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Cardiogenetics, Volume 16, Issue 4

2026 December - 8 articles

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Articles (8)

  • Article
  • Open Access
105 Views
19 Pages

Beyond Traditional Risk Factors: The Role of the CYP11B2 C(-344)T Polymorphism in Atherosclerosis and Cardiorenal Syndrome Phenotypes in Diabetes Mellitus

  • Volha Vasilkova,
  • Ivan Pchelin,
  • Tatsiana Mokhort,
  • Natalia Hudiakova and ,
  • Kseniia Lukianets,
  • Hussein Yousif Khalid Hussein,
  • Arkadi Silin and
  • Valentina Bayrasheva
  • + 3 authors+ 0 author

Background: This study aimed to evaluate the association of the CYP11B2 C(-344)T polymorphism with cardiorenal phenotypes and atherosclerosis in patients with DM. Methods: A total of 269 patients with DM (180 with type 2 and 89 with type 1 diabetes)...

(This article belongs to the Section Cardiovascular Genetics in Clinical Practice)
  • Review
  • Open Access
190 Views
34 Pages

Somatic hematopoietic mutations, particularly clonal hematopoiesis of indeterminate potential (CHIP), represent an emerging link between aging, inflammation and cardiovascular disease beyond their established relevance in hematology. This narrative r...

(This article belongs to the Section Molecular & Translational Genetics)
  • Review
  • Open Access
338 Views
20 Pages

Clinical and Prognostic Spectrum of Non-Dilated Left Ventricular Cardiomyopathy: The Role of Genetic Status

  • Chiara Castelli,
  • Roberta Rossini,
  • Antonella Maffè,
  • Andrea Faggiano and ,
  • Rossella Manai,
  • Federica Toto,
  • Marco Matteo Cingolani and
  • Federico Landra
  • + 3 authors+ 0 author

Non-dilated left ventricular cardiomyopathy (NDLVC) presents a unique clinical paradox: patients with nearly identical phenotypes can face radically different clinical outcomes. NDLVC has been recently recognized as a distinct dynamic phenotype withi...

(This article belongs to the Special Issue Genetic Insights into Sudden Cardiac Death: From Risk Stratification to Precision Prevention)
  • Article
  • Open Access
889 Views
18 Pages

Generation and Functional Characterization of Cadaver-Derived iPSC-Cardiomyocytes: A Feasibility Study Toward Functional Molecular Autopsy in Sudden Cardiac Death

  • Lijo Cherian Ozhathil,
  • Mikkel Eriksen Dupont,
  • Emma H. Meibom,
  • Iben Bache and ,
  • Isabella Mengarelli,
  • Connie R. Bezzina,
  • Luca Soattin,
  • Bo Hjorth Bentzen,
  • Jytte Banner and
  • Thomas Jespersen
  • + 6 authors+ 1 author

Sudden cardiac death (SCD) accounts for a substantial share of deaths in young individuals. Despite postmortem pathological, toxicological, and forensic examination and molecular autopsy, many cases remain unexplained, highlighting the need for compl...

(This article belongs to the Section Molecular & Translational Genetics)
  • Review
  • Open Access
392 Views
12 Pages

Trends in Preventing Sudden Cardiac Death in Hypertrophic Cardiomyopathy

  • Noemí Ramos-López,
  • María Ximena Reyes Cabrera,
  • Juan Ramón Gimeno-Blanes and
  • María Sabater Molina

Background: Contemporary series report declining sudden cardiac death (SCD) in hypertrophic cardiomyopathy (HCM), but whether this reflects fewer arrhythmic events or a greater proportion of deaths successfully prevented is unclear. We examined the p...

(This article belongs to the Section Cardiovascular Genetics in Clinical Practice)
  • Article
  • Open Access
279 Views
17 Pages

Mosaic Loss of Y Chromosome: Temporal Variance and Association with Various Features in Patients at High Risk of Cardiovascular Disease

  • Margarita Gundobina,
  • Daria Azarova,
  • Mark Jain,
  • Yulia Begrambekova and ,
  • Petr Poletskov,
  • Larisa Samokhodskaya and
  • Iana Orlova
  • + 2 authors+ 0 author

Mosaic loss of the Y chromosome (mLOY) is a common karyotype alteration. The accumulation of LOY cells leads to genetic mosaicism and affects the development of pathological conditions in elderly men. Emerging data suggest that this phenomenon might...

(This article belongs to the Section Molecular & Translational Genetics)
  • Article
  • Open Access
621 Views
21 Pages

Background: Hypertrophic cardiomyopathy (HCM) exhibits clinical heterogeneity and age-related penetrance, yet its molecular basis across adulthood remains incompletely understood. This study aimed to characterize age-dependent transcriptomic signatur...

(This article belongs to the Special Issue Contemporary and Future Approaches to Inherited Cardiomyopathies)
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Cardiogenetics - ISSN 2035-8148