Dynamic functional connectivity reveals altered variability in functional connectivity among patients with major depressive disorder von Demirtaş, Murat, Tornador, Cristian, Falcón, Carles, López-Solà, Marina, Hernández-Ribas, Rosa, Pujol, Jesús, Menchón, José M., Ritter, Petra, Cardoner, Narcis, Soriano-Mas, Carles, Deco, Gustavo

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New Cases of Hypochromic Microcytic Anemia Due to Mutations in the SLC11A2 Gene and Functional Characterization of the G75R Mutation von Romero-Cortadellas, Lídia, Hernández, Gonzalo, Ferrer-Cortès, Xènia, Zalba-Jadraque, Laura, Fuster, José Luis, Bermúdez-Cortés, Mar, Galera-Miñarro, Ana María, Pérez-Montero, Santiago, Tornador, Cristian, Sánchez, Mayka

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Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III von Hernández, Gonzalo, Romero-Cortadellas, Lídia, Ferrer-Cortès, Xènia, Venturi, Veronica, Dessy-Rodriguez, Mercedes, Olivella, Mireia, Husami, Ammar, De Soto, Concepción Pérez, Morales-Camacho, Rosario M, Villegas, Ana, González-Fernández, Fernando-Ataulfo, Morado, Marta, Kalfa, Theodosia A, Quintana-Bustamante, Oscar, Pérez-Montero, Santiago, Tornador, Cristian, Segovia, Jose-Carlos, Sánchez, Mayka

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BID expression determines the apoptotic fate of cancer cells after abrogation of the spindle assembly checkpoint by AURKB or TTK inhibitors von Bertran-Alamillo, Jordi, Giménez-Capitán, Ana, Román, Ruth, Talbot, Sara, Whiteley, Rebecca, Floc'h, Nicolas, Martínez-Pérez, Elizabeth, Martin, Matthew J, Smith, Paul D, Sullivan, Ivana, Terp, Mikkel G, Saeh, Jamal, Marino-Buslje, Cristina, Fabbri, Giulia, Guo, Grace, Xu, Man, Tornador, Cristian, Aguilar-Hernández, Andrés, Reguart, Noemí, Ditzel, Henrik J, Martínez-Bueno, Alejandro, Nabau-Moretó, Núria, Gascó, Amaya, Rosell, Rafael, Pease, J Elizabeth, Polanska, Urszula M, Travers, Jon, Urosevic, Jelena, Molina-Vila, Miguel A

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New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II von Musri, Melina Mara, Venturi, Veronica, Ferrer-Cortès, Xènia, Romero-Cortadellas, Lídia, Hernández, Gonzalo, Leoz, Pilar, Ricard Andrés, María Pilar, Morado, Marta, Fernández Valle, María Del Carmen, Beneitez Pastor, David, Ortuño Cabrero, Ana, Moreno Gamiz, Maite, Senent Peris, Leonor, Perez-Valencia, Amanda Isabel, Pérez-Montero, Santiago, Tornador, Cristian, Sánchez, Mayka

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Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New Cases von Celma Nos, Ferran, Hernandez, Gonzalo, Ferrer-Cortes, Xenia, Hernandez-Rodriguez, Ines, Navarro-Almenzar, Begona, Fuster, Jose Luis, Bermudez Cortes, Mar, Perez-Montero, Santiago, Tornador, Cristian, Sanchez, Mayka

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P1475: MUTATIONS IN THE GAP DOMAIN OF RACGAP1 CAUSE DEVELOPMENTAL AND ERYTHROID DEFECTS IN ZEBRAFISH von Romero‐Cortadellas, Lídia, Bañón, Aitor, Hernández, Gonzalo, Pérez‐Montero, Santiago, Tornador, Cristian, Alsina, Berta, Sanchez, Mayka

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CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic Anemia von Tornador, Cristian, Sánchez-Prados, Edgar, Cadenas, Beatriz, Russo, Roberta, Venturi, Veronica, Andolfo, Immacolata, Hernández-Rodriguez, Ines, Iolascon, Achille, Sánchez, Mayka

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L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia-Report of New Cases von Cadenas, Beatriz, Fita-Torró, Josep, Bermúdez-Cortés, Mar, Hernandez-Rodriguez, Inés, Fuster, José Luis, Llinares, María Esther, Galera, Ana María, Romero, Julia Lee, Pérez-Montero, Santiago, Tornador, Cristian, Sanchez, Mayka

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Environmental factors linked to depression vulnerability are associated with altered cerebellar resting-state synchronization von Córdova-Palomera, Aldo, Tornador, Cristian, Falcón, Carles, Bargalló, Nuria, Brambilla, Paolo, Crespo-Facorro, Benedicto, Deco, Gustavo, Fañanás, Lourdes

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Altered amygdalar resting-state connectivity in depression is explained by both genes and environment von Córdova-Palomera, Aldo, Tornador, Cristian, Falcón, Carles, Bargalló, Nuria, Nenadic, Igor, Deco, Gustavo, Fañanás, Lourdes

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PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data von Escaramís, Geòrgia, Tornador, Cristian, Bassaganyas, Laia, Rabionet, Raquel, Tubio, Jose M C, Martínez-Fundichely, Alexander, Cáceres, Mario, Gut, Marta, Ossowski, Stephan, Estivill, Xavier

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Altered resting-state whole-brain functional networks of neonates with intrauterine growth restriction von Batalle, Dafnis, Muñoz-Moreno, Emma, Tornador, Cristian, Bargallo, Nuria, Deco, Gustavo, Eixarch, Elisenda, Gratacos, Eduard

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Evolutionary dynamics of the Ty3/gypsy LTR retrotransposons in the genome of Anopheles gambiae von Tubio, Jose Manuel C, Tojo, Marta, Bassaganyas, Laia, Escaramis, Georgia, Sharakhov, Igor V, Sharakhova, Maria V, Tornador, Cristian, Unger, Maria F, Naveira, Horacio, Costas, Javier, Besansky, Nora J

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Genomic insights into the Ixodes scapularis tick vector of Lyme disease von Gulia-Nuss, Monika, Nuss, Andrew B., Meyer, Jason M., Sonenshine, Daniel E., Roe, R. Michael, Waterhouse, Robert M., Sattelle, David B., de la Fuente, José, Ribeiro, Jose M., Megy, Karine, Thimmapuram, Jyothi, Miller, Jason R., Walenz, Brian P., Koren, Sergey, Hostetler, Jessica B., Thiagarajan, Mathangi, Joardar, Vinita S., Hannick, Linda I., Bidwell, Shelby, Hammond, Martin P., Young, Sarah, Zeng, Qiandong, Abrudan, Jenica L., Almeida, Francisca C., Ayllón, Nieves, Bhide, Ketaki, Bissinger, Brooke W., Bonzon-Kulichenko, Elena, Buckingham, Steven D., Caffrey, Daniel R., Caimano, Melissa J., Croset, Vincent, Driscoll, Timothy, Gilbert, Don, Gillespie, Joseph J., Giraldo-Calderón, Gloria I., Grabowski, Jeffrey M., Jiang, David, Khalil, Sayed M. S., Kim, Donghun, Kocan, Katherine M., Koči, Juraj, Kuhn, Richard J., Kurtti, Timothy J., Lees, Kristin, Lang, Emma G., Kennedy, Ryan C., Kwon, Hyeogsun, Perera, Rushika, Qi, Yumin, Radolf, Justin D., Sakamoto, Joyce M., Sánchez-Gracia, Alejandro, Severo, Maiara S., Silverman, Neal, Šimo, Ladislav, Tojo, Marta, Tornador, Cristian, Van Zee, Janice P., Vázquez, Jesús, Vieira, Filipe G., Villar, Margarita, Wespiser, Adam R., Yang, Yunlong, Zhu, Jiwei, Arensburger, Peter, Pietrantonio, Patricia V., Barker, Stephen C., Shao, Renfu, Zdobnov, Evgeny M., Hauser, Frank, Grimmelikhuijzen, Cornelis J. P., Park, Yoonseong, Rozas, Julio, Benton, Richard, Pedra, Joao H. F., Nelson, David R., Unger, Maria F., Tubio, Jose M. C., Tu, Zhijian, Robertson, Hugh M., Shumway, Martin, Sutton, Granger, Wortman, Jennifer R., Lawson, Daniel, Wikel, Stephen K., Nene, Vishvanath M., Fraser, Claire M., Collins, Frank H., Birren, Bruce, Nelson, Karen E., Caler, Elisabet, Hill, Catherine A.

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Increased methylation at an unexplored glucocorticoid responsive element within exon 1 D of NR3C1 gene is related to anxious-depressive disorders and decreased hippocampal connecti... von Palma-Gudiel, Helena, Córdova-Palomera, Aldo, Tornador, Cristian, Falcón, Carles, Bargalló, Núria, Deco, Gustavo, Fañanás, Lourdes

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Lentiviral Gene Therapy for the Correction of Congenital Dyserythropoietic Anemia Type II von Dessy-Rodriguez, Mercedes, Fañanas-Baquero, Sara, Venturi, Veronica, Payan, Salvador, Tornador, Cristian, Hernández, Gonzalo, Bianchi, Paola, Sanchez, Mayka, Ramirez, Juan Carlos, Segovia, José C, Quintana Bustamante, Oscar

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Modelling Congenital Dyserythropoietic Anemia Type II through Gene Editing in Hematopoietic Stem and Progenitor Cells von Dessy-Rodriguez, Mercedes, Fañanas-Baquero, Sara, Venturi, Veronica, Payán-Pernía, Salvador, Tornador, Cristian, Hernandez, Gonzalo, Sanchez, Mayka, Segovia, José C, Quintana Bustamante, Oscar

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Autosomal Recessive Congenital Dyserythropoietic Anemia Type III Is Caused By Mutations in the Centralspindlin RACGAP1 Component von Romero-Cortadellas, Lídia, Hernández, Gonzalo, Ferrer-Cortès, Xènia, Venturi, Veronica, Olivella, Mireia, Pérez de Soto, Concepción, Morales-Camacho, Rosario M., Villegas, Ana, Gonzalez-Fernandez, F. Ataulfo, Morado, Marta, Pérez-Montero, Santiago, Tornador, Cristian, Sánchez, Mayka

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Increased methylation at an unexplored glucocorticoid responsive element within exon 1D of NR3C1 gene is related to anxious-depressive disorders and decreased hippocampal connectiv... von Palma-Gudiel, Helena, Córdova-Palomera, Aldo, Tornador, Cristian, Falcón, Carles, Bargalló, Núria, Deco, Gustavo, Fañanás, Lourdes

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