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Autism-specific copy number variants further implicate the phosphatidylinositol signaling pathway and the glutamatergic synapse in the etiology of the disorder

Febrero 1, 2009

Cuscó I, Medrano A, Gener B, Vilardell M, Gallastegui F, Villa O, González E, Rodríguez-Santiago B, Vilella E, Del Campo M, Pérez-Jurado LA. Hum Mol Genet. 2009 May 15;18(10):1795-804. Epub 2009 Feb 26

Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia

Junio 1, 2009

Rodríguez-Santiago B, Brunet A, Sobrino B, Serra-Juhé C, Flores R, Armengol L, Vilella E, Gabau E, Guitart M, Guillamat R, Martorell L, Valero J, Gutiérrez-Zotes A, Labad A, Carracedo A, Estivill X, Pérez-Jurado LA. Mol Psychiatry. 2010 Oct;15(10):1023-33. Epub 2009 Jun 16

Array-CGH in patients with Kabuki-like phenotype: identification of two patients with complex rearrangements including 2q37 deletions and no other recurrent aberration

Abril 1, 2008

Cuscó I, del Campo M, Vilardell M, González E, Gener B, Galán E, Toledo L, Pérez-Jurado LA. BMC Med Genet. 2008 Apr 11;9:27

Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A

Abril 1, 2008

Venceslá A, Baena M, Fares Taie L, Cornet M, Baiget M, Tizzano EF. Haemophilia. 2008 May;14(3):489-93. Epub 2008 Apr 1