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Cited by in F6Publishing
For: Martínez-barrios E, Cesar S, Cruzalegui J, Hernandez C, Arbelo E, Fiol V, Brugada J, Brugada R, Campuzano O, Sarquella-brugada G. Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population. Biomedicines 2022;10:106. [DOI: 10.3390/biomedicines10010106] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Martinez-Barrios E, Sarquella-Brugada G, Perez-Serra A, Fernandez-Falgueras A, Cesar S, Alcalde M, Coll M, Puigmulé M, Iglesias A, Ferrer-Costa C, Del Olmo B, Picó F, Lopez L, Fiol V, Cruzalegui J, Hernandez C, Arbelo E, Díez-Escuté N, Cerralbo P, Grassi S, Oliva A, Toro R, Brugada J, Brugada R, Campuzano O. Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort. Int J Legal Med 2023. [PMID: 36693943 DOI: 10.1007/s00414-023-02951-0] [Reference Citation Analysis]
2 Johnson MJ, Kelson M, Ruparel H, Simons K, Vincent P. QT and the beast: A case of valproate monotherapy for schizoaffective disorder-bipolar type with comorbid congenital long QT syndrome. Psychiatry Research Case Reports 2022;1:100076. [DOI: 10.1016/j.psycr.2022.100076] [Reference Citation Analysis]
3 Huang H, Jing S, Wu S, Wei L, Zhang Q, Hua Y, Li Y, Yu H, Zhou K. Case Report: A novel KNCH2 variant-induced fetal heart block and the advantages of fetal genomic sequencing in prenatal long-term dexamethasone exposure. Front Genet 2022;13. [DOI: 10.3389/fgene.2022.1010078] [Reference Citation Analysis]
4 Martínez-barrios E, Cruzalegui J, Cesar S, Chipa F, Arbelo E, Fiol V, Brugada J, Sarquella-brugada G, Campuzano O. Short QT Syndrome: Update on Genetic Basis. Rare Diseases - Recent Advances [Working Title] 2022. [DOI: 10.5772/intechopen.106808] [Reference Citation Analysis]
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