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Search for publications relevant for "genome-wide association study (GWAS)"
genome-wide association study (GWAS)
Publication
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Person
Publication
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publication
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma
2012 |
First Faculty of Medicine
publication
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B
2022 |
First Faculty of Medicine, Second Faculty of Medicine, Faculty of Physical Education and Sport
publication
A genome-wide association study of anorexia nervosa
2014 |
First Faculty of Medicine
publication
Mendelian randomisation studies: principle and selected examples from cardiovascular medicine
2020 |
First Faculty of Medicine
publication
Inherited variability in a master regulator polymorphism (rs4846126) associates with survival in 5-FU treated colorectal cancer patients
2014 |
First Faculty of Medicine
publication
Association between intake of the n-3 polyunsaturated fatty acid docosahexaenoic acid (n-3 PUFA DHA) and reduced risk of ovarian cancer: A systematic Mendelian Randomization study
2023 |
Faculty of Medicine in Pilsen
publication
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for
2015 |
First Faculty of Medicine
publication
A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium
2011 |
First Faculty of Medicine
publication
LD Score regression distinguishes confounding from polygenicity in genome-wide association studies
2015 |
Second Faculty of Medicine
publication
TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study
2021 |
Second 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
Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1
2011 |
First Faculty of Medicine
publication
A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23
2012 |
First Faculty of Medicine
publication
Broad genetic issues in lung cancer
2009 |
First Faculty of Medicine
publication
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling
Publication without faculty affiliation
publication
Validation and functional characterization of GWAS-identified variants for chronic lymphocytic leukemia: a CRuCIAL study
2022 |
Faculty of Medicine in Pilsen
publication
Gene expression variations: potentialities of master regulator polymorphisms in colorectal cancer risk
2012 |
First Faculty of Medicine
publication
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
2014 |
First Faculty of Medicine
publication
Genetic background in common forms of obesity - from studies on identical twins to candidate genes of obesity
2014 |
Faculty of Science, Central Library of Charles University
publication
Relationships between some genetic polymorphisms and clinical features of Alzheimer's disease
2015 |
First Faculty of Medicine
publication
Genome-wide association study identifies multiple risk loci for renal cell carcinoma
2017 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk
2018 |
First Faculty of Medicine
publication
A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis
2019 |
First Faculty of Medicine
publication
Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis
2015 |
Second Faculty of Medicine
publication
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa
Publication without faculty affiliation
publication
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
2019 |
Second Faculty of Medicine
publication
The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
2020 |
First Faculty of Medicine
publication
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma
2012 |
Second Faculty of Medicine
publication
Polymorphisms within Autophagy-Related Genes Influence the Risk of Developing Colorectal Cancer: A Meta-Analysis of Four Large Cohorts
2021 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Genome-wide association study identifies an early onset pancreatic cancer risk locus
2020 |
First Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine