Publicacions
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Fernandez-Castillo N, Cabana-Domínguez J, Soriano J, Sànchez-Mora C, Roncero C, Grau-López L, Ros-Cucurull E, Daigre C, van Donkelaar MM, Franke B, Casas M, Ribasés M and Cormand B.
Transcriptomic and genetic studies identify NFAT5 as a candidate gene for cocaine dependence.
TRANSLATIONAL PSYCHIATRY . 5(10): . Nº de cites: 13
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Sánchez-Mora C, Richarte V, Garcia-Martínez I, Pagerols M, Corrales M, Bosch R, Vidal R, Viladevall L, Casas M, Cormand B, Ramos-Quiroga JA and Ribasés M.
Dopamine receptor DRD4 gene and stressful life events in persistent attention deficit hyperactivity disorder.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS . 168(6): 480-491. Nº de cites: 12
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Alemany S, Ribasés M, Vilor-Tejedor N, Bustamante M, Sánchez-Mora C, Bosch R, Richarte V, Cormand B, Casas M, Ramos-Quiroga JA and Sunyer J.
New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS . 168(6): 459-470. Nº de cites: 57
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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. Nº de cites: 16
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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): . Nº de cites: 28
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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. Nº de cites: 23
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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: 16
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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: 51
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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: 17
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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: 28