Cèlia Sintas

Genome-wide association analysis identifies susceptibility loci for migraine without aura

Tobias Freilinger, Verneri Anttila, Boukje de Vries et al. · Nature Genetics · 2012 · 339 citations · Full text

Genome-wide Association Study, Cluster Headache, Neurogenomics +5

Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

Katherine M. Siewert, Derek Klarin, Scott M. Damrauer et al. · International Journal of Epidemiology · 2020 · 82 citations · Full text

Genetic analysis for a shared biological basis between migraine and coronary artery disease

Bendik S. Winsvold, Christopher P. Nelson, Rainer Malik et al. · Neurology Genetics · 2015 · 73 citations · Full text

Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia

Cèlia Sintas, Oriel Carreño, Noèlia Fernàndez‐Castillo et al. · Scientific Reports · 2017 · 57 citations · Full text

A loss-of-function CACNA1A mutation causing benign paroxysmal torticollis of infancy

Marta Vila‐Pueyo, Gemma G. Gené, Marina Flotats-Bastardes et al. · European Journal of Paediatric Neurology · 2014 · 43 citations

Biology, Genetics, Loss-of-function Cacna1a Mutation