Two novel variants of the ABCG5 gene cause xanthelasmas and macrothrombocytopenia: a brief review of hematologic abnormalities of sitosterolemia von Bastida, J. M., Benito, R., Janusz, K., Díez‐Campelo, M., Hernández‐Sánchez, J. M., Marcellini, S., Girós, M., Rivera, J., Lozano, M. L., Hortal, A., Hernández‐Rivas, J. M., González‐Porras, J. R.

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Exome sequencing reveals novel and recurrent mutations with clinical impact in blastic plasmacytoid dendritic cell neoplasm von Menezes, J, Acquadro, F, Wiseman, M, Gómez-López, G, Salgado, R N, Talavera-Casañas, J G, Buño, I, Cervera, J V, Montes-Moreno, S, Hernández-Rivas, J M, Ayala, R, Calasanz, M J, Larrayoz, M J, Brichs, L F, Gonzalez-Vicent, M, Pisano, D G, Piris, M A, Álvarez, S, Cigudosa, J C

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SNP-based mapping arrays reveal high genomic complexity in monoclonal gammopathies, from MGUS to myeloma status von López-Corral, L, Sarasquete, M E, Beà, S, García-Sanz, R, Mateos, M V, Corchete, L A, Sayagués, J M, García, E M, Bladé, J, Oriol, A, Hernández-García, M T, Giraldo, P, Hernández, J, González, M, Hernández-Rivas, J M, San Miguel, J F, Gutiérrez, N C

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Both expanded and uncultured mesenchymal stem cells from MDS patients are genomically abnormal, showing a specific genetic profile for the 5q− syndrome von Lopez-Villar, O, Garcia, J L, Sanchez-Guijo, F M, Robledo, C, Villaron, E M, Hernández-Campo, P, Lopez-Holgado, N, Diez-Campelo, M, Barbado, M V, Perez-Simon, J A, Hernández-Rivas, J M, San-Miguel, J F, del Cañizo, M-C

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Prognostic impact and landscape of NOTCH1 mutations in chronic lymphocytic leukemia (CLL): a study on 852 patients von Weissmann, S, Roller, A, Jeromin, S, Hernández, M, Abáigar, M, Hernández-Rivas, J M, Grossmann, V, Haferlach, C, Kern, W, Haferlach, T, Schnittger, S, Kohlmann, A

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Design and application of a 23-gene panel by next-generation sequencing for inherited coagulation bleeding disorders von Bastida, J. M., del Rey, M., Lozano, M. L., Sarasquete, M. E., Benito, R., Fontecha, M. E., Fisac, R., García-Frade, L. J., Aguilar, C., Martínez, M. P., Pardal, E., Aguilera, C., Pérez, B., Ramos, R., Cardesa, M. R., Martin-Antorán, J. M., Silvestre, L. A., Cebeira, M. J., Bermejo, N., Riesco, S., Mendoza, M. C., García-Sanz, R., González-Díaz, M., Hernández-Rivas, J. M., González-Porras, J. R.

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The immunophenotype of different immature, myeloid and B-cell lineage-committed CD34 hematopoietic cells allows discrimination between normal reactive and myelodysplastic syndrome... von Matarraz, S, López, A, Barrena, S, Fernandez, C, Jensen, E, Flores, J, Bárcena, P, Rasillo, A, Sayagues, J M, Sánchez, M L, Hernandez-Campo, P, Hernandez Rivas, J M, Salvador, C, Fernandez-Mosteirín, N, Giralt, M, Perdiguer, L, Orfao, A

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miR-146a rs2431697 identifies myeloproliferative neoplasm patients with higher secondary myelofibrosis progression risk von Ferrer-Marín, F., Arroyo, A. B., Bellosillo, B., Cuenca, E. J., Zamora, L., Hernández-Rivas, J. M., Hernández-Boluda, J. C., Fernandez-Rodriguez, C., Luño, E., García Hernandez, C., Kerguelen, A., Fiallo-Suárez, D. V., Gómez-Casares, M. T., Ayala, R., Vélez, P., Boqué, C., García-Gutierrez, V., Arrizabalaga, B., Estrada, N., Cifuentes, R., Arcas, I., de los Reyes-García, A. M., Besses, C., Vicente, V., Alvarez-Larrán, A., Teruel-Montoya, R., González-Conejero, R., Martínez, C.

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Uniparental disomy causes deficiencies of vitamin K‐dependent proteins von Dasi, M. A., Gonzalez‐Conejero, R., Izquierdo, S., Padilla, J., Garcia, J. L., Garcia‐Barberá, N., Argilés, B., Morena‐Barrio, M. E., Hernández‐Sánchez, J. M., Hernández‐Rivas, J. M., Vicente, V., Corral, J.

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Aggressive systemic mastocytosis with the co-occurrence of PRKG2::PDGFRB, KAT6A::NCOA2, and RXRA::NOTCH1 fusion transcripts and a heterozygous RUNX1 frameshift mutation von Poscente, M, Tolomeo, D, Arshadi, A, Agostini, A, L'Abbate, A, Solimando, A.G., Palumbo, O, Carella, M, Palumbo, P, González, T, Hernández-Rivas, JM, Bassi, L, Isidori, R, Dell'Aquila, M, Trapè, G, Latagliata, R, Pessina, G, Natoni, F, Storlazzi, CT

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Genome-wide profiling of methylation identifies novel targets with aberrant hypermethylation and reduced expression in low-risk myelodysplastic syndromes von del Rey, M, O'Hagan, K, Dellett, M, Aibar, S, Colyer, H A A, Alonso, M E, Díez-Campelo, M, Armstrong, R N, Sharpe, D J, Gutiérrez, N C, García, J L, De Las Rivas, J, Mills, K I, Hernández-Rivas, J M

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Gene expression profiling in MDS and AML: potential and future avenues von Theilgaard-Mönch, K, Boultwood, J, Ferrari, S, Giannopoulos, K, Hernandez-Rivas, J M, Kohlmann, A, Morgan, M, Porse, B, Tagliafico, E, Zwaan, C M, Wainscoat, J, Van den Heuvel-Eibrink, M M, Mills, K, Bullinger, L

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Mapping quantitative trait loci controlling fatty acid composition in olive von Hernández, M. L., Belaj, A., Sicardo, M. D., León, L., de la Rosa, R., Martín, A., Martínez-Rivas, J. M., Atienza, S. G.

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6q deletion in Waldenström macroglobulinemia is associated with features of adverse prognosis von Ocio, E. M., Schop, R. F. J., Gonzalez, B., Van Wier, S. A., Hernandez‐Rivas, J. M., Gutierrez, N. C., Garcia‐Sanz, R., Moro, M. J., Aguilera, C., Hernandez, J., Xu, R., Greipp, P. R., Dispenzieri, A., Jalal, S. M., Lacy, M. Q., Gonzalez‐Paz, N., Gertz, M. A., San Miguel, J. F., Fonseca, R.

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Mutation Status and Immunoglobulin Gene Rearrangements in Patients from Northwest and Central Region of Spain with Chronic Lymphocytic Leukemia von Sarasquete, M. E., Alcoceba, M., Martín, A., Hernández Rivas, José Ángel, González-Gascón y Marín, I., Rodríguez-Vicente, Ana Eugenia, Heras, C., de las Heras, N., Fisac, R., García de Coca, A., de la Fuente, I., Hernández-Sánchez, María, Recio, I., Galende, J., Martín-Núñez, G., Alonso, J. M., Hernández-Rivas, Jesús-María, González, Marcos

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Outcome after relapse of acute lymphoblastic leukemia in adult patients included in four consecutive risk-adapted trials by the PETHEMA Study Group von ORIOL, Albert, VIVES, Susana, DEL POTRO, Eloy, GUARDIA, Ramon, BRUNET, Salut, BERGUA, Juan, BERNAL, Teresa, MORENO, Maria-José, CALVO, Carlota, BASTIDA, Pilar, FELIU, Evarist, RIBERA, Josep-Maria, HERNANDEZ-RIVAS, Jesús-María, TORMO, Mar, HERAS, Inmaculada, RIVAS, Concepción, BETHENCOURT, Concepción, MOSCARDO, Federico, BUENO, Javier, GRANDE, Carlos

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P622: DOUBLE‐HIT TRAF3 DELETION AND MUTATION IDENTIFIED BY HIGH‐THROUGHPUT SEQUENCING DEFINE A NEW INDEPENDENT PROGNOSTIC FACTOR IN CHRONIC LYMPHOCYTIC LEUKEMIA von Perez‐Carretero, C., Hernández‐Sánchez, M., Quijada‐Álamo, M., González, T., Rodríguez‐Sánchez, A., Martín‐Izquierdo, M., Matías‐Martín, J., Rubio, A., Dávila, J., García de Coca, A., Galende, J., Jimenez‐Montero, P., Queizán, J.‐A., González‐Gascón y Marín, I., Hernández‐Rivas, J.‐Á., Benito, R., Hernández‐Rivas, J.‐M., Rodríguez‐Vicente, A.‐E.

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High-Frequency Resonant SEPIC Converter With Wide Input and Output Voltage Ranges von Jingying Hu, Sagneri, A. D., Rivas, J. M., Yehui Han, Davis, S. M., Perreault, D. J.

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Micro-macro consistency in multiscale modeling: Score-based model assisted sampling of fast/slow dynamical systems von Crabtree, E. R., Bello-Rivas, J. M., Kevrekidis, I. G.

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Locating saddle points using gradient extremals on manifolds adaptively revealed as point clouds von Georgiou, A., Vandecasteele, H., Bello-Rivas, J. M., Kevrekidis, I.

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