Roser Corominas - Publications

2005-2009 Genetics, Microbiology and Statistics University of Barcelona, Spain 

26 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Chau KK, Zhang P, Urresti J, Amar M, Pramod AB, Chen J, Thomas A, Corominas R, Lin GN, Iakoucheva LM. Full-length isoform transcriptome of the developing human brain provides further insights into autism. Cell Reports. 36: 109631. PMID 34469739 DOI: 10.1016/j.celrep.2021.109631  0.306
2021 Fernàndez-Castillo N, Cabana-Domínguez J, Corominas R, Cormand B. Molecular genetics of cocaine use disorders in humans. Molecular Psychiatry. PMID 34453125 DOI: 10.1038/s41380-021-01256-1  0.662
2019 Wang W, Corominas R, Lin GN. Mutations From Whole Exome Sequencing in Neurodevelopmental and Psychiatric Disorders: From Discovery to Application. Frontiers in Genetics. 10: 258. PMID 31001316 DOI: 10.3389/Fgene.2019.00258  0.424
2018 Brandler WM, Antaki D, Gujral M, Kleiber ML, Whitney J, Maile MS, Hong O, Chapman TR, Tan S, Tandon P, Pang T, Tang SC, Vaux KK, Yang Y, Harrington E, ... ... Corominas R, et al. Paternally inherited cis-regulatory structural variants are associated with autism. Science (New York, N.Y.). 360: 327-331. PMID 29674594 DOI: 10.1126/Science.Aan2261  0.732
2017 Lin GN, Corominas R, Nam HJ, Urresti J, Iakoucheva LM. Comprehensive Analyses of Tissue-Specific Networks with Implications to Psychiatric Diseases. Methods in Molecular Biology (Clifton, N.J.). 1613: 371-402. PMID 28849569 DOI: 10.1007/978-1-4939-7027-8_15  0.321
2017 Sintas C, Carreño O, Fernàndez-Castillo N, Corominas R, Vila-Pueyo M, Toma C, Cuenca-León E, Barroeta I, Roig C, Volpini V, Macaya A, Cormand B. Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia. Scientific Reports. 7: 2514. PMID 28566750 DOI: 10.1038/S41598-017-02554-X  0.697
2015 Lin GN, Corominas R, Lemmens I, Yang X, Tavernier J, Hill DE, Vidal M, Sebat J, Iakoucheva LM. Spatiotemporal 16p11.2 protein network implicates cortical late mid-fetal brain development and KCTD13-Cul3-RhoA pathway in psychiatric diseases. Neuron. 85: 742-54. PMID 25695269 DOI: 10.1016/J.Neuron.2015.01.010  0.404
2014 Corominas R, Yang X, Lin GN, Kang S, Shen Y, Ghamsari L, Broly M, Rodriguez M, Tam S, Trigg SA, Fan C, Yi S, Tasan M, Lemmens I, Kuang X, et al. Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism. Nature Communications. 5: 3650. PMID 24722188 DOI: 10.1038/Ncomms4650  0.341
2014 Iakoucheva LM, Lin NG, Corominas R, Yang X, Hao T, Hill D, Vidal M. Poster #S138 SPATIO-TEMPORAL PROTEIN INTERACTION NETWORK DYNAMICS OF 16P11.2 GENES Schizophrenia Research. 153: S138. DOI: 10.1016/S0920-9964(14)70417-7  0.318
2013 Carreño O, Corominas R, Serra SA, Sintas C, Fernández-Castillo N, Vila-Pueyo M, Toma C, Gené GG, Pons R, Llaneza M, Sobrido MJ, Grinberg D, Valverde MÁ, Fernández-Fernández JM, Macaya A, et al. Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies. Molecular Genetics & Genomic Medicine. 1: 206-22. PMID 24498617 DOI: 10.1186/1129-2377-14-S1-P26  0.688
2013 Sánchez-Mora C, Cormand B, Ramos-Quiroga JA, Hervás A, Bosch R, Palomar G, Nogueira M, Gómez-Barros N, Richarte V, Corrales M, Garcia-Martinez I, Corominas R, Guijarro S, Bigorra A, Bayés M, et al. Evaluation of common variants in 16 genes involved in the regulation of neurotransmitter release in ADHD. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. 23: 426-35. PMID 22939005 DOI: 10.1016/J.Euroneuro.2012.07.014  0.692
2012 Michaelson JJ, Shi Y, Gujral M, Zheng H, Malhotra D, Jin X, Jian M, Liu G, Greer D, Bhandari A, Wu W, Corominas R, Peoples A, Koren A, Gore A, et al. Whole-genome sequencing in autism identifies hot spots for de novo germline mutation. Cell. 151: 1431-42. PMID 23260136 DOI: 10.1016/J.Cell.2012.11.019  0.497
2012 Carreño O, Corominas R, Fernández-Morales J, Camiña M, Sobrido MJ, Fernández-Fernández JM, Pozo-Rosich P, Cormand B, Macaya A. SNP variants within the vanilloid TRPV1 and TRPV3 receptor genes are associated with migraine in the Spanish population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 94-103. PMID 22162417 DOI: 10.1002/Ajmg.B.32007  0.743
2012 Fernàndez-Castillo N, Cormand B, Roncero C, Sánchez-Mora C, Grau-Lopez L, Gonzalvo B, Miquel L, Corominas R, Ramos-Quiroga JA, Casas M, Ribasés M. Candidate pathway association study in cocaine dependence: the control of neurotransmitter release. The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry. 13: 126-34. PMID 21426264 DOI: 10.3109/15622975.2010.551406  0.685
2011 Vacic V, McCarthy S, Malhotra D, Murray F, Chou HH, Peoples A, Makarov V, Yoon S, Bhandari A, Corominas R, Iakoucheva LM, Krastoshevsky O, Krause V, Larach-Walters V, Welsh DK, et al. Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia. Nature. 471: 499-503. PMID 21346763 DOI: 10.1038/Nature09884  0.368
2011 Vacic V, McCarthy S, Malhotra D, Murray F, Chou HH, Peoples A, Makarov V, Yoon S, Bhandari A, Corominas R, Iakoucheva LM, Krastoshevsky O, Krause V, Larach-Walters V, Welsh DK, et al. Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia (Nature (2011) 471 (499-501)) Nature. 474: 114. DOI: 10.1038/Nature10088  0.321
2010 Serra SA, Cuenca-León E, Llobet A, Rubio-Moscardo F, Plata C, Carreño O, Fernàndez-Castillo N, Corominas R, Valverde MA, Macaya A, Cormand B, Fernández-Fernández JM. A mutation in the first intracellular loop of CACNA1A prevents P/Q channel modulation by SNARE proteins and lowers exocytosis. Proceedings of the National Academy of Sciences of the United States of America. 107: 1672-7. PMID 20080591 DOI: 10.1073/Pnas.0908359107  0.713
2010 Corominas R, Sobrido MJ, Ribasés M, Cuenca-León E, Blanco-Arias P, Narberhaus B, Roig M, Leira R, López-González J, Macaya A, Cormand B. Association study of the serotoninergic system in migraine in the Spanish population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 177-84. PMID 19455600 DOI: 10.1002/Ajmg.B.30972  0.755
2009 Corominas R, Ribases M, Camiña M, Cuenca-León E, Pardo J, Boronat S, Sobrido MJ, Cormand B, Macaya A. Two-stage case-control association study of dopamine-related genes and migraine. Bmc Medical Genetics. 10: 95. PMID 19772578 DOI: 10.1186/1471-2350-10-95  0.722
2009 Corominas R, Ribasés M, Cuenca-León E, Narberhaus B, Serra SA, del Toro M, Roig M, Fernández-Fernández JM, Macaya A, Cormand B. Contribution of syntaxin 1A to the genetic susceptibility to migraine: a case-control association study in the Spanish population. Neuroscience Letters. 455: 105-9. PMID 19368856 DOI: 10.1016/J.Neulet.2009.03.011  0.746
2009 Cuenca-León E, Banchs I, Serra SA, Latorre P, Fernàndez-Castillo N, Corominas R, Valverde MA, Volpini V, Fernández-Fernández JM, Macaya A, Cormand B. Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene. Journal of the Neurological Sciences. 280: 10-4. PMID 19232643 DOI: 10.1016/J.Jns.2009.01.005  0.747
2009 Corominas R, Ribasés M, Cuenca-León E, Cormand B, Macaya A. Lack of association of hormone receptor polymorphisms with migraine. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 16: 413-5. PMID 19175383 DOI: 10.1111/J.1468-1331.2008.02499.X  0.716
2009 Cuenca-León E, Corominas R, Montfort M, Artigas J, Roig M, Bayés M, Cormand B, Macaya A. Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred. Neurogenetics. 10: 191-8. PMID 19153782 DOI: 10.1007/S10048-008-0169-6  0.738
2008 Cuenca-León E, Corominas R, Fernàndez-Castillo N, Volpini V, Del Toro M, Roig M, Macaya A, Cormand B. Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes. Cephalalgia : An International Journal of Headache. 28: 1039-47. PMID 18644040 DOI: 10.1111/J.1468-2982.2008.01645.X  0.765
2008 Cuscó I, Corominas R, Bayés M, Flores R, Rivera-Brugués N, Campuzano V, Pérez-Jurado LA. Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion. Genome Research. 18: 683-94. PMID 18292220 DOI: 10.1101/Gr.073197.107  0.438
2005 Macaya A, Brunso L, Fernández-Castillo N, Arranz JA, Ginjaar HB, Cuenca-León E, Corominas R, Roig M, Cormand B. Molybdenum cofactor deficiency presenting as neonatal hyperekplexia: a clinical, biochemical and genetic study. Neuropediatrics. 36: 389-94. PMID 16429380 DOI: 10.1055/S-2005-872877  0.738
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