- Paediatric diabetes subtypes in a consanguineous population: a single-centre cohort study from Kurdistan, Iraq2024 | Second Faculty of Medicine
- Louis-Bar Syndrome of Ataxia Telangiectasia in Consanguinous Family2006 | Second Faculty of Medicine
- The invaluable role of consanguinity in providing insight into paediatric endocrine conditions: Lessons learned from congenital hyperinsulinism, monogenic diabetes, and short stature2022 | Second Faculty of Medicine
- A novel variant of C12orf4 in a consanguineous Armenian family confirms the etiology of autosomal recessive intellectual disability type 66 with delineation of the phenotype2019 | Second Faculty of Medicine, First Faculty of Medicine
- Phantom of consanguineousness1999 | Faculty of Science
- Congenital hyperinsulinism caused by novel homozygous katp channel gene variants may be linked to unexplained neonatal deaths among kurdish consanguineous families2020 | Second Faculty of Medicine
- DFNB35 due to a novel mutation in the ESRRB gene in a Czech consanguineous family2012 | Second Faculty of Medicine, Central Library of Charles University
- Appreciating the otherness2022 | Faculty of Social Sciences
- A founder COL4A4 pathogenic variant resulting in autosomal recessive Alport syndrome accounts for most genetic kidney failure in Romani people2023 | Second Faculty of Medicine, Central Library of Charles University, Third Faculty of Medicine, Faculty of Medicine in Pilsen
- 150 Years of Anthropology: Tylor, Morgan and Miklouho-Maclay or Culture, Comparison and Field Research in 18712021 | Faculty of Social Sciences
- Contiguous hemizygous deletion of TBX5, TBX3, and RBM19 resulting in a combined phenotype of Holt-Oram and ulnar-mammary syndromes2006 | Second Faculty of Medicine
- Evidence of occupational following among politicians in Victoria2015 | Faculty of Arts
- Reflexion of Institutions of Roman Law of Persons in Modern Codifications2015 | Faculty of Law
- The Power of kith and kin: Empirical evidence of kin among public administrators, judges and notaries, in the Czech Republic2016 | Faculty of Arts
- Biological relationships and frontal sinus similarity in skeletal remains with known genealogical data2020 | Faculty of Science, First Faculty of Medicine
- A progressive KY myopathy could be caused by a missense pathogenic variant2023 | Second Faculty of Medicine
- Hereditary haemochromatosis caused by homozygous HJV mutation evolved through paternal disomy2015 | Central Library of Charles University, First Faculty of Medicine
- Kinship terminology in Czech Sign Language2016 | Faculty of Arts
- The homozygous KCNQ1 gene mutation associated with recessive Romano-Ward syndrome2006 | Publication without faculty affiliation
- Psycho-organic symptoms as early manifestation of adult onset POMT1 - related limb girdle muscular dystrophy2014 | Second Faculty of Medicine
- Recessive ITPA Mutations Cause an Early Infantile Encephalopathy2015 | First Faculty of Medicine
- Joint Closing Workshop of the IGCP/UNESCO/SIDA Projects 594 and 6062014 | Faculty of Science
- Women of Abencerrajes (Ibn al-Sarrāj): Kinship Strategies in Fifteenth Century Granada2023 | Faculty of Arts
- DFNB49 is an important cause of non-syndromic deafness in Czech Roma patients but not in the general Czech population2012 | Second Faculty of Medicine
- Homozygosity mapping in a family with microcephaly, mental retardation, and short stature to a Cohen syndrome region on 8q21.3-8q22.1: Redefining a clinical entity2000 | Central Library of Charles University
- Recessive mutations in SLC35A3 cause early onset epileptic encephalopathy with skeletal defects2017 | Second Faculty of Medicine
- Premature chromosome condensation in humans associated with microcephaly and mental retardation: A novel autosomal recessive condition2002 | Central Library of Charles University
- An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome2015 | Second Faculty of Medicine
- Franz Köstl, the first-ever professor of psychiatry in Prague (on ocassion of the 200th birth anniversary)2011 | Third Faculty of Medicine
- Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia2022 | Second Faculty of Medicine