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Publications

  • 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.

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

  • Fernandez 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 . 30: 44-55. Number of citations: 13

    [doi:10.1016/j.euroneuro.2017.11.012]

  • Cross-Disorder Group of the Psychiatric Genomics Consortium. Electronic address: and Cross-Disorder Group of the Psychiatric Genomics Consortium.

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

    Cell . 179(7): 1469. Number of citations: 157

    [doi:10.1016/j.cell.2019.11.020]

  • Zhang-James Y, Fernandez 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. Number of citations: 22

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

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

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

    TRANSLATIONAL PSYCHIATRY . 9(1): 242-242. Number of citations: 8

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

  • Torrico B, Shaw AD, Mosca R, Vivó-Luque N, Hervás A, Fernandez 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

    J PSYCHIATR NEUROSCI . 44(5): 350-359. Number of citations: 9

    [doi:10.1503/jpn.180184]

  • Cabana J, Shivalikanjli A, Fernandez N and Cormand B.

    Genome-wide association meta-analysis of cocaine dependence: Shared genetics with comorbid conditions.

    PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY . 94: 109667-109667. Number of citations: 11

    [doi:10.1016/j.pnpbp.2019.109667]

  • Chelban V, Wilson MP, Warman Chardon J, Vandrovcova J, Zanetti MN, Zamba-Papanicolaou E, Efthymiou S, Pope S, Conte MR, Abis G, Liu YT, Tribollet E, Haridy NA, Botía JA, Ryten M, Nicolaou P, Minaidou A, Christodoulou K, Kernohan KD, Eaton A, Osmond M, Ito Y, Bourque P, Jepson JEC, Bello O, Bremner F, Cordivari C, Reilly MM, Foiani M, Heslegrave A, Zetterberg H, Heales SJR, Wood NW, Rothman JE, Boycott KM, Mills PB, Clayton PT, Houlden H and Care4Rare Canada Consortium and the SYNaPS Study Group.

    PDXK mutations cause polyneuropathy responsive to pyridoxal 5'-phosphate supplementation.

    ANNALS OF NEUROLOGY . 86(2): 225-240. Number of citations: 9

    [doi:10.1002/ana.25524]

  • Salpietro V, Malintan NT, Llano-Rivas I, Spaeth CG, Efthymiou S, Striano P, Vandrovcova J, Cutrupi MC, Chimenz R, David E, Di Rosa G, Marce-Grau A, Raspall-Chaure M, Martin-Hernandez E, Zara F, Minetti C, Deciphering Developmental Disorders Study, SYNAPS Study Group, Bello OD, De Zorzi R, Fortuna S, Dauber A, Alkhawaja M, Sultan T, Mankad K, Vitobello A, Thomas Q, Mau-Them FT, Faivre L, Martinez-Azorin F, Prada CE, Alfons Macaya, Kullmann DM, Rothman JE, Krishnakumar SS and Houlden H.

    Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment.

    AMERICAN JOURNAL OF HUMAN GENETICS . 104(4): 721-730. Number of citations: 27

    [doi:10.1016/j.ajhg.2019.02.016]

  • Arcos-Burgos M, Vélez JI, Martinez AF, Ribasés M, Ramos-Quiroga JA, Sánchez-Mora C, Richarte V, Roncero C, Cormand B, Fernandez N, Casas M, Lopera F, Pineda DA, Palacio JD, Acosta-López JE, Cervantes-Henriquez ML, Sánchez-Rojas MG, Puentes-Rozo PJ, Molina BSG, MTA Cooperative Group, Boden MT, Wallis D, Lidbury B, Newman S, Easteal S, Swanson J, Patel H, Volkow N, Acosta MT, Castellanos FX, de Leon J, Mastronardi CA and Muenke M.

    ADGRL3 (LPHN3) variants predict substance use disorder

    TRANSLATIONAL PSYCHIATRY . 9: 42-42. Number of citations: 9

    [doi:10.1038/s41398-019-0396-7]