Personas / Equipo Humano

Bru Cormand Rifà

Buscador de publicaciones

Publicaciones

  • 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 citas: 18

    [doi:10.1016/j.jmoldx.2020.06.008]

  • 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 citas: 14

    [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 citas: 3

    [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 citas: 30

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

  • Esteller-Cucala P, Maceda I, Børglum AD, Demontis D, Faraone SV, Cormand B and Lao O.

    Genomic analysis of the natural history of attention-deficit/hyperactivity disorder using Neanderthal and ancient Homo sapiens samples.

    Scientific Reports . 10(1): 8622-8622. Nº de citas: 15

    [doi:10.1038/s41598-020-65322-4]

  • Fernandez-Castillo N, Gan G, van Donkelaar MMJ, Vaht M, Weber H, Retz W, Meyer-Lindenberg A, Franke B, Harro J, Reif A, Faraone SV and Cormand B.

    RBFOX1, encoding a splicing regulator, is a candidate gene for aggressive behavior.

    European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology . 30: 44-55. Nº de citas: 44

    [doi:10.1016/j.euroneuro.2017.11.012]

  • .

    Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders.

    CELL . 179(7): 1469. Nº de citas: 916

    [doi:10.1016/j.cell.2019.11.020]

  • Zhang-James Y, Fernandez-Castillo N, Hess JL, Malki K, Glatt SJ, Cormand B and Faraone SV.

    An integrated analysis of genes and functional pathways for aggression in human and rodent models.

    MOLECULAR PSYCHIATRY . 24(11): 1655-1667. Nº de citas: 62

    [doi:10.1038/s41380-018-0068-7]

  • Pineda L, Shivalikanjli A, Cabana-Domínguez J, Demontis D, Rajagopal VM, Børglum AD, Faraone SV, Cormand B and Fernandez-Castillo N.

    Exploring genetic variation that influences brain methylation in attention-deficit/hyperactivity disorder

    Translational Psychiatry . 9(1): 242-242. Nº de citas: 22

    [doi:10.1038/s41398-019-0574-7]

  • Torrico B, Shaw AD, Mosca R, Vivó-Luque N, Hervás A, Fernandez-Castillo N, Aloy P, Bayés M, Fullerton JM, Cormand B and Toma C.

    Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes.

    JOURNAL OF PSYCHIATRY & NEUROSCIENCE . 44(5): 350-359. Nº de citas: 20

    [doi:10.1503/jpn.180184]