Héctor San Nicolás

Heterozygous <i>STUB1</i> mutation causes familial ataxia with cognitive affective syndrome (SCA48)

Sara Ortega‐Cubero, Héctor San Nicolás, Jordi Corral et al. · Neurology · 2018 · 101 citations

The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2.

Isabelle Henry, Georges Uzan, Dominique Weil et al. · PubMed · 1984 · 63 citations

New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32

Carmen Serrano, Marc Corral‐Juan, Giovanni Stévanin et al. · JAMA Neurology · 2013 · 45 citations

Genotype of an individual single nucleotide polymorphism regulates DNA methylation at the<i>TRPC3</i>alternative promoter

Álex Martín-Trujillo, Isabel Iglesias‐Platas, Eliécer Coto et al. · Epigenetics · 2011 · 20 citations · Full text

Transcriptional Regulation, Systems Biology, Ataxia Patients +15

Giant SCA8 alleles in nine children whose mother has two moderately large ones

Jordi Corral, Isabel Banchs, Héctor San Nicolás et al. · Annals of Neurology · 2005 · 15 citations