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fine mapping
Publication
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Person
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publication
Fine mapping of MHC region in lung cancer highlights independent susceptibility loci by ethnicity
2018 |
Second Faculty of Medicine
publication
Fine mapping of autosomal dominant nonsyndromic hearing impairment DFNA21 to chromosome 6p24.1-22.3
2005 |
Central Library of Charles University
publication
Fine-Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies
2020 |
First Faculty of Medicine
publication
Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
2015 |
Second 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
Functionally distinct regions of the locus Leishmania major response 15 control IgE or IFNγ level in addition to skin lesions
2023 |
First Faculty of Medicine, Central Library of Charles University, Faculty of Science, Third Faculty of Medicine
publication
Implication of synapse-related genes in bipolar disorder by linkage and gene expression analyses
2010 |
Publication without faculty affiliation
publication
The chromosome 2p21 region harbors a complex genetic architecture for association with risk for renal cell carcinoma
2012 |
First Faculty of Medicine
publication
Mapping genomic loci implicates genes and synaptic biology in schizophrenia
2022 |
First Faculty of Medicine, Second Faculty of Medicine
publication
Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results
2009 |
Second Faculty of Medicine
publication
Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia
2015 |
First Faculty of Medicine
publication
Common variants in P2RY11 are associated with narcolepsy
2011 |
First Faculty of Medicine
publication
Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels
2019 |
First Faculty of Medicine
publication
Multiancestry analysis of the HLA locus in Alzheimer's and Parkinson's diseases uncovers a shared adaptive immune response mediated by HLA-DRB1*04 subtypes
2023 |
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
A catalog of genetic loci associated with kidney function from analyses of a million individuals
2019 |
First Faculty of Medicine
publication
FMR1 Gene Expansion, Large Deletion of Xp, and Skewed X-Inactivation in a Girl With Mental Retardation and Autism
2010 |
Second Faculty of Medicine
publication
Identification of Novel Associations and Localization of Signals in Idiopathic Inflammatory Myopathies Using Genome-Wide Imputation
2023 |
First Faculty of Medicine
publication
Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy
2023 |
First Faculty of Medicine
publication
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
2023 |
First Faculty of Medicine
publication
Multi-omics approach dissects cis-regulatory mechanisms underlying North Carolina macular dystrophy, a retinal enhanceropathy
2022 |
First Faculty of Medicine
publication
Differential effects of 5-HT3 receptor antagonist on lipid profile in spontaneously hypertensive rat and chromosome 8 congenic strain
2012 |
First Faculty of Medicine