A Baxová

800 total citations
40 papers, 416 citations indexed

About

A Baxová is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, A Baxová has authored 40 papers receiving a total of 416 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 18 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in A Baxová's work include Connective tissue disorders research (4 papers), RNA regulation and disease (3 papers) and Renal and related cancers (3 papers). A Baxová is often cited by papers focused on Connective tissue disorders research (4 papers), RNA regulation and disease (3 papers) and Renal and related cancers (3 papers). A Baxová collaborates with scholars based in Czechia, Australia and Slovakia. A Baxová's co-authors include Štěpán Kutílek, Andrew O.M. Wilkie, Chong Ae Kim, Lampros A. Mavrogiannis, Gillian Morriss‐Kay, Steven A. Wall, K. Kozlowski, J Zeman, Pavel Calda and Sheila Unger and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

A Baxová

37 papers receiving 414 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A Baxová Czechia 10 246 243 49 39 33 40 416
Emma Hobson United Kingdom 9 256 1.0× 213 0.9× 30 0.6× 40 1.0× 42 1.3× 24 405
Maria Luigia Cavaliere Italy 13 171 0.7× 257 1.1× 36 0.7× 34 0.9× 28 0.8× 19 372
Nina Bögershausen Germany 11 234 1.0× 280 1.2× 46 0.9× 28 0.7× 16 0.5× 13 444
Marjan M. Nezarati Canada 10 198 0.8× 232 1.0× 23 0.5× 57 1.5× 40 1.2× 17 447
Maria Rosaria Piemontese Italy 12 141 0.6× 248 1.0× 111 2.3× 31 0.8× 17 0.5× 23 393
Wim Brussel Netherlands 6 115 0.5× 241 1.0× 32 0.7× 23 0.6× 41 1.2× 8 363
Natalie C. Butterfield Australia 12 162 0.7× 332 1.4× 22 0.4× 33 0.8× 55 1.7× 16 482
Eri Imagawa Japan 13 170 0.7× 250 1.0× 24 0.5× 41 1.1× 26 0.8× 30 418
Florian Witte Germany 12 158 0.6× 525 2.2× 70 1.4× 37 0.9× 66 2.0× 12 620
Olivier Pichon France 13 258 1.0× 416 1.7× 22 0.4× 43 1.1× 25 0.8× 30 576

Countries citing papers authored by A Baxová

Since Specialization
Citations

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

Fields of papers citing papers by A Baxová

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Baxová

This figure shows the co-authorship network connecting the top 25 collaborators of A Baxová. A scholar is included among the top collaborators of A Baxová 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 A Baxová. A Baxová 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.
Zikánová, Marie, A Baxová, Lenka Nosková, et al.. (2020). Age Dependent Progression of Multiple Epiphyseal Dysplasia and Pseudoachondroplasia Due to Heterozygous Mutations in COMP Gene. SHILAP Revista de lepidopterología. 121(3). 153–162. 3 indexed citations
2.
Tesařová, Markéta, J Zeman, Viktor Stránecký, et al.. (2020). Fatal neonatal nephrocutaneous syndrome in 18 Roma children with EGFR deficiency. The Journal of Dermatology. 47(6). 663–668. 6 indexed citations
3.
Čechová, Anna, A Baxová, J Zeman, et al.. (2019). Attenuated Type of Asphyxiating Thoracic Dysplasia due to Mutations in DYNC2H1 Gene. SHILAP Revista de lepidopterología. 120(4). 124–130. 1 indexed citations
4.
Elišáková, Veronika, M Merta, Jana Reiterová, et al.. (2018). Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease – a case report. BMC Nephrology. 19(1). 163–163. 8 indexed citations
5.
Magner, Martin, et al.. (2018). The Age Dependent Progression of Hajdu-Cheney Syndrome in Two Families. Prague Medical Report. 119(4). 156–164. 6 indexed citations
6.
Včelák, Josef, et al.. (2016). Mutation analysis of TRPS1 gene including core promoter, 5′UTR, and 3′UTR regulatory sequences with insight into their organization. Clinica Chimica Acta. 464. 30–36. 6 indexed citations
7.
Baxová, A, et al.. (2014). Analysis of common SHOX gene sequence variants and ∼4.9-kb PAR1 deletion in ISS patients. Journal of Genetics. 93(2). 505–508. 3 indexed citations
8.
Baxová, A, et al.. (2011). Cryptic Chromosomal Rearrangements in Children with Idiopathic Mental Retardation in the Czech Population. Genetic Testing and Molecular Biomarkers. 15(9). 607–611. 4 indexed citations
9.
10.
Campos‐Xavier, Belinda, Danielle Martinet, John F. Bateman, et al.. (2009). Mutations in the Heparan-Sulfate Proteoglycan Glypican 6 (GPC6) Impair Endochondral Ossification and Cause Recessive Omodysplasia. The American Journal of Human Genetics. 84(6). 760–770. 84 indexed citations
11.
Hadač, Jan, Alena Zumrová, Vladimı́r Bzdúch, et al.. (2007). Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms. Journal of Human Genetics. 52(4). 342–348. 19 indexed citations
12.
Mavrogiannis, Lampros A., A Baxová, Štěpán Kutílek, et al.. (2001). Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects. Nature Genetics. 27(1). 17–18. 109 indexed citations
13.
Mavrogiannis, Lampros A., et al.. (2000). Mutations of the homeobox gene ALX4 in parietal foramina and cranium bifidum: a component of DEFECT 11 syndrome.. The American Journal of Human Genetics. 67. 40–40. 2 indexed citations
14.
Žižka, Ján, et al.. (1998). Brachytelephalangic chondrodysplasia punctata with distinctive phenotype and normal karyotype. American Journal of Medical Genetics. 76(3). 213–216. 11 indexed citations
15.
Zeman, J, et al.. (1997). Opsismodysplasia: A case report. Australasian Radiology. 41(1). 35–37. 3 indexed citations
16.
Vasiľ, M., A Baxová, & K. Kozlowski. (1997). Severe limb abnormalities: Nievergelt or new syndrome?. American Journal of Medical Genetics. 70(1). 48–51. 6 indexed citations
17.
Kutílek, Štěpán, et al.. (1997). Foramina parietalia permagna: Report of nine cases in one family. Journal of Paediatrics and Child Health. 33(2). 168–170. 9 indexed citations
18.
Baxová, A, et al.. (1996). Lethal kyphomelic dysplasia. Journal of Paediatrics and Child Health. 32(2). 188–190. 2 indexed citations
19.
Baxová, A, et al.. (1994). Mesomelic dysplasia: Langer type. Australasian Radiology. 38(1). 58–60. 1 indexed citations
20.
Baxová, A, et al.. (1994). Parental consanguinity in two sibs with omodysplasia. American Journal of Medical Genetics. 49(3). 263–265. 12 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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