Anna Křepelová

739 total citations
26 papers, 465 citations indexed

About

Anna Křepelová is a scholar working on Genetics, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, Anna Křepelová has authored 26 papers receiving a total of 465 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Pathology and Forensic Medicine and 6 papers in Molecular Biology. Recurrent topics in Anna Křepelová's work include Genetic Neurodegenerative Diseases (5 papers), Immunodeficiency and Autoimmune Disorders (4 papers) and Mitochondrial Function and Pathology (3 papers). Anna Křepelová is often cited by papers focused on Genetic Neurodegenerative Diseases (5 papers), Immunodeficiency and Autoimmune Disorders (4 papers) and Mitochondrial Function and Pathology (3 papers). Anna Křepelová collaborates with scholars based in Czechia, United Kingdom and United States. Anna Křepelová's co-authors include Zdeněk Sedláček, I Žofková, Kateřina Zajíčková, Zuzana Mušová, Markéta Havlovičová, Radim Mazanec, T Maríková, Josef Kraus, Tomáš Procházka and Petra Lišková and has published in prestigious journals such as PLoS ONE, Journal of Bone and Mineral Research and Journal of Cellular Physiology.

In The Last Decade

Anna Křepelová

24 papers receiving 452 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Anna Křepelová Czechia 13 238 133 93 82 73 26 465
Akihide Kondo Japan 15 138 0.6× 133 1.0× 36 0.4× 70 0.9× 58 0.8× 100 646
Dania S. Khalil Saudi Arabia 8 142 0.6× 35 0.3× 140 1.5× 44 0.5× 16 0.2× 11 322
Corinne Bouvier‐Labit France 11 102 0.4× 58 0.4× 23 0.2× 51 0.6× 51 0.7× 16 576
Cécile Cauquil France 14 363 1.5× 67 0.5× 110 1.2× 20 0.2× 89 1.2× 40 579
Helen Marshall United States 7 267 1.1× 24 0.2× 121 1.3× 36 0.4× 100 1.4× 11 595
Yasuyuki Hitoshi Japan 10 267 1.1× 55 0.4× 80 0.9× 27 0.3× 41 0.6× 18 454
Ri-ichiro Kohno Japan 13 439 1.8× 40 0.3× 58 0.6× 23 0.3× 107 1.5× 21 700
Hung‐Lin Lin Taiwan 11 96 0.4× 54 0.4× 24 0.3× 77 0.9× 137 1.9× 20 515
T. Schweitzer Germany 10 179 0.8× 50 0.4× 147 1.6× 28 0.3× 44 0.6× 15 504
Chen Qiu China 10 110 0.5× 42 0.3× 25 0.3× 57 0.7× 25 0.3× 41 359

Countries citing papers authored by Anna Křepelová

Since Specialization
Citations

This map shows the geographic impact of Anna Křepelová'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 Anna Křepelová with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Křepelová more than expected).

Fields of papers citing papers by Anna Křepelová

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anna Křepelová. 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 Anna Křepelová. The network helps show where Anna Křepelová may publish in the future.

Co-authorship network of co-authors of Anna Křepelová

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Křepelová. A scholar is included among the top collaborators of Anna Křepelová 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 Anna Křepelová. Anna Křepelová 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
1.
Schwarz, Martin, Eva Froňková, Michael Svatoň, et al.. (2024). Functional studies associate novel DUOX2 gene variants detected in heterozygosity to Crohn’s disease. Molecular Biology Reports. 51(1). 399–399.
2.
Zieg, Jakub, M. Balaščaková, Katalin Štěrbová, et al.. (2023). Schimke immunoosseous dysplasia: an ultra-rare disease. a 20-year case series from the tertiary hospital in the Czech Republic. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 49(1). 11–11. 4 indexed citations
3.
Paděrová, Jana, Markéta Vlčková, Markéta Havlovičová, et al.. (2018). Under the mask of Kabuki syndrome: Elucidation of genetic-and phenotypic heterogeneity in patients with Kabuki-like phenotype. European Journal of Medical Genetics. 61(6). 315–321. 21 indexed citations
4.
Lišková, Petra, Ľubica Ďuďáková, Anna Křepelová, Jǐŕı Kléma, & Pirro G. Hysi. (2017). Replication of SNP associations with keratoconus in a Czech cohort. PLoS ONE. 12(2). e0172365–e0172365. 18 indexed citations
5.
Křepelová, Anna, et al.. (2016). Analysis of FOXL2 detects three novel mutations and an atypical phenotype of blepharophimosis‐ptosis‐epicanthus inversus syndrome. Clinical and Experimental Ophthalmology. 44(9). 757–762. 8 indexed citations
6.
Ďuďáková, Ľubica, Kateřina Jirsová, Viktor Stránecký, et al.. (2015). Validation of rs2956540:G>C and rs3735520:G>A association with keratoconus in a population of European descent. European Journal of Human Genetics. 23(11). 1581–1583. 28 indexed citations
7.
Mušová, Zuzana, Michaela Kaiserová, Eva Kriegová, et al.. (2013). A Novel Frameshift Mutation in the AFG3L2 Gene in a Patient with Spinocerebellar Ataxia. The Cerebellum. 13(3). 331–337. 15 indexed citations
8.
Mušová, Zuzana, Zdeněk Sedláček, Radim Mazanec, et al.. (2012). Spinocerebellar Ataxias Type 8, 12, and 17 and Dentatorubro-Pallidoluysian Atrophy in Czech Ataxic Patients. The Cerebellum. 12(2). 155–161. 14 indexed citations
9.
Zieg, Jakub, Anna Křepelová, Alireza Baradaran‐Heravi, et al.. (2011). Rituximab resistant evans syndrome and autoimmunity in Schimke immuno-osseous dysplasia. Pediatric Rheumatology. 9(1). 27–27. 15 indexed citations
10.
Sedláček, Zdeněk, et al.. (2011). Molecular Genetic Analysis of 103 Sporadic Colorectal Tumours in Czech Patients. PLoS ONE. 6(8). e24114–e24114. 33 indexed citations
11.
Mušová, Zuzana, Radim Mazanec, Anna Křepelová, et al.. (2009). Highly unstable sequence interruptions of the CTG repeat in the myotonic dystrophy gene. American Journal of Medical Genetics Part A. 149A(7). 1365–1374. 110 indexed citations
12.
Bendová, Šárka, et al.. (2007). Novel mutations in the NF1 gene in Czech patients with neurofibromatosis type 1. Journal of Molecular Neuroscience. 31(3). 273–279. 3 indexed citations
13.
Zumrová, Alena, et al.. (2007). Autosomálně dominantní spinocerebelární ataxie. Neurologie pro praxi. 8(5). 277–282.
14.
Plevová, Pavlína, et al.. (2006). Elejalde syndrome—A case report. American Journal of Medical Genetics Part A. 140A(20). 2223–2226. 6 indexed citations
15.
Zumrová, Alena, Radim Mazanec, Martin Vyhnálek, et al.. (2005). Concomitancy of mutation in FRDA gene and FMR1 premutation in 58 year-old woman.. PubMed. 26(1). 71–4. 3 indexed citations
16.
Trková, Marie, Julie Fleitz, Anna Křepelová, et al.. (2005). Identification of five new families strengthens the link between childhood choroid plexus carcinoma and germline TP53 mutations. European Journal of Cancer. 41(11). 1597–1603. 54 indexed citations
17.
Hájek, Milan, Miriam Adamovičová, Vı́t Herynek, et al.. (2004). MR relaxometry and 1H MR spectroscopy for the determination of iron and metabolite concentrations in PKAN patients. European Radiology. 15(5). 1060–1068. 24 indexed citations
18.
Černý, Jan, et al.. (2003). Biallelic IgH rearrangements in patients with indolent lymphoproliferative disorders: Molecular and practical implications. Journal of Cellular Physiology. 199(2). 217–226. 9 indexed citations
19.
Zajíčková, Kateřina, et al.. (2002). Vitamin D receptor gene polymorphisms, bone mineral density and bone turnover: FokI genotype is related to postmenopausal bone mass. Physiological Research. 51(5). 501–509. 50 indexed citations
20.
Křepelová, Anna, et al.. (1992). Factor VIII gene deletions in haemophilia A patients in Czechoslovakia. British Journal of Haematology. 81(2). 271–276. 5 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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