Persones / Equip Humà

Bru Cormand Rifà

Buscador de publicacions

Publicacions

  • Welander NZ, Rukh G, Rask-Andersen M, Harder AVE, van den Maagdenberg AMJM, Schiöth HB and Mwinyi J.

    Migraine, inflammatory bowel disease and celiac disease: A Mendelian randomization study.

    Headache . 63(5): 642-651. Nº de cites: 5

    [doi:10.1111/head.14470]

  • Zhao L, Zhao W, Cao J and Tu Y.

    Causal relationships between migraine and microstructural white matter: a Mendelian randomization study.

    JOURNAL OF HEADACHE AND PAIN . 24(1): 10-10. Nº de cites: 13

    [doi:10.1186/s10194-023-01550-z]

  • Vila-Pueyo M, Cuenca-León E, Queirós AC, Kulis M, Sintas C, Cormand B, Martín-Subero JI, Pozo-Rosich P, Fernandez-Castillo N and Macaya A.

    Genome-wide DNA methylation analysis in an antimigraine-treated preclinical model of cortical spreading depolarization

    Cephalalgia . 43(2): . Nº de cites: 6

    [doi:10.1177/03331024221146317]

  • Demontis D, Walters GB, Athanasiadis G, Walters R, Therrien K, Nielsen TT, Farajzadeh L, Voloudakis G, Bendl J, Zeng B, Zhang W, Grove J, Als TD, Duan J, Satterstrom FK, Bybjerg-Grauholm J, Bækved-Hansen M, Gudmundsson OO, Magnusson SH, Baldursson G, Davidsdottir K, Haraldsdottir GS, Agerbo E, Hoffman GE, Dalsgaard S, Martin J, Ribasés M, Boomsma DI, Soler Artigas M, Roth Mota N, Howrigan D, Medland SE, Zayats T, Rajagopal VM, Nordentoft M, Mors O, Hougaard DM, Mortensen PB, Daly MJ, Faraone SV, Stefansson H, Roussos P, Franke B, Werge T, Neale BM, Stefansson K and Børglum AD.

    Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains.

    NATURE GENETICS . 55(2): 198-208. Nº de cites: 165

    [doi:10.1038/s41588-022-01285-8]

  • Cabana-Domínguez J, Anton-Galindo E, Fernandez-Castillo N, Singgih EL, O'Leary A, Norton WH, Strekalova T, Schenck A, Reif A, Lesch KP, Slattery D and Cormand B.

    The translational genetics of ADHD and related phenotypes in model organisms

    NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS . 144: 104949-104949. Nº de cites: 4

    [doi:10.1016/j.neubiorev.2022.104949]

  • O'Leary, A, Fernandez-Castillo N, Gan, G, Yang, YB, Yotova, AY, Kranz, TM, Grunewald, L, Freudenberg, F, Anton-Galindo, E, Cabana-Domínguez J, Harneit, A, Schweiger, JI, Schwarz, K, Ma, R, Chen, JF, Schwarz, E, Rietschel, M, Tost, H, Meyer-Lindenberg, A, Pane-Farre, CA, Kircher, T, Hamm, AO, Burguera, D, Mota, NR, Franke, B, Schweiger, S, Winter, J, Heinz, A, Erk, S, Romanczuk-Seiferth, N, Walter, H, Ströhle A, Fehm, L, Fydrich, T, Lueken, U, Weber, H, Lang, T, Gerlach, AL, Nöthen MM, Alpers, GW, Arolt, V, Witt, S, Richter, J, Straube, B, Cormand B, Slattery, DA and Reif, A.

    Behavioural and functional evidence revealing the role of RBFOX1 variation in multiple psychiatric disorders and traits

    MOLECULAR PSYCHIATRY . 27(11): 4464-4473. Nº de cites: 18

    [doi:10.1038/s41380-022-01722-4]

  • Weiner DJ, Ling E, Erdin S, Tai DJC, Yadav R, Grove J, Fu JM, Nadig A, Carey CE, Baya N, Bybjerg-Grauholm J, Berretta S, Macosko EZ, Sebat J, O'Connor LJ, Hougaard DM, Børglum AD, Talkowski ME, McCarroll SA and Robinson EB.

    Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p.

    NATURE GENETICS . 54(11): 1630-1639. Nº de cites: 15

    [doi:10.1038/s41588-022-01203-y]

  • Mattheisen, M, Grove, J, Als, TD, Martin, J, Voloudakis, G, Meier, S, Demontis, D, Bendl, J, Walters, R, Carey, CE, Rosengren, A, Strom, NI, Hauberg, ME, Zeng, B, Hoffman, G, Zhang, W, Bybjerg-Grauholm, J, Bækvad-Hansen M, Agerbo, E, Cormand B, Nordentoft, M, Werge, T, Mors, O, Hougaard, DM, Buxbaum, JD, Faraone, SV, Franke, B, Dalsgaard, S, Mortensen, PB, Robinson, EB, Roussos, P, Neale, BM, Daly, MJ and Børglum AD.

    Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups

    NATURE GENETICS . 54(10): 1470-1478. Nº de cites: 27

    [doi:10.1038/s41588-022-01171-3]

  • Vainieri I, Martin J, Rommel AS, Asherson P, Banaschewski T, Buitelaar J, Cormand B, Crosbie J, Faraone SV, Franke B, Loo SK, Miranda A, Manor I, Oades RD, Purves KL, Ramos-Quiroga JA, Ribasés M, Roeyers H, Rothenberger A, Schachar R, Sergeant J, Steinhausen HC, Vuijk PJ, Doyle AE and Kuntsi J.

    Polygenic association between attention-deficit/hyperactivity disorder liability and cognitive impairments.

    PSYCHOLOGICAL MEDICINE . 52(14): 3150-3158. Nº de cites: 7

    [doi:10.1017/S0033291720005218]

  • Mitchell BL, Diaz-Torres S, Bivol S, Cuellar-Partida G, Gerring ZF, Martin NG, Medland SE, Grasby KL, Nyholt DR and Rentería ME.

    Elucidating the relationship between migraine risk and brain structure using genetic data.

    BRAIN . 145(9): 3214-3224. Nº de cites: 15

    [doi:10.1093/brain/awac105]