Publicaciones en las que colabora con LUIS ANTONIO CASTAÑO GONZÁLEZ (64)

2024

  1. Risk for progression to type 1 diabetes in first-degree relatives under 50 years of age

    Frontiers in Endocrinology, Vol. 15

2012

  1. Consumption of cows' milk is associated with lower risk of type 2 diabetes mellitus. A cross-sectional study

    International Dairy Journal, Vol. 26, Núm. 2, pp. 162-165

2011

  1. Accuracy in copy number calling by qPCR and PRT: A matter of DNA

    PLoS ONE, Vol. 6, Núm. 12

  2. Revisiting genome wide association studies (GWAS) in coeliac disease: Replication study in Spanish population and expression analysis of candidate genes

    Journal of Medical Genetics, Vol. 48, Núm. 7, pp. 493-496

2010

  1. A regulatory single nucleotide polymorphism in the ubiquitin D gene associated with celiac disease

    Human Immunology, Vol. 71, Núm. 1, pp. 96-99

  2. Analysis of β-defensin and Toll-like receptor gene copy number variation in celiac disease

    Human Immunology, Vol. 71, Núm. 8, pp. 833-836

  3. Long-term and acute effects of gliadin on small intestine of patients on potentially pathogenic networks in celiac disease

    Autoimmunity, Vol. 43, Núm. 2, pp. 131-139

2009

  1. Exploring the diabetogenicity of the HLA-B18-DR3 CEH: Independent association with T1D genetic risk close to HLA-DOA

    Genes and Immunity, Vol. 10, Núm. 6, pp. 596-600

  2. Los anticuerpos antitransglutaminasa. Una herramienta en el seguimiento de los pacientes celiacos

    Revista Espanola de Pediatria, Vol. 65, Núm. 3, pp. 272-276

  3. TH17 (and TH1) signatures of intestinal biopsies of CD patients in response to gliadin

    Autoimmunity, Vol. 42, Núm. 1, pp. 69-73

2008

  1. Combined Functional and Positional Gene Information for the Identification of Susceptibility Variants in Celiac Disease

    Gastroenterology, Vol. 134, Núm. 3, pp. 738-746

  2. Evidence that the COMTVal158Met polymorphism moderates subclinical psychotic and affective symptoms in unaffected first-degree relatives of patients with schizophrenia

    European Psychiatry, Vol. 23, Núm. 3, pp. 219-222

  3. Reply

    Gastroenterology

  4. The functional R620W variant of the PTPN22 gene is associated with celiac disease

    Tissue Antigens, Vol. 71, Núm. 3, pp. 247-249

2007

  1. Association of KIR2DL5B gene with celiac disease supports the susceptibility locus on 19q13.4

    Genes and Immunity, Vol. 8, Núm. 2, pp. 171-176

  2. Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright's hereditary osteodystrophy

    Journal of Clinical Endocrinology and Metabolism, Vol. 92, Núm. 6, pp. 2370-2373

  3. Mutations in GCK and HNF-1α explain the majority of cases with clinical diagnosis of MODY in Spain

    Clinical Endocrinology, Vol. 67, Núm. 4, pp. 538-546

  4. The majority of cases of neonatal diabetes in Spain can be explained by known genetic abnormalities

    Diabetic Medicine, Vol. 24, Núm. 7, pp. 707-713

  5. Toll-like receptor 4 (TLR4) gene polymorphisms in celiac disease

    Tissue Antigens, Vol. 70, Núm. 6, pp. 495-498

  6. Two-year follow-up of anti-transglutaminase autoantibodies among celiac children on gluten-free diet: Comparison of IgG and IgA

    Autoimmunity, Vol. 40, Núm. 2, pp. 117-121