Research map: Applications of genetic testing in cardiovascular disease
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Papers in this map
2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death
· Katja Zeppenfeld · 2022 · 3137 citations · Cited by this paper
Sodium reduction and salt substitutes: impact on blood pressure and recurrent stroke
· 2026 · Related
2024 ESC Guidelines for the management of atrial fibrillation developed in collaboration with the European Association for Cardio-Thoracic Surgery (EACTS)
· Isabelle C. Van Gelder · 2024 · 2934 citations · Cited by this paper
Artificial intelligence for right ventricular assessment: current evidence and future directions
· 2026 · Related
2023 ESC Guidelines for the management of cardiomyopathies
· Elena Arbelo · 2023 · 2720 citations · Cited by this paper
Postoperative atrial fibrillation after cardiac surgery: what is new?
· 2025 · Related
2024 ESC Guidelines for the management of peripheral arterial and aortic diseases
· Lucia Mazzolai · 2024 · 999 citations · Cited by this paper
Artificial intelligence for left ventricular strain
· 2026 · Related
Limitations of next-generation genome sequence assembly
· Can Alkan · 2010 · 795 citations · Cited by this paper
Impact of social determinants of health on cardiovascular health
· 2026 · Related
A robust benchmark for detection of germline large deletions and insertions
· Justin M. Zook · 2020 · 495 citations · Cited by this paper
Current opinion in cardiology, epigenetics of heart failure
· 2026 · Related
Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young
· Sian Ellard · 2008 · 439 citations · Cited by this paper
Weight loss as the optimal cardiometabolic management strategy for preventing and treating heart failure
· 2026 · Related
2025 ESC Guidelines for the management of myocarditis and pericarditis
· Jeanette Schulz‐Menger · 2025 · 410 citations · Cited by this paper
Optimizing conduits and intraoperative graft quality in coronary artery bypass graft surgery
· 2026 · Related
A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants
· Stephen F. Kingsmore · 2019 · 367 citations · Cited by this paper
Fetal MRI for cardiopulmonary anomalies: what the pediatric cardiologist and surgeon need to know
· 2026 · Related
2023 Update on European Atherosclerosis Society Consensus Statement on Homozygous Familial Hypercholesterolaemia: new treatments and clinical guidance
· Marina Cuchel · 2023 · 364 citations · Cited by this paper
Aldosterone synthase inhibition in hypertension: an evolving therapeutic strategy
· 2026 · Related
Recent Advances in Mitochondrial Disease
· Lyndsey Craven · 2017 · 301 citations · Cited by this paper
Recommendations for the management of autoinflammatory diseases
· Nienke M. ter Haar · 2015 · 278 citations · Cited by this paper
Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
· Jeffrey S. Dungan · 2022 · 212 citations · Cited by this paper
European guidelines for constitutional cytogenomic analysis
· Marisa Silva · 2018 · 183 citations · Cited by this paper
The 2021 EULAR/American College of Rheumatology points to consider for diagnosis, management and monitoring of the interleukin-1 mediated autoinflammatory diseases: cryopyrin-associated periodic syndromes, tumour necrosis factor receptor-associated periodic syndrome, mevalonate kinase deficiency, and deficiency of the interleukin-1 receptor antagonist
· Micol Romano · 2022 · 139 citations · Cited by this paper
Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic)
· Mireille Claustres · 2013 · 129 citations · Cited by this paper
Position statement from the International Society for Prenatal Diagnosis on the use of non‐invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies
· Lisa Hui · 2023 · 110 citations · Cited by this paper
Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity
· Gregory Costain · 2020 · 100 citations · Cited by this paper
Evaluation and Management of Deficiency of Adenosine Deaminase 2
· Pui Y. Lee · 2023 · 93 citations · Cited by this paper
Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines
· Eleni Mavraki · 2022 · 88 citations · Cited by this paper
Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics
· Eloisa Arbustini · 2021 · 75 citations · Cited by this paper
EULAR/PReS endorsed recommendations for the management of familial Mediterranean fever (FMF): 2024 update
· Seza Özen · 2025 · 69 citations · Cited by this paper
An Evidence Framework for Genetic Testing
· Sharon F. Terry · 2017 · 48 citations · Cited by this paper
Mitochondrial Donation and Preimplantation Genetic Testing for mtDNA Disease
· Louise Hyslop · 2025 · 48 citations · Cited by this paper
Whole gene sequencing identifies deep-intronic variants with potential functional impact in patients with hypertrophic cardiomyopathy
· Rita Mendes de Almeida · 2017 · 47 citations · Cited by this paper
Integration of genetic testing into diagnostic pathways for cardiomyopathies: a clinical consensus statement by the ESC Council on Cardiovascular Genomics
· Perry Mark Elliott · 2024 · 40 citations · Cited by this paper
Solving the unsolved rare diseases in Europe
· Holm Graeßner · 2021 · 36 citations · Cited by this paper
Whole MYBPC3 NGS sequencing as a molecular strategy to improve the efficiency of molecular diagnosis of patients with hypertrophic cardiomyopathy
· Alexandre Janin · 2019 · 29 citations · Cited by this paper
Tuberous Sclerosis Complex (TSC): Expert Recommendations for Provision of Coordinated Care
· Nicholas M. P. Annear · 2019 · 27 citations · Cited by this paper
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