Publicacions
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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. Nº de cites: 17
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Sánchez-Mora C, Ramos-Quiroga JA, Bosch R, Corrales M, Garcia-Martínez I, Nogueira M, Pagerols M, Palomar G, Richarte V, Vidal R, Arias-Vasquez A, Bustamante M, Forns J, Gross-Lesch S, Guxens M, Hinney A, Hoogman M, Jacob C, Jacobsen KK, Kan CC, Kiemeney L, Kittel-Schneider S, Klein M, Onnink M, Rivero O, Zayats T, Buitelaar J, Faraone SV, Franke B, Haavik J, Johansson S, Lesch KP, Reif A, Sunyer J, Bayés M, Casas M, Cormand B and Ribasés M.
Case-Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the Disorder
NEUROPSYCHOPHARMACOLOGY . 40(4): 915-926. Nº de cites: 52
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Vila-Pueyo M, Pons R, Raspall-Chaure M, Marcé-Grau A, Carreño O, Sintas C, Cormand B, Pineda M and Macaya A.
Clinical and genetic analysis in alternating hemiplegia of childhood: ten new patients from Southern Europe.
JOURNAL OF THE NEUROLOGICAL SCIENCES . 344(1-2): 37-42. Nº de cites: 18
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Vila-Pueyo M, Gené GG, Flotats-Bastardes M, Elorza X, Sintas C, Valverde MA, Cormand B, Fernández-Fernández JM and Macaya A.
A loss-of-function CACNA1A mutation causing benign paroxysmal torticollis of infancy.
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY . 18(3): 430-433. Nº de cites: 29
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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: 47
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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
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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.
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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: 31
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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: 47
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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: 51