Publicacións nas que colabora con Noa Carrera Cachaza (8)

2018

  1. Identification of putative second genetic hits in schizophrenia carriers of high-risk copy number variants and resequencing in additional samples

    European Archives of Psychiatry and Clinical Neuroscience, Vol. 268, Núm. 6, pp. 585-592

2016

  1. Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia

    Translational Psychiatry, Vol. 6, Núm. 3

2015

  1. An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders

    Clinica Chimica Acta, Vol. 445, pp. 34-40

2013

  1. Role of DISC1 interacting proteins in schizophrenia risk from genome-wide analysis of missense SNPs

    Annals of Human Genetics, Vol. 77, Núm. 6, pp. 504-512

2012

  1. Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia

    Biological Psychiatry, Vol. 71, Núm. 2, pp. 169-177

2010

  1. Testing the antagonistic pleiotropy model of schizophrenia susceptibility by analysis of DAOA, PPP1R1B, and APOL1 genes

    Psychiatry Research, Vol. 179, Núm. 2, pp. 126-129

2009

  1. A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia

    Human Genetics, Vol. 124, Núm. 6, pp. 607-613

  2. Recent adaptive selection at MAOB and ancestral susceptibility to schizophrenia

    American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, Vol. 150, Núm. 3, pp. 369-374