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Perez-Sanchez I, Sabater-Molina M, Rocamora MEN, Glover G, Escudero F, de Mingo Casado P, Gimeno-Blanes JR. Phenotypic Characterization of a Family With An In-frame Deletion in the DMD Gene and Variable Penetrance. Curr Gene Ther. 2018;18(4):246-251. doi: 10.2174/1566523218666180709125346. PubMed PMID: 29984652.
AÑO: 2018; IF: 2.218
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29984652
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Pérez-Sánchez I, Sabater-Molina M, Muñoz-Esparza C, Gimeno-Blanes JR. Phenotype-modifying Factors in Hypertrophic Cardiomyopathy. Response. Rev Esp Cardiol (Engl Ed). 2018 Sep;71(9):770-771. doi: 10.1016/j.rec.2018.04.023. Epub 2018 Jun 25. English, Spanish. PubMed PMID: 29954718.
AÑO: 2018; IF: 5.126
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Garcia-Molina E, Sabater-Molina M, Lopez-Cuenca D, Olmo MC, Perez I, Munoz Esparza C, Gimeno Blanes JR. A study of the pathogenicity of variants in familial heart disease. The value of cosegregation. Am J Transl Res. 2019 Mar 15;11(3):1724-1735. eCollection 2019. PubMed PMID: 30972196; PubMed Central PMCID: PMC6456527.
AÑO: 2019; IF: 3.375
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Gil-Ortuno C, Sebastian-Marcos P, Sabater-Molina M, Nicolas-Rocamora E, Gimeno-Blanes JR, Fernandez Del Palacio MJ. Genetics of feline hypertrophic cardiomyopathy. Clin Genet. 2020 Sep;98(3):203-214. doi: 10.1111/cge.13743. Epub 2020 Apr 1. PubMed PMID: 32215921.
AÑO: 2020; IF: 4.438
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Ochoa JP, Sabater-Molina M, García-Pinilla JM, Mogensen J, Restrepo-Córdoba A, Palomino-Doza J, Villacorta E, Martinez-Moreno M, Ramos-Maqueda J, Zorio E, Peña-Peña ML, García-Granja PE, Rodríguez-Palomares JF, Cárdenas-Reyes IJ, de la Torre-Carpente MM, Bautista-Pavés A, Akhtar MM, Cicerchia MN, Bilbao-Quesada R, Mogollón-Jimenez MV, Salazar-Mendiguchía J, Mesa Latorre JM, Arnaez B, Olavarri-Miguel I, Fuentes-Cañamero ME, Lamounier A Jr, Pérez Ruiz JM, Climent-Payá V, Pérez-Sanchez I, Trujillo-Quintero JP, Lopes LR, Repáraz-Andrade A, Marín-Iglesias R, Rodriguez-Vilela A, Sandín-Fuentes M, Garrote JA, Cortel-Fuster A, Lopez-Garrido M, Fontalba-Romero A, Ripoll-Vera T, Llano-Rivas I, Fernandez-Fernandez X, Isidoro-García M, Garcia-Giustiniani D, Barriales-Villa R, Ortiz-Genga M, García-Pavía P, Elliott PM, Gimeno JR, Monserrat L. Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy. J Am Coll Cardiol. 2018 Nov 13;72(20):2457-2467. doi: 10.1016/j.jacc.2018.10.001. PubMed PMID: 30442288.
AÑO: 2018; IF: 18.639
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