E. Martín

The genetic architecture of Parkinson disease in Spain: characterizing population-specific risk, differential haplotype structures, and providing etiologic insight

Sonja W. Scholz, D. Hernandez, M. Nalls, 2019, bioRxiv.

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. Neurology.

Idiopathic delayed-onset oedema associated with deep brain stimulation

E. Martín, A. Ayala, P. García, 2020, Neurología (English Edition).

Familial clustering and genetic heterogeneity in Meniere's disease

T. Requena, J. Lopez-Escamez, E. Martín, 2014, Clinical genetics.