Publicacions
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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
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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: 12
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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: 100
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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
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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: 15
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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: 60
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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