JUAN RAMÓN GIMENO BLANES

Siguero-Alvarez M, Salguero-Jimenez A, Grego-Bessa J, de la Barrera J, MacGrogan D, Prados B, Sanchez-Saez F, Pineiro-Sabaris R, Felipe-Medina N, Torroja C, Gomez MJ, Sabater-Molina M, Escriba R, Richaud-Patin I, Iglesias-Garcia O, Sbroggio M, Callejas S, O'Regan DP, McGurk KA, Dopazo A, Giovinazzo G, Ibanez B, Monserrat L, Perez-Pomares JM, Sanchez-Cabo F, Pendas AM, Raya A, Gimeno-Blanes JR, de la Pompa JL. A Human Hereditary Cardiomyopathy Shares a Genetic Substrate With Bicuspid Aortic Valve. Circulation. 2023 Jan 3;147(1):47-65. doi: 10.1161/CIRCULATIONAHA.121.058767. Epub 2022 Nov 3. Erratum In: Circulation. 2023 Jan 17;147(3):e63. PubMed PMID: 36325906.

AÑO: 2023; IF: 37.8

36325906

Parisi V, Baldassarre R, Ferrara V, Ditaranto R, Barlocco F, Lillo R, Re F, Marchi G, Chiti C, Di Nicola F, Catalano C, Barile L, Schiavo MA, Ponziani A, Saturi G, Caponetti AG, Berardini A, Graziosi M, Pasquale F, Salamon I, Ferracin M, Nardi E, Capelli I, Girelli D, Gimeno Blanes JR, Biffi M, Galie N, Olivotto I, Graziani F, Biagini E. Electrocardiogram analysis in Anderson-Fabry disease: a valuable tool for progressive phenotypic expression tracking. Front Cardiovasc Med. 2023 Jun 21;10:1184361. doi: 10.3389/fcvm.2023.1184361. eCollection 2023. PubMed PMID: 37416917; PubMed Central PMCID: PMC10320218.

AÑO: 2023; IF: 3.6

37416917

Robles-Mezcua A, Ruiz-Salas A, Medina-Palomo C, Robles-Mezcua M, Diaz-Exposito A, Ortega-Jimenez MV, Gimeno-Blanes JR, Jimenez-Navarro MF, Garcia-Pinilla JM. The Novel Variant NP_00454563.2 (p.Glu259Glyfs*77) in Gene PKP2 Associated with Arrhythmogenic Cardiomyopathy in 8 Families from Malaga, Spain. Genes (Basel). 2023 Jul 19;14(7):1468. doi: 10.3390/genes14071468. PubMed PMID: 37510372; PubMed Central PMCID: PMC10379208.

AÑO: 2023; IF: 4.141

37510372

Bermudez-Jimenez FJ, Carriel V, Santos-Mateo JJ, Fernandez A, Garcia-Hernandez S, Ramos KA, Piqueras-Flores J, Cabrera-Romero E, Barriales-Villa R, de la Higuera Romero L, Alcala Lopez JE, Gimeno Blanes JR, Sanchez-Porras D, Campos F, Alaminos M, Oyonarte-Ramirez JM, Alvarez M, Tercedor L, Brodehl A, Jimenez-Jaimez J. ROD2 domain filamin C missense mutations exhibit a distinctive cardiac phenotype with restrictive/hypertrophic cardiomyopathy and saw-tooth myocardium. Rev Esp Cardiol (Engl Ed). 2023 May;76(5):301-311. doi: 10.1016/j.rec.2022.08.002. Epub 2022 Aug 8. English, Spanish. PubMed PMID: 35952944.

AÑO: 2023; IF: 6.975

35952944

Lopez-Palop R, Carrillo P, Leithold G, Lozano I, Nieto A, Frutos A, Garcia J, Freites A, Lacunza J, Duran JM, Hurtado J, Gimeno JR, Valdesuso R, Pinar E, Pascual D. Accuracy of the angiography-based quantitative flow ratio in intermediate left main coronary artery lesions and comparison with visual estimation. Int J Cardiol. 2023 Jul 15;383:8-14. doi: 10.1016/j.ijcard.2023.04.035. Epub 2023 Apr 20. PubMed PMID: 37085119.

AÑO: 2023; IF: 3.5

37085119