Oriel Carreño

SNP variants within the vanilloid<i>TRPV1</i>and<i>TRPV3</i>receptor genes are associated with migraine in the Spanish population

Oriel Carreño, Roser Corominas, Jessica Fernández‐Morales et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2011 · 80 citations · Full text

Life Sciences, Genetics, Neuroscience +16

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

Cèlia Sintas, Oriel Carreño, Noèlia Fernàndez‐Castillo et al. · Scientific Reports · 2017 · 60 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Screening of <scp><i>CACNA1A</i></scp> and <scp><i>ATP1A2</i></scp> genes in hemiplegic migraine: clinical, genetic, and functional studies

Oriel Carreño, Roser Corominas, Selma A. Serra et al. · Molecular Genetics & Genomic Medicine · 2013 · 46 citations · Full text

Life Sciences, Genetics, Neurology +16

A mutation in the first intracellular loop of CACNA1A prevents P/Q channel modulation by SNARE proteins and lowers exocytosis

Selma A. Serra, Ester Cuenca-León, Artur Llobet et al. · Proceedings of the National Academy of Sciences · 2010 · 30 citations · Full text

Life Sciences, Neurology, Neuroscience +17

Clinical and genetic analysis in alternating hemiplegia of childhood: Ten new patients from Southern Europe

Marta Vila‐Pueyo, Roser Pons, Miquel Raspall‐Chaure et al. · Journal of the Neurological Sciences · 2014 · 24 citations

Life Sciences, Genetics, Neurology +11