Publicacións nas que colabora con Ángel Carracedo Álvarez (14)

2021

  1. Genome-wide association study of stage III/IV grade C periodontitis (former aggressive periodontitis) in a Spanish population

    Journal of Clinical Periodontology, Vol. 48, Núm. 7, pp. 896-906

2019

  1. Novel truncating variants expand the phenotypic spectrum of KAT6B-related disorders

    American Journal of Medical Genetics, Part A, Vol. 179, Núm. 2, pp. 290-294

2018

  1. Assessment of genotyping tools applied in genetic susceptibility studies of periodontal disease: A systematic review

    Archives of Oral Biology, Vol. 92, pp. 38-50

  2. Genética y medicina de familia

    Semergen: revista española de medicina de familia, Núm. 1, pp. 54-60

  3. 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

2017

  1. Copy number variation analysis of patients with intellectual disability from North-West Spain

    Gene, Vol. 626, pp. 189-199

2016

  1. Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive states

    Schizophrenia Research, Vol. 174, Núm. 1-3, pp. 10-16

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

  2. Caracterización molecular y descripción fenotípica de dos casos con aberraciones cromosómicas recíprocas en la region de los síndromes de microdeleción/microduplicación 3q29

    Revista de Neurologia, Vol. 61, Núm. 6, pp. 255-260

  3. Resequencing and association analysis of coding regions at twenty candidate genes suggest a role for rare risk variation at AKAP9 and protective variation at NRXN1 in schizophrenia susceptibility

    Journal of Psychiatric Research, Vol. 66-67, pp. 38-44

2012

  1. Family history and breast cancer hormone receptor status in a Spanish cohort

    PLoS ONE, Vol. 7, Núm. 1

2011

  1. A novel mutation in the OFD1 (Cxorf5) gene may contribute to oral phenotype in patients with oral-facial-digital syndrome type 1

    Oral Diseases, Vol. 17, Núm. 6, pp. 610-614

2010

  1. The genomics serving pediatrics in the investigation of the multifactorial disease

    Acta Pediatrica Espanola, Vol. 68, Núm. 2, pp. 55-60

2007

  1. Extensive linkage disequilibrium mapping at HTR2A and DRD3 for schizophrenia susceptibility genes in the Galician population

    Schizophrenia Research, Vol. 90, Núm. 1-3, pp. 123-129