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Genetic Variation
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MUDr. Pavel Vodička CSc., DrSc.
Academic staff at First Faculty of Medicine
183 publications
Publications
publication
Single Nucleotide Polymorphisms within Interferon Signaling Pathway Genes Are Associated with Colorectal Cancer Susceptibility and Survival
2014 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Association of serum bilirubin and promoter variations in HMOX1 and UGT1A1 genes with sporadic colorectal cancer
2012 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Polymorphisms in miRNA-binding sites of nucleotide excision repair genes and colorectal cancer risk
2012 |
First Faculty of Medicine
publication
Gene expression variations: potentialities of master regulator polymorphisms in colorectal cancer risk
2012 |
First Faculty of Medicine
publication
Association Between TAS2R38 Gene Polymorphisms and Colorectal Cancer Risk: A Case-Control Study in Two Independent Populations of Caucasian Origin
2011 |
First Faculty of Medicine
publication
Genotype and haplotype analysis of TP53 gene and the risk of pancreatic cancer: an association study in the Czech Republic
2010 |
First Faculty of Medicine, Central Library of Charles University, Second Faculty of Medicine
publication
Genetic variants in selenoprotein genes increase risk of colorectal cancer
2010 |
First Faculty of Medicine, Third Faculty of Medicine
publication
Insulin pathway related genes and risk of colorectal cancer: INSR promoter polymorphism shows a protective effect
2007 |
First Faculty of Medicine, Central Library of Charles University
publication
Novel insights into genetic susceptibility for colorectal cancer from transcriptome-wide association and functional investigation
2024 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
MUC13-miRNA-4647 axis in colorectal cancer: Prospects to identifications of risk factors and clinical outcomes
2023 |
First Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine, Faculty of Medicine in Hradec Králové
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