Publikationen in Zusammenarbeit mit Forschern von Universidad de Extremadura (61)

2016

  1. GC gene polymorphism and unbound serum retinol-binding protein 4 are related to the risk of insulin resistance in patients with chronic hepatitis c: A prospective cross-sectional study

    Medicine (United States), Vol. 95, Núm. 10

2013

  1. Influence of Vitamin D-Related Gene Polymorphisms (CYP27B and VDR) on the Response to Interferon/Ribavirin Therapy in Chronic Hepatitis C

    PLoS ONE, Vol. 8, Núm. 9

  2. Vitamin D deficiency and vitamin D therapy in chronic hepatitis C

    Annals of Hepatology, Vol. 12, Núm. 2, pp. 199-204

2012

  1. Analysis of the functional polymorphism in the cytochrome P450 CYP2C8 gene rs11572080 with regard to colorectal cancer risk

    Frontiers in Genetics, Vol. 3, Núm. DEC

  2. Polymorphism of the TLR4 gene reduces the risk of hepatitis C virus-induced hepatocellular carcinoma

    Oncology, Vol. 82, Núm. 1, pp. 35-40

  3. Predicting response to therapy in chronic hepatitis C: An approach combining interleukin-28B gene polymorphisms and clinical data

    Journal of Gastroenterology and Hepatology (Australia), Vol. 27, Núm. 2, pp. 279-285

  4. Relation of IL28b gene polymorphism with biochemical and histological features in hepatitis C virus-induced liver disease

    PLoS ONE, Vol. 7, Núm. 5

2010

  1. CYP2W1 variant alleles in Caucasians and association of the CYP2W1 G541A (Ala181Thr) polymorphism with increased colorectal cancer risk

    Pharmacogenomics, Vol. 11, Núm. 7, pp. 919-925

2009

  1. Analysis of a non-synonymous single nucleotide polymorphism of the human diamine oxidase gene (ref. SNP ID: Rs1049793) in patients with Crohn's disease

    Scandinavian Journal of Gastroenterology, Vol. 44, Núm. 10, pp. 1207-1212

2008

  1. A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

    Nature Genetics, Vol. 40, Núm. 5, pp. 623-630

  2. Glutathione S-transferase GSTT1 and GSTM1 allozymes: Beyond null alleles

    Pharmacogenomics, Vol. 9, Núm. 3, pp. 359-363

  3. Interaction of CYP2C8 and CYP2C9 genotypes modifies the risk for nonsteroidal anti-inflammatory drugs-related acute gastrointestinal bleeding

    Pharmacogenetics and Genomics, Vol. 18, Núm. 1, pp. 37-43

  4. Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer

    Human Molecular Genetics, Vol. 17, Núm. 23, pp. 3720-3727

2007

  1. Cytochrome P450 CYP2C9 Polymorphism and NSAID-Related Acute Gastrointestinal Bleeding

    Gastroenterology

  2. GSTT1 and GSTM1 null genotypes may facilitate hepatitis C virus infection becoming chronic

    Journal of Infectious Diseases, Vol. 195, Núm. 9, pp. 1320-1323

  3. Genetic variability in CYP3A4 and CYP3A5 in primary liver, gastric and colorectal cancer patients

    BMC Cancer, Vol. 7

  4. Glutathione S-transferases π1, α1 and μ3 genetic polymorphisms and the risk of hepatocellular carcinoma in humans

    Pharmacogenomics, Vol. 8, Núm. 8, pp. 895-899

2006

  1. Glutathione S-transferase M1 and T1 genetic polymorphisms are not related to the risk of hepatocellular carcinoma: A study in the Spanish population

    European Journal of Cancer, Vol. 42, Núm. 1, pp. 73-77

  2. Glutathione S-transferases μ1, θ1, π1 α1 and μ3 genetic polymorphisms and the risk of colorectal and gastric cancers in humans

    Pharmacogenomics, Vol. 7, Núm. 5, pp. 711-718

  3. Interethnic and intraethnic variability of CYP2C8 and CYP2C9 polymorphisms in healthy individuals

    Molecular Diagnosis and Therapy, Vol. 10, Núm. 1, pp. 29-40