| Multicenter analysis of the SLC6A3/DAT1 VNTR haplotype in persistent ADHD suggests differential involvement of the gene in childhood and persistent ADHD B Franke, AA Vasquez, S Johansson, M Hoogman, J Romanos, ... Neuropsychopharmacology 35 (3), 656-664, 2010 | 231 | 2010 |
| Genetics of aggressive behavior: an overview K Veroude, Y Zhang‐James, N Fernàndez‐Castillo, MJ Bakker, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 …, 2016 | 181 | 2016 |
| Aggressive behavior in humans: Genes and pathways identified through association studies N Fernàndez‐Castillo, B Cormand American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 171 …, 2016 | 106 | 2016 |
| An integrated analysis of genes and functional pathways for aggression in human and rodent models Y Zhang-James, N Fernàndez-Castillo, JL Hess, K Malki, SJ Glatt, ... Molecular psychiatry 24 (11), 1655-1667, 2019 | 89 | 2019 |
| Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes E Cuenca-Leon, R Corominas, N Fernandez-Castillo, V Volpini, ... Cephalalgia 28 (10), 1039-1047, 2008 | 75 | 2008 |
| Genome-wide association meta-analysis of cocaine dependence: Shared genetics with comorbid conditions J Cabana-Domínguez, A Shivalikanjli, N Fernàndez-Castillo, B Cormand Progress in Neuro-Psychopharmacology and Biological Psychiatry 94, 109667, 2019 | 65 | 2019 |
| Association study between the DAT1, DBH and DRD2 genes and cocaine dependence in a Spanish sample N Fernandez-Castillo, M Ribases, C Roncero, M Casas, B Gonzalvo, ... Psychiatric genetics 20 (6), 317-320, 2010 | 55 | 2010 |
| RBFOX1, encoding a splicing regulator, is a candidate gene for aggressive behavior N Fernàndez-Castillo, G Gan, MMJ van Donkelaar, M Vaht, H Weber, ... European Neuropsychopharmacology 30, 44-55, 2020 | 54 | 2020 |
| 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 SA Serra, N Fernàndez-Castillo, A Macaya, B Cormand, MA Valverde, ... Pflügers Archiv-European Journal of Physiology 458, 489-502, 2009 | 50 | 2009 |
| Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability B Torrico, N Fernàndez-Castillo, A Hervás, M Milà, M Salgado, I Rueda, ... European Journal of Human Genetics 23 (12), 1694-1701, 2015 | 46 | 2015 |
| Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia C Sintas, O Carreño, N Fernàndez-Castillo, R Corominas, M Vila-Pueyo, ... Scientific reports 7 (1), 2514, 2017 | 44 | 2017 |
| Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies O Carreño, R Corominas, SA Serra, C Sintas, N Fernández‐Castillo, ... Molecular genetics & genomic medicine 1 (4), 206-222, 2013 | 42 | 2013 |
| ADGRL3 (LPHN3) variants predict substance use disorder M Arcos-Burgos, JI Vélez, AF Martinez, M Ribasés, JA Ramos-Quiroga, ... Translational psychiatry 9 (1), 42, 2019 | 41 | 2019 |
| Evaluation of single nucleotide polymorphisms in the miR-183–96–182 cluster in adulthood attention-deficit and hyperactivity disorder (ADHD) and substance use disorders (SUDs) C Sánchez-Mora, JA Ramos-Quiroga, I Garcia-Martínez, ... European Neuropsychopharmacology 23 (11), 1463-1473, 2013 | 40 | 2013 |
| Molecular genetics of cocaine use disorders in humans N Fernàndez-Castillo, J Cabana-Domínguez, R Corominas, B Cormand Molecular psychiatry 27 (1), 624-639, 2022 | 37 | 2022 |
| Association study of 37 genes related to serotonin and dopamine neurotransmission and neurotrophic factors in cocaine dependence N Fernàndez‐Castillo, C Roncero, L Grau‐Lopez, C Barral, G Prat, ... Genes, Brain and Behavior 12 (1), 39-46, 2013 | 36 | 2013 |
| Molybdenum cofactor deficiency presenting as neonatal hyperekplexia: a clinical, biochemical and genetic study A Macaya, L Brunso, N Fernandez-Castillo, JA Arranz, HB Ginjaar, ... Neuropediatrics, 389-394, 2005 | 36 | 2005 |
| Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene E Cuenca-León, I Banchs, SA Serra, P Latorre, N Fernàndez-Castillo, ... Journal of the neurological sciences 280 (1-2), 10-14, 2009 | 34 | 2009 |
| Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: A meta‐analysis in four European populations C Sánchez‐Mora, M Ribasés, M Casas, M Bayés, R Bosch, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 156 …, 2011 | 33 | 2011 |
| A mutation in the first intracellular loop of CACNA1A prevents P/Q channel modulation by SNARE proteins and lowers exocytosis SA Serra, E Cuenca-León, A Llobet, F Rubio-Moscardo, C Plata, ... Proceedings of the National Academy of Sciences 107 (4), 1672-1677, 2010 | 33 | 2010 |
