Publikationen, an denen er mitarbeitet ANGEL MARIA CARRACEDO ALVAREZ (18)

2024

  1. A genome-wide association study meta-analysis in a European sample of stage III/IV grade C periodontitis patients ≤35 years of age identifies new risk loci

    Journal of Clinical Periodontology, Vol. 51, Núm. 4, pp. 431-440

2023

  1. RSPO4 is a potential risk gene of stages III–IV, grade C periodontitis through effects on innate immune response and oral barrier integrity

    Journal of Clinical Periodontology, Vol. 50, Núm. 4, pp. 476-486

2021

  1. Do periodontal disease and alzheimer’s disease share a background of genetic susceptibility?

    Medicina Oral Patologia Oral y Cirugia Bucal, Vol. 26, pp. 4

  2. Genetic susceptibility to periodontal disease in down syndrome: A case-control study

    International Journal of Molecular Sciences, Vol. 22, Núm. 12

  3. 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

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. Whole exome sequencing approach to analysis of the origin of cancer stem cells in patients with head and neck squamous cell carcinoma

    Journal of Oral Pathology and Medicine, Vol. 47, Núm. 10, pp. 938-944

2014

  1. Identification of a novel PNPLA1 mutation in a Spanish family with autosomal recessive congenital ichthyosis

    British Journal of Dermatology

2013

  1. Genetic Variations in SMAD7 Are Associated with Colorectal Cancer Risk in the Colon Cancer Family Registry

    PLoS ONE, Vol. 8, Núm. 4

2012

  1. Characterization of TGM1 c.984+1G>A mutation identified in a homozygous carrier of lamellar ichthyosis

    International Journal of Dermatology, Vol. 51, Núm. 4, pp. 427-430

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

  2. Analysis of TGM1, ALOX12B, ALOXE3, NIPAL4 and CYP4F22 in autosomal recessive congenital ichthyosis from Galicia (NW Spain): Evidence of founder effects

    British Journal of Dermatology, Vol. 165, Núm. 4, pp. 906-911

2007

  1. Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES)

    International Journal of Dermatology, Vol. 46, Núm. 1, pp. 61-63

2001

  1. Identification of Mycobacterium marinum in sea-urchin granulomas

    British Journal of Dermatology, Vol. 145, Núm. 1, pp. 114-116

1997

  1. Síndrome de Gorlin: Manifestaciones clínicas y su relación con alteraciones genéticas en el cromosoma 9

    Revista española de cirugía oral y maxilofacial: Publicación Oficial de la Sociedad Española de Cirugía Oral y Maxilofacial, Vol. 19, Núm. 4, pp. 210-216

1996

  1. Mapa ligamento del cromosoma 1: aplicación a la genética de la miopía

    Archivos de la Sociedad Española de Oftalmologia, Vol. 71, Núm. 3, pp. 269-274

1993

  1. Marcadores genético-moleculares en miopía

    Archivos de la Sociedad Española de Oftalmologia, Vol. 65, Núm. 5, pp. 393-398

1992

  1. Two different genetic markers for high and low myopia.

    European journal of ophthalmology, Vol. 2, Núm. 4, pp. 196-199