Publications
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Weber H, Kittel-Schneider S, Heupel J, Weißflog L, Kent L, Freudenberg F, Alttoa A, Post A, Herterich S, Haavik J, Halmøy A, Fasmer OB, Landaas ET, Johansson S, Cormand B, Ribasés M, Sánchez-Mora C, Ramos-Quiroga JA, Franke B, Lesch KP and Reif A.
On the role of NOS1 ex1f-VNTR in ADHD-allelic, subgroup, and meta-analysis.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS . 168(6): 445-458. Number of citations: 17
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Gómez-Grau M, Garrido E, Cozar M, Rodriguez-Sureda V, Domínguez C, Arenas C, Gatti RA, Cormand B, Grinberg-Vaisman DR and Vilageliu L.
Evaluation of Aminoglycoside and Non-Aminoglycoside Compounds for Stop-Codon Readthrough Therapy in Four Lysosomal Storage Diseases.
PLoS One . 10(8): . Number of citations: 30
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Sintas C, Fernández-Morales J, Vila-Pueyo M, Narberhaus B, Arenas C, Pozo-Rosich P, Macaya A and Cormand B.
Replication study of previous migraine genome-wide association study findings in a Spanish sample of migraine with aura
CEPHALALGIA . 35(9): 776-782. Number of citations: 26
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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. Number of citations: 19
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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. Number of citations: 54
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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. Number of citations: 19
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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. Number of citations: 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. Number of citations: 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. Number of citations: 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.
