Found: 18
Select item for more details and to access through your institution.
Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation.
- Published in:
- Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-06618-y
- By:
- 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
- By:
- Publication type:
- Article
Association of DIO2 and MCT10 Polymorphisms With Persistent Symptoms in LT4-Treated Patients in the UK Biobank.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 2, p. e613, doi. 10.1210/clinem/dgad556
- By:
- Publication type:
- Article
Early-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66671-w
- By:
- Publication type:
- Article
Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.806429
- By:
- Publication type:
- Article
Explaining deep neural networks for knowledge discovery in electrocardiogram analysis.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-90285-5
- By:
- Publication type:
- Article
Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 2, p. 372, doi. 10.3390/jcm9020372
- By:
- Publication type:
- Article
Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and Death.
- Published in:
- Journal of the American Heart Association, 2024, v. 13, n. 9, p. 1, doi. 10.1161/JAHA.123.034439
- By:
- Publication type:
- Article
Association of Common and Rare Genetic Variation in the 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Gene and Cataract Risk.
- Published in:
- 2022
- By:
- Publication type:
- journal article
DeepFake electrocardiograms using generative adversarial networks are the beginning of the end for privacy issues in medicine.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-01295-2
- By:
- Publication type:
- Article
Genetically predicted adipose tissue distribution influences the risk of atherosclerosis.
- Published in:
- European Journal of Preventive Cardiology, 2023, v. 30, n. 7, p. e41, doi. 10.1093/eurjpc/zwad041
- By:
- Publication type:
- Article
Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest.
- Published in:
- Frontiers in Physiology, 2018, p. N.PAG, doi. 10.3389/fphys.2018.00894
- By:
- Publication type:
- Article
Genome-wide association study identifies 18 novel loci associated with left atrial volume and function.
- Published in:
- European Heart Journal, 2021, v. 42, n. 44, p. 4523, doi. 10.1093/eurheartj/ehab466
- By:
- Publication type:
- Article
Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy.
- Published in:
- Molecular Genetics & Genomic Medicine, 2016, v. 4, n. 6, p. 617, doi. 10.1002/mgg3.245
- By:
- Publication type:
- Article
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.
- Published in:
- European Heart Journal, 2015, v. 36, n. 37, p. 2523, doi. 10.1093/eurheartj/ehv297
- By:
- Publication type:
- Article
Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of I<sub>f</sub> and I<sub>CaL</sub> in patient-derived cardiomyocytes.
- Published in:
- Cardiovascular Research, 2020, v. 116, n. 6, p. 1147, doi. 10.1093/cvr/cvz217
- By:
- Publication type:
- Article
Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse.
- Published in:
- Cardiovascular Research, 2020, v. 116, n. 1, p. 138, doi. 10.1093/cvr/cvz106
- By:
- Publication type:
- Article
Effect of Loss-of-Function Genetic Variants in PCSK9 on Glycemic Traits, Neurocognitive Impairment, and Hepatobiliary Function.
- Published in:
- 2022
- By:
- Publication type:
- journal article