Works matching AU Stefansson, Kari
Results: 137
Personalized genomic information: preparing for the future of genetic medicine.
- Published in:
- 2010
- By:
- Publication type:
- review
Monoclonal Antibodies and Lectins as Probes for Investigation of the Cell Biology of Human Trabecular Meshwork: A Preliminary Report.
- Published in:
- Ophthalmic Research, 1989, v. 21, n. 1, p. 27, doi. 10.1159/000266763
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- Publication type:
- Article
Transformers significantly improve splice site prediction.
- Published in:
- Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-07298-9
- By:
- Publication type:
- Article
Publisher Correction: Transformers significantly improve splice site prediction.
- Published in:
- 2024
- By:
- Publication type:
- Correction Notice
Transformers significantly improve splice site prediction.
- Published in:
- Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-07298-9
- By:
- Publication type:
- Article
Transformers significantly improve splice site prediction.
- Published in:
- Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-07298-9
- By:
- Publication type:
- Article
A population-based familial aggregation analysis indicates genetic contribution in a majority of renal cell carcinomas.
- Published in:
- International Journal of Cancer, 2002, v. 100, n. 4, p. 476, doi. 10.1002/ijc.10513
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- Publication type:
- Article
Assessing population differentiation and isolation from single–nucleotide polymorphism data.
- Published in:
- Journal of the Royal Statistical Society: Series B (Statistical Methodology), 2002, v. 64, n. 4, p. 695, doi. 10.1111/1467-9868.00357
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- Publication type:
- Article
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.
- Published in:
- Frontiers in Endocrinology, 2023, v. 14, p. 1, doi. 10.3389/fendo.2023.1081741
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- Publication type:
- Article
Genetic Risk Score and Cardiovascular Events in Women.
- Published in:
- 2010
- By:
- Publication type:
- Letter
An Icelandic saga on a centralized healthcare database and democratic decision making.
- Published in:
- Nature Biotechnology, 1999, v. 17, n. 7, p. 620, doi. 10.1038/10796
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- Publication type:
- Article
Expression of the Oligodendrocyte-Myelin Glycoprotein by Neurons in the Mouse Central Nervous System.
- Published in:
- Journal of Neurochemistry, 1998, v. 70, n. 4, p. 1704, doi. 10.1046/j.1471-4159.1998.70041704.x
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- Publication type:
- Article
Molecular Evolution of τ Protein: Implications for Alzheimer's Disease.
- Published in:
- Journal of Neurochemistry, 1996, v. 67, n. 4, p. 1622, doi. 10.1046/j.1471-4159.1996.67041622.x
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- Publication type:
- Article
The Icelandic Man Cometh.
- Published in:
- 2003
- By:
- Publication type:
- Interview
Fine-scale recombination rate differences between sexes, populations and individuals.
- Published in:
- Nature, 2010, v. 467, n. 7319, p. 1099, doi. 10.1038/nature09525
- By:
- Publication type:
- Article
Icelandic genetic database not at risk from bankruptcy.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas.
- Published in:
- Human Genetics, 2016, v. 135, n. 4, p. 425, doi. 10.1007/s00439-016-1638-x
- By:
- Publication type:
- Article
Comparing migraine with and without aura to healthy controls using RNA sequencing.
- Published in:
- 2019
- By:
- Publication type:
- journal article
The influence of genetic constitution on migraine drug responses.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Rare variant associations with birth weight identify genes involved in adipose tissue regulation, placental function and insulin-like growth factor signalling.
- Published in:
- Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-024-55761-2
- By:
- Publication type:
- Article
DG-041 inhibits the EP3 prostanoid receptor—A new target for inhibition of platelet function in atherothrombotic disease.
- Published in:
- Platelets, 2008, v. 19, n. 8, p. 605, doi. 10.1080/09537100802351073
- By:
- Publication type:
- Article
Blocking the EP3 receptor for PGE2 with DG-041 decreases thrombosis without impairing haemostatic competence.
- Published in:
- Cardiovascular Research, 2014, v. 101, n. 3, p. 482, doi. 10.1093/cvr/cvt276
- By:
- Publication type:
- Article
Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility.
- Published in:
- American Journal of Epidemiology, 2017, v. 185, n. 3, p. 162, doi. 10.1093/aje/kww120
- By:
- Publication type:
- Article
Association Between IL-1 β/TNF-α-Induced Glucocorticoid-Sensitive Changes in Multiple Gene Expression and Altered Responsiveness in Airway Smooth Muscle.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2001, v. 25, n. 6, p. 761, doi. 10.1165/ajrcmb.25.6.4628
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- Publication type:
- Article
Developmental Changes in the Molecular Weights of Polypeptides in the Human CNS That Carry the HNK-1 Epitope and Bind Phaseolus vulgaris Lectins.
- Published in:
- Journal of Neurochemistry, 1988, v. 50, n. 6, p. 1924, doi. 10.1111/j.1471-4159.1988.tb02498.x
- By:
- Publication type:
- Article
The Hexabrachion Gene as a Candidate for a Tuberous Sclerosis Gene.
- Published in:
- Annals of the New York Academy of Sciences, 1991, v. 615, n. 1, p. 220, doi. 10.1111/j.1749-6632.1991.tb37763.x
- By:
- Publication type:
- Article
Prion susceptibility and protective alleles exhibit marked geographic differences (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #628 (2003) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/628.pdf)
- Published in:
- Human Mutation, 2003, v. 22, n. 1, p. 104, doi. 10.1002/humu.9157
- By:
- Publication type:
- Article
Prion susceptibility and protective alleles exhibit marked geographic differencesCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #628 (2003) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/628.pdf.
- Published in:
- Human Mutation, 2003, v. 22, n. 1, p. 104, doi. 10.1002/humu.9157
- By:
- Publication type:
- Article
GORpipe: a query tool for working with sequence data based on a Genomic Ordered Relational (GOR) architecture.
- Published in:
- 2016
- By:
- Publication type:
- Product Review
GORpipe: a query tool for working with sequence data based on a Genomic Ordered Relational (GOR) architecture.
- Published in:
- Bioinformatics, 2015, v. 31, n. 20, p. 3081, doi. 10.1093/bioinformatics/btw199
- By:
- Publication type:
- Article
The OMgp gene, a second growth suppressor within the NF1 gene.
- Published in:
- Oncogene, 1998, v. 16, n. 12, p. 1525, doi. 10.1038/sj.onc.1201683
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- Publication type:
- Article
Rare mutations associating with serum creatinine and chronic kidney disease.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 25, p. 1, doi. 10.1093/hmg/ddu399
- By:
- Publication type:
- Article
A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration).
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 9, p. 975, doi. 10.1093/hmg/ddh106
- By:
- Publication type:
- Article
Increased absorption of phytosterols is the simplest and most plausible explanation for coronary artery disease risk not accounted for by non-HDL cholesterol in high cholesterol absorbers.
- Published in:
- European Heart Journal, 2021, v. 42, n. 3, p. 283, doi. 10.1093/eurheartj/ehaa902
- By:
- Publication type:
- Article
Two Rare Mutations in the COL1A2 Gene Associate With Low Bone Mineral Density and Fractures in Iceland.
- Published in:
- Journal of Bone & Mineral Research, 2016, v. 31, n. 1, p. 173, doi. 10.1002/jbmr.2604
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- Publication type:
- Article
Cloning of cDNA for Two Large Polypeptides Found in Myelinating Oligodendrocytes.
- Published in:
- Annals of the New York Academy of Sciences, 1988, v. 540, n. 1, p. 405, doi. 10.1111/j.1749-6632.1988.tb27116.x
- By:
- Publication type:
- Article
A Peanut Agglutinin Binding Glycoprotein in CNS Myelin and Oligodendrocytes.
- Published in:
- Annals of the New York Academy of Sciences, 1988, v. 540, n. 1, p. 409, doi. 10.1111/j.1749-6632.1988.tb27118.x
- By:
- Publication type:
- Article
A 70-Kd Polypeptide Secreted by Human Peripheral Blood Mononuclear Cells That Suppresses Proliferation of a Human Glioblastoma Cell Line.
- Published in:
- Annals of the New York Academy of Sciences, 1988, v. 540, n. 1, p. 333, doi. 10.1111/j.1749-6632.1988.tb27090.x
- By:
- Publication type:
- Article
Sharing of Epitopes by Bacteria and the Nicotinic Acetylcholine Receptor: A Possible Role in the Pathogenesis of Myasthenia Gravis.
- Published in:
- Annals of the New York Academy of Sciences, 1987, v. 505, n. 1, p. 451, doi. 10.1111/j.1749-6632.1987.tb51315.x
- By:
- Publication type:
- Article
Role of pharmacogenomics in drug development.
- Published in:
- Drug Development Research, 2004, v. 62, n. 2, p. 86, doi. 10.1002/ddr.10367
- By:
- Publication type:
- Article
Cartilage Acidic Protein 1 in Plasma Associates With Prevalent Osteoarthritis and Predicts Future Risk as Well as Progression to Joint Replacements: Results From the UK Biobank Resource.
- Published in:
- Arthritis & Rheumatology, 2023, v. 75, n. 4, p. 544, doi. 10.1002/art.42376
- By:
- Publication type:
- Article
The CRTAC1 Protein in Plasma Is Associated With Osteoarthritis and Predicts Progression to Joint Replacement: A Large‐Scale Proteomics Scan in Iceland.
- Published in:
- Arthritis & Rheumatology, 2021, v. 73, n. 11, p. 2025, doi. 10.1002/art.41793
- By:
- Publication type:
- Article
Genome-wide investigation of persistence with methotrexate treatment in early rheumatoid arthritis.
- Published in:
- Rheumatology, 2024, v. 63, n. 5, p. 1221, doi. 10.1093/rheumatology/kead301
- By:
- Publication type:
- Article
Reproductive fitness and genetic risk of psychiatric disorders in the general population.
- Published in:
- Nature Communications, 2017, v. 8, n. 6, p. 1, doi. 10.1038/ncomms15833
- By:
- Publication type:
- Article
Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis.
- Published in:
- Nature Communications, 2016, v. 7, n. 7, p. 12350, doi. 10.1038/ncomms12350
- By:
- Publication type:
- Article
Common and rare variants associated with kidney stones and biochemical traits.
- Published in:
- Nature Communications, 2015, v. 6, n. 8, p. 7975, doi. 10.1038/ncomms8975
- By:
- Publication type:
- Article
Neuregulin 1 and schizophrenia.
- Published in:
- Annals of Medicine, 2004, v. 36, n. 1, p. 62, doi. 10.1080/07853890310017585
- By:
- Publication type:
- Article
Evaluating differences in linkage disequilibrium between populations.
- Published in:
- Annals of Human Genetics, 2010, v. 74, n. 3, p. 233, doi. 10.1111/j.1469-1809.2010.00571.x
- By:
- Publication type:
- Article
The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease.
- Published in:
- European Heart Journal, 2010, v. 31, n. 24, p. 3017, doi. 10.1093/eurheartj/ehq272
- By:
- Publication type:
- Article
Familial aggregation of atrial fibrillation in Iceland.
- Published in:
- European Heart Journal, 2006, v. 27, n. 6, p. 708, doi. 10.1093/eurheartj/ehi727
- By:
- Publication type:
- Article