G. Bjornsdottir

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Aliases
G. Bjornsdottir, Gyda Bjornsdottir
Publication record
93 papers · 19,521 citations · H-index 41

PAPERS

Variant in a Taste Receptor Locus Tied to Changes in the Use of Insomnia Medication
20250 citationsauthor #4
The genetic architecture of fibromyalgia across 2.5 million individuals
20250 citationsauthor #2
Correction: Uncovering drug targets for cluster headache through proteome-wide Mendelian randomization analysis
20250 citationsauthor #26
Missense variants in FRS3 affect body mass index in populations of diverse ancestries
20251 citationsauthor #15
Robust inference and widespread genetic correlates from a large-scale genetic association study of human personality
20257 citationsauthor #28
Rare loss-of-function variants in HECTD2 and AKAP11 confer risk of bipolar disorder
20255 citationsauthor #13
Trans-ancestry genome-wide study of depression identifies 697 associations implicating cell types and pharmacotherapies
2025113 citationsauthor #54
Uncovering drug targets for cluster headache through proteome-wide Mendelian randomization analysis
20254 citationsauthor #26
HMG-CoA reductase is a potential therapeutic target for migraine: a mendelian randomization study
20245 citationsauthor #29
GWAS meta-analysis reveals key risk loci in essential tremor pathogenesis
202411 citationsauthor #11
Homozygosity for R47H in TREM2 and the Risk of Alzheimer's Disease.
20247 citationsauthor #23
Sequence variants associated with BMI affect disease risk through BMI itself
20245 citationsauthor #24
Loss-of-function variants in ITSN1 confer high risk of Parkinson’s disease
202410 citationsauthor #18
Rare variants with large effects provide functional insights into the pathology of migraine subtypes, with and without aura
202340 citationsauthor #1
Cluster Headache Genomewide Association Study and Meta‐Analysis Identifies Eight Loci and Implicates Smoking as Causal Risk Factor
202349 citationsauthor #15
A causal effects of gut microbiota in the development of migraine
202339 citationsauthor #13
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study
202322 citationsauthor #8
Physical and cognitive impact following SARS-CoV-2 infection in a large population-based case-control study
20232 citationsauthor #18
Migraine, chronic kidney disease and kidney function: observational and genetic analyses
20237 citationsauthor #28
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria
20232 citationsauthor #23
Genetic diversity fuels gene discovery for tobacco and alcohol use
2022349 citationsauthor #26
A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome
202214 citationsauthor #2
A genome-wide meta-analysis identifies 53 sequence variants associating with carpal tunnel syndrome
20220 citationsauthor #2
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
20222 citationsauthor #1
Thirty novel sequence variants impacting human intracranial volume
20225 citationsauthor #8
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology
202240 citationsauthor #1
Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals
2022523 citationsauthor #63
A genome-wide meta-analysis identi es 53 sequence variants associating with carpal tunnel syndrome
20220 citationsauthor #2
Genetic propensities for verbal and spatial ability have opposite effects on body mass index and risk of schizophrenia
20218 citationsauthor #26
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
20215 citationsauthor #16
The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland
202152 citationsauthor #9
A meta-analysis uncovers the first sequence variant conferring risk of Bell’s palsy
202113 citationsauthor #2
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
2021286 citationsauthor #4
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
2021388 citationsauthor #16
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo
202127 citationsauthor #2
Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database
20214 citationsauthor #18
A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis
2021133 citationsauthor #6
Model-based assessment of replicability for genome-wide association meta-analysis
202130 citationsauthor #51
Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming.
202028 citationsauthor #20
Brain age prediction using deep learning uncovers associated sequence variants
2019350 citationsauthor #3
A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis
201999 citationsauthor #31
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
2019640 citationsauthor #152
CONTRIBUTOR LIST FOR THE SOCIAL SCIENCE GENETIC ASSOCIATION CONSORTIUM RESEARCH TEAM:
20190 citationsauthor #44
Common and Rare Sequence Variants Influencing Tumor Biomarkers in Blood
201914 citationsauthor #18
Data Related to Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
20194 citationsauthor #43
Deep learning based brain age prediction uncovers associated sequence variants
201913 citationsauthor #3
A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy
20199 citationsauthor #1
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
20182,100 citationsauthor #64
Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis
2018142 citationsauthor #16
Rare and Common Variants Conferring Risk of Tooth Agenesis
201847 citationsauthor #35
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
20181,596 citationsauthor #86
Relatedness disequilibrium regression estimates heritability without environmental bias
2018162 citationsauthor #5
The nature of nurture: Effects of parental genotypes
2017817 citationsauthor #13
Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation
201741 citationsauthor #1
Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations (vol 156, pg 2337, 2015)
20171 citationsauthor #5
Selection against variants in the genome associated with educational attainment
2017146 citationsauthor #13
15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia
201775 citationsauthor #14
Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction
2017107 citationsauthor #4
Sequence variant at 8 q 24 . 21 associates with sciatica caused by lumbar disc herniation
20173 citationsauthor #1
Estimating heritability without environmental bias
20175 citationsauthor #5
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
2016116 citationsauthor #34
Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses
2016977 citationsauthor #58
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
2016408 citationsauthor #16
The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals
2016394 citationsauthor #58
A rare missense mutation in CHRNA4 associates with smoking behavior and its consequences
201630 citationsauthor #4
Correction: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
201616 citationsauthor #58
Genome-wide association study identifies 74 loci associated with educational attainment
20161,277 citationsauthor #20
Large-scale whole-genome sequencing of the Icelandic population
2015775 citationsauthor #33
Adult Reading History Questionnaire--Icelandic Version
20150 citationsauthor #1
Neuropathic pain phenotyping by international consensus (NeuroPPIC) for genetic studies: a NeuPSIG systematic review, Delphi survey, and expert panel recommendations
201573 citationsauthor #5
Polygenic risk scores for schizophrenia and bipolar disorder predict creativity
2015375 citationsauthor #3
The Adult Reading History Questionnaire (ARHQ) in Icelandic
201448 citationsauthor #1
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.
20148 citationsauthor #1
From paper to web: Mode equivalence of the ARHQ and NEO-FFI
20146 citationsauthor #1
CNVs conferring risk of autism or schizophrenia affect cognition in controls
2013655 citationsauthor #7
A mutation in APP protects against Alzheimer’s disease and age-related cognitive decline
20121,695 citationsauthor #18
Identification of low-frequency variants associated with gout and serum uric acid levels
2011163 citationsauthor #9
Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption.
2011137 citationsauthor #24
Tailoring health information on the web: The role of knowledge representation and formal vocabularies
20110 citationsauthor #2
Prevalence and clinical characteristics of ankylosing spondylitis in Iceland - a nationwide study.
201044 citationsauthor #3
Addictions and their familiality in Iceland
201029 citationsauthor #6
New common variants affecting susceptibility to basal cell carcinoma
2009323 citationsauthor #48
Variant in the sequence of the LINGO1 gene confers risk of essential tremor
2009219 citationsauthor #10
Corrigendum: Variant in the sequence of the LINGO1 gene confers risk of essential tremor
20092 citationsauthor #10
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits
2008124 citationsauthor #35
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease
20081,545 citationsauthor #20
Genetics of gene expression and its effect on disease
20081,406 citationsauthor #14
The Nursing Specialist Group
20080 citationsauthor #2
An Internet‐Based Survey of Icelandic Nurses on Their Use of and Attitudes Toward NANDA, NIC, and NOC
20035 citationsauthor #1
Assuring Standardized Nursing Documentation in the Development of an Electronic Patient Record: The Human Factor
20010 citationsauthor #2
HeartCare: an Internet-based information and support system for patient home recovery after coronary artery bypass graft (CABG) surgery.
2001131 citationsauthor #3
Human Centred Design Considerations for Multidisciplinary Chronic Heart Failure Disease Management Technology
20000 citationsauthor #1
Online social support for individuals concerned with heart disease: observing gender differences
199922 citationsauthor #1

TIMELINE

1999 22 citations

2000 0 citations

2001 131 citations

2003 5 citations

2008 3,075 citations

2009 544 citations

2010 73 citations

2011 300 citations

2012 1,695 citations

2013 655 citations

2014 62 citations

2015 1,223 citations

2016 3,218 citations

2017 1,195 citations

2018 4,047 citations

2019 1,129 citations

2020 28 citations

2021 946 citations

2022 933 citations

2023 161 citations

2024 38 citations

2025 130 citations

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