Roser Corominas

3.8k total citations
26 papers, 731 citations indexed

About

Roser Corominas is a scholar working on Molecular Biology, Psychiatry and Mental health and Cellular and Molecular Neuroscience. According to data from OpenAlex, Roser Corominas has authored 26 papers receiving a total of 731 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Psychiatry and Mental health and 7 papers in Cellular and Molecular Neuroscience. Recurrent topics in Roser Corominas's work include Migraine and Headache Studies (10 papers), Neuroscience of respiration and sleep (5 papers) and Attention Deficit Hyperactivity Disorder (3 papers). Roser Corominas is often cited by papers focused on Migraine and Headache Studies (10 papers), Neuroscience of respiration and sleep (5 papers) and Attention Deficit Hyperactivity Disorder (3 papers). Roser Corominas collaborates with scholars based in Spain, United States and Greece. Roser Corominas's co-authors include Bru Cormand, Alfons Macaya, Noèlia Fernàndez‐Castillo, Guan Ning Lin, Ester Cuenca-León, Lilia M. Iakoucheva, José M. Fernández‐Fernández, Weidi Wang, Marta Ribasès and Luis A. Pérez‐Jurado and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neuron and Scientific Reports.

In The Last Decade

Roser Corominas

25 papers receiving 724 citations

Peers

Countries citing papers authored by Roser Corominas

Since Specialization

Citations

This map shows the geographic impact of Roser Corominas's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Roser Corominas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roser Corominas more than expected).

Fields of papers citing papers by Roser Corominas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roser Corominas. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Roser Corominas. The network helps show where Roser Corominas may publish in the future.

Co-authorship network of co-authors of Roser Corominas

This figure shows the co-authorship network connecting the top 25 collaborators of Roser Corominas. A scholar is included among the top collaborators of Roser Corominas based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Roser Corominas. Roser Corominas is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	The pleiotropic contribution of genes in dopaminergic and serotonergic pathways to addiction and related behavioral traits 2023 ·Frontiers in Psychiatry ·(unknown), Judit Cabana‐Domínguez, Bàrbara Torrico, Roser Corominas, Bru Cormand, Noèlia Fernàndez‐Castillo	5
2	Molecular genetics of cocaine use disorders in humans 2021 ·Molecular Psychiatry ·Noèlia Fernàndez‐Castillo, Judit Cabana‐Domínguez, Roser Corominas, Bru Cormand	37
3	Generation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering Williams-Beuren syndrome (7q11.23 deletion) 2020 ·Stem Cell Research ·Bernd Kuebler, Begoña Arán, Raquel Flores, Luis A. Pérez‐Jurado, Anna Veiga, Roser Corominas, Ivon Cuscó	2
4	Derivation of induced pluripotent stem cells (iPSCs) by retroviral transduction of skin fibroblasts from four patients suffering 7q11.23 microduplication syndrome 2020 ·Stem Cell Research ·Bernd Kuebler, Begoña Arán, Raquel Flores, Luis A. Pérez‐Jurado, Anna Veiga, Ivon Cuscó, Roser Corominas	0
5	Isoform Transcriptome of Developing Human Brain Provides New Insights into Autism Risk Variants 2020 ·SSRN Electronic Journal ·Kevin Chau, Pan Zhang, Jorge Urresti, (unknown), Akula Bala Pramod, (unknown), Roser Corominas, Guan Ning Lin, Lilia M. Iakoucheva	1
6	De novo Mutations From Whole Exome Sequencing in Neurodevelopmental and Psychiatric Disorders: From Discovery to Application 2019 ·Frontiers in Genetics ·Weidi Wang, Roser Corominas, Guan Ning Lin	43
7	bigSCale: an analytical framework for big-scale single-cell data 2018 ·Genome Research ·Giovanni Iacono, Elisabetta Mereu, Amy Guillaumet-Adkins, Roser Corominas, Ivon Cuscó, Gustavo Rodríguez-Esteban, Marta Gut, Luis A. Pérez‐Jurado, Holger Heyn	49
8	Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia 2017 ·Scientific Reports ·Cèlia Sintas, (unknown), Noèlia Fernàndez‐Castillo, Roser Corominas, Marta Vila‐Pueyo, Claudio Toma, Ester Cuenca-León, Isabel Barroeta, (unknown), Vı́ctor Volpini, Alfons Macaya, Bru Cormand	37
9	Spatiotemporal 16p11.2 Protein Network Implicates Cortical Late Mid-Fetal Brain Development and KCTD13-Cul3-RhoA Pathway in Psychiatric Diseases 2015 ·Neuron ·Guan Ning Lin, Roser Corominas, Irma Lemmens, Xinping Yang, Jan Tavernier, David E. Hill, Marc Vidal, Jonathan Sebat, Lilia M. Iakoucheva	103
10	Evaluation of common variants in 16 genes involved in the regulation of neurotransmitter release in ADHD 2012 ·European Neuropsychopharmacology ·Cristina Sánchez‐Mora, Bru Cormand, Josep Antoni Ramos‐Quiroga, Amaia Hervás, Rosa Bosch, Glòria Palomar, Mariana Nogueira, Núria Gómez-Barros, Vanesa Richarte, Montse Corrales, Iris Garcia‐Martínez, Roser Corominas, Silvina Guijarro, Aitana Bigorra, Mónica Bayés, Miguel Casas, Marta Ribasès	26
11	SNP variants within the vanilloidTRPV1andTRPV3receptor genes are associated with migraine in the Spanish population 2011 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·(unknown), Roser Corominas, Jessica Fernández‐Morales, (unknown), María‐Jesús Sobrido, José M. Fernández‐Fernández, Patricia Pozo‐Rosich, Bru Cormand, Alfons Macaya	66
12	Candidate pathway association study in cocaine dependence: The control of neurotransmitter release 2011 ·The World Journal of Biological Psychiatry ·Noèlia Fernàndez‐Castillo, Bru Cormand, Carlos Roncero, Cristina Sánchez‐Mora, Lara Grau‐López, Begoña Gonzalvo, Laia Miquel‐Serra, Roser Corominas, Josep Antoni Ramos‐Quiroga, Miguel Casas, Marta Ribasès	11
13	Two-stage case-control association study of dopamine-related genes and migraine 2009 ·BMC Medical Genetics ·Roser Corominas, Marta Ribasès, (unknown), Ester Cuenca-León, Julio Pardo, Susana Boronat, María‐Jesús Sobrido, Bru Cormand, Alfons Macaya	25
14	Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred 2009 ·Neurogenetics ·Ester Cuenca-León, Roser Corominas, Magda Montfort, J Artigas-Pallarés, Manuel G. Roig, Mónica Bayés, Bru Cormand, Alfons Macaya	11
15	Association study of the serotoninergic system in migraine in the spanish population 2009 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Roser Corominas, María‐Jesús Sobrido, Marta Ribasès, Ester Cuenca-León, Patricia Blanco, (unknown), Manuel G. Roig, Rogelio Leira, Javier López-González, Alfons Macaya, Bru Cormand	35
16	Contribution of syntaxin 1A to the genetic susceptibility to migraine: A case–control association study in the Spanish population 2009 ·Neuroscience Letters ·Roser Corominas, Marta Ribasès, Ester Cuenca-León, (unknown), Selma A. Serra, Mireia del Toro, Manuel G. Roig, José M. Fernández‐Fernández, Alfons Macaya, Bru Cormand	11
17	Lack of association of hormone receptor polymorphisms with migraine 2009 ·European Journal of Neurology ·Roser Corominas, Marta Ribasès, Ester Cuenca-León, Bru Cormand, Alfons Macaya	21
18	Late-onset episodic ataxia type 2 associated with a novel loss-of-function mutation in the CACNA1A gene 2009 ·Journal of the Neurological Sciences ·Ester Cuenca-León, Isabel Banchs, Selma A. Serra, Pilar Latorre, Noèlia Fernàndez‐Castillo, Roser Corominas, Miguel A. Valverde, Vı́ctor Volpini, José M. Fernández‐Fernández, Alfons Macaya, Bru Cormand	29
19	Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion 2008 ·Genome Research ·Ivon Cuscó, Roser Corominas, Mónica Bayés, Raquel Flores, (unknown), Victoria Campuzano, Luis A. Pérez‐Jurado	56
20	Molybdenum Cofactor Deficiency Presenting as Neonatal Hyperekplexia: A Clinical, Biochemical and Genetic Study 2005 ·Neuropediatrics ·Alfons Macaya, (unknown), Noèlia Fernàndez‐Castillo, José Antonio Arranz, H.B. Ginjaar, Ester Cuenca-León, Roser Corominas, (unknown), Bru Cormand	21

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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