Persones / Equip Humà

Bru Cormand Rifà

Buscador de publicacions

Publicacions

  • Ramos-Quiroga JA, Sánchez-Mora C, Casas M, Garcia-Martínez I, Bosch R, Nogueira M, Corrales M, Palomar G, Vidal R, Coll-Tané M, Bayés M, Cormand B and Ribasés M.

    Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder.

    JOURNAL OF PSYCHIATRIC RESEARCH . 49: 60-67. Nº de cites: 44

    [doi:10.1016/j.jpsychires.2013.10.022]

  • Tristan-Noguero A, Fernandez-Castillo N, Roncero C, Sánchez-Mora C, Ramos-Quiroga JA, Daigre C, Egido A, Alvarós J, GEMMA PRAT VIGUÉ, Casas M, Cormand B and Ribasés M.

    Lack of association between the LPR and VNTR polymorphisms of the serotonin transporter gene and cocaine dependence in a Spanish sample

    PSYCHIATRY RESEARCH . 210(3): 1287-1289. Nº de cites: 4

    [doi:10.1016/j.psychres.2013.09.004]

  • Carreño O, Corominas R, Serra SA, Sintas C, Fernández-Castillo N, Vila-Pueyo M, Toma C, Gené GG, Pons R, Llaneza M, Sobrido MJ, Grinberg-Vaisman DR, Valverde MÁ, Fernández-Fernández JM, Macaya A and Cormand B.

    Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies.

    Molecular genetics & genomic medicine . 1(4): 206-222.

    [doi:10.1002/mgg3.24]

  • Toma C, Hervás A, Balmaña N, Salgado M, Maristany M, Vilella E, Aguilera F, Orejuela C, Cuscó I, Gallastegui F, Pérez-Jurado LA, Caballero-Andaluz R, Diego-Otero Yd, Guzmán-Alvarez G, Ramos-Quiroga JA, Ribasés M, Bayés M and Cormand B.

    Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC.

    WORLD JOURNAL OF BIOLOGICAL PSYCHIATRY . 14(7): 516-527. Nº de cites: 30

    [doi:10.3109/15622975.2011.602719]

  • Toma C, Hervás A, Torrico B, Balmaña N, Salgado M, Maristany M, Vilella E, Martínez-Leal R, Planelles MI, Cuscó I, del Campo M, Pérez-Jurado LA, Caballero-Andaluz R, de Diego-Otero Y, Pérez-Costillas L, Ramos-Quiroga JA, Ribasés M, Bayés M and Cormand B.

    Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2

    PSYCHIATRIC GENETICS . 23(2): 82-85. Nº de cites: 45

    [doi:10.1097/YPG.0b013e32835d6fc6]

  • Sánchez-Mora C, Ribasés M, Ramos-Quiroga JA, Casas M, Bosch R, Boreatti-Hümmer A, Heine M, Jacob CP, Lesch KP, Fasmer OB, Knappskog PM, Kooij JJS, Kan C, Buitelaar JK, Mick E, Asherson P, Faraone SV, Franke B, Johansson S, Haavik J, Reif A, Bayés M and Cormand B.

    Meta-analysis of brain-derived neurotrophic factor p.Val66Met in adult ADHD in four European populations.

    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS . 153B(2): 512-523. Nº de cites: 50

    [doi:10.1002/ajmg.b.31008]

  • Chabás A, Cormand B, Balcells S, Gonzalez R, Casanova C, Colomer J, Vilageliu L and Grinberg-Vaisman DR.

    Neuronopathic and non-neuronopathic presentation of Gaucher disease in patients with the third most common mutation (D409H) in Spain.

    JOURNAL OF INHERITED METABOLIC DISEASE . 19(6): 798-800. Nº de cites: 15

    [doi:10.1007/BF01799179]

  • Cormand B, Vilageliu L, Balcells S, Gonzalez R, Chabás A and Grinberg-Vaisman DR.

    Two novel (1098insA and Y313H) and one rare (R359Q) mutations detected in exon 8 of the beta-glucocerebrosidase gene in Gaucher's disease patients.

    HUMAN MUTATION . 7(3): 272-274.

    [doi:10.1002/(SICI)1098-1004(1996)7:3272::AID-HUMU143.0.CO;2-#]

  • Chabás A, Cormand B, Grinberg-Vaisman DR, Burguera JM, Balcells S, Merino JL, Mate I, Sobrino JA, Gonzalez R and Vilageliu L.

    Unusual expression of Gaucher's disease: cardiovascular calcifications in three sibs homozygous for the D409H mutation.

    JOURNAL OF MEDICAL GENETICS . 32(9): 740-742. Nº de cites: 91

    [doi:10.1136/jmg.32.9.740]

  • Cormand B, Vilageliu L, Burguera JM, Balcells S, Gonzalez R, Grinberg-Vaisman DR and Chabás A.

    Gaucher disease in Spanish patients: analysis of eight mutations.

    HUMAN MUTATION . 5(4): 303-309. Nº de cites: 47

    [doi:10.1002/humu.1380050406]