| Year |
Citation |
Score |
| 2023 |
Antón-Galindo E, Cabana-Domínguez J, Torrico B, Corominas R, Cormand B, Fernàndez-Castillo N. The pleiotropic contribution of genes in dopaminergic and serotonergic pathways to addiction and related behavioral traits. Frontiers in Psychiatry. 14: 1293663. PMID 37937232 DOI: 10.3389/fpsyt.2023.1293663 |
0.716 |
|
| 2022 |
Cabana-Domínguez J, Torrico B, Reif A, Fernàndez-Castillo N, Cormand B. Comprehensive exploration of the genetic contribution of the dopaminergic and serotonergic pathways to psychiatric disorders. Translational Psychiatry. 12: 11. PMID 35013130 DOI: 10.1038/s41398-021-01771-3 |
0.782 |
|
| 2021 |
Fernàndez-Castillo N, Cabana-Domínguez J, Kappel DB, Torrico B, Weber H, Lesch KP, Lao O, Reif A, Cormand B. Exploring the Contribution to ADHD of Genes Involved in Mendelian Disorders Presenting with Hyperactivity and/or Inattention. Genes. 13. PMID 35052433 DOI: 10.3390/genes13010093 |
0.776 |
|
| 2020 |
Torrico B, Antón-Galindo E, Fernàndez-Castillo N, Rojo-Francàs E, Ghorbani S, Pineda-Cirera L, Hervás A, Rueda I, Moreno E, Fullerton JM, Casadó V, Buitelaar JK, Rommelse N, Franke B, Reif A, et al. Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses. Journal of Clinical Medicine. 9. PMID 32545830 DOI: 10.3390/Jcm9061851 |
0.79 |
|
| 2020 |
Roth Mota N, Poelmans G, Klein M, Torrico B, Fernàndez-Castillo N, Cormand B, Reif A, Franke B, Arias Vásquez A. Cross-disorder genetic analyses implicate dopaminergic signaling as a biological link between Attention-Deficit/Hyperactivity Disorder and obesity measures. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 31896117 DOI: 10.1038/S41386-019-0592-4 |
0.721 |
|
| 2019 |
Torrico B, Shaw AD, Mosca R, Vivó-Luque N, Hervás A, Fernàndez-Castillo N, Aloy P, Bayés M, Fullerton JM, Cormand B, Toma C. Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes Journal of Psychiatry & Neuroscience : Jpn. 44: 1-10. PMID 31094488 DOI: 10.1503/Jpn.180184 |
0.785 |
|
| 2019 |
Torrico B, Cabana-Domínguez J, Shivalikanjli A, Fernàndez-Castillo N, Cormand B. S68EXPLORING DOPAMINERGIC AND SEROTONERGIC PATHWAYS IN PSYCHIATRIC DISORDERS European Neuropsychopharmacology. 29: S148-S149. DOI: 10.1016/J.Euroneuro.2019.08.069 |
0.723 |
|
| 2019 |
Fernàndez-Castillo N, Cabana J, Torrico B, Cormand B. EXPLORING THE CONTRIBUTION TO ADHD OF GENES INVOLVED IN MENDELIAN DISORDERS (OMIM) PRESENTING WITH HYPERACTIVITY AND/OR INATTENTION European Neuropsychopharmacology. 29: S52. DOI: 10.1016/J.Euroneuro.2019.07.105 |
0.76 |
|
| 2019 |
Mota NR, Poelmans G, Klein M, Torrico B, Fernàndez-Castillo N, Cormand B, Reif A, Franke B, Arias-Vásquez A. All Roads Lead To Dopamine: Exploring The Genetic Link Between Adhd, Obesity Measures And Brain Volumes European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2019.07.103 |
0.668 |
|
| 2019 |
Torrico B, Shaw A, Mosca R, Vivó-Luque N, Hervas A, Fernàndez-Castillo N, Aloy P, Bayés M, Fullerton J, Cormand B, Toma C. F21WHOLE EXOME SEQUENCING IDENTIFIES LRP1 AS NOVEL CANDIDATE GENE ACROSS PSYCHIATRIC DISORDERS European Neuropsychopharmacology. 29: S1120-S1121. DOI: 10.1016/J.Euroneuro.2018.08.101 |
0.785 |
|
| 2019 |
Mota NR, Klein M, Poelmans G, Fernàndez-Castillo N, Torrico B, Galesloot TE, Kiemeney LA, Cormand B, Arias-Vásquez A, Franke B. F2Elucidating The Genetic And Biological Factors Underlying The Relationship Between Adhd And Bmi Variation European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2018.08.082 |
0.674 |
|
| 2019 |
Mota NR, Klein M, Galesloot TE, Kiemeney LA, Fernàndez-Castillo N, Torrico B, Cormand B, Franke B, Arias-Vásquez A. Attention Deficit Hyperactivity Disorder and Obesity: The Weight of Shared Genetic Risk Factors European Neuropsychopharmacology. 29. DOI: 10.1016/J.Euroneuro.2017.06.108 |
0.706 |
|
| 2017 |
Cormand B, Torrico B, Ghorbani S, Fernàndez-Castillo N, Pineda L, Hervás A, Franke B, Buitelaar J, Freitag C, Reif A, Rueda I, Kleppe R, Haavik J, Toma C. Contribution of The 14-3-3 Gene Family To Autism Spectrum Disorder European Neuropsychopharmacology. 27: S374-S375. DOI: 10.1016/J.Euroneuro.2016.09.404 |
0.782 |
|
| 2016 |
Cabana-Domínguez J, Roncero C, Grau-López L, Rodríguez-Cintas L, Barral C, Abad AC, Erikson G, Wineinger NE, Torrico B, Arenas C, Casas M, Ribasés M, Cormand B, Fernàndez-Castillo N. A Highly Polymorphic Copy Number Variant in the NSF Gene is Associated with Cocaine Dependence. Scientific Reports. 6: 31033. PMID 27498889 DOI: 10.1038/Srep31033 |
0.686 |
|
| 2016 |
Torrico B, Chiocchetti AG, Bacchelli E, Trabetti E, Hervás A, Franke B, Buitelaar JK, Rommelse N, Yousaf A, Duketis E, Freitag CM, Caballero-Andaluz R, Martinez-Mir A, Scholl FG, Ribasés M, et al. Lack of replication of previous autism spectrum disorder GWAS hits in European populations. Autism Research : Official Journal of the International Society For Autism Research. PMID 27417655 DOI: 10.1002/Aur.1662 |
0.741 |
|
| 2015 |
Toma C, Torrico B, Hervás A, Salgado M, Rueda I, Valdés-Mas R, Buitelaar JK, Rommelse N, Franke B, Freitag C, Reif A, Pérez-Jurado LA, Battaglia A, Mazzone L, Bacchelli E, et al. Common and rare variants of microRNA genes in autism spectrum disorders. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 1-11. PMID 25903372 DOI: 10.3109/15622975.2015.1029518 |
0.761 |
|
| 2015 |
Torrico B, Fernàndez-Castillo N, Hervás A, Milà M, Salgado M, Rueda I, Buitelaar JK, Rommelse N, Oerlemans AM, Bralten J, Freitag CM, Reif A, Battaglia A, Mazzone L, Maestrini E, et al. Contribution of common and rare variants of the PTCHD1 gene to autism spectrum disorders and intellectual disability. European Journal of Human Genetics : Ejhg. PMID 25782667 DOI: 10.1038/Ejhg.2015.37 |
0.781 |
|
| 2014 |
Toma C, Torrico B, Hervás A, Valdés-Mas R, Tristán-Noguero A, Padillo V, Maristany M, Salgado M, Arenas C, Puente XS, Bayés M, Cormand B. Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations. Molecular Psychiatry. 19: 784-90. PMID 23999528 DOI: 10.1038/Mp.2013.106 |
0.777 |
|
| 2013 |
Toma C, Hervás A, Torrico B, Balmaña N, Salgado M, Maristany M, Vilella E, Martínez-Leal R, Planelles MI, Cuscó I, del Campo M, Pérez-Jurado LA, Caballero-Andaluz R, de Diego-Otero Y, Pérez-Costillas L, et al. Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2. Psychiatric Genetics. 23: 82-5. PMID 23277129 DOI: 10.1097/Ypg.0B013E32835D6Fc6 |
0.753 |
|
| 2011 |
Pérez-Dueñas B, Ormazábal A, Toma C, Torrico B, Cormand B, Serrano M, Sierra C, De Grandis E, Marfa MP, García-Cazorla A, Campistol J, Pascual JM, Artuch R. Cerebral folate deficiency syndromes in childhood: clinical, analytical, and etiologic aspects. Archives of Neurology. 68: 615-21. PMID 21555636 DOI: 10.1001/Archneurol.2011.80 |
0.742 |
|
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