Publicacions
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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: 27
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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: 18
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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: 36
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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: 22
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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: 51
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Brevik EJ, van Donkelaar MM, Weber H, Sánchez-Mora C, Jacob C, Rivero O, Kittel-Schneider S, Garcia-Martínez I, Aebi M, van Hulzen K, Cormand B, Ramos-Quiroga JA, IMAGE Consortium, Lesch KP, Reif A, Ribasés M, Franke B, Posserud MB, Johansson S, Lundervold AJ, Haavik J and Zayats T.
Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS . 171(5): 733-747. Nº de cites: 32
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Asherson P and Cormand B.
The genetics of aggression: Where are we now?
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS . 171(5): 559-561. Nº de cites: 10
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Veroude K, Zhang-James Y, Fernandez-Castillo N, Bakker MJ, Cormand B and Faraone SV.
Genetics of aggressive behavior: An overview.
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS . 171B(1): 3-43. Nº de cites: 94
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Urreizti R, Roca N, Trepat J, Garcia-Garcia F, Aleman A, Orteschi D, Marangi G, Neri G, Opitz JM, Dopazo J, Cormand B, Vilageliu L, Balcells S and Grinberg-Vaisman DR.
Screening of CD96 and ASXL1 in 11 patients with Opitz C or Bohring-Opitz syndromes.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A . 170A(1): 24-31. Nº de cites: 11