M. Kohoutová

741 total citations
55 papers, 577 citations indexed

About

M. Kohoutová is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, M. Kohoutová has authored 55 papers receiving a total of 577 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 12 papers in Genetics and 7 papers in Pathology and Forensic Medicine. Recurrent topics in M. Kohoutová's work include Genetic and Kidney Cyst Diseases (7 papers), MicroRNA in disease regulation (6 papers) and Cancer-related molecular mechanisms research (6 papers). M. Kohoutová is often cited by papers focused on Genetic and Kidney Cyst Diseases (7 papers), MicroRNA in disease regulation (6 papers) and Cancer-related molecular mechanisms research (6 papers). M. Kohoutová collaborates with scholars based in Czechia, United States and Netherlands. M. Kohoutová's co-authors include Jitka Štekrová, Jana Reiterová, M Merta, Vít Weinberger, Eva Jandáková, E. Günther, O Stark, Vladimı́r Tesař, Luboš Minář and P. Tichý and has published in prestigious journals such as Nature, Biochemical and Biophysical Research Communications and Journal of Bacteriology.

In The Last Decade

M. Kohoutová

51 papers receiving 556 citations

Peers

M. Kohoutová
Xianming Chen United States
Robert Chin United States
Yumei Yang China
Jianyong Liu China
Michael Nazimiec United States
Wendi Zhou China
Bingjie Chen China
Yuhuan Meng China
Michael Jen Jie Chu New Zealand
Xianming Chen United States
M. Kohoutová
Citations per year, relative to M. Kohoutová M. Kohoutová (= 1×) peers Xianming Chen

Countries citing papers authored by M. Kohoutová

Since Specialization
Citations

This map shows the geographic impact of M. Kohoutová's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by M. Kohoutová with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Kohoutová more than expected).

Fields of papers citing papers by M. Kohoutová

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Kohoutová. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by M. Kohoutová. The network helps show where M. Kohoutová may publish in the future.

Co-authorship network of co-authors of M. Kohoutová

This figure shows the co-authorship network connecting the top 25 collaborators of M. Kohoutová. A scholar is included among the top collaborators of M. Kohoutová based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with M. Kohoutová. M. Kohoutová is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
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Jandáková, Eva, et al.. (2024). Human Endogenous Retroviruses in Breast Cancer: Altered Expression Pattern Implicates Divergent Roles in Carcinogenesis. Oncology. 102(10). 858–867. 7 indexed citations
4.
Jandáková, Eva, et al.. (2017). Cell-Free Urinary MicroRNAs Expression in Small-Scale Experiments. Methods in molecular biology. 1580. 99–106. 2 indexed citations
5.
Jandáková, Eva, Vít Weinberger, Lenka Záveská Drábková, et al.. (2015). Evaluation of Cell-Free Urine microRNAs Expression for the Use in Diagnosis of Ovarian and Endometrial Cancers. A Pilot Study. Pathology & Oncology Research. 21(4). 1027–1035. 61 indexed citations
6.
Elišáková, Veronika, Jitka Štekrová, Jana Reiterová, et al.. (2014). Novel mutations of PKD genes in the Czech population with autosomal dominant polycystic kidney disease. BMC Medical Genetics. 15(1). 41–41. 21 indexed citations
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Šípek, A, et al.. (2014). Heterochromatin variants in human karyotypes: a possible association with reproductive failure. Reproductive BioMedicine Online. 29(2). 245–250. 21 indexed citations
8.
Reiterová, Jana, et al.. (2013). Mutational Analysis of ACTN4, Encoding α-Actinin 4, in Patients with Focal Segmental Glomerulosclerosis Using HRM Method. Folia Biologica. 59(3). 110–115. 5 indexed citations
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Reiterová, Jana, et al.. (2012). TRPC6 Gene Variants in Czech Adult Patients with Focal Segmental Glomerulosclerosis and Minimal Change Disease. Folia Biologica. 58(4). 173–176. 12 indexed citations
10.
Schwarzová, Lucie, Jitka Štekrová, Martina Florianová, et al.. (2012). Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families. Familial Cancer. 12(1). 35–42. 8 indexed citations
11.
Hošek, Petr, Martin Kubeš, Petre I. Dobrev, et al.. (2012). Auxin transport at cellular level: new insights supported by mathematical modelling. Journal of Experimental Botany. 63(10). 3815–3827. 42 indexed citations
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Štekrová, Jitka, et al.. (2009). New mutations in the PKD1 gene in Czech population with autosomal dominant polycystic kidney disease. BMC Medical Genetics. 10(1). 78–78. 9 indexed citations
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Štekrová, Jitka, et al.. (2007). Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects. BMC Medical Genetics. 8(1). 16–16. 22 indexed citations
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Kleibl, Zdeněk, et al.. (2007). Mutation analysis of the MYH gene in unrelated Czech APC mutation-negative polyposis patients. European Journal of Cancer. 43(10). 1617–1621. 8 indexed citations
16.
Štekrová, Jitka, et al.. (2004). PKD2 mutations in a Czech population with autosomal dominant polycystic kidney disease. Nephrology Dialysis Transplantation. 19(5). 1116–1122. 15 indexed citations
17.
Reiterová, Jana, Jitka Štekrová, M. Kohoutová, et al.. (2004). The Influence of G‐Protein β3‐Subunit Gene and Endothelial Nitric Oxide Synthase Gene in Exon 7 Polymorphisms on Progression of Autosomal Dominant Polycystic Kidney Disease. Renal Failure. 26(2). 119–125. 6 indexed citations
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Vandrovcová, Jana, et al.. (2004). Molecular analysis of theAPCandMYHgenes in Czech families affected by FAP or multiple adenomas: 13 novel mutations. Human Mutation. 23(4). 397–397. 26 indexed citations
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Kohoutová, M., et al.. (2002). APCgermline mutations identified in Czech patients with familial adenomatous polyposis. Human Mutation. 19(4). 460–461. 11 indexed citations
20.
Reiterová, Jana, et al.. (2002). Four novel mutations of the PKD2 gene in czech families with autosomal dominant polycystic kidney disease. Human Mutation. 19(5). 573–573. 11 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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