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Publications

  • Brevik EJ, van Donkelaar MM, Weber H, Sánchez-Mora C, Jacob C, Rivero O, Kittel-Schneider S, Garcia-Martínez I, Aebi M, van Hulzen K, Cormand B, Ramos-Quiroga JA, IMAGE Consortium, Lesch KP, Reif A, Ribasés M, Franke B, Posserud MB, Johansson S, Lundervold AJ, Haavik J and Zayats T.

    Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder.

    AM J MED GENET B . 171(5): 733-747. Number of citations: 26

    [doi:10.1002/ajmg.b.32434]

  • Fernandez N and Cormand B.

    Aggressive behavior in humans: Genes and pathways identified through association studies.

    AM J MED GENET B . 171(5): 676-696. Number of citations: 39

    [doi:10.1002/ajmg.b.32419]

  • Urreizti R, Roca N, Trepat J, Garcia-Garcia F, Aleman A, Orteschi D, Marangi G, Neri G, Opitz JM, Dopazo J, Cormand B, Vilageliu L, Balcells S and Grinberg-Vaisman DR.

    Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes.

    AMERICAN JOURNAL OF MEDICAL GENETICS PART A . 170A(1): 24-31. Number of citations: 9

    [doi:10.1002/ajmg.a.37418]

  • Veroude K, Zhang-James Y, Fernandez N, Bakker MJ, Cormand B and Faraone SV.

    Genetics of aggressive behavior: An overview.

    AM J MED GENET B . 171B(1): 3-43. Number of citations: 64

    [doi:10.1002/ajmg.b.32364]

  • Alemany S, Ribasés M, Vilor-Tejedor N, Bustamante M, Sánchez-Mora C, Bosch R, Richarte V, Cormand B, Casas M, Ramos-Quiroga JA and Sunyer J.

    New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder.

    AM J MED GENET B . 168(6): 459-470. Number of citations: 32

    [doi:10.1002/ajmg.b.32341]

  • Sánchez-Mora C, Richarte V, Garcia-Martínez I, Pagerols M, Corrales M, Bosch R, Vidal R, Viladevall L, Casas M, Cormand B, Ramos-Quiroga JA and Ribasés M.

    Dopamine receptor DRD4 gene and stressful life events in persistent attention deficit hyperactivity disorder.

    AM J MED GENET B . 168(6): 480-491. Number of citations: 11

    [doi:10.1002/ajmg.b.32340]

  • Weber H, Kittel-Schneider S, Heupel J, Weißflog L, Kent L, Freudenberg F, Alttoa A, Post A, Herterich S, Haavik J, Halmøy A, Fasmer OB, Landaas ET, Johansson S, Cormand B, Ribasés M, Sánchez-Mora C, Ramos-Quiroga JA, Franke B, Lesch KP and Reif A.

    On the role of NOS1 ex1f-VNTR in ADHD-allelic, subgroup, and meta-analysis.

    AM J MED GENET B . 168(6): 445-458. Number of citations: 13

    [doi:10.1002/ajmg.b.32326]

  • Gómez-Grau M, Garrido E, Cozar M, Rodriguez-Sureda V, Domínguez C, Arenas C, Gatti RA, Cormand B, Grinberg-Vaisman DR and Vilageliu L.

    Evaluation of Aminoglycoside and Non-Aminoglycoside Compounds for Stop-Codon Readthrough Therapy in Four Lysosomal Storage Diseases.

    PLoS One . 10(8): e0135873. Number of citations: 21

    [doi:10.1371/journal.pone.0135873]

  • Sintas C, Fernández-Morales J, Vila-Pueyo M, Narberhaus B, Arenas C, Pozo-Rosich P, Macaya A and Cormand B.

    Replication study of previous migraine genome-wide association study findings in a Spanish sample of migraine with aura

    Cephalalgia . 35(9): 776-782. Number of citations: 17

    [doi:10.1177/0333102414557841]

  • Louter MA, Fernandez-Morales J, de Vries B, Winsvold B, Anttila V, Fernandez-Cadenas I, Vila-Pueyo M, Sintas C, van Duijn CM, Cormand B, Álvarez-Sabin J, Montaner J, Ferrari MD, van den Maagdenberg A, Palotie A, Zwart JA, Macaya A, Terwindt GM and Pozo-Rosich P.

    Candidate-gene association study searching for genetic factors involved in migraine chronification

    Cephalalgia . 35(6): 500-507. Number of citations: 11

    [doi:10.1177/0333102414547141]