José María Millán (J M Millan, José M Millán, Jose M Millan, Jose M Millán)

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 16

Top Topics

Bioinformatics Analysis

Top Venues

International journal of molecular sciences

Journal of clinical medicine

Antioxidants (Basel, Switzerland)

This page only lists publications with an associated author ORCID identifier.

Publications

Raquel Baviera-Muñoz, Lidón Carretero-Vilarroig, Nuria Muelas, Rafael Sivera, Pablo Sopena-Novales, Begoña Martínez-Sanchis, Isabel Sastre-Bataller, Marina Campins-Romeu, Irene Martínez-Torres, Jose Manuel García-Verdugo, José María Millán, Teresa Jaijo, Elena Aller, Luis Bataller
Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain. Movement disorders clinical practice 10 (6) (2023)
Elisa González-Romero, Cristina Martínez-Valiente, Gema García-García, Antonio Rosal-Vela, José María Millán, Miguel Angel Sanz, Guillermo F Sanz, Alessandro Liquori, José Vicente Cervera, Rafael Pascual Vázquez-Manrique
PCR-Based Strategy for Introducing CRISPR/Cas9 Machinery into Hematopoietic Cell Lines. Cancers 15 (17) (2023)
Ana Pilar Gómez-Escribano, Carlos Mora-Martinez, Marta Isabel Roca-Marugán, Denise S Walker, Joaquín Panadero, Maria D Sequedo, Ratni Saini, Hans-Joachim Knölker, Jose Blanca, Juan Burguera, Agustin Lahoz, Joaquin Cañizares, José María Millán, Nick O Burton, William R Schafer, Rafael Pascual Vázquez-Manrique
Changes in lipid metabolism driven by steroid signalling modulate proteostasis in C. elegans. EMBO reports (2023)
María Del Carmen Ortuño-Costela, Victoria Cerrada, Ana Moreno-Izquierdo, Inés García-Consuegra, Camille Laberthonnière, Mégane Delourme, Rafael Garesse, Joaquín Arenas, Carla Fuster-García, Gema García-García, José María Millán, Frédérique Magdinier, María Esther Gallardo
Generation of the First Human In Vitro Model for McArdle Disease Based on iPSC Technology. International journal of molecular sciences 23 (22) (2022)
Laura Blasco-Pérez, Mar Costa-Roger, Jordi Leno-Colorado, Sara Bernal, Laura Alias, Marta Codina Solà, Desirée Martínez-Cruz, Claudia Castiglioni, Enrico Bertini, Lorena Travaglini, José María Millán, Elena Aller, Javier Sotoca, Raúl Juntas, Christina Engel Hoei-Hansen, Antonio Moreno-Escribano, Encarna Guillén-Navarro, Laura Costa-Comellas, Francina Munell, Susana Boronat, Ricardo Rojas-García, Mónica Povedano, Ivon Cusco, Eduardo F Tizzano
Deep Molecular Characterization of Milder Spinal Muscular Atrophy Patients Carrying the c.859G>C Variant in SMN2 . International journal of molecular sciences 23 (15) (2022)
Juan Luque, Ingrid Mendes, Beatriz Gómez, Beatriz Morte, Miguel López de Heredia, Enrique Herreras, Virginia Corrochano, Juan Bueren, Pía Gallano, Rafael Artuch, Cristina Fillat, Luis A Pérez-Jurado, Lluis Montoliu, Ángel Carracedo, José María Millán, Susan M Webb, Francesc Palau, null null, Pablo Lapunzina
CIBERER: Spanish national network for research on rare diseases: A highly productive collaborative initiative. Clinical genetics 101 (5-6) (2022)
José María Millán, Gema García-García
Genetic Testing for Rare Diseases. Diagnostics (Basel, Switzerland) 12 (4) (2022)
Jorge Raga-Cervera, Jose M Bolarin, José María Millán, José Javier García-Medina, Laia Pedrola, Javier Abellán-Abenza, Mar Valero-Vello, Silvia M Sanz-González, José E O'Connor, David Galarreta-Mira, Elena Bendala-Tufanisco, Aloma Mayordomo-Febrer, Maria D Pinazo-Durán, Vicente C Zanón-Moreno
miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks. Journal of clinical medicine 10 (11) (2021)
Lilián Galbis-Martínez, Fiona Blanco-Kelly, Gema García-García, Almudena Ávila-Fernández, Teresa Jaijo, Carla Fuster-García, Irene Perea-Romero, Olga Zurita-Muñoz, Belén Jimenez-Rolando, Ester Carreño, Blanca García-Sandoval, José María Millán, Carmen Ayuso
Genotype-phenotype correlation in patients with Usher syndrome and pathogenic variants in MYO7A: implications for future clinical trials. Acta ophthalmologica 99 (8) (2021)
Brais Bea-Mascato, Carlos Solarat, Irene Perea-Romero, Teresa Jaijo, Fiona Blanco-Kelly, José María Millán, Carmen Ayuso, Diana Valverde
Prevalent ALMS1 Pathogenic Variants in Spanish Alström Patients. Genes 12 (2) (2021)
M Stemerdink, B García-Bohórquez, R Schellens, G Garcia-Garcia, E Van Wijk, José María Millán
Genetics, pathogenesis and therapeutic developments for Usher syndrome type 2. Human genetics (2021)
Carla Fuster-García, Belén García-Bohórquez, Ana Rodríguez-Muñoz, Elena Aller, Teresa Jaijo, José María Millán, Gema García-García
Usher Syndrome: Genetics of a Human Ciliopathy. International journal of molecular sciences 22 (13) (2021)
Carla Fuster-García, Belén García-Bohórquez, Ana Rodríguez-Muñoz, José María Millán, Gema García-García
Application of CRISPR Tools for Variant Interpretation and Disease Modeling in Inherited Retinal Dystrophies. Genes 11 (5) (2020)
Gema García-García, Alba Berzal-Serrano, Piedad García-Díaz, Rebeca Villanova-Aparisi, Sara Juárez-Rodríguez, Carlos de Paula-Vernetta, Laura Cavallé-Garrido, Teresa Jaijo, Miguel Armengot-Carceller, José María Millán, Elena Aller
Improving the Management of Patients with Hearing Loss by the Implementation of an NGS Panel in Clinical Practice. Genes 11 (12) (2020)
José Bono-Yagüe, Ana Pilar Gómez-Escribano, José María Millán, Rafael Pascual Vázquez-Manrique
Reactive Species in Huntington Disease: Are They Really the Radicals You Want to Catch? Antioxidants (Basel, Switzerland) 9 (7) (2020)
Fred Schwaller, Valérie Bégay, Gema García-García, Francisco J Taberner, Rabih Moshourab, Brennan McDonald, Trevor Docter, Johannes Kühnemund, Julia Ojeda-Alonso, Ricardo Paricio-Montesinos, Stefan G Lechner, James F A Poulet, José María Millán, Gary R Lewin
USH2A is a Meissner's corpuscle protein necessary for normal vibration sensing in mice and humans. Nature neuroscience 24 (1) (2020)