Acceder Registro /

FRANCISCO RUIZ

Buscador

Castillo-Guardiola V, Rosado-Jimenez L, Sarabia-Meseguer MD, Marin-Vera M, Macias-Cerrolaza JA, Garcia-Hernandez R, Zafra-Poves M, Sanchez-Henarejos P, Moreno-Locubiche MA, Cuevas-Tortosa E, Arnaldos-Carrillo M, Ayala de la Pena F, Alonso-Romero JL, Noguera-Velasco JA, Ruiz-Espejo F. Next step in molecular genetics of hereditary breast/ovarian cancer: Multigene panel testing in clinical actionably genes and prioritization algorithms in the study of variants of uncertain significance. Eur J Med Genet. 2022 Apr;65(4):104468. doi: 10.1016/j.ejmg.2022.104468. Epub 2022 Mar 1. PubMed PMID: 35245693.
AÑO: 2022; IF: 1.9
Sánchez-Bermúdez AI, Sarabia-Meseguer MD, García-Aliaga Á, Marín-Vera M, Macías-Cerrolaza JA, Henaréjos PS, Guardiola-Castillo V, Peña FA, Alonso-Romero JL, Noguera-Velasco JA, Ruiz-Espejo F. Mutational analysis of RAD51C and RAD51D genes in hereditary breast and ovarian cancer families from Murcia (southeastern Spain). Eur J Med Genet. 2018 Jun;61(6):355-361. doi: 10.1016/j.ejmg.2018.01.015. Epub 2018 Feb 2. PubMed PMID: 29409816.
AÑO: 2018; IF: 2.022
Castillo-Guardiola V, Sarabia-Meseguer MD, Marín-Vera M, Sánchez-Bermúdez AI, Alonso-Romero JL, Noguera-Velasco JA, Ruiz-Espejo F. New insights into the performance of multigene panel testing: Two novel nonsense variants in BRIP1 and TP53 in a young woman with breast cancer. Cancer Genet. 2018 Dec;228-229:1-4. doi: 10.1016/j.cancergen.2018.06.002. Epub 2018 Jun 23. PubMed PMID: 30553462.
AÑO: 2018; IF: 2.183
Lozano-Rivas, N; Linares, LF; Marras-Fernandez-Cid, C; Garcia-Hernandez, AM; Alguero, MDC; Iniesta, F; Sanchez-Salinas, D; Lopez-Lucas, MD; Rodriguez-Valiente, M; Cabanas, V; Garcia-Bernal, D; Molina, MDM; Lopez, S; Ramirez-Tovar, F; Sara, JER; Garcia, B; Blanquer, M; Fernandez-Delgado, JAO; Espinosa, M; Zamarro, J; Becerra-Ratia, J; Peris, JL; Lopez-Exposito, I; Bafalliu, JA; Ruiz-Espejo, F; Domenech, E; Morales-Cano, MD; Arrabal, PM; Soler, G; Vera, A; Guzman-Aroca, F; Moraleda, JM; Sackstein, R. CLINICAL TRIAL OF INTRAVENOUS INFUSION OF FUCOSYLATED BONE MARROW MESENCHYMAL STEM CELLS IN PATIENTS WITH OSTEOPOROSIS. ANNALS OF THE RHEUMATIC DISEASES. 2018; 77:1625-1625. 10.1136/annrheumdis-2018-eular.4728
AÑO: 2018; IF: 14.299
García-Molina E, Sabater-Molina M, Muñoz C, Ruiz-Espejo F, Gimeno JR. An R1632C variant in the SCN5A gene causing Brugada syndrome. Mol Med Rep. 2016 Jun;13(6):4677-80. doi: 10.3892/mmr.2016.5100. Epub 2016 Apr 11. PubMed PMID: 27082542.
AÑO: 2016; IF: 1.692

Instituto de Investigación Sanitaria Acreditado

ISCII

Fondo Social Europeo "El FSE Invierte en tu futuro"

Fondo Social Europeo

Sello de Calidad Europeo "HR Excellence in Research"

HRS4R