| A proteome-scale map of the human interactome network T Rolland, M Taşan, B Charloteaux, SJ Pevzner, Q Zhong, N Sahni, S Yi, ... Cell 159 (5), 1212-1226, 2014 | 1505 | 2014 |
| Whole-genome sequencing in autism identifies hot spots for de novo germline mutation JJ Michaelson, Y Shi, M Gujral, H Zheng, D Malhotra, X Jin, M Jian, G Liu, ... Cell 151 (7), 1431-1442, 2012 | 683 | 2012 |
| Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia V Vacic, S McCarthy, D Malhotra, F Murray, HH Chou, A Peoples, ... Nature 471 (7339), 499-503, 2011 | 377 | 2011 |
| Paternally inherited cis-regulatory structural variants are associated with autism WM Brandler, D Antaki, M Gujral, ML Kleiber, J Whitney, MS Maile, ... Science 360 (6386), 327-331, 2018 | 222 | 2018 |
| Spatiotemporal 16p11. 2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases GN Lin, R Corominas, I Lemmens, X Yang, J Tavernier, DE Hill, M Vidal, ... Neuron 85 (4), 742-754, 2015 | 177 | 2015 |
| Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism R Corominas, X Yang, GN Lin, S Kang, Y Shen, L Ghamsari, M Broly, ... Nature communications 5 (1), 3650, 2014 | 170 | 2014 |
| Copy number variation at the 7q11. 23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion I Cuscó, R Corominas, M Bayés, R Flores, N Rivera-Brugués, ... Genome research 18 (5), 683-694, 2008 | 102 | 2008 |
| SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population O Carreno, R Corominas, J Fernández‐Morales, M Camina, MJ Sobrido, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159 …, 2012 | 88 | 2012 |
| bigSCale: an analytical framework for big-scale single-cell data G Iacono, E Mereu, A Guillaumet-Adkins, R Corominas, I Cuscó, ... Genome research 28 (6), 878-890, 2018 | 77 | 2018 |
| 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 | 77 | 2008 |
| De novo Mutations From Whole Exome Sequencing in Neurodevelopmental and Psychiatric Disorders: From Discovery to Application W Wang, R Corominas, GN Lin Frontiers in genetics 10, 258, 2019 | 65 | 2019 |
| Association study of the serotoninergic system in migraine in the Spanish population R Corominas, MJ Sobrido, M Ribases, E Cuenca‐León, P Blanco‐Arias, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153 …, 2010 | 62 | 2010 |
| Molecular genetics of cocaine use disorders in humans N Fernandez-Castillo, J Cabana-Dominguez, R Corominas, B Cormand Molecular psychiatry 27 (1), 624-639, 2022 | 54 | 2022 |
| 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 | 54 | 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 | 47 | 2013 |
| Evaluation of common variants in 16 genes involved in the regulation of neurotransmitter release in ADHD C Sánchez-Mora, B Cormand, JA Ramos-Quiroga, A Hervás, R Bosch, ... European Neuropsychopharmacology 23 (6), 426-435, 2013 | 47 | 2013 |
| Two-stage case-control association study of dopamine-related genes and migraine R Corominas, M Ribases, M Camiña, E Cuenca-León, J Pardo, S Boronat, ... BMC medical genetics 10, 1-9, 2009 | 42 | 2009 |
| 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 36 (06), 389-394, 2005 | 39 | 2005 |
| Lack of association of hormone receptor polymorphisms with migraine R Corominas, M Ribases, E Cuenca‐Leon, B Cormand, A Macaya European journal of neurology 16 (3), 413-415, 2009 | 36 | 2009 |
| 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 | 35 | 2009 |
