Persones / Equip Humà

Bru Cormand Rifà

Buscador de publicacions

Publicacions

  • Pineda L, Cabana-Domínguez J, Grau-López L, Daigre C, Sánchez-Mora C, Palma-Álvarez RF, Ramos-Quiroga JA, Ribasés M, Cormand B and Fernandez-Castillo N.

    Exploring allele specific methylation in drug dependence susceptibility.

    JOURNAL OF PSYCHIATRIC RESEARCH . 136: 474-482. Nº de cites: 1

    [doi:10.1016/j.jpsychires.2020.07.044]

  • Demontis, Ditte, Walters, Raymond K, Rajagopal, Veera M, Waldman, Irwin D, Grove, Jakob, Als, Thomas D, Dalsgaard, Soren, Ribasas, Marta, Bybjerg-Grauholm, Jonas, Bakvad-Hansen, Maria, Werge, Thomas, Nordentoft, Merete, Mors, Ole, Mortensen, Preben Bo, Cormand B, Hougaard, David M, Neale, Benjamin M, Franke, Barbara, Faraone, Stephen V and Borglum, Anders D.

    Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

    NATURE COMMUNICATIONS . 12(1): 576-576. Nº de cites: 19

    [doi:10.1038/s41467-020-20443-2]

  • Vaht M, Laas K, Fernandez-Castillo N, Kurrikoff T, Kanarik M, Faraone SV, Tooding LM, Veidebaum T, Franke B, Reif A, Cormand B and Harro J.

    Variants of the Aggression-Related RBFOX1 Gene in a Population Representative Birth Cohort Study: Aggressiveness, Personality, and Alcohol Use Disorder.

    Frontiers in Psychiatry . 11: 501847-501847. Nº de cites: 2

    [doi:10.3389/fpsyt.2020.501847]

  • Navas-Pérez E, Vicente-García C, Mirra S, Burguera D, Fernandez-Castillo N, Ferrán JL, López-Mayorga M, Alaiz-Noya M, Suárez-Pereira I, Antón-Galindo E, Ulloa F, Herrera-Úbeda C, Cuscó P, Falcón-Moya R, Rodríguez-Moreno A, D'Aniello S, Cormand B, Marfany G, Soriano E, Carrión ÁM, Carvajal JJ and Garcia-Fernàndez J.

    Characterization of an eutherian gene cluster generated after transposon domestication identifies Bex3 as relevant for advanced neurological functions.

    Genome Biology . 21(1): 267-267. Nº de cites: 12

    [doi:10.1186/s13059-020-02172-3]

  • Matalonga L, Laurie S, Papakonstantinou A, Piscia D, Mereu E, Bullich G, Thompson R, Horvath R, Pérez-Jurado L, Riess O, Gut I, van Ommen GJ, Lochmüller H, Beltran S and RD–Connect Genome-Phenome Analysis Platform and URD-Cat Data Contributors.

    Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity

    JOURNAL OF MOLECULAR DIAGNOSTICS . 22(9): 1205-1215. Nº de cites: 15

    [doi:10.1016/j.jmoldx.2020.06.008]

  • Rovira P, Demontis D, Sánchez-Mora C, Zayats T, Klein M, Mota NR, Weber H, Garcia-Martínez I, Pagerols M, Vilar L, Arribas L, Richarte V, Corrales M, Fadeuilhe C, Bosch R, Martin GE, Almos P, Doyle AE, Grevet EH, Grimm O, Halmøy A, Hoogman M, Hutz M, Jacob CP, Kittel-Schneider S, Knappskog PM, Lundervold AJ, Rivero O, Rovaris DL, Salatino-Oliveira A, da Silva BS, Svirin E, Sprooten E, Strekalova T, ADHD Working Group of the Psychiatric Genomics Consortium, 23andMe Research team, Arias-Vasquez A, Sonuga-Barke EJS, Asherson P, Bau CHD, Buitelaar JK, Cormand B, Faraone SV, Haavik J, Johansson SE, Kuntsi J, Larsson H, Lesch KP, Reif A, Rohde LA, Casas M, Børglum AD, Franke B, Ramos-Quiroga JA, Artigas MS and Ribasés M.

    Shared genetic background between children and adults with attention deficit/hyperactivity disorder.

    NEUROPSYCHOPHARMACOLOGY . 45(10): 1617-1626. Nº de cites: 64

    [doi:10.1038/s41386-020-0664-5]

  • Corominas J, Klein M, Zayats T, Rivero O, Ziegler GC, Pauper M, Neveling K, Poelmans G, Jansch C, Svirin E, Geissler J, Weber H, Reif A, Arias Vasquez A, Galesloot TE, Kiemeney LALM, Buitelaar JK, Ramos-Quiroga JA, Cormand B, Ribasés M, Hveem K, Gabrielsen ME, Hoffmann P, Cichon S, Haavik J, Johansson S, Jacob CP, Romanos M, Franke B and Lesch KP.

    Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing.

    MOLECULAR PSYCHIATRY . 25(9): 2047-2057. Nº de cites: 17

    [doi:10.1038/s41380-018-0210-6]

  • Torrico B, Antón-Galindo E, Fernandez-Castillo N, Rojo-Francàs E, Ghorbani S, Pineda L, Hervás A, Rueda I, Moreno E, Fullerton JM, Casadó V, Buitelaar JK, Rommelse N, Franke B, Reif A, Chiocchetti AG, Freitag C, Kleppe R, Haavik J, Toma C and Cormand B.

    Involvement of the 14-3-3 Gene Family in Autism Spectrum Disorder and Schizophrenia: Genetics, Transcriptomics and Functional Analyses.

    Journal of Clinical Medicine . 9(6): . Nº de cites: 12

    [doi:10.3390/jcm9061851]

  • Pineda L, Cabana-Domínguez J, Beneto N, Diez H, Arenas C, Cormand B and Fernandez-Castillo N.

    DDC expression is not regulated by NFAT5 (TonEBP) in dopaminergic neural cell lines.

    Gene . 742: 144569-144569. Nº de cites: 1

    [doi:10.1016/j.gene.2020.144569]

  • Roth Mota N, Poelmans G, Klein M, Torrico B, Fernandez-Castillo N, Cormand B, Reif A, Franke B and Arias Vásquez A.

    Cross-disorder genetic analyses implicate dopaminergic signaling as a biological link between Attention-Deficit/Hyperactivity Disorder and obesity measures.

    NEUROPSYCHOPHARMACOLOGY . 45(7): 1188-1195. Nº de cites: 26

    [doi:10.1038/s41386-019-0592-4]