Ana Victoria Marco Hernández (Ana Victoria Marco-Hernández)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 5

Top Topics

Molecular Docking

Intellectual Disability

Dna Methylation

Top Venues

Journal of inherited metabolic disease

American journal of medical genetics. Part A

International journal of molecular sciences

Clinical genetics

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

Publications

María Alcázar Fabra, Abraham J Paredes-Fuentes, Manuel Torralba Carnerero, Daniel José Moreno Fernández-Ayala, Antonio Arroyo Luque, Ana Sánchez-Cuesta, Carmine Staiano, Paula Sánchez-Pintos, Maria-Luz Couce, Miguel Tomás Vila, Ana Victoria Marco Hernández, Carmen Orellana, Francisco Martínez, Mónica Roselló, Alfonso Caro, Juan Silvestre Oltra Soler, Sandra Monfort, Alejandro Sánchez, Dolores Rausell, Isidro Vitoria, Mireia Del Toro, Ángeles García-Cazorla, Natalia A Julia-Palacios, Cristina Jou, Delia Yubero, Luis Carlos López, Juan Diego Hernández Camacho, Guillermo Lopez-Lluch, Manuel Ballesteros Simarro, Juan Carlos Rodríguez-Aguilera, Gloria Brea Calvo, María Victoria Cascajo Almenara, Rafael Artuch, Carlos Santos-Ocaña
New variants expand the neurological phenotype of COQ7 deficiency. Journal of inherited metabolic disease (2024)
Dolores Martínez-Rubio, Isabel Hinarejos, Herminia Argente-Escrig, Clara Marco-Marin, María Ana Lozano, Nerea Gorría-Redondo, Vincenzo Lupo, Itxaso Martí-Carrera, Concepción Miranda, María Vázquez-López, Asunción García-Pérez, Ana Victoria Marco Hernández, Miguel Tomás-Vila, Sergio Aguilera-Albesa, Carmen Espinós
Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy. International journal of molecular sciences 24 (22) (2023)
Ana Victoria Marco Hernández, Alfonso Caro-Llopis, Pilar Rubio Sánchez, Juan Carlos Martínez Martínez, Miguel Tomás Vila, Sandra Monfort, Francisco Martínez
Extending the Phenotype Related to SCN1A Gene: Arthrogryposis, Movement Disorders, and Malformations of Cortical Development. Journal of child neurology 37 (5) (2022)
Ana Victoria Marco Hernández, Alfonso Caro, Alejandro Montoya Filardi, Miguel Tomás Vila, Sandra Monfort, Beatriz Beseler Soto, Juan José Nieto-Barceló, Francisco Martinez Castellano
Extending the clinical phenotype of SPTAN1: From DEE5 to migraine, epilepsy, and subependymal heterotopias without intellectual disability. American journal of medical genetics. Part A (2021)
Ana Victoria Marco Hernández, Miguel Tomás-Vila, Alejandro Montoya-Filardi, Honorio Barranco-González, Juan Jesus Vilchez Padilla, Inmaculada Azorín, Patricia Smeyers Dura, Sandra Monfort-Membrado, Inmaculada Pitarch Castellano, Francisco Martínez-Castellano
Mitochondrial developmental encephalopathy with bilateral optic neuropathy related to homozygous variants in IMMT gene. Clinical genetics (2021)