- Charcot-Marie-Tooth neuropathy due to a novel EGR2 gene mutation with mild phenotype - Usefulness of human mapping chip linkage analysis in a Czech family2012 | First Faculty of Medicine
- Charcot-Marie-Tooth neuropathy due to a novel EGR2 gene mutation with mild phenotype - Usefulness of human mapping chip linkage analysis in a Czech family2012 | Second Faculty of Medicine
- Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease2005 | First Faculty of Medicine
- Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease2005 | Faculty of Physical Education and Sport
- Integrated gene expression profiling and linkage analysis in the rat2006 | First Faculty of Medicine
- Integrated gene expression profiling and linkage analysis in the rat2006 | Faculty of Physical Education and Sport
- Integrated transcriptional profiling and linkage analysis for disease gene identificationPublication without faculty affiliation
- Genomewide differential linkage analysis of SHR chromosome 4q11 role in metabolit syndromePublication without faculty affiliation
- Suggestive evidence for linkage for restless legs syndrome on chromosome 19p132008 | First Faculty of Medicine
- Familial juvenile hyperuricaemic nephropathy (FJHN): linkage analysis in 15 families, physical and transcriptional characterisation of the FJHN critical region on chromosome 16p11.2 and the analysis of seven candidate genes2003 | First Faculty of Medicine
- Dynamic linkage analysis of 1018 single nucleotide polymorphisms in 214 candidate genes reveals novel risk haplotype associated with higher prevalence of hypertension in French CanadiansPublication without faculty affiliation
- Bioinformatic perspectives in the neuronal ceroid lipofuscinoses2013 | First Faculty of Medicine
- Phenotypic Variability in a Large Czech Family with a Dynamin 2-Associated Charcot-Marie-Tooth Neuropathy2011 | Second Faculty of Medicine
- Homozygosity mapping of a second gene locus for hereditary combined deficiency of vitamin K-dependent clotting factors to the centromeric region of chromosome 162002 | Central Library of Charles University
- Modifier gene study of meconium ileus in cystic fibrosis: statistical considerations and gene mapping results2009 | Second Faculty of Medicine
- Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia2016 | First Faculty of Medicine
- DCDC2 Mutations Cause a Renal-Hepatic Ciliopathy by Disrupting Wnt Signaling2015 | First Faculty of Medicine
- Human leukocyte antigen association with familial steroid-sensitive nephrotic syndrome2020 | Second Faculty of Medicine
- Genomic Determinants of Triglyceride and Cholesterol Distribution into Lipoprotein Fractions in the Rat2014 | First Faculty of Medicine
- Quantitative trait loci for stress and candidate gene sof Essentials hypertension2005 | First Faculty of Medicine
- Quantitative trait loci for stress and candidate gene sof Essentials hypertension2005 | Faculty of Physical Education and Sport
- Quantitative founder effect analysis of French-Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension2005 | First Faculty of Medicine
- Quantitative founder effect analysis of French-Canadian families identifies specific loci contributing to metabolic phenotypes of hypertension2005 | Faculty of Physical Education and Sport
- Suggestive evidence for linkage for restless legs syndrome on chromosome 19p132008 | Publication without faculty affiliation
- Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 22003 | First Faculty of Medicine
- Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 22003 | Faculty of Physical Education and Sport
- PKD1 and PKD2 mutations in Slovenian families with autosomal dominant polycystic kidney disease2006 | First Faculty of Medicine
- PKD1 and PKD2 mutations in Slovenian families with autosomal dominant polycystic kidney disease2006 | Faculty of Physical Education and Sport
- Structural compatibility of novel nucleotide modifications with shortened linkages designed for antigene/antisense therapy2004 | Faculty of Mathematics and Physics, Central Library of Charles University
- Analysis of SYNJI, a candidate gene for 21q22 linked bipolar disorder. A replication study2004 | First Faculty of Medicine