Persones / Equip Humà

Bru Cormand Rifà

Buscador de publicacions

Publicacions

  • Martin J, Walters RK, Demontis D, Mattheisen M, Lee SH, Robinson E, Brikell I, Ghirardi L, Larsson H, Lichtenstein P, Eriksson N, 23andMe Research Team, Psychiatric Genomics Consortium: ADHD Subgroup, iPSYCH–Broad ADHD Workgroup, Werge T, Mortensen PB, Pedersen MG, Mors O, Nordentoft M, Hougaard DM, Bybjerg-Grauholm J, Wray NR, Franke B, Faraone SV, O'Donovan MC, Thapar A, Børglum AD and Neale BM.

    A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder

    BIOLOGICAL PSYCHIATRY . 83(12): 1044-1053. Nº de cites: 97

    [doi:10.1016/j.biopsych.2017.11.026]

  • Pineda L, Cabana-Domínguez J, Roncero C, Cozar M, Grau-López L, Abad AC, Martínez-Luna N, Robles-Martínez M, Sánchez-Mora C, Ramos-Quiroga JA, Casas M, Ribasés M, Fernandez-Castillo N and Cormand B.

    Evaluation of previous substance dependence genome-wide significant findings in a Spanish sample.

    DRUG AND ALCOHOL DEPENDENCE . 187: 358-362. Nº de cites: 3

    [doi:10.1016/j.drugalcdep.2018.03.013]

  • Gormley P, Kurki MI, Hiekkala ME, Veerapen K, Häppölä P, Mitchell AA, Lal D, Palta P, Surakka I, Kaunisto MA, Hämäläinen E, Vepsäläinen S, Havanka H, Harno H, Ilmavirta M, Nissilä M, Säkö E, Sumelahti ML, Liukkonen J, Sillanpää M, Metsähonkala L, Koskinen S, Lehtimäki T, Raitakari O, Männikkö M, Ran C, Belin AC, Jousilahti P, Anttila V, Salomaa V, Artto V, Färkkilä M, 23andMe Research Team, International Headache Genetics Consortium (IHGC), Runz H, Daly MJ, Neale BM, Ripatti S, Kallela M, Wessman M and Palotie A.

    Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families.

    Neuron . 98(4): 743. Nº de cites: 32

    [doi:10.1016/j.neuron.2018.04.014]

  • Brandler WM, Antaki D, Gujral M, Kleiber ML, Whitney J, Maile MS, Hong O, Chapman TR, Tan S, Tandon P, Pang T, Tang SC, Vaux KK, Yang Y, Harrington E, Juul S, Turner DJ, Thiruvahindrapuram B, Kaur G, Wang Z, Kingsmore SF, Gleeson JG, Bisson D, Kakaradov B, Telenti A, Venter JC, Corominas R, Toma C, Cormand B, Rueda I, Guijarro S, Messer KS, Nievergelt CM, Arranz MJ, Courchesne E, Pierce K, Muotri AR, Iakoucheva LM, Hervás A, Scherer SW, Corsello C and Sebat J.

    Paternally inherited cis-regulatory structural variants are associated with autism.

    SCIENCE . 360(6386): 327-331. Nº de cites: 118

    [doi:10.1126/science.aan2261]

  • Pagerols M, Richarte V, Sánchez-Mora C, Rovira P, Soler Artigas M, Garcia-Martínez I, Calvo-Sánchez E, Corrales M, da Silva BS, Mota NR, Victor MM, Rohde LA, Grevet EH, Bau CHD, Cormand B, Casas M, Ramos-Quiroga JA and Ribasés M.

    Integrative genomic analysis of methylphenidate response in attention-deficit/hyperactivity disorder.

    SCIENTIFIC REPORTS . 8(1): 1881-1881. Nº de cites: 11

    [doi:10.1038/s41598-018-20194-7]

  • Urreizti R, Damanti S, Esteve-Matanza C, Franco-Valls H, Castilla-Vallmanya L, Tonda R, Cormand B, Vilageliu L, Opitz JM, Neri G, Grinberg-Vaisman DR and Balcells S.

    A De Novo FOXP1 Truncating Mutation in a Patient Originally Diagnosed as C Syndrome

    SCIENTIFIC REPORTS . 8: 694-694. Nº de cites: 11

    [doi:10.1038/s41598-017-19109-9]

  • Cabana-Domínguez J, Roncero C, Pineda L, Palma-Álvarez RF, Ros-Cucurull E, Grau-López L, Esojo A, Casas M, Arenas C, Ramos-Quiroga JA, Ribasés M, Fernandez-Castillo N and Cormand B.

    Association of the PLCB1 gene with drug dependence.

    SCIENTIFIC REPORTS . 7(1): 10110-10110. Nº de cites: 12

    [doi:10.1038/s41598-017-10207-2]

  • Garcia-Martínez I, Sánchez-Mora C, Soler Artigas M, Rovira P, Pagerols M, Corrales M, Calvo-Sánchez E, Richarte V, Bustamante M, Sunyer J, Cormand B, Casas M, Ramos-Quiroga JA and Ribasés M.

    Gene-wide Association Study Reveals RNF122 Ubiquitin Ligase as a Novel Susceptibility Gene for Attention Deficit Hyperactivity Disorder.

    SCIENTIFIC REPORTS . 7(1): 5407-5407. Nº de cites: 10

    [doi:10.1038/s41598-017-05514-7]

  • Sintas C, Carreño O, Fernandez-Castillo N, Corominas R, Vila-Pueyo M, Toma C, Cuenca-León E, Barroeta I, Roig C, Volpini V, Macaya A and Cormand B.

    Mutation Spectrum in the CACNA1A Gene in 49 Patients with Episodic Ataxia.

    SCIENTIFIC REPORTS . 7(1): 2514-2514. Nº de cites: 26

    [doi:10.1038/s41598-017-02554-x]

  • Sintas C, Fernàndez-Castillo N, Vila-Pueyo M, Pozo-Rosich P, Macaya A and Cormand B.

    Transcriptomic Changes in Rat Cortex and Brainstem After Cortical Spreading Depression With or Without Pretreatment With Migraine Prophylactic Drugs.

    JOURNAL OF PAIN . 18(4): 366-375. Nº de cites: 3

    [doi:10.1016/j.jpain.2016.11.007]