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- 2024
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Mark
Haplotype analysis identifies functional elements in monoclonal gammopathy of unknown significance
(
- Contribution to journal › Article
- 2022
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Mark
Genome-wide meta-analysis of monoclonal gammopathy of undetermined significance (MGUS) identifies risk loci impacting IRF-6
(
- Contribution to journal › Letter
- 2021
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Mark
DNA Repair Gene Polymorphisms and Chromosomal Aberrations in Exposed Populations
(
- Contribution to journal › Article
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Mark
DNA repair gene polymorphisms and chromosomal aberrations in healthy, nonsmoking population
(
- Contribution to journal › Article
- 2020
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Mark
Epistatic effect of TLR3 and cGAS-STING-IKKε-TBK1-IFN signaling variants on colorectal cancer risk
(
- Contribution to journal › Article
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Mark
Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans
(
- Contribution to journal › Article
- 2019
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Mark
Single nucleotide polymorphisms within MUC4 are associated with colorectal cancer survival
(
- Contribution to journal › Article
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Mark
Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population
(
- Contribution to journal › Article
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Mark
Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS) : comparison with multiple myeloma
2019) In Leukemia(
- Contribution to journal › Letter
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Mark
Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance
(
- Contribution to journal › Letter
- 2018
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Mark
Genetic variation of acquired structural chromosomal aberrations
(
- Contribution to journal › Article
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Mark
Short article : Influence of regulatory NLRC5 variants on colorectal cancer survival and 5-fluorouracil-based chemotherapy
(
- Contribution to journal › Article
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Mark
Investigation of single and synergic effects of NLRC5 and PD-L1 variants on the risk of colorectal cancer
(
- Contribution to journal › Article
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Mark
Genetic variation associated with chromosomal aberration frequency : A genome-wide association study
2018) In Environmental and Molecular Mutagenesis(
- Contribution to journal › Article
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Mark
Coding variants in NOD-like receptors : An association study on risk and survival of colorectal cancer
(
- Contribution to journal › Article
- 2017
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Mark
Genomewide association study on monoclonal gammopathy of unknown significance (MGUS)
(
- Contribution to journal › Article
- 2016
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Mark
Genetic variation in the major mitotic checkpoint genes associated with chromosomal aberrations in healthy humans
(
- Contribution to journal › Article
- 2015
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Mark
Metabolic gene variants associated with chromosomal aberrations in healthy humans.
(
- Contribution to journal › Article
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Mark
Interactions of DNA repair gene variants modulate chromosomal aberrations in healthy subjects.
(
- Contribution to journal › Article
- 2014
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Mark
Colorectal cancer risk and patients' survival: influence of polymorphisms in genes somatically mutated in colorectal tumors
(
- Contribution to journal › Article
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Mark
Single Nucleotide Polymorphisms within Interferon Signaling Pathway Genes Are Associated with Colorectal Cancer Susceptibility and Survival.
(
- Contribution to journal › Article
- 2013
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Mark
Genetic variants in C-type lectin genes are associated with colorectal cancer susceptibility and clinical outcome
(
- Contribution to journal › Article
- 2012
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Mark
Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases
(
- Contribution to journal › Article
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Mark
A Comprehensive Investigation on Common Polymorphisms in the MDR1/ABCB1 Transporter Gene and Susceptibility to Colorectal Cancer
(
- Contribution to journal › Article
- 2011
-
Mark
MTHFR and MTRR genotype and haplotype analysis and colorectal cancer susceptibility in a case?control study from the Czech Republic
(
- Contribution to journal › Article
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Mark
Association Between TAS2R38 Gene Polymorphisms and Colorectal Cancer Risk: A Case-Control Study in Two Independent Populations of Caucasian Origin
(
- Contribution to journal › Article
- 2010
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Mark
Chromosomal damage in peripheral blood lymphocytes of newly diagnosed cancer patients and healthy controls
(
- Contribution to journal › Article
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Mark
Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study
(
- Contribution to journal › Article
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Mark
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility
(
- Contribution to journal › Article