Noèlia Fernàndez‐Castillo

Author

Also Known As

C Matera, Fernàndez Castillo, Noèlia, N Fernàndez-Castillo, N Fernández-Castillo, N. Fernandez-Castillo, N. Fernàndez-Castillo, N. Fernàndez‐Castillo, N. Fernández-Castillo, Noelia Fernàndez-Castillo, Noelia Fernàndez‐Castillo

115

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Universitat de Barcelona Institut de Biomedicina de la Universitat de Barcelona Centre for Biomedical Network Research on Rare Diseases Centro de Investigación Biomédica en Red Instituto de Salud Carlos III

About

Noèlia Fernàndez‐Castillo is an author at Universitat de Barcelona specializing in medicine, neuroscience, and social sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	344
2	Social Sciences	6	6	157
3	Health Sciences	1	1	43
4	Natural Sciences	1	1	26
5	Behavioral Sciences	1	1	17

Noèlia Fernàndez‐Castillo

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
An integrated analysis of genes and functional pathways for aggression in human and rodent models Yanli Zhang‐James, Noèlia Fernàndez‐Castillo, Jonathan Hess, Molecular Psychiatry	2018	97
Genetic Analysis of 27 Spanish Patients with Hemiplegic Migraine, Basilar-Type Migraine and Childhood Periodic Syndromes Ester Cuenca-León, Roser Corominas, Noèlia Fernàndez‐Castillo, Cephalalgia	2008	65
Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia Cèlia Sintas, Oriel Carreño, Noèlia Fernàndez‐Castillo, Scientific Reports	2017	57
Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits Aet O’Leary, Noèlia Fernàndez‐Castillo, Gabriela Gan, Molecular Psychiatry	2022	56
The hemiplegic migraine-associated Y1245C mutation in CACNA1A results in a gain of channel function due to its effect on the voltage sensor and G-protein-mediated inhibition Selma A. Serra, Noèlia Fernàndez‐Castillo, Alfons Macaya, Pflügers Archiv - European Journal of Physiology Channel FunctionMolecular NeuroscienceVoltage SensorNeurophysiologyPhysiology	2009	45
Association study between the DAT1, DBH and DRD2 genes and cocaine dependence in a Spanish sample Noèlia Fernàndez‐Castillo, Marta Ribasès, Carlos Roncero, Psychiatric Genetics Substance UseGeneticsGenetic EpidemiologyHuman PolymorphismDopaminergic Genes	2010	43
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, Molecular Genetics & Genomic Medicine	2013	43
ADGRL3 (LPHN3) variants predict substance use disorder Mauricio Arcos‐Burgos, Jorge I. Vélez, Ariel F. Martinez, Translational Psychiatry	2019	43
Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability Bàrbara Torrico, Noèlia Fernàndez‐Castillo, Amaia Hervás, European Journal of Human Genetics Neurodevelopmental DisordersRare VariantsSyndromic AutismGenetic DisorderGenetics	2015	42
Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene Ester Cuenca-León, Isabel Banchs, Selma A. Serra, Journal of the Neurological Sciences Novel Loss-of-function MutationCacna1a GeneMendelian DisorderGenetic DisorderGenetics	2009	41

Page 1