Publications
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                        Mollá B, Riveiro F, Bolinches-Amorós A, Muñoz-Lasso DC, Palau F and González-Cabo P. Two different pathogenic mechanisms, dying-back axonal neuropathy and pancreatic senescence, are present in the YG8R mouse model of Friedreich's ataxiaDISEASE MODELS & MECHANISMS . 9(6): 647-657. Number of citations: 24 
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                        Yubero-Siles D, Brandi-Tarrau N, Ormazabal-Herrero A, Garcia-Cazorla A, Pérez-Dueñas B, Campistol-Plana J, Ribes A, Palau F, Artuch-Iriberri R, Armstrong-Moron J and Working Group. Targeted Next Generation Sequencing in Patients with Inborn Errors of MetabolismPLoS One . 11(5): . Number of citations: 44 
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                        Ponce G, Quiñones-Lombraña A, Martín-Palanco NG, Rubio-Solsona E, Jiménez-Arriero MÁ, Palomo T and Hoenicka J. The Addiction-Related Gene Ankk1 is Oppositely Regulated by D1R-and D2R-Like Dopamine ReceptorsNEUROTOXICITY RESEARCH . 29(3): 345-350. Number of citations: 16 
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                        Sáez MA, Fernández-Rodríguez J, Moutinho C, Sanchez-Mut JV, Gomez A, Vidal E, Petazzi P, Szczesna K, Lopez-Serra P, Lucariello M, Lorden P, Delgado-Morales R, de la Caridad OJ, Huertas D, Gelpí JL, Orozco M, López-Doriga A, Milà M, Perez-Jurado LA, Pineda M, Armstrong-Moron J, Lázaro C and Esteller M. Mutations in JMJD1C are involved in Rett syndrome and intellectual disabilityGENETICS IN MEDICINE . 18(4): 378-385. Number of citations: 41 
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                        Sevilla T, Lupo V, Martínez-Rubio D, Sancho P, Sivera R, Chumillas MJ, García-Romero M, Pascual-Pascual SI, Muelas N, Dopazo J, Vílchez JJ, Palau F and Espinós C. Mutations in the MORC2 gene cause axonal Charcot-Marie-Tooth diseaseBRAIN . 139: 62-72. Number of citations: 95 
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                        Prieto J, León M, Ponsoda X, García-García F, Bort R, Serna E, Barneo-Muñoz M, Palau F, Dopazo J, López-García C and Torres J. Dysfunctional mitochondrial fission impairs cell reprogrammingCell Cycle . 15(23): 3240-3250. Number of citations: 38 
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                        Cassis L, Cortés-Saladelafont E, Molero M, Yubero-Siles D, González MJ, Ormazabal-Herrero A, Fons-Estupina C, Jou-Munoz C, Sierra-March C, Castejón Ponce E, Ramos F, Armstrong-Moron J, O'Callaghan-Gordo M, Casado-Rio M, Montero-Sanchez R, Meavilla-Olivas SM, Artuch-Iriberri R, Baric I, Bartoloni F, Bellettato CM, Bonifazi F, Ceci A, Cvitanovic-Šojat L, Dali CI, D'Avanzo F, Fumic K, Giannuzzi V, Lampe C, Scarpa M and Garcia-Cazorla A. Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disordersORPHANET JOURNAL OF RARE DISEASES . 10: 164-164. Number of citations: 19 
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                        Cortés-Saladelafont E, Molero M, Ormazabal-Herrero A, Tristan-Noguero A, Sierra-March C, Armstrong-Moron J, Artuch-Iriberri R and Garcia-Cazorla A. Diagnosis of Biogenic Amines Synthesis DefectsJournal of Pediatric Neurology . 13(4): 186-197. Number of citations: 2 
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                        Koeneke A, Ponce G, Hoenicka J and Huertas E. The ANKK1/DRD2 locus is a genomic substrate for affective priming and recognition of angry facesBRAIN AND BEHAVIOR . 5(11): . Number of citations: 2 
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                        Fernandes TG, Duarte ST, Ghazvini M, Gaspar C, Santos DC, Porteira AR, Rodrigues GM, Haupt S, Rombo DM, Armstrong-Moron J, Sebastião AM, Gribnau J, Garcia-Cazorla A, Brüstle O, Henrique D, Cabral JM and Diogo MM. Neural commitment of human pluripotent stem cells under defined conditions recapitulates neural development and generates patient-specific neural cellsBIOTECHNOLOGY JOURNAL . 10(10): 1578-1588. Number of citations: 28 
