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:
Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation
Óscar Campuzano, Geòrgia Sarquella-Brugada, Elena Arbelo, et al.
Journal of Clinical Medicine (2020) Vol. 9, Iss. 6, pp. 1866-1866
Open Access | Times Cited: 7
Óscar Campuzano, Geòrgia Sarquella-Brugada, Elena Arbelo, et al.
Journal of Clinical Medicine (2020) Vol. 9, Iss. 6, pp. 1866-1866
Open Access | Times Cited: 7
Showing 7 citing articles:
Clinical impact of rare variants associated with inherited channelopathies: a 5-year update
Geòrgia Sarquella-Brugada, Anna Fernàndez-Falgueras, Sergi César, et al.
Human Genetics (2021) Vol. 141, Iss. 10, pp. 1579-1589
Open Access | Times Cited: 25
Geòrgia Sarquella-Brugada, Anna Fernàndez-Falgueras, Sergi César, et al.
Human Genetics (2021) Vol. 141, Iss. 10, pp. 1579-1589
Open Access | Times Cited: 25
Modeling genetic cardiac channelopathies using induced pluripotent stem cells – Status quo from an electrophysiological perspective
Michelle Vanessa Kapchoup Kamga, Michael Reppel, Jürgen Hescheler, et al.
Biochemical Pharmacology (2021) Vol. 192, pp. 114746-114746
Closed Access | Times Cited: 10
Michelle Vanessa Kapchoup Kamga, Michael Reppel, Jürgen Hescheler, et al.
Biochemical Pharmacology (2021) Vol. 192, pp. 114746-114746
Closed Access | Times Cited: 10
Whole exome sequencing of FFPE samples—expanding the horizon of forensic molecular autopsies
Emma Adolfsson, Daniel Kling, Cecilia Gunnarsson, et al.
International Journal of Legal Medicine (2022) Vol. 137, Iss. 4, pp. 1215-1234
Open Access | Times Cited: 4
Emma Adolfsson, Daniel Kling, Cecilia Gunnarsson, et al.
International Journal of Legal Medicine (2022) Vol. 137, Iss. 4, pp. 1215-1234
Open Access | Times Cited: 4
The link between abnormalities of calcium handling proteins and catecholaminergic polymorphic ventricular tachycardia
Ding-Jyun Lin, Wen-Sen Lee, Yu-Chung Chien, et al.
Tzu Chi Medical Journal (2021) Vol. 33, Iss. 4, pp. 323-331
Open Access | Times Cited: 4
Ding-Jyun Lin, Wen-Sen Lee, Yu-Chung Chien, et al.
Tzu Chi Medical Journal (2021) Vol. 33, Iss. 4, pp. 323-331
Open Access | Times Cited: 4
Cardiac channelopathies in pediatrics: a genetic update
Estefanía Martinez-Barrios, Óscar Campuzano, Andrea Greco, et al.
European Journal of Pediatrics (2024) Vol. 183, Iss. 11, pp. 4635-4640
Closed Access
Estefanía Martinez-Barrios, Óscar Campuzano, Andrea Greco, et al.
European Journal of Pediatrics (2024) Vol. 183, Iss. 11, pp. 4635-4640
Closed Access
Anatomical-MRI Correlations in Adults and Children with Arrhythmogenic Right Ventricular Cardiomyopathy
Simona-Sorana Căinap, Ilana Kovalenko, Edoardo Bonamano, et al.
Diagnostics (2021) Vol. 11, Iss. 8, pp. 1388-1388
Open Access | Times Cited: 2
Simona-Sorana Căinap, Ilana Kovalenko, Edoardo Bonamano, et al.
Diagnostics (2021) Vol. 11, Iss. 8, pp. 1388-1388
Open Access | Times Cited: 2
Clinical Impact of Rare Variants Associated with Inherited Channelopathies: A Five-Year Update
Geòrgia Sarquella-Brugada, Anna Fernández‐Arévalo, Sergi César, et al.
Research Square (Research Square) (2021)
Closed Access | Times Cited: 2
Geòrgia Sarquella-Brugada, Anna Fernández‐Arévalo, Sergi César, et al.
Research Square (Research Square) (2021)
Closed Access | Times Cited: 2
