

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

Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

Tom R. Gaunt, Laurent F. Thomas, A. Uitterlinden, 2021, Cell.

Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations

Blair H. Smith, T. Thorgeirsson, R. Freeman, 2015, Pain.

Psychometric properties of the Icelandic NEO-FFI in a general population sample compared to a sample recruited for a study on the genetics of addiction.

H. Stefánsson, T. Thorgeirsson, K. Kristjánsson, 2014, Personality and individual differences.

Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2019, Nature Genetics.

Addictions and their familiality in Iceland

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2010, Annals of the New York Academy of Sciences.

From paper to web: Mode equivalence of the ARHQ and NEO-FFI

Patricia Flatley Brennan, Fanney Thorsdottir, Gyda Bjornsdottir, 2014, Comput. Hum. Behav..

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.

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

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

A causal effects of gut microbiota in the development of migraine

M. Pirinen, T. Lehtimäki, H. Stefánsson, 2023, The Journal of Headache and Pain.

Online social support for individuals concerned with heart disease: observing gender differences

Gyda Bjornsdottir, G. Bjornsdottir, 1999, AMIA.

Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses

Joseph K. Pickrell, Sara M. Willems, Toshiko Tanaka, 2016, Nature Genetics.

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

M. P. Concas, N. Eriksson, M. Nalls, 2016, Nature Genetics.

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Joseph K. Pickrell, Sara M. Willems, C. Gieger, 2016 .

Migraine, chronic kidney disease and kidney function: observational and genetic analyses

M. Pirinen, T. Lehtimäki, H. Stefánsson, 2023, Human Genetics.

Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption.

R. Mägi, D. Gudbjartsson, T. Thorgeirsson, 2011, Human molecular genetics.

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.

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

Jonathan P. Beauchamp, Gerardus A. Meddens, Joseph K. Pickrell, 2018, 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.

Cluster Headache Genomewide Association Study and Meta‐Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor

Laurent F. Thomas, M. Pirinen, H. Stefánsson, 2023, Annals of neurology.

Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations

Tom R. Gaunt, Alexander E. Lopez, Laurent F. Thomas, 2021, Cell.

Correction: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Joseph K. Pickrell, Sara M. Willems, C. Gieger, 2016, Nature Genetics.

Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations

Blair H. Smith, T. Thorgeirsson, R. Freeman, 2015, Pain.

Variant in the sequence of the LINGO1 gene confers risk of essential tremor

H. Stefánsson, S. Steinberg, J. Gulcher, 2009, Nature Genetics.

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals

Gerardus A. Meddens, Joseph K. Pickrell, Steven F. Lehrer, 2018, Nature Genetics.

HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study

M. Pirinen, T. Lehtimäki, H. Stefánsson, 2024, Scientific reports.

Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease

H. Stefánsson, D. Gudbjartsson, T. Thorgeirsson, 2024, NPJ Parkinson's disease.

GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis

Jens K. Boldsen, H. Stefánsson, D. Gudbjartsson, 2024, Communications biology.