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rs41291957 controls miR-143 and miR-145 expression and impacts coronary artery disease risk.
- Published in:
- EMBO Molecular Medicine, 2021, v. 13, n. 10, p. 1, doi. 10.15252/emmm.202114060
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- Article
Unravelling the Neospora caninum secretome through the secreted fraction (ESA) and quantification of the discharged tachyzoite using high-resolution mass spectrometry-based proteomics.
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- Parasites & Vectors, 2013, v. 6, n. 1, p. 1, doi. 10.1186/1756-3305-6-335
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- Article
Obesity Variants in the GIPR Gene Are not Associated With Risk of Fracture or Bone Mineral Density.
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- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 8, p. e1608, doi. 10.1210/clinem/dgad734
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- Article
Instance-level accuracy versus bag-level accuracy in multi-instance learning.
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- Data Mining & Knowledge Discovery, 2016, v. 30, n. 2, p. 313, doi. 10.1007/s10618-015-0416-z
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- Article
Genetic architecture of band neutrophil fraction in Iceland.
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- Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03462-1
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- Article
Genetic variants associated with platelet count are predictive of human disease and physiological markers.
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- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02642-9
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- Article
The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis.
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- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02224-9
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- Article
Effect of tissue-grouped regulatory variants associated to type 2 diabetes in related secondary outcomes.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-30369-6
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- Article
Gene Set Enrichment Analyses: lessons learned from the heart failure phenotype.
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- BioData Mining, 2017, v. 10, p. 1, doi. 10.1186/s13040-017-0137-5
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- Article
Discovery and replication of SNP-SNP interactions for quantitative lipid traits in over 60,000 individuals.
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- BioData Mining, 2017, v. 10, p. 1, doi. 10.1186/s13040-017-0145-5
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- Article
Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.
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- 2023
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- Correction Notice
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38951-2
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- Publication type:
- Article
Gene-Centric Meta-Analysis of Lipid Traits in African, East Asian and Hispanic Populations.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0050198
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- Article
Genetic variants associated with syncope implicate neural and autonomic processes.
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- European Heart Journal, 2023, v. 44, n. 12, p. 1070, doi. 10.1093/eurheartj/ehad016
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- Article
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
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- European Heart Journal, 2022, v. 43, n. 45, p. 4707, doi. 10.1093/eurheartj/ehac322
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- Article
Genetically determined NLRP3 inflammasome activation associates with systemic inflammation and cardiovascular mortality.
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- European Heart Journal, 2021, v. 42, n. 18, p. 1742, doi. 10.1093/eurheartj/ehab107
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- Article
Genetic variability in the absorption of dietary sterols affects the risk of coronary artery disease.
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- European Heart Journal, 2020, v. 41, n. 28, p. 2618, doi. 10.1093/eurheartj/ehaa531
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- Article
Identifying gene-gene interactions that are highly associated with four quantitative lipid traits across multiple cohorts.
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- Human Genetics, 2017, v. 136, n. 2, p. 165, doi. 10.1007/s00439-016-1738-7
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- Article
Harnessing publicly available genetic data to prioritize lipid modifying therapeutic targets for prevention of coronary heart disease based on dysglycemic risk.
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- Human Genetics, 2016, v. 135, n. 5, p. 453, doi. 10.1007/s00439-016-1647-9
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- Article
Sequence variants with large effects on cardiac electrophysiology and disease.
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- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12682-9
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- Article
Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA.
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- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06920-9
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- Article
Association of the coronary artery disease risk gene GUCY1A3 with ischaemic events after coronary intervention.
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- Cardiovascular Research, 2019, v. 115, n. 10, p. 1512, doi. 10.1093/cvr/cvz015
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- Publication type:
- Article
Loss-of-function variants in ITSN1 confer high risk of Parkinson's disease.
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- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00752-9
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- Publication type:
- Article
Polygenic risk scores associate with blood pressure traits across the lifespan.
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- European Journal of Preventive Cardiology, 2024, v. 31, n. 6, p. 644, doi. 10.1093/eurjpc/zwad365
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- Article
Erratum: Genetic loci associated with heart rate variability and their effects on cardiac disease risk.
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- Nature Communications, 2017, v. 8, n. 8, p. 16140, doi. 10.1038/ncomms16140
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- Publication type:
- Article
Genetic loci associated with heart rate variability and their effects on cardiac disease risk.
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- Nature Communications, 2017, v. 8, n. 6, p. 15805, doi. 10.1038/ncomms15805
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- Article
Polygenic Interactions With Environmental Exposures in Blood Pressure Regulation: The HUNT Study.
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- Journal of the American Heart Association, 2024, v. 13, n. 19, p. 1, doi. 10.1161/JAHA.123.034612
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- Article
Screening for Rare Coding Variants That Associate With the QTc Interval in Iceland.
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- Journal of the American Heart Association, 2023, v. 12, n. 14, p. 1, doi. 10.1161/JAHA.123.029845
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- Article
Sequence variants associating with urinary biomarkers.
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- Human Molecular Genetics, 2019, v. 28, n. 7, p. 1199, doi. 10.1093/hmg/ddy409
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- Article
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
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- Human Molecular Genetics, 2013, v. 22, n. 16, p. 3394
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- Article
Loci influencing blood pressure identified using a cardiovascular gene-centric array.
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- Human Molecular Genetics, 2013, v. 22, n. 8, p. 1663
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- Article
Coding variants in RPL3L and MYZAP increase risk of atrial fibrillation.
- Published in:
- Communications Biology, 2018, v. 1, n. 1, p. N.PAG, doi. 10.1038/s42003-018-0068-9
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- Article
Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05428-6
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- Article
Sequence variant affects GCSAML splicing, mast cell specific proteins, and risk of urticaria.
- Published in:
- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-05079-4
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- Article
Associations of Polymorphisms in the Peroxisome Proliferator-Activated Receptor Gamma Coactivator-1 Alpha Gene With Subsequent Coronary Heart Disease: An Individual-Level Meta-Analysis.
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- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.909870
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- Article
Controle da diversidade da população em algoritmos genéticos aplicados na predição de estruturas de prote-ínas.
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- Scientia, 2009, v. 20, n. 2, p. 83, doi. 10.4013/sct.2009.20.2.02
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- 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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- Article
Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies.
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- Genome Medicine, 2015, v. 7, n. 1, p. 1, doi. 10.1186/s13073-015-0211-x
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- Article
Mendelian randomization of blood lipids for coronary heart disease.
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- European Heart Journal, 2015, v. 36, n. 9, p. 539
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- Article
The impact of susceptibility loci for coronary artery disease on other vascular domains and recurrence risk.
- Published in:
- European Heart Journal, 2013, v. 34, n. 37, p. 2896
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- Article
A comparison of two workflows for regulome and transcriptome‐based prioritization of genetic variants associated with myocardial mass.
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- Genetic Epidemiology, 2019, v. 43, n. 6, p. 717, doi. 10.1002/gepi.22215
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- Article
The ENCODE Project and Perspectives on Pathways.
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- Genetic Epidemiology, 2014, v. 38, n. 4, p. 275, doi. 10.1002/gepi.21802
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- Article
Genomic correlates of glatiramer acetate adverse cardiovascular effects lead to a novel locus mediating coronary risk.
- Published in:
- PLoS ONE, 2017, v. 12, n. 8, p. 1, doi. 10.1371/journal.pone.0182999
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- Publication type:
- Article