<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Greene, Daniel</style></author><author><style face="normal" font="default" size="100%">De Wispelaere, Koenraad</style></author><author><style face="normal" font="default" size="100%">Lees, Jon</style></author><author><style face="normal" font="default" size="100%">Codina-Solà, Marta</style></author><author><style face="normal" font="default" size="100%">Jensson, Brynjar O.</style></author><author><style face="normal" font="default" size="100%">Hales, Emma</style></author><author><style face="normal" font="default" size="100%">Katrinecz, Andrea</style></author><author><style face="normal" font="default" size="100%">Nieto Molina, Esther</style></author><author><style face="normal" font="default" size="100%">Sevilla Porras, Marta</style></author><author><style face="normal" font="default" size="100%">Pascoal, Sonia</style></author><author><style face="normal" font="default" size="100%">Valenzuela, Irene</style></author><author><style face="normal" font="default" size="100%">Pfundt, Rolph</style></author><author><style face="normal" font="default" size="100%">Schot, Rachel</style></author><author><style face="normal" font="default" size="100%">Sleutels, Frank</style></author><author><style face="normal" font="default" size="100%">Wijngaard, Robin</style></author><author><style face="normal" font="default" size="100%">Arroyo Carrera, Ignacio</style></author><author><style face="normal" font="default" size="100%">Duat Rodríguez, Anna</style></author><author><style face="normal" font="default" size="100%">Atton, Giles</style></author><author><style face="normal" font="default" size="100%">Casas-Alba, Didac</style></author><author><style face="normal" font="default" size="100%">Donnelly, Deirdre</style></author><author><style face="normal" font="default" size="100%">Fernández Garoz, Bárbara</style></author><author><style face="normal" font="default" size="100%">Foulds, Nicola</style></author><author><style face="normal" font="default" size="100%">García-Navas Núñez, Deyanira</style></author><author><style face="normal" font="default" size="100%">González Alguacil, Elena</style></author><author><style face="normal" font="default" size="100%">Jarvis, Joanna</style></author><author><style face="normal" font="default" size="100%">Kant, Sarina G.</style></author><author><style face="normal" font="default" size="100%">Madrigal Bajo, Irene</style></author><author><style face="normal" font="default" size="100%">Martinez-Monseny, Antonio F.</style></author><author><style face="normal" font="default" size="100%">McKee, Shane</style></author><author><style face="normal" font="default" size="100%">Sariego Jamardo, Andrea</style></author><author><style face="normal" font="default" size="100%">Stefansson, Kari</style></author><author><style face="normal" font="default" size="100%">Rodríguez-Revenga Bodi, Laia</style></author><author><style face="normal" font="default" size="100%">Ortiz Cabrera, Nelmar Valentina</style></author><author><style face="normal" font="default" size="100%">Sulem, Patrick</style></author><author><style face="normal" font="default" size="100%">Suri, Mohnish</style></author><author><style face="normal" font="default" size="100%">Van Karnebeek, Clara</style></author><author><style face="normal" font="default" size="100%">Vasudevan, Pradeep</style></author><author><style face="normal" font="default" size="100%">Vega Pajares, Ana Isabel</style></author><author><style face="normal" font="default" size="100%">Carracedo, Ángel</style></author><author><style face="normal" font="default" size="100%">Engelen, Marc</style></author><author><style face="normal" font="default" size="100%">Lapunzina, Pablo</style></author><author><style face="normal" font="default" size="100%">Morgan, Natasha P.</style></author><author><style face="normal" font="default" size="100%">Morte, Beatriz</style></author><author><style face="normal" font="default" size="100%">Rump, Patrick</style></author><author><style face="normal" font="default" size="100%">Stirrups, Kathy</style></author><author><style face="normal" font="default" size="100%">Tizzano, Eduardo F.</style></author><author><style face="normal" font="default" size="100%">Barakat, Tahsin Stefan</style></author><author><style face="normal" font="default" size="100%">O’Donoghue, Michael</style></author><author><style face="normal" font="default" size="100%">Pérez-Jurado, Luis Alberto</style></author><author><style face="normal" font="default" size="100%">Freson, Kathleen</style></author><author><style face="normal" font="default" size="100%">Mumford, Andrew D.</style></author><author><style face="normal" font="default" size="100%">Turro, Ernest</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy</style></title><secondary-title><style face="normal" font="default" size="100%">Nature Genetics</style></secondary-title><short-title><style face="normal" font="default" size="100%">Nat Genet</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Oct-04-2025</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.nature.com/articles/s41588-025-02159-5https://www.nature.com/articles/s41588-025-02159-5.pdfhttps://www.nature.com/articles/s41588-025-02159-5.pdfhttps://www.nature.com/articles/s41588-025-02159-5</style></url></web-urls></urls><language><style face="normal" font="default" size="100%">eng</style></language></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Luque, Juan</style></author><author><style face="normal" font="default" size="100%">Mendes, Ingrid</style></author><author><style face="normal" font="default" size="100%">Gómez, Beatriz</style></author><author><style face="normal" font="default" size="100%">Morte, Beatriz</style></author><author><style face="normal" font="default" size="100%">de Heredia, Miguel López</style></author><author><style face="normal" font="default" size="100%">Herreras, Enrique</style></author><author><style face="normal" font="default" size="100%">Corrochano, Virginia</style></author><author><style face="normal" font="default" size="100%">Bueren, Juan</style></author><author><style face="normal" font="default" size="100%">Gallano, Pia</style></author><author><style face="normal" font="default" size="100%">Artuch, Rafael</style></author><author><style face="normal" font="default" size="100%">Fillat, Cristina</style></author><author><style face="normal" font="default" size="100%">Pérez-Jurado, Luis A</style></author><author><style face="normal" font="default" size="100%">Montoliu, Lluis</style></author><author><style face="normal" font="default" size="100%">Carracedo, Ángel</style></author><author><style face="normal" font="default" size="100%">Millán, José M</style></author><author><style face="normal" font="default" size="100%">Webb, Susan M</style></author><author><style face="normal" font="default" size="100%">Palau, Francesc</style></author><author><style face="normal" font="default" size="100%">Lapunzina, Pablo</style></author></authors><translated-authors><author><style face="normal" font="default" size="100%">CIBERER Network</style></author></translated-authors></contributors><titles><title><style face="normal" font="default" size="100%">CIBERER: Spanish National Network for Research on Rare Diseases: a highly productive collaborative initiative.</style></title><secondary-title><style face="normal" font="default" size="100%">Clin Genet</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Clin Genet</style></alt-title></titles><dates><year><style  face="normal" font="default" size="100%">2022</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2022 Jan 20</style></date></pub-dates></dates><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;CIBER (Center for Biomedical Network Research; Centro de Investigación Biomédica En Red) is a public national consortium created in 2006 under the umbrella of the Spanish National Institute of Health Carlos III (ISCIII). This innovative research structure comprises 11 different specific areas dedicated to the main public health priorities in the National Health System. CIBERER, the thematic area of CIBER focused on Rare Diseases currently consists of 75 research groups belonging to universities, research centers and hospitals of the entire country. CIBERER's mission is to be a center prioritizing and favoring collaboration and cooperation between biomedical and clinical research groups, with special emphasis on the aspects of genetic, molecular, biochemical and cellular research of rare diseases. This research is the basis for providing new tools for the diagnosis and therapy of low-prevalence diseases, in line with the International Rare Diseases Research Consortium (IRDiRC) objectives, thus favoring translational research between the scientific environment of the laboratory and the clinical setting of health centers. In this paper, we intend to review CIBERER's 15-year journey and summarize the main results obtained in terms of internationalization, scientific production, contributions towards the discovery of new therapies and novel genes associated to diseases, cooperation with patients' associations and many other topics related to rare disease research. This article is protected by copyright. All rights reserved.&lt;/p&gt;</style></abstract></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Peña-Chilet, Maria</style></author><author><style face="normal" font="default" size="100%">Roldán, Gema</style></author><author><style face="normal" font="default" size="100%">Perez-Florido, Javier</style></author><author><style face="normal" font="default" size="100%">Ortuno, Francisco M</style></author><author><style face="normal" font="default" size="100%">Carmona, Rosario</style></author><author><style face="normal" font="default" size="100%">Aquino, Virginia</style></author><author><style face="normal" font="default" size="100%">López-López, Daniel</style></author><author><style face="normal" font="default" size="100%">Loucera, Carlos</style></author><author><style face="normal" font="default" size="100%">Fernandez-Rueda, Jose L</style></author><author><style face="normal" font="default" size="100%">Gallego, Asunción</style></author><author><style face="normal" font="default" size="100%">Garcia-Garcia, Francisco</style></author><author><style face="normal" font="default" size="100%">González-Neira, Anna</style></author><author><style face="normal" font="default" size="100%">Pita, Guillermo</style></author><author><style face="normal" font="default" size="100%">Núñez-Torres, Rocío</style></author><author><style face="normal" font="default" size="100%">Santoyo-López, Javier</style></author><author><style face="normal" font="default" size="100%">Ayuso, Carmen</style></author><author><style face="normal" font="default" size="100%">Minguez, Pablo</style></author><author><style face="normal" font="default" size="100%">Avila-Fernandez, Almudena</style></author><author><style face="normal" font="default" size="100%">Corton, Marta</style></author><author><style face="normal" font="default" size="100%">Moreno-Pelayo, Miguel Ángel</style></author><author><style face="normal" font="default" size="100%">Morin, Matías</style></author><author><style face="normal" font="default" size="100%">Gallego-Martinez, Alvaro</style></author><author><style face="normal" font="default" size="100%">Lopez-Escamez, Jose A</style></author><author><style face="normal" font="default" size="100%">Borrego, Salud</style></author><author><style face="normal" font="default" size="100%">Antiňolo, Guillermo</style></author><author><style face="normal" font="default" size="100%">Amigo, Jorge</style></author><author><style face="normal" font="default" size="100%">Salgado-Garrido, Josefa</style></author><author><style face="normal" font="default" size="100%">Pasalodos-Sanchez, Sara</style></author><author><style face="normal" font="default" size="100%">Morte, Beatriz</style></author><author><style face="normal" font="default" size="100%">Carracedo, Ángel</style></author><author><style face="normal" font="default" size="100%">Alonso, Ángel</style></author><author><style face="normal" font="default" size="100%">Dopazo, Joaquin</style></author></authors><translated-authors><author><style face="normal" font="default" size="100%">Spanish Exome Crowdsourcing Consortium</style></author></translated-authors></contributors><titles><title><style face="normal" font="default" size="100%">CSVS, a crowdsourcing database of the Spanish population genetic variability.</style></title><secondary-title><style face="normal" font="default" size="100%">Nucleic Acids Res</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Nucleic Acids Res</style></alt-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Alleles</style></keyword><keyword><style  face="normal" font="default" size="100%">Chromosome Mapping</style></keyword><keyword><style  face="normal" font="default" size="100%">Crowdsourcing</style></keyword><keyword><style  face="normal" font="default" size="100%">Databases, Genetic</style></keyword><keyword><style  face="normal" font="default" size="100%">Exome</style></keyword><keyword><style  face="normal" font="default" size="100%">Gene Frequency</style></keyword><keyword><style  face="normal" font="default" size="100%">Genetic Variation</style></keyword><keyword><style  face="normal" font="default" size="100%">Genetics, Population</style></keyword><keyword><style  face="normal" font="default" size="100%">Genome, Human</style></keyword><keyword><style  face="normal" font="default" size="100%">Genomics</style></keyword><keyword><style  face="normal" font="default" size="100%">Humans</style></keyword><keyword><style  face="normal" font="default" size="100%">Internet</style></keyword><keyword><style  face="normal" font="default" size="100%">Precision Medicine</style></keyword><keyword><style  face="normal" font="default" size="100%">Software</style></keyword><keyword><style  face="normal" font="default" size="100%">Spain</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2021 01 08</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">49</style></volume><pages><style face="normal" font="default" size="100%">D1130-D1137</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The knowledge of the genetic variability of the local population is of utmost importance in personalized medicine and has been revealed as a critical factor for the discovery of new disease variants. Here, we present the Collaborative Spanish Variability Server (CSVS), which currently contains more than 2000 genomes and exomes of unrelated Spanish individuals. This database has been generated in a collaborative crowdsourcing effort collecting sequencing data produced by local genomic projects and for other purposes. Sequences have been grouped by ICD10 upper categories. A web interface allows querying the database removing one or more ICD10 categories. In this way, aggregated counts of allele frequencies of the pseudo-control Spanish population can be obtained for diseases belonging to the category removed. Interestingly, in addition to pseudo-control studies, some population studies can be made, as, for example, prevalence of pharmacogenomic variants, etc. In addition, this genomic data has been used to define the first Spanish Genome Reference Panel (SGRP1.0) for imputation. This is the first local repository of variability entirely produced by a crowdsourcing effort and constitutes an example for future initiatives to characterize local variability worldwide. CSVS is also part of the GA4GH Beacon network. CSVS can be accessed at: http://csvs.babelomics.org/.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">D1</style></issue><custom1><style face="normal" font="default" size="100%">https://www.ncbi.nlm.nih.gov/pubmed/32990755?dopt=Abstract</style></custom1></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Tenorio-Castaño, Jair</style></author><author><style face="normal" font="default" size="100%">Morte, Beatriz</style></author><author><style face="normal" font="default" size="100%">Nevado, Julián</style></author><author><style face="normal" font="default" size="100%">Martínez-Glez, Víctor</style></author><author><style face="normal" font="default" size="100%">Santos-Simarro, Fernando</style></author><author><style face="normal" font="default" size="100%">García-Miñaur, Sixto</style></author><author><style face="normal" font="default" size="100%">Palomares-Bralo, María</style></author><author><style face="normal" font="default" size="100%">Pacio-Míguez, Marta</style></author><author><style face="normal" font="default" size="100%">Gómez, Beatriz</style></author><author><style face="normal" font="default" size="100%">Arias, Pedro</style></author><author><style face="normal" font="default" size="100%">Alcochea, Alba</style></author><author><style face="normal" font="default" size="100%">Carrión, Juan</style></author><author><style face="normal" font="default" size="100%">Arias, Patricia</style></author><author><style face="normal" font="default" size="100%">Almoguera, Berta</style></author><author><style face="normal" font="default" size="100%">López-Grondona, Fermina</style></author><author><style face="normal" font="default" size="100%">Lorda-Sanchez, Isabel</style></author><author><style face="normal" font="default" size="100%">Galán-Gómez, Enrique</style></author><author><style face="normal" font="default" size="100%">Valenzuela, Irene</style></author><author><style face="normal" font="default" size="100%">Méndez Perez, María</style></author><author><style face="normal" font="default" size="100%">Cuscó, Ivón</style></author><author><style face="normal" font="default" size="100%">Barros, Francisco</style></author><author><style face="normal" font="default" size="100%">Pié, Juan</style></author><author><style face="normal" font="default" size="100%">Ramos, Sergio</style></author><author><style face="normal" font="default" size="100%">Ramos, Feliciano</style></author><author><style face="normal" font="default" size="100%">Kuechler, Alma</style></author><author><style face="normal" font="default" size="100%">Tizzano, Eduardo</style></author><author><style face="normal" font="default" size="100%">Ayuso, Carmen</style></author><author><style face="normal" font="default" size="100%">Kaiser, Frank</style></author><author><style face="normal" font="default" size="100%">Pérez-Jurado, Luis</style></author><author><style face="normal" font="default" size="100%">Carracedo, Ángel</style></author><author><style face="normal" font="default" size="100%">Lapunzina, Pablo</style></author></authors><translated-authors><author><style face="normal" font="default" size="100%">The ENoD-CIBERER Consortium</style></author><author><style face="normal" font="default" size="100%">The SIDE Consortium</style></author></translated-authors></contributors><titles><title><style face="normal" font="default" size="100%">Schuurs–Hoeijmakers Syndrome (PACS1 Neurodevelopmental Disorder): Seven Novel Patients and a Review</style></title><secondary-title><style face="normal" font="default" size="100%">Genes</style></secondary-title><short-title><style face="normal" font="default" size="100%">Genes</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2021</style></year><pub-dates><date><style  face="normal" font="default" size="100%">Jan-05-2021</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.mdpi.com/2073-4425/12/5/738https://www.mdpi.com/2073-4425/12/5/738/pdf</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">12</style></volume><pages><style face="normal" font="default" size="100%">738</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">5</style></issue></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Gil-Ibañez, Pilar</style></author><author><style face="normal" font="default" size="100%">Garcia-Garcia, Francisco</style></author><author><style face="normal" font="default" size="100%">Dopazo, Joaquin</style></author><author><style face="normal" font="default" size="100%">Bernal, Juan</style></author><author><style face="normal" font="default" size="100%">Morte, Beatriz</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Global Transcriptome Analysis of Primary Cerebrocortical Cells: Identification of Genes Regulated by Triiodothyronine in Specific Cell Types.</style></title><secondary-title><style face="normal" font="default" size="100%">Cereb Cortex</style></secondary-title><alt-title><style face="normal" font="default" size="100%">Cereb Cortex</style></alt-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">Animals</style></keyword><keyword><style  face="normal" font="default" size="100%">Astrocytes</style></keyword><keyword><style  face="normal" font="default" size="100%">Cells, Cultured</style></keyword><keyword><style  face="normal" font="default" size="100%">Cerebral Cortex</style></keyword><keyword><style  face="normal" font="default" size="100%">Fluorescent Antibody Technique</style></keyword><keyword><style  face="normal" font="default" size="100%">Gene Expression Profiling</style></keyword><keyword><style  face="normal" font="default" size="100%">Mice, 129 Strain</style></keyword><keyword><style  face="normal" font="default" size="100%">Mice, Inbred BALB C</style></keyword><keyword><style  face="normal" font="default" size="100%">Mice, Inbred C57BL</style></keyword><keyword><style  face="normal" font="default" size="100%">Neurons</style></keyword><keyword><style  face="normal" font="default" size="100%">Piperazines</style></keyword><keyword><style  face="normal" font="default" size="100%">Transcriptome</style></keyword><keyword><style  face="normal" font="default" size="100%">Triiodothyronine</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2017</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2017 01 01</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">27</style></volume><pages><style face="normal" font="default" size="100%">706-717</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;Thyroid hormones, thyroxine, and triiodothyronine (T3) are crucial for cerebral cortex development acting through regulation of gene expression. To define the transcriptional program under T3 regulation, we have performed RNA-Seq of T3-treated and untreated primary mouse cerebrocortical cells. The expression of 1145 genes or 7.7% of expressed genes was changed upon T3 addition, of which 371 responded to T3 in the presence of cycloheximide indicating direct transcriptional regulation. The results were compared with available transcriptomic datasets of defined cellular types. In this way, we could identify targets of T3 within genes enriched in astrocytes and neurons, in specific layers including the subplate, and in specific neurons such as prepronociceptin, cholecystokinin, or cortistatin neurons. The subplate and the prepronociceptin neurons appear as potentially major targets of T3 action. T3 upregulates mostly genes related to cell membrane events, such as G-protein signaling, neurotransmission, and ion transport and downregulates genes involved in nuclear events associated with the M phase of cell cycle, such as chromosome organization and segregation. Remarkably, the transcriptomic changes induced by T3 sustain the transition from fetal to adult patterns of gene expression. The results allow defining in molecular terms the elusive role of thyroid hormones on neocortical development.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><custom1><style face="normal" font="default" size="100%">https://www.ncbi.nlm.nih.gov/pubmed/26534908?dopt=Abstract</style></custom1></record></records></xml>