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Search for publications relevant for "Single nucleotide polymorphisms (SNP)"
Single nucleotide polymorphisms (SNP)
Publication
Class
Person
Publication
Programmes
publication
Molecular epidemiology of VZV
2010 |
Faculty of Medicine in Hradec Králové
publication
Association of atherothrombosis and thrombophilias - genetic aspects
2014 |
First Faculty of Medicine
publication
Fulminant hepatitis and death associated with disseminated varicella in an immunocompromised adult from the Czech Republic caused by a wild-type clade 4 varicella-zoster virus strain
2011 |
Faculty of Medicine in Hradec Králové
publication
Single Nucleotide Polymorphisms from CSF2, FLT1, TFPI and TLR9 Genes Are Associated with Prelabor Rupture of Membranes
2021 |
Faculty of Medicine in Hradec Králové
publication
Pregnancy-Associated Plasma Protein A Polymorphisms in Patients with Risk Pregnancies
2011 |
First Faculty of Medicine
publication
Massively Parallel Sequencing Detected a Mutation in the MFN2 Gene Missed by Sanger Sequencing Due to a Primer Mismatch on an SNP Site
2016 |
Second Faculty of Medicine
publication
Electrochemical Detection of Single-Nucleotide Polymorphism Associated with Rifampicin Resistance in Mycobacterium tuberculosis Using Solid-Phase Primer Elongation with Ferrocene-Linked Redox-Labeled Nucleotides
2021 |
Faculty of Science
publication
Several obesity- and nutrient-related gene polymorphisms but not FTO and UCP variants modulate postabsorptive resting energy expenditure and fat-induced thermogenesis in obese individuals: the NUGENOB Study
2009 |
Third Faculty of Medicine
publication
Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers
2010 |
First Faculty of Medicine
publication
Association of polymorphisms of platelet receptors GPIa (807C>T), GPVI (13254T>C), and P2Y12 (34C>T and H1/H2 haplotype) with increased risk of periprocedural bleeding in patients undergoing coronary angiography/percutaneous coronary intervention
2017 |
Third Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Comparison of Y-chromosomal haplogroup predictors
2017 |
Second Faculty of Medicine, Faculty of Science, Faculty of Education
publication
Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility
2010 |
First Faculty of Medicine
publication
SNPman: a program for genotype calling using run data from TaqMan allelic discrimination
2011 |
Central Library of Charles University, Second Faculty of Medicine
publication
Using Prior Information from the Medical Literature in GWAS of Oral Cancer Identifies Novel Susceptibility Variant on Chromosome 4-the AdAPT Method
2012 |
First Faculty of Medicine
publication
Association between a 15q25 gene variant, smoking quantity and tobacco-related cancers among 17 000 individuals
2010 |
First Faculty of Medicine
publication
The frequencies of thrombophilic alleles known from GWAS studies in healthy population and in group of patients with venous thromboembolism (VTE) in the Czech Republic
2016 |
Publication without faculty affiliation
publication
A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23
2012 |
First Faculty of Medicine
publication
Common Breast Cancer Susceptibility Alleles and the Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Implications for Risk Prediction
2010 |
First Faculty of Medicine
publication
Charcot-Marie-Tooth neuropathy due to a novel EGR2 gene mutation with mild phenotype - Usefulness of human mapping chip linkage analysis in a Czech family
2012 |
First Faculty of Medicine
publication
Analysis of synapsin III-196 promoter mutation in schizophrenia and bipolar disorder
2006 |
Publication without faculty affiliation
publication
Charcot-Marie-Tooth neuropathy due to a novel EGR2 gene mutation with mild phenotype - Usefulness of human mapping chip linkage analysis in a Czech family
2012 |
Second Faculty of Medicine
publication
Validation and functional characterization of GWAS-identified variants for chronic lymphocytic leukemia: a CRuCIAL study
2022 |
Faculty of Medicine in Pilsen
publication
Distribution of varicella-zoster virus (VZV) wild-type genotypes in northern and southern Europe: evidence for high conservation of circulating genotypes
2009 |
Publication without faculty affiliation
publication
Molecular genetic investigation of polymorfisms and STR loci in patients with nonsmall cell lung cancer
2009 |
First Faculty of Medicine
publication
Replication of restless legs syndrome loci in three European populations
2009 |
First Faculty of Medicine, Central Library of Charles University
publication
Distribution of varicella-zoster virus (VZV) wild-type genotypes in northern and southern Europe: evidence for high conservation of circulating genotypes
2009 |
Central Library of Charles University
publication
Novel dysfunctional variant in ABCG2 as a cause of severe tophaceous gout: biochemical, molecular genetics and functional analysis
2016 |
First Faculty of Medicine
publication
Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype: results from the IBDchip European Project
2013 |
First Faculty of Medicine
publication
ABO blood groups and pancreatic cancer risk and survival: Results from the PANcreatic Disease ReseArch (PANDoRA) consortium
2013 |
First Faculty of Medicine
publication
Scrimer: designing primers from transcriptome data
2015 |
Faculty of Science