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European Journal of Clinical Investigation|March 10, 2017
Delta-amino-levulinic acid dehydratase gene and essential tremorJosé A G Agúndez, Elena García-Martín, Hortensia Alonso-Navarro, et al.
Frontiers in Neuroscience|April 26, 2018
Pleiotropic Effects of Variants in Dementia Genes in Parkinson DiseaseLaura Ibanez, Umber Dube, Albert A Davis, et al.
Acta Neurochirurgica|March 22, 2021
Volumetric growth rate of incidental asymptomatic meningiomas: a single-center prospective cohort studyPedro David Delgado-López, Antonio Montalvo-Afonso, Javier Martín-Alonso, et al.
Pharmacogenetics and Genomics|August 17, 2013
No association of the SLC1A2 rs3794087 allele with risk for essential tremor in the Spanish populationElena García-Martín, Carmen Martínez, Hortensia Alonso-Navarro, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 29, 2014
No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish populationLaura Fachal, Ana Mosquera-Miguel, Pau Pastor, et al.
Medicine|June 20, 2015
Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential TremorPedro Ayuso, José A G Agúndez, Hortensia Alonso-Navarro, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 17, 2015
Automated neuromelanin imaging as a diagnostic biomarker for Parkinson's diseaseGabriel Castellanos, María A Fernández-Seara, Oswaldo Lorenzo-Betancor, et al.
Neurobiology of Aging|June 12, 2018
Pooled-DNA target sequencing of Parkinson genes reveals novel phenotypic associations in Spanish populationMonica Diez-Fairen, Bruno A Benitez, Sara Ortega-Cubero, et al.
Neurobiology of Aging|February 6, 2018
Target-enriched sequencing of chromosome 17q21.31 in sporadic tauopathies reveals no candidate variantsCristina Razquin, Sara Ortega-Cubero, Estefania Rojo-Bustamante, et al.
Neurology|November 2, 2018
Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48)David Genis, Sara Ortega-Cubero, Hector San Nicolás, et al.
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