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GWAS
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Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis
2012 |
First 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
Mendelian randomisation studies: principle and selected examples from cardiovascular medicine
2020 |
First Faculty of Medicine
publication
Association of atherothrombosis and thrombophilias - genetic aspects
2014 |
First 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
Do GWAS-Identified Risk Variants for Chronic Lymphocytic Leukemia Influence Overall Patient Survival and Disease Progression?
2023 |
Faculty of Medicine in Pilsen
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
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes
2017 |
First Faculty of Medicine
publication
Broad genetic issues in lung cancer
2009 |
First Faculty of Medicine
publication
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for
2015 |
First Faculty of Medicine
publication
GWAS-Identified Variants for Obesity Do Not Influence the Risk of Developing Multiple Myeloma: A Population-Based Study and Meta-Analysis
2023 |
Faculty of Medicine in Pilsen
publication
Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness
2016 |
Second Faculty of Medicine
publication
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia
2019 |
Second Faculty of Medicine
publication
Beyond GWAS of Colorectal Cancer: Evidence of Interaction with Alcohol Consumption and Putative Causal Variant for the 10q24.2 Region
2022 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium
2011 |
First Faculty of Medicine
publication
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21
2016 |
Faculty of Medicine in Pilsen
publication
Identification of novel loci and new risk variant in known loci for colorectal cancer risk in East Asians
2020 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Genetic variation in gonadal impairment in female survivors of childhood cancer: a PanCareLIFE study protocol
2018 |
Second 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
Circulating Levels of Insulin-like Growth Factor 1 and Insulin-like Growth Factor Binding Protein 3 Associate With Risk of Colorectal Cancer Based on Serologic and Mendelian Randomization Analyses
2020 |
First Faculty of Medicine, Faculty of Medicine in Pilsen
publication
Variants influencing age at diagnosis of HNF1A-MODY
2022 |
Second 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
Genetic and non-genetic risk factors for early-onset pancreatic cancer
2023 |
First Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine
publication
Genetic variation associated with chromosomal aberration frequency: A genome-wide association study
2019 |
First Faculty of Medicine, Faculty of Medicine in Pilsen, Third Faculty of Medicine
publication
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma
2012 |
First Faculty of Medicine
publication
Kleine-Levin syndrome is associated with birth difficulties and genetic variants in the TRANK1 gene loci
2021 |
First Faculty of Medicine
publication
Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
2022 |
Faculty of Science
publication
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa
Publication without faculty affiliation
publication
Impact of genetic polymorphisms in kinetochore and spindle assembly genes on chromosomal aberration frequency in healthy humans
2020 |
First Faculty of Medicine, Faculty of Medicine in Pilsen