Works matching AU Bayés, Mònica

Results: 18
    1
    2

    The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases.

    Published in:
    Human Mutation, 2022, v. 43, n. 6, p. 717, doi. 10.1002/humu.24353
    By:
    • Laurie, Steven;
    • Piscia, Davide;
    • Matalonga, Leslie;
    • Corvó, Alberto;
    • Fernández‐Callejo, Marcos;
    • Garcia‐Linares, Carles;
    • Hernandez‐Ferrer, Carles;
    • Luengo, Cristina;
    • Martínez, Inés;
    • Papakonstantinou, Anastasios;
    • Picó‐Amador, Daniel;
    • Protasio, Joan;
    • Thompson, Rachel;
    • Tonda, Raul;
    • Bayés, Mònica;
    • Bullich, Gemma;
    • Camps‐Puchadas, Jordi;
    • Paramonov, Ida;
    • Trotta, Jean‐Rémi;
    • Alonso, Angel
    Publication type:
    Article
    3
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    Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy.

    Published in:
    Nature Genetics, 2013, v. 45, n. 12, p. 1464, doi. 10.1038/ng.2799
    By:
    • Balbás-Martínez, Cristina;
    • Sagrera, Ana;
    • Carrillo-de-Santa-Pau, Enrique;
    • Earl, Julie;
    • Márquez, Mirari;
    • Vazquez, Miguel;
    • Lapi, Eleonora;
    • Castro-Giner, Francesc;
    • Beltran, Sergi;
    • Bayés, Mònica;
    • Carrato, Alfredo;
    • Cigudosa, Juan C;
    • Domínguez, Orlando;
    • Gut, Marta;
    • Herranz, Jesús;
    • Juanpere, Núria;
    • Kogevinas, Manolis;
    • Langa, Xavier;
    • López-Knowles, Elena;
    • Lorente, José A
    Publication type:
    Article
    5

    Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor.

    Published in:
    BMC Genomics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2164-14-371
    By:
    • Llorens, Franc;
    • Hummel, Manuela;
    • Pantano, Lorena;
    • Pastor, Xavier;
    • Vivancos, Ana;
    • Castillo, Ester;
    • Mattlin, Heidi;
    • Ferrer, Anna;
    • Ingham, Matthew;
    • Noguera, Marc;
    • Kofler, Robert;
    • Dohm, Juliane C.;
    • Pluvinet, Raquel;
    • Bayés, Mònica;
    • Himmelbauer, Heinz;
    • del Rio, José Antonio;
    • Martí, Eulàlia;
    • Sumoy, Lauro
    Publication type:
    Article
    6

    Multiple platform assessment of the EGF dependent transcriptome by microarray and deep tag sequencing analysis.

    Published in:
    BMC Genomics, 2011, v. 12, n. 1, p. 326, doi. 10.1186/1471-2164-12-326
    By:
    • Llorens, Franc;
    • Hummel, Manuela;
    • Pastor, Xavier;
    • Ferrer, Anna;
    • Pluvinet, Raquel;
    • Vivancos, Ana;
    • Castillo, Ester;
    • Iraola, Susana;
    • Mosquera, Ana M.;
    • González, Eva;
    • Lozano, Juanjo;
    • Ingham, Matthew;
    • Dohm, Juliane C.;
    • Noguera, Marc;
    • Kofler, Robert;
    • Río, Jose Antonio del;
    • Bayés, Mònica;
    • Himmelbauer, Heinz;
    • Sumoy, Lauro
    Publication type:
    Article
    7

    Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC.

    Published in:
    World Journal of Biological Psychiatry, 2013, v. 14, n. 7, p. 516, doi. 10.3109/15622975.2011.602719
    By:
    • Toma, Claudio;
    • Hervás, Amaia;
    • Balmaña, Noemí;
    • Salgado, Marta;
    • Maristany, Marta;
    • Vilella, Elisabet;
    • Aguilera, Francisco;
    • Orejuela, Carmen;
    • Cuscó, Ivon;
    • Gallastegui, Fátima;
    • Pérez-Jurado, Luis Alberto;
    • Caballero-Andaluz, Rafaela;
    • Diego-Otero, Yolanda de;
    • Guzmán-Alvarez, Guadalupe;
    • Ramos-Quiroga, Josep Antoni;
    • Ribasés, Marta;
    • Bayés, Mònica;
    • Cormand, Bru
    Publication type:
    Article
    8

    Candidate system analysis in ADHD: Evaluation of nine genes involved in dopaminergic neurotransmission identifies association with DRD1.

    Published in:
    World Journal of Biological Psychiatry, 2012, v. 13, n. 4, p. 281, doi. 10.3109/15622975.2011.584905
    By:
    • RibaséS, Marta;
    • Ramos-Quiroga, Josep Antoni;
    • HerváS, Amaia;
    • Sánchez-Mora, Cristina;
    • Bosch, Rosa;
    • Bielsa, Anna;
    • Gastaminza, Xavier;
    • Lesch, Klaus-Peter;
    • Reif, Andreas;
    • Renner, Tobias J.;
    • Romanos, Marcel;
    • Warnke, Andreas;
    • Walitza, Susanne;
    • Freitag, Christine;
    • Meyer, Jobst;
    • Palmason, Haukur;
    • Casas, Miquel;
    • Bayés, Mònica;
    • Cormand, Bru
    Publication type:
    Article
    9
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    11

    Case-Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the Disorder.

    Published in:
    Neuropsychopharmacology, 2015, v. 40, n. 4, p. 915, doi. 10.1038/npp.2014.267
    By:
    • Sánchez-Mora, Cristina;
    • Ribasés, Marta;
    • Hinney, Anke;
    • Hoogman, Martine;
    • Klein, Marieke;
    • Jacobsen, Kaya K;
    • Zayats, Tetyana;
    • Haavik, Jan;
    • Johansson, Stefan;
    • Kan, Cornelis C;
    • Kiemeney, Lambertus;
    • Onnink, Marten;
    • Franke, Barbara;
    • Rivero, Olga;
    • Lesch, Klaus-Peter;
    • Buitelaar, Jan;
    • Faraone, Stephen V;
    • Bayés, Mònica;
    • Ramos-Quiroga, Josep A;
    • Casas, Miguel
    Publication type:
    Article
    12

    Differential Association of Circadian Genes with Mood Disorders: CRY1 and NPAS2 are Associated with Unipolar Major Depression and CLOCK and VIP with Bipolar Disorder.

    Published in:
    Neuropsychopharmacology, 2010, v. 35, n. 6, p. 1279, doi. 10.1038/npp.2009.230
    By:
    • Soria, ,3Virginia;
    • Martínez-Amorós, Èrika;
    • Escaramís, Geòrgia;
    • Valero, Joaquín;
    • Pérez-Egea, Rosario;
    • García, Cecilia;
    • Gutiérrez-Zotes, Alfonso;
    • Puigdemont, Dolors;
    • Bayés, Mònica;
    • Crespo, José M.;
    • Martorell, Lourdes;
    • Vilella, Elisabet;
    • Labad, Antonio;
    • Vallejo, Julio;
    • Pérez, Víctor;
    • Menchón, José M.;
    • Estivill, Xavier;
    • Gratacòs, Mònica;
    • Urretavizcaya, Mikel
    Publication type:
    Article
    13

    Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD.

    Published in:
    Neuropsychopharmacology, 2010, v. 35, n. 3, p. 656, doi. 10.1038/npp.2009.170
    By:
    • Franke, Barbara;
    • Vasquez, Alejandro Arias;
    • Johansson, Stefan;
    • Hoogman, Martine;
    • Romanos, Jasmin;
    • Boreatti-Hümmer, Andrea;
    • Heine, Monika;
    • Jacob, Christian P.;
    • Lesch, Klaus-Peter;
    • Casas, Miguel;
    • Ribasés, Marta;
    • Bosch, Rosa;
    • Sánchez-Mora, Cristina;
    • Gómez-Barros, Núria;
    • Fernàndez-Castillo, Noèlia;
    • Bayés, Mònica;
    • Halmøy, Anne;
    • Halleland, Helene;
    • Landaas, Elisabeth T.;
    • Fasmer, Ole B.
    Publication type:
    Article
    14

    Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders.

    Published in:
    Human Molecular Genetics, 2008, v. 17, n. 9, p. 1234, doi. 10.1093/hmg/ddn013
    By:
    • Mercader, Josep Maria;
    • Saus, Ester;
    • Agüera, Zaida;
    • Bayés, Mònica;
    • Boni, Claudette;
    • Carreras, Anna;
    • Cellini, Elena;
    • de Cid, Rafael;
    • Dierssen, Mara;
    • Escaramís, Geòrgia;
    • Fernández-Aranda, Fernando;
    • Forcano, Laura;
    • Gallego, Xavier;
    • González, Juan Ramón;
    • Gorwood, Philip;
    • Hebebrand, Johannes;
    • Hinney, Anke;
    • Nacmias, Benedetta;
    • Puig, Anna;
    • Ribasés, Marta
    Publication type:
    Article
    15
    16

    Resequencing and association analysis of arylalkylamine N-acetyltransferase ( AANAT) gene and its contribution to major depression susceptibility.

    Published in:
    Journal of Pineal Research, 2010, v. 49, n. 1, p. 35, doi. 10.1111/j.1600-079X.2010.00763.x
    By:
    • Soria, Virginia;
    • Martínez-Amorós, Èrika;
    • Escaramís, Geòrgia;
    • Valero, Joaquín;
    • Crespo, José M.;
    • Gutiérrez-Zotes, Alfonso;
    • Bayés, Mònica;
    • Martorell, Lourdes;
    • Vilella, Elisabet;
    • Estivill, Xavier;
    • Menchón, José M.;
    • Gratacòs, Mònica;
    • Urretavizcaya, Mikel
    Publication type:
    Article
    17

    The Catalan initiative for the Earth BioGenome Project: contributing local data to global biodiversity genomics.

    Published in:
    NAR Genomics & Bioinformatics, 2024, v. 6, n. 3, p. 1, doi. 10.1093/nargab/lqae075
    By:
    • Corominas, Montserrat;
    • Marquès-Bonet, Tomàs;
    • Arnedo, Miquel A;
    • Bayés, Mònica;
    • Belmonte, Jordina;
    • Escrivà, Hector;
    • Fernández, Rosa;
    • Gabaldón, Toni;
    • Garnatje, Teresa;
    • Germain, Josep;
    • Niell, Manel;
    • Palero, Ferran;
    • Pons, Joan;
    • Puigdomènech, Pere;
    • Project, The Catalan initiative for the Earth BioGenome;
    • Arroyo, Vanesa;
    • Cuevas-Caballé, Cristian;
    • Obiol, Joan Ferrer;
    • Gut, Ivo;
    • Gut, Marta
    Publication type:
    Article
    18

    Homozygous tandem duplication within the gene encoding the β-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa.

    Published in:
    Human Mutation, 1995, v. 5, n. 3, p. 228, doi. 10.1002/humu.1380050307
    By:
    • Bayés, Mònica;
    • Giordano, Mara;
    • Balcells, Susana;
    • Grinberg, Daniel;
    • Vilageliu, Llusïsa;
    • Martínez, Immaculada;
    • Ayuso, Carmen;
    • Benítez, Javier;
    • Ramos-Arroyo, María A.;
    • Chivelet, Pilar;
    • Solans, Teresa;
    • Valverde, Diana;
    • Amselem, Serge;
    • Goossens, Michel;
    • Baiget, Montserrat;
    • Gonzàlez-Duarte, Roser;
    • Besmond, Claude
    Publication type:
    Article