2022 - Research.com Genetics and Molecular Biology in Czech Republic Leader Award
The scientist’s investigation covers issues in Genetics, Colorectal cancer, Single-nucleotide polymorphism, Internal medicine and Genotype. His Colorectal cancer study is related to the wider topic of Cancer. His work deals with themes such as Untranslated region and Locus, which intersect with Single-nucleotide polymorphism.
His Internal medicine study integrates concerns from other disciplines, such as Personalized medicine, Bioinformatics and Oncology. When carried out as part of a general Oncology research project, his work on Adjuvant is frequently linked to work in Molecular level, therefore connecting diverse disciplines of study. His work is dedicated to discovering how Genotype, Odds ratio are connected with Endocrinology and Polymorphism and other disciplines.
Pavel Vodicka spends much of his time researching Colorectal cancer, Internal medicine, Oncology, Genetics and Single-nucleotide polymorphism. His Colorectal cancer study is concerned with the field of Cancer as a whole. Pavel Vodicka has included themes like Gastroenterology and Endocrinology in his Internal medicine study.
His Oncology research incorporates elements of Epidemiology, Proportional hazards model, Treatment response, Breast cancer and Cohort. His Single-nucleotide polymorphism research is multidisciplinary, relying on both Locus, Pancreatic disease and Bioinformatics. His Genome-wide association study study combines topics in areas such as Genetic association and Medical genetics.
His main research concerns Colorectal cancer, Internal medicine, Oncology, Cancer and Cancer research. His Colorectal cancer research integrates issues from Cancer cell, Genome-wide association study, Carcinogenesis and Primary tumor. His Genome-wide association study study results in a more complete grasp of Genetics.
His Oncology research is multidisciplinary, incorporating perspectives in Odds ratio, Epidemiology, Breast cancer, Single-nucleotide polymorphism and Pancreatic disease. His work focuses on many connections between Cancer and other disciplines, such as Mendelian Randomization Analysis, that overlap with his field of interest in Biobank. The various areas that Pavel Vodicka examines in his Cancer research study include DNA damage, Expression quantitative trait loci, Metastasis, DNA repair and Epigenetics.
His primary areas of investigation include Colorectal cancer, Internal medicine, Oncology, Cancer and Genome-wide association study. His study in Colorectal cancer is interdisciplinary in nature, drawing from both Cancer research, Fluorouracil, DNA damage and Genotype. His study in the field of Odds ratio, Treatment response, Family history and Liquid biopsy also crosses realms of Cell-free fetal DNA.
His Oncology study combines topics in areas such as Pancreatic cancer, Single-nucleotide polymorphism, Linkage disequilibrium, Disease and Pancreatic disease. His studies deal with areas such as Telomere, Transcriptome, Computational biology and DNA repair as well as Cancer. His research integrates issues of Unknown Significance, Case-control study and Mutation in his study of Genome-wide association study.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3
Ian P.M. Tomlinson;Emily Webb;Luis Carvajal-Carmona;Peter Broderick.
Nature Genetics (2008)
Polymorphisms within micro-RNA-binding sites and risk of sporadic colorectal cancer
Debora Landi;Federica Gemignani;Alessio Naccarati;Barbara Pardini.
Genetic polymorphisms in DNA repair genes and possible links with DNA repair rates, chromosomal aberrations and single-strand breaks in DNA
Pavel Vodicka;Rajiv Kumar;Rajiv Kumar;Rudolf Stetina;Somali Sanyal.
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.
Barbara Schormair;David Kemlink;Darina Roeske;Gertrud Eckstein.
Nature Genetics (2008)
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer
Brian M. Wolpin;Cosmeri Rizzato;Peter Kraft;Charles Kooperberg.
Nature Genetics (2014)
Association of DNA repair polymorphisms with DNA repair functional outcomes in healthy human subjects.
Pavel Vodicka;Rudolf Stetina;Veronika Polakova;Elena Tulupova.
HOTAIR long non-coding RNA is a negative prognostic factor not only in primary tumors, but also in the blood of colorectal cancer patients.
Miroslav Svoboda;Jana Slyskova;Michaela Schneiderova;Peter Makovicky.
The role of ABC transporters in progression and clinical outcome of colorectal cancer.
I. Hlavata;B. Mohelnikova-Duchonova;R. Vaclavikova;V. Liska.
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer
Erica J Childs;Evelina Mocci;Daniele Campa;Daniele Campa;Paige M Bracci.
Nature Genetics (2015)
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.
Juliane Winkelmann;Darina Czamara;Barbara Schormair;Franziska Knauf.
PLOS Genetics (2011)
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