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No Clinically Relevant Effect of Heart Rate Increase and Heart Rate Recovery During Exercise on Cardiovascular Disease: A Mendelian Randomization Analysis.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. N.PAG, doi. 10.3389/fgene.2021.569323
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- Article
Causal Inference for Genetic Obesity, Cardiometabolic Profile and COVID-19 Susceptibility: A Mendelian Randomization Study.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.586308
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- Article
State of the Art Review on Genetics and Precision Medicine in Arrhythmogenic Cardiomyopathy.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 18, p. 6615, doi. 10.3390/ijms21186615
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- Article
Fine mapping of candidate effector genes for heart rate.
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- Human Genetics, 2024, v. 143, n. 9/10, p. 1207, doi. 10.1007/s00439-024-02684-z
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- Article
A Novel Two-Stage Heart Arrhythmia Ensemble Classifier.
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- Computers (2073-431X), 2021, v. 10, n. 5, p. 60, doi. 10.3390/computers10050060
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- Article
Vitamin D and high blood pressure: causal association or epiphenomenon?
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- European Journal of Epidemiology, 2014, v. 29, n. 1, p. 1, doi. 10.1007/s10654-013-9874-z
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- Article
The effects of polygenic risk for psychiatric disorders and smoking behaviour on psychotic experiences in UK Biobank.
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- Translational Psychiatry, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41398-020-01009-8
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- Article
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
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- Nature Genetics, 2014, v. 46, n. 8, p. 826, doi. 10.1038/ng.3014
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- Article
The role of GRIP1 and ephrin B3 in blood pressure control and vascular smooth muscle cell contractility.
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- Scientific Reports, 2016, p. 38976, doi. 10.1038/srep38976
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- Article
Analysing electrocardiographic traits and predicting cardiac risk in UK biobank.
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- JRSM Cardiovascular Disease, 2021, p. 1, doi. 10.1177/20480040211023664
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- Article
The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction.
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- Frontiers in Pharmacology, 2022, v. 12, p. 1, doi. 10.3389/fphar.2021.679857
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- Article
Greater risk of severe COVID-19 in Black, Asian and Minority Ethnic populations is not explained by cardiometabolic, socioeconomic or behavioural factors, or by 25(OH)-vitamin D status: study of 1326 cases from the UK Biobank.
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- Journal of Public Health, 2020, v. 42, n. 3, p. 451, doi. 10.1093/pubmed/fdaa095
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- Article
Progress in Determining the Genes for Hypertension, Insulin Resistance, and Dyslipidemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1997, v. 827, n. 1, p. 110, doi. 10.1111/j.1749-6632.1997.tb51826.x
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- Article
Polygenic risk scores for schizophrenia and major depression are associated with socio-economic indicators of adversity in two British community samples.
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- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-02247-8
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- Publication type:
- Article
Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-45703-0
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- Article
Reaching the End-Game for GWAS: Machine Learning Approaches for the Prioritization of Complex Disease Loci.
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- Frontiers in Genetics, 2020, p. 1, doi. 10.3389/fgene.2020.00350
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- Publication type:
- Article
Age, sex and disease-specific associations between resting heart rate and cardiovascular mortality in the UK BIOBANK.
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- PLoS ONE, 2020, v. 15, n. 5, p. 1, doi. 10.1371/journal.pone.0233898
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- Article
Machine Learning of Gut Microbiome Composition for Diagnostic Classification of Inflammatory Bowel Diseases.
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- FASEB Journal, 2021, v. 35, p. N.PAG, doi. 10.1096/fasebj.2021.35.S1.04113
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- Article
Hypertension genetics past, present and future applications.
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- Journal of Internal Medicine, 2021, v. 290, n. 6, p. 1130, doi. 10.1111/joim.13352
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- Article
Light to moderate coffee consumption is associated with lower risk of death: a UK Biobank study.
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- European Journal of Preventive Cardiology, 2022, v. 29, n. 6, p. 982, doi. 10.1093/eurjpc/zwac008
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- Publication type:
- Article
Left atrial structure and function are associated with cardiovascular outcomes independent of left ventricular measures: a UK Biobank CMR study.
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- European Heart Journal - Cardiovascular Imaging, 2022, v. 23, n. 9, p. 1191, doi. 10.1093/ehjci/jeab266
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- Publication type:
- Article
Corrigendum to: Left atrial structure and function are associated with cardiovascular outcomes independent of left ventricular measures: a UK Biobank CMR study.
- Published in:
- European Heart Journal - Cardiovascular Imaging, 2022, v. 23, n. 9, p. e331, doi. 10.1093/ehjci/jeac119
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- Article
ECG T-Wave Morphologic Variations Predict Ventricular Arrhythmic Risk in Low- and Moderate-Risk Populations.
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- 2022
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- Publication type:
- journal article
Genome-Wide Meta-Analysis of Blood Pressure Response to β<sub>1</sub>-Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies).
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- 2019
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- Publication type:
- journal article
Genomic and pleiotropic analyses of resting QT interval identifies novel loci and overlap with atrial electrical disorders.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 24, p. 2513, doi. 10.1093/hmg/ddab197
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- Publication type:
- Article
Genome-wide association study of cardiac troponin I in the general population.
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- Human Molecular Genetics, 2021, v. 30, n. 21, p. 2027, doi. 10.1093/hmg/ddab124
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- Publication type:
- Article
Genetic variants in TRPM7 associated with unexplained stillbirth modify ion channel function.
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- Human Molecular Genetics, 2020, v. 29, n. 11, p. 1797, doi. 10.1093/hmg/ddz198
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- Publication type:
- Article
Over 1000 genetic loci influencing blood pressure with multiple systems and tissues implicated.
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- Human Molecular Genetics, 2019, v. 28, p. R151, doi. 10.1093/hmg/ddz197
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- Publication type:
- Article
The biological impact of blood pressure-associated genetic variants in the natriuretic peptide receptor C gene on human vascular smooth muscle.
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- Human Molecular Genetics, 2018, v. 27, n. 1, p. 199, doi. 10.1093/hmg/ddx375
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- Publication type:
- Article
Quantifying the extent to which index event biases influence large genetic association studies.
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- Human Molecular Genetics, 2017, v. 26, n. 5, p. 1018, doi. 10.1093/hmg/ddw433
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- Publication type:
- Article
Variation in left ventricular cardiac magnetic resonance normal reference ranges: systematic review and meta-analysis.
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- European Heart Journal - Cardiovascular Imaging, 2021, v. 22, n. 5, p. 494, doi. 10.1093/ehjci/jeaa089
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- Publication type:
- Article
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
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- Nature, 2011, v. 478, n. 7367, p. 103, doi. 10.1038/nature10405
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- Article
Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04148-1
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- Publication type:
- Article
Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans.
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- Human Mutation, 2011, v. 32, n. 7, p. 806, doi. 10.1002/humu.21508
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- Publication type:
- Article
Polygenic scores for schizophrenia and major depression are associated with psychosocial risk factors in children: evidence of gene–environment correlation.
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- Journal of Child Psychology, 2022, v. 63, n. 10, p. 1140, doi. 10.1111/jcpp.13657
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- Publication type:
- Article
Gene-educational attainment interactions in a multi-population genome-wide meta-analysis identify novel lipid loci.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1235337
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- Publication type:
- Article
Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.
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- Human Molecular Genetics, 2006, v. 15, n. 8, p. 1365, doi. 10.1093/hmg/ddl058
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- Publication type:
- Article
Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.
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- Human Molecular Genetics, 2005, v. 14, n. 13, p. 1805, doi. 10.1093/hmg/ddi187
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- Article
Genetics of essential hypertension.
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- Human Molecular Genetics, 2004, v. 13, n. suppl_1, p. R169
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- Publication type:
- Article
Gene–Environment Correlation over Time: A Longitudinal Analysis of Polygenic Risk Scores for Schizophrenia and Major Depression in Three British Cohorts Studies.
- Published in:
- Genes, 2022, v. 13, n. 7, p. 1136, doi. 10.3390/genes13071136
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- Publication type:
- Article
Meta-Analysis of Dilated Cardiomyopathy Using Cardiac RNA-Seq Transcriptomic Datasets.
- Published in:
- Genes, 2020, v. 11, n. 1, p. 60, doi. 10.3390/genes11010060
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- Publication type:
- Article
Poor Bone Quality is Associated With Greater Arterial Stiffness: Insights From the UK Biobank.
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- Journal of Bone & Mineral Research, 2021, v. 36, n. 1, p. 90, doi. 10.1002/jbmr.4164
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- Article
Mutations in the gene encoding the human matrix Gla protein cause Keutel syndrome.
- Published in:
- Nature Genetics, 1999, v. 21, n. 1, p. 142, doi. 10.1038/5102
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- Article
Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.
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- PLoS Genetics, 2022, v. 18, n. 4, p. 1, doi. 10.1371/journal.pgen.1010068
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- Publication type:
- Article
SLC2A9 Is a High-Capacity Urate Transporter in Humans.
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- PLoS Medicine, 2008, v. 5, n. 10, p. 1509, doi. 10.1371/journal.pmed.0050197
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- Article
Molecular basis of the neuronal ceroid lipofuscinoses: Mutations in CLN1, CLN2, CLN3, and CLN5.
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- Human Mutation, 1999, v. 14, n. 3, p. 199, doi. 10.1002/(SICI)1098-1004(1999)14:3<199::AID-HUMU3>3.0.CO;2-A
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- Publication type:
- Article
NMR metabolomic modeling of age and lifespan: A multicohort analysis.
- Published in:
- Aging Cell, 2024, v. 23, n. 7, p. 1, doi. 10.1111/acel.14164
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- Article
Absence of linkage of the epithelial sodium channel to hypertension in black Caribbeans<sup>*</sup>.
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- American Journal of Hypertension, 1998, v. 11, n. 8, p. 942, doi. 10.1016/S0895-7061(98)00092-2
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- Publication type:
- Article
Long-term association of ultra-short heart rate variability with cardiovascular events.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-45988-2
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- Publication type:
- Article
Mutations in the palmitoyl-protein thioesterase gene ( PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 2, p. 291, doi. 10.1093/hmg/7.2.291
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- Article