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Mónica Roldan Molina

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Publications

  • Rey-Barroso L, Roldan-Molina M, Frías M, Burgos-Fernández FJ, Isola I, Ruiz-Llobet A, Sarrate E and Vilaseca M.

    Optimized protocol for intracellular labeling of red blood cells with anti-hemoglobin F for confocal microscopy analysis

    MICRON . 199: 103913-103913.

    [doi:10.1016/j.micron.2025.103913]

  • Amato ME, Frías M, Cerisola A, Roldan-Molina M and Ortigoza-Escobar JD.

    Novel CYFIP2 Frameshift Variant Linked to Dyskinetic Crises: Functional Studies Show Impaired Cell Motility

    CLINICAL GENETICS . 108(6): 708-712.

    [doi:10.1111/cge.14774]

  • López-Marquez A, Badosa-Gallego MC, Enjuanes-Ruiz L, Hernández-Carabias P, Sánchez-Martín M, Cadot B, Guesmia Z, Georvasilis I, Balsells S, Blanco-Ramos M, Puighermanal E, Quintana A, Roldan-Molina M, Allamand V and Jimenez-Mallebrera C.

    Generation and characterization of Col6a1 knock-in mice: A promising pre-clinical model for collagen VI-Related dystrophies.

    DISEASE MODELS & MECHANISMS . : .

    [doi:10.1242/dmm.052460]

  • Pascual-Rodriguez A, Moulka, T, de Fàbregues, O, Repossi, R, García-Ruiz, PJ, Ortolano, S, De Lucca, M, Vela-Desojo, L, Alves-Villar, M, Frías, M, Feliz-Feliz, C, Roldan-Molina M, Olival, J, Fernandez-Isern G, Palau F, Pijuan-Marquilles J and Hoenicka J.

    Lysosomal Network Defects in Early-Onset Parkinson's Disease Patients Carrying Rare Variants in Lysosomal Hydrolytic Enzyme Genes

    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 26(19): .

    [doi:10.3390/ijms26199454]

  • Nolasco-Tovar GA, Roldan-Molina M, Jamshidi Y, Georvasilis I, Rodríguez RJ, Boostani R, Shoeibi A, Armengol L, Codina-Bergadà A, Karimiani EG, Hernando-Davalillo C, Martorell-Sampol L, Ramírez Almaraz ML, Muchart-Lopez J, Ortez-Gonzalez CI, Nascimento-Osorio A, Urreizti R, Natera-de Benito D and Serrano M.

    Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

    Annals of Clinical and Translational Neurology . : .

    [doi:10.1002/acn3.70206]

  • Frías M, Badosa-Gallego MC, Jimenez-Mallebrera C, Porta JM and Roldan-Molina M.

    The artificial intelligence challenge in rare disease diagnosis: A case study on collagen VI muscular dystrophy.

    Computers in biology and medicine . 196(Pt A): 110610-110610. Number of citations: 1

    [doi:10.1016/j.compbiomed.2025.110610]

  • CastilloSD, Perosanz X, Ressler AK, Ivars M, Rodriguez J, Rovira-Zurriaga C, Nola EM, Llena J, Grego-Bessa J, Roldan-Molina M, Arnau R, Martínez-Romero A, Barber-Martínez de la Torre I, Miguel Bejarano Serrano, Vicente-Villa MA, Celis-Passini V, Salvador-Hernandez H, Mora J, Marchuk DA, Baselga E and Graupera M.

    Somatic Uniparental Disomy of PTEN in Endothelial Cells Causes Vascular Malformations in Patients with PTEN Hamartoma Tumor Syndrome

    Cancer Discovery . 15(7): 1350-1362. Number of citations: 5

    [doi:10.1158/2159-8290.CD-24-0807]

  • Palau F, Cantarero-Abad L, Roldan-Molina M, Rodríguez-Sanz M, Mathison A, Díaz-Osorio Y, Pijuan-Marquilles J, Frías M, Urrutia R and Hoenicka J.

    Abnormal Redox Balance at Membrane Contact Sites Causes Axonopathy in Gdap1-related Charcot-marie-tooth Disease.

    research square . : .

    [doi:10.21203/rs.3.rs-5682984/v1]

  • Mora J, Climent A, Roldan-Molina M, Flores MC, Varo A, Pérez-Jaume S, Jou-Munoz C, Celma MS, Lazaro JJ, Cheung I, Castañeda-Heredia A, Gorostegui M, Rodriguez E, Chamorro S, Muñoz JP and Cheung NK.

    Desensitizing the autonomic nervous system to mitigate anti-GD2 monoclonal antibody side effects

    Frontiers in oncology . 14: 1380917-1380917.

    [doi:10.3389/fonc.2024.1380917]

  • Badosa-Gallego MC, Roldan-Molina M, Fernández-Irigoyen J, Santamaria E and Jimenez-Mallebrera C.

    Proteomic and functional characterisation of extracellular vesicles from collagen VI deficient human fibroblasts reveals a role in cell motility

    SCIENTIFIC REPORTS . 13(1): 14622-14622. Number of citations: 5

    [doi:10.1038/s41598-023-41632-1]