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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death
Estefanía Martinez-Barrios, Simone Grassi, Marı́a Brión, et al.
Frontiers in Medicine (2023) Vol. 10
Open Access | Times Cited: 32

Showing 1-25 of 32 citing articles:

Inherited Arrhythmias in the Pediatric Population: An Updated Overview
Marco Valerio Mariani, Nicola Pierucci, Francesca Fanisio, et al.
Medicina (2024) Vol. 60, Iss. 1, pp. 94-94
Open Access | Times Cited: 26
Sudden Cardiac Death in the Young: State-of-the-Art Review in Molecular Autopsy
Cecilia Salzillo, Vincenza Sansone, Francesco Napolitano
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 4, pp. 3313-3327
Open Access | Times Cited: 9
Fatal intoxications and inherited cardiac disorders in the young: where to draw the line?
Simone Grassi, Fabio Vaiano, Alexandra Dimitrova, et al.
International Journal of Legal Medicine (2025)
Open Access | Times Cited: 1
Establishment of performance parameters for the Qubit™ 1X dsDNA HS Assay for use in forensic genetics casework
A. Naidoo, Donna‐Lee Pamela Martin, Laura Jane Heathfield
Forensic Science International Reports (2025), pp. 100405-100405
Open Access
Quantification of Myocardial Biomarkers in Sudden Cardiac Deaths Using a Rapid Immunofluorescence Method for Simultaneous Biomarker Analysis
Matteo Antonio Sacco, Valerio Riccardo Aquila, Saverio Gualtieri, et al.
Biomedicines (2025) Vol. 13, Iss. 1, pp. 193-193
Open Access
Expanding the Concept of Iron Deficiency Using a Mitochondrial Metabolic Approach: Explaining and Preventing Sudden Death
Christineil Thompson
Pediatric Blood & Cancer (2025)
Closed Access
RBM20 p.Arg636Cys: A Pathogenic Variant Identified in a Family with Several Cases of Unexpected Sudden Deaths
Rebeca Lorca, Alberto Alén, Maria Cristina de Oliveira Salgado, et al.
Journal of Clinical Medicine (2025) Vol. 14, Iss. 3, pp. 743-743
Open Access
Challenges of genetics in the diagnosis of sudden cardiac death. Interest of forensic and legal medicine
Alejandro Blanco‐Verea, Ángel Carracedo, Marı́a Brión
Medicina Clínica (English Edition) (2025)
Closed Access
Sudden Cardiac Death: The Role of Molecular Autopsy with Next-Generation Sequencing
Jennifer Fadoni, Agostinho Santos, António Amorim, et al.
Diagnostics (2025) Vol. 15, Iss. 4, pp. 460-460
Open Access
Sudden cardiac death: the role of molecular autopsy with next-generation sequencing
Jennifer Fadoni, Agostinho Santos, Laura Cainé, et al.
Journal of Forensic and Legal Medicine (2025), pp. 102837-102837
Closed Access
Whole exome sequence reveals genetic profiles of primary cardiomyopathy and genotype-phenotype association in Chinese population
Ruilin Liu, Yifeng Yang, Ke Wei Gong, et al.
BMC Genomics (2025) Vol. 26, Iss. 1
Open Access
Are pre-analytical factors fully considered in forensic FFPE molecular analyses? A systematic review reveals the need for standardised procedures
Carlo Previderé, Serena Bonin, Calogero Cuttaia, et al.
International Journal of Legal Medicine (2025)
Open Access
Sudden Cardiac Death in Pregnant Women—Literature Review and Autopsy Findings
Ioana Radu, Anca Otilia Farcas, Laura Cimpan, et al.
Diagnostics (2025) Vol. 15, Iss. 9, pp. 1108-1108
Open Access
Investigating cardiac genetic background in sudden infant death syndrome (SIDS)
Francesca Cazzato, Mónica Coll, Simone Grassi, et al.
International Journal of Legal Medicine (2024)
Open Access | Times Cited: 2
Postmortale Genetik nach einem plötzlichen Herztod
Silke Kauferstein, Britt-Maria Beckmann
Herzschrittmachertherapie + Elektrophysiologie (2024) Vol. 35, Iss. 1, pp. 31-38
Closed Access | Times Cited: 1
Novel Gain-of-Function Mutation in the Kv11.1 Channel Found in the Patient with Brugada Syndrome and Mild QTc Shortening
Denis V. Abramochkin, Bowen Li, Han Zhang, et al.
Biochemistry (Moscow) (2024) Vol. 89, Iss. 3, pp. 543-552
Open Access | Times Cited: 1
Congenital heart diseases (CHDs) and forensic investigations: Searching for the cause of death
Francesco Sessa, Mario Giuseppe Chisari, Monica Salerno, et al.
Experimental and Molecular Pathology (2024) Vol. 137, pp. 104907-104907
Open Access | Times Cited: 1
“Acquired” sudden cardiac death high-risk genetic mutation in a heart transplant recipient
Luca Fazzini, Trista Brown, Matteo Castrichini, et al.
American Journal of Transplantation (2024) Vol. 24, Iss. 10, pp. 1916-1918
Closed Access | Times Cited: 1
Fentanyl and Sudden Death—A Postmortem Perspective for Diagnosing and Predicting Risk
Ines Strenja-Linić, Elizabeta Dadić-Hero, Manuela Perković, et al.
Diagnostics (2024) Vol. 14, Iss. 17, pp. 1995-1995
Open Access | Times Cited: 1
Molecular autopsy for sudden death in Japan
Takuma YAMAMOTO, Yuko Emoto, Takehiko Murase, et al.
Journal of Toxicologic Pathology (2023)
Open Access | Times Cited: 2
The Role of miRNA Expression Profile in Sudden Cardiac Death Cases
Alessia Bernini Di Michele, Valerio Onofri, Mauro Pesaresi, et al.
Genes (2023) Vol. 14, Iss. 10, pp. 1954-1954
Open Access | Times Cited: 2
DNA Extraction from Postmortem Blood: A Pilot Study for Advancing Molecular Diagnostics in Forensic Medicine Casework
Sadhu Rama Mohana Rao, Sravani Yandava, T. Mohit Kumar Moses, et al.
Indian Journal of Forensic Medicine & Toxicology (2024) Vol. 18, Iss. 1, pp. 124-129
Open Access
Postmortem Molecular Autopsy in Heritable Channelopathies and Selected Cardiomyopathies
Kathryn A. Glatter, Anum Bashir
Elsevier eBooks (2024), pp. 910-919
Closed Access
Molecular autopsy by proxy: relevance for genetic counseling in rare genetic disorders
Cristina Skrypnyk, Rawan AlHarmi
Frontiers in Genetics (2024) Vol. 15
Open Access
Molecular autopsy in Chinese sudden cardiac death in the young
Sit‐Yee Kwok, Stephanie Ho, F. Jin Shih, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 11
Open Access
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