Roser Corominas
Affiliations: | 2005-2009 | Genetics, Microbiology and Statistics | University of Barcelona, Spain |
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"Roser Corominas"Parents
Sign in to add mentor| Bru Cormand | grad student | 2005-2009 | University of Barcelona, Spain |
| Bru Cormand | post-doc | 2018- | University of Barcelona, Spain |
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Publications
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| Antón-Galindo E, Cabana-Domínguez J, Torrico B, et al. (2023) The pleiotropic contribution of genes in dopaminergic and serotonergic pathways to addiction and related behavioral traits. Frontiers in Psychiatry. 14: 1293663 |
| Fernàndez-Castillo N, Cabana-Domínguez J, Corominas R, et al. (2021) Molecular genetics of cocaine use disorders in humans. Molecular Psychiatry |
| Wang W, Corominas R, Lin GN. (2019) Mutations From Whole Exome Sequencing in Neurodevelopmental and Psychiatric Disorders: From Discovery to Application. Frontiers in Genetics. 10: 258 |
| Brandler WM, Antaki D, Gujral M, et al. (2018) Paternally inherited cis-regulatory structural variants are associated with autism. Science (New York, N.Y.). 360: 327-331 |
| Lin GN, Corominas R, Nam HJ, et al. (2017) Comprehensive Analyses of Tissue-Specific Networks with Implications to Psychiatric Diseases. Methods in Molecular Biology (Clifton, N.J.). 1613: 371-402 |
| Sintas C, Carreño O, Fernàndez-Castillo N, et al. (2017) Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia. Scientific Reports. 7: 2514 |
| Lin GN, Corominas R, Lemmens I, et al. (2015) Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases. Neuron. 85: 742-54 |
| Corominas R, Yang X, Lin GN, et al. (2014) Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism. Nature Communications. 5: 3650 |
| Iakoucheva LM, Lin NG, Corominas R, et al. (2014) Poster #S138 SPATIO-TEMPORAL PROTEIN INTERACTION NETWORK DYNAMICS OF 16P11.2 GENES Schizophrenia Research. 153: S138 |
| Carreño O, Corominas R, Serra SA, et al. (2013) Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies. Molecular Genetics & Genomic Medicine. 1: 206-22 |