Publicacións nas que colabora con Ángel Carracedo Álvarez (14)
2021
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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
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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
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Assessment of genotyping tools applied in genetic susceptibility studies of periodontal disease: A systematic review
Archives of Oral Biology, Vol. 92, pp. 38-50
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Genética y medicina de familia
Semergen: revista española de medicina de familia, Núm. 1, pp. 54-60
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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
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Copy number variation analysis of patients with intellectual disability from North-West Spain
Gene, Vol. 626, pp. 189-199
2016
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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
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An efficient screening method for simultaneous detection of recurrent copy number variants associated with psychiatric disorders
Clinica Chimica Acta, Vol. 445, pp. 34-40
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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
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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
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Family history and breast cancer hormone receptor status in a Spanish cohort
PLoS ONE, Vol. 7, Núm. 1
2011
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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
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The genomics serving pediatrics in the investigation of the multifactorial disease
Acta Pediatrica Espanola, Vol. 68, Núm. 2, pp. 55-60
2007
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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