Found: 49
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Histopathology and levels of proteins in plasma associate with survival after colorectal cancer diagnosis.
- Published in:
- British Journal of Cancer, 2023, v. 129, n. 7, p. 1142, doi. 10.1038/s41416-023-02374-z
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- Publication type:
- Article
Sequence variants affecting the genome-wide rate of germline microsatellite mutations.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39547-6
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- 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
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- Publication type:
- Article
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
- Published in:
- European Heart Journal, 2022, v. 43, n. 45, p. 4707, doi. 10.1093/eurheartj/ehac322
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- Publication type:
- Article
Effect of booster vaccination against Delta and Omicron SARS-CoV-2 variants in Iceland.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33076-4
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- Publication type:
- Article
Comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics".
- Published in:
- Science Translational Medicine, 2021, v. 13, n. 622, p. 1, doi. 10.1126/scitranslmed.abe8497
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- 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
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- Publication type:
- Article
Design of experiments for development and optimization of a liquid chromatography coupled to tandem mass spectrometry bioanalytical assay.
- Published in:
- Journal of Mass Spectrometry, 2021, v. 56, n. 9, p. 1, doi. 10.1002/jms.4566
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- Publication type:
- Article
Design of experiments for development and optimization of a liquid chromatography coupled to tandem mass spectrometry bioanalytical assay.
- Published in:
- Journal of Mass Spectrometry, 2021, v. 56, n. 9, p. 1, doi. 10.1002/jms.4566
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- Publication type:
- Article
Predicting the probability of death using proteomics.
- Published in:
- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02289-6
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- Publication type:
- Article
Sequence variants with large effects on cardiac electrophysiology and disease.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12682-9
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- Publication type:
- Article
Transcriptome-wide association study of multiple myeloma identifies candidate susceptibility genes.
- Published in:
- Human Genomics, 2019, v. 13, n. 1, p. N.PAG, doi. 10.1186/s40246-019-0231-5
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- Publication type:
- Article
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-09304-9
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- Publication type:
- Article
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters.
- Published in:
- 2017
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- Publication type:
- Case Study
Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 19, p. 3850, doi. 10.1093/hmg/ddx285
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- Publication type:
- Article
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.
- Published in:
- Nature Communications, 2017, v. 8, n. 6, p. 15789, doi. 10.1038/ncomms15789
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- Publication type:
- Article
Multi-nucleotide de novo Mutations in Humans.
- Published in:
- PLoS Genetics, 2016, v. 12, n. 11, p. 1, doi. 10.1371/journal.pgen.1006315
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- Publication type:
- Article
Erratum: A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.
- Published in:
- Nature Communications, 2016, v. 7, n. 9, p. 12869, doi. 10.1038/ncomms12869
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- Publication type:
- Article
A protein-truncating R179X variant in RNF186 confers protection against ulcerative colitis.
- Published in:
- Nature Communications, 2016, v. 7, n. 8, p. 12342, doi. 10.1038/ncomms12342
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- 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
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- 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
Protolichesterinic Acid, Isolated from the Lichen Cetraria islandica, Reduces LRRC8A Expression and Volume-Sensitive Release of Organic Osmolytes in Human Lung Epithelial Cancer Cells.
- Published in:
- 2016
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- Publication type:
- journal 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
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- Publication type:
- Article
Association Analysis of 29,956 Individuals Confirms That a Low-Frequency Variant at CCND2 Halves the Risk of Type 2 Diabetes by Enhancing Insulin Secretion.
- Published in:
- Diabetes, 2015, v. 64, n. 6, p. 2279, doi. 10.2337/db14-1456
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- Publication type:
- Article
Identification of a large set of rare complete human knockouts.
- Published in:
- Nature Genetics, 2015, v. 47, n. 5, p. 448, doi. 10.1038/ng.3243
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- Publication type:
- Article
Rare mutations associating with serum creatinine and chronic kidney disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 25, p. 6935, doi. 10.1093/hmg/ddu399
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- Publication type:
- Article
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma.
- Published in:
- Nature Genetics, 2014, v. 46, n. 10, p. 1126, doi. 10.1038/ng.3087
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- Publication type:
- Article
Common and low-frequency variants associated with genome-wide recombination rate.
- Published in:
- Nature Genetics, 2014, v. 46, n. 1, p. 11, doi. 10.1038/ng.2833
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- Publication type:
- Article
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization.
- Published in:
- Nature Genetics, 2013, v. 45, n. 8, p. 902, doi. 10.1038/ng.2694
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- Publication type:
- Article
Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity.
- Published in:
- PLoS ONE, 2013, v. 8, n. 3, p. 1, doi. 10.1371/journal.pone.0058048
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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
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- Publication type:
- Article
Rate of de novo mutations and the importance of father's age to disease risk.
- Published in:
- Nature, 2012, v. 488, n. 7412, p. 471, doi. 10.1038/nature11396
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- Publication type:
- Article
Novel aspects of the pathogenesis of aneurysms of the abdominal aorta in humans.
- Published in:
- Cardiovascular Research, 2011, v. 90, n. 1, p. 18
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- Publication type:
- Article
Fine-scale recombination rate differences between sexes, populations and individuals.
- Published in:
- Nature, 2010, v. 467, n. 7319, p. 1099, doi. 10.1038/nature09525
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- Publication type:
- Article
Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones-Role of Age and Comorbid Diseases.
- Published in:
- PLoS Genetics, 2010, v. 6, n. 7, p. 1, doi. 10.1371/journal.pgen.1001039
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- Publication type:
- Article
Several common variants modulate heart rate, PR interval and QRS duration.
- Published in:
- Nature Genetics, 2010, v. 42, n. 2, p. 117, doi. 10.1038/ng.511
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- Publication type:
- Article
New sequence variants associated with bone mineral density.
- Published in:
- Nature Genetics, 2009, v. 41, n. 1, p. 15, doi. 10.1038/ng.284
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- Publication type:
- Article
Male-pattern baldness susceptibility locus at 20p11.
- Published in:
- Nature Genetics, 2008, v. 40, n. 11, p. 1282, doi. 10.1038/ng.255
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- Publication type:
- Article
A Drastic Reduction in the Life Span of Cystatin C L68Q Carriers Due to Life-Style Changes during the Last Two Centuries.
- Published in:
- PLoS Genetics, 2008, v. 4, n. 6, p. 1, doi. 10.1371/journal.pgen.1000099
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- Publication type:
- Article
Support for involvement of the AHI1 locus in schizophrenia.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 9, p. 988, doi. 10.1038/sj.ejhg.5201848
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- Publication type:
- Article
The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts.
- Published in:
- PLoS Genetics, 2007, v. 3, n. 4, p. e61, doi. 10.1371/journal.pgen.0030061
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- Publication type:
- Article
The BARD1 Cys557Ser variant and breast cancer risk in Iceland.
- Published in:
- 2006
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- Publication type:
- journal article
A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction.
- Published in:
- Nature Genetics, 2006, v. 38, n. 1, p. 68, doi. 10.1038/ng1692
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- Publication type:
- Article
Familial Risk of Lung Carcinoma in the Icelandic Population.
- Published in:
- JAMA: Journal of the American Medical Association, 2004, v. 292, n. 24, p. 2977, doi. 10.1001/jama.292.24.2977
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- Publication type:
- Article
Cancer as a Complex Phenotype: Pattern of Cancer Distribution within and beyond the Nuclear Family.
- Published in:
- PLoS Medicine, 2004, v. 1, n. 3, p. 229, doi. 10.1371/journal.pmed.0010065
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- Publication type:
- Article
Interstitial deletions including chromosome 3 common eliminated region 1 (C3CER1) prevail in human solid tumors from 10 different tissues.
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 232
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- Publication type:
- Article
The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke.
- Published in:
- Nature Genetics, 2004, v. 36, n. 3, p. 233, doi. 10.1038/ng1311
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- Publication type:
- Article
NUP98-HOXA9 expression in hemopoietic stem cells induces chronic and acute myeloid leukemias in mice.
- Published in:
- EMBO Journal, 2001, v. 20, n. 3, p. 350, doi. 10.1093/emboj/20.3.350
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- Publication type:
- Article
Hoxa9 transforms primary bone marrow cells through specific collaboration with Meis1a but not Pbx1b.
- Published in:
- EMBO Journal, 1998, v. 17, n. 13, p. 3714, doi. 10.1093/emboj/17.13.3714
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- Publication type:
- Article