V. Cantarín

Epigenetic profiling linked to multisystem inflammatory syndrome in children (MIS-C): A multicenter, retrospective study

M. Esteller, E. López-Granados, P. Soler-Palacín, 2022, eClinicalMedicine.

Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients

F. Ramos, O. Moldovan, M. Couce, 2019, Front. Neurosci..

Hashimoto encephalopathy as manifestation of central nervous system chronic graft‐versus‐host disease after hematopoietic stem cell transplantation

M. Díaz, C. Guerrero, B. Molina, 2019, Pediatric blood & cancer.

Clinical and genetic features of 13 Spanish patients with KCNQ2 mutations

J. García-Peñas, J. Armstrong, M. Couce, 2016, Journal of Human Genetics.