Publicacions
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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
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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: 11
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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: 31
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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: 4
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Urreizti R, Cueto-Gonzalez, Ana Maria, Franco-Valls, Héctor, Mort-Farre, Silvia, Roca N, Ponomarenko, Julia, Cozzuto, Luca, Company, Carlos, Bosio M, Ossowski, Stephan, Montfort, Magda, Hecht, Jochen, Tizzano, Eduardo, Cormand B, Vilageliu L, Opitz, John, Neri, Giovanni, Grinberg-Vaisman DR and Balcells S.
A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes.
SCIENTIFIC REPORTS . 7: 44138-44138. Nº de cites: 28
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Pagerols M, Richarte V, Sánchez-Mora C, Garcia-Martínez I, Corrales M, Corominas M, Cormand B, Casas M, Ribasés M and Ramos-Quiroga JA.
Pharmacogenetics of methylphenidate response and tolerability in attention-deficit/hyperactivity disorder.
PHARMACOGENOMICS JOURNAL . 17(1): 98-104. Nº de cites: 19
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De-Castro M, Tonda R, Escudero-Ferruz P, Andres R, Mayor-Lorenzo A, Castro J, Ciccioli M, Hidalgo DA, Rodríguez-Ezcurra JJ, Farrando J, Pérez-Santonja JJ, Cormand B, Marfany G and Gonzalez R.
Novel Candidate Genes and a Wide Spectrum of Structural and Point Mutations Responsible for Inherited Retinal Dystrophies Revealed by Exome Sequencing.
PLoS One . 11(12): . Nº de cites: 43
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Zayats T, Jacobsen KK, Kleppe R, Jacob CP, Kittel-Schneider S, Ribasés M, Ramos-Quiroga JA, Richarte V, Casas M, Mota NR, Grevet EH, Klein M, Corominas J, Bralten J, Galesloot T, Vasquez AA, Herms S, Forstner AJ, Larsson H, Breen G, Asherson P, Gross-Lesch S, Lesch KP, Cichon S, Gabrielsen MB, Holmen OL, Bau CH, Buitelaar J, Kiemeney L, Faraone SV, Cormand B, Franke B, Reif A, Haavik J and Johansson S.
Exome chip analyses in adult attention deficit hyperactivity disorder.
TRANSLATIONAL PSYCHIATRY . 6(10): . Nº de cites: 24
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Klein M, Berger S, Hoogman M, Dammers J, Makkinje R, Heister AJ, Galesloot TE, Kiemeney LA, Weber H, Kittel-Schneider S, Lesch KP, Reif A, Ribase´s M, Ramos-Quiroga JA, Cormand B, Zayats T, Hegvik TA, Jacobsen KK, Johansson S, Haavik J, Mota NR, Bau CH, Grevet EH, Doyle A, Faraone SV, Arias-Va´squez A and Franke B.
Meta-analysis of the DRD5 VNTR in persistent ADHD
EUROPEAN NEUROPSYCHOPHARMACOLOGY . 26(9): 1527-1532. Nº de cites: 3
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Fernandez-Castillo N and Cormand B.
Aggressive behavior in humans: Genes and pathways identified through association studies.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS . 171(5): 676-696. Nº de cites: 55