| Antiproliferative and Pro-Apoptotic Effect of Uvaol in Human Hepatocarcinoma HepG2 Cells by Affecting G0/G1 Cell Cycle Arrest, ROS Production and AKT/PI3K … GC Bonel-Pérez, A Pérez-Jiménez, I Gris-Cárdenas, AM Parra-Pérez, ... Molecules 25 (18), 4254, 2020 | 22 | 2020 |
| Defective α‐tectorin may involve tectorial membrane in familial Meniere disease P Roman‐Naranjo, AM Parra‐Perez, A Escalera‐Balsera, A Soto‐Varela, ... Clinical and Translational Medicine 12 (6), 2022 | 16 | 2022 |
| Involvement of the PI3K/AKT Intracellular Signaling Pathway in the AntiCancer Activity of Hydroxytyrosol, a Polyphenol from Olea europaea, in Hematological Cells and … AM Parra-Perez, A Pérez-Jiménez, I Gris-Cárdenas, GC Bonel-Pérez, ... International Journal of Molecular Sciences 23 (13), 7053, 2022 | 10 | 2022 |
| A systematic review on machine learning approaches in the diagnosis and prognosis of rare genetic diseases P Roman-Naranjo, AM Parra-Perez, JA Lopez-Escamez Journal of biomedical informatics, 104429, 2023 | 9 | 2023 |
| Types of inheritance and genes associated with familial Meniere disease AM Parra-Perez, JA Lopez-Escamez Journal of the Association for Research in Otolaryngology 24 (3), 269-279, 2023 | 8 | 2023 |
| 3DBionotes Covid JR Macias, R Sanchez-Garcia, P Conesa, E Ramirez-Aportela, ... Bioinformatics 37 (22), 4258-4260, 2021 | 4 | 2021 |
| A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss P Robles-Bolivar, D Bächinger, AM Parra-Perez, P Román-Naranjo, ... European Journal of Human Genetics 30 (11), 1301-1305, 2022 | 2 | 2022 |
| A rare haplotype of the GJD3 gene segregating in familial Meniere Disease interferes with connexin assembly A Escalera-Balsera, P Robles-Bolivar, AM Parra-Perez, S Murillo-Cuesta, ... medRxiv, 2024.01. 16.24300842, 2024 | 1 | 2024 |
| Rare Deletions or Large Duplications Contribute to Genetic Variation in Patients with Severe Tinnitus and Meniere Disease A Escalera-Balsera, AM Parra-Perez, A Gallego-Martinez, L Frejo, ... Genes 15 (1), 22, 2023 | 1 | 2023 |
| Ultrarare missense and frameshift variants in the TECTA gene may involve tectorial membrane in familial Meniere disease P Román-Naranjo, AM Parra-Perez, A Escalera-Balsera, A Soto-Varela, ... medRxiv, 2022.02. 18.22270926, 2022 | 1 | 2022 |
| An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population AM Parra-Perez, A Gallego-Martinez, JA Lopez-Escamez Human Genetics, 1-13, 2024 | | 2024 |
| Identification of ADAMTS18 and SDK1 genes in patients with Meniere Disease with endolymphatic sac hypoplasia P Robles, D Baechinger, A Escalera-Balsera, A Gallego-Martinez, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 376-377, 2024 | | 2024 |
| Involvement of GJD3 variants in familial Meniere disease and tectorial membrane attachment A Escalera-Balsera, A Gallego-Martinez, AM Parra-Perez, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 376-376, 2024 | | 2024 |
| A systematic review on machine learning approaches in the diagnosis of rare genetic diseases P Roman-Naranjo, AM Parra-Perez, JA Lopez-Escamez medRxiv, 2023.01. 30.23285203, 2023 | | 2023 |
| Rare missense variants and frameshift deletions in TECTA gene in familial Meniere disease AM Parra-Perez, P Román-Naranjo SATELLITE-07-SATURDAY, 0 | | |
Jose Antonio Lopez-Escamez MD, PhDUniversidad de Granada, University of Sydney, GENyO, ibs.GRANADADirección de correo verificada de go.ugr.es
