A Baxová
Impact in
- Genetics top 10%
- Craniofacial Disorders and Treatments
- Connective tissue disorders research
- Cleft Lip and Palate Research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 21
- Genetic and Kidney Cyst Diseases 3
- Connective tissue disorders research 3
- Craniofacial Disorders and Treatments 3
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- RNA regulation and disease 3
- Renal and related cancers 2
- Wnt/β-catenin signaling in development and cancer 2
- Co-authors
- Štěpán Kutílek (3 shared papers)Andrew O.M. Wilkie (1 shared paper)Gillian Morriss‐Kay (1 shared paper)Steven A. Wall (1 shared paper)Chong Ae Kim (2 shared papers)Lampros A. Mavrogiannis (2 shared papers)K. Kozlowski (10 shared papers)J Zeman (10 shared papers)
In The Last Decade
A Baxová
36 papers receiving 335 citations
Peers
Comparison fields: 5 of 64
- Genetics 205
- Developmental Biology 15
- Molecular Biology 175
- Genetics 21
- Rheumatology 25
Countries citing papers authored by A Baxová
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
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-authors
The 25 scholars most cited alongside A Baxová, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 109 | |
| 2 | 2011 | 37 | |
| 3 | FGFR2 gene mutation (Tyr375Cys) in a new case of Beare-Stevenson syndrome. | 1998 | 23 |
| 4 | 2007 | 19 | |
| 5 | 2014 | 16 | |
| 6 | 1994 | 12 | |
| 7 | 1998 | 11 | |
| 8 | 1997 | 10 | |
| 9 | 2018 | 9 | |
| 10 | 2009 | 9 | |
| 11 | X-linked dominant chondrodysplasia punctata (CDPX2): multisystemic impact of the defect in cholesterol biosynthesis. | 2007 | 7 |
| 12 | 2018 | 6 | |
| 13 | 2016 | 6 | |
| 14 | 1997 | 6 | |
| 15 | 2020 | 6 | |
| 16 | 2015 | 5 | |
| 17 | 1994 | 4 | |
| 18 | 2014 | 4 | |
| 19 | 2011 | 4 | |
| 20 | 1993 | 3 |
About A Baxová
A Baxová is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 39 papers that have together received 337 indexed citations. Recurring topics across this work include Fetal and Pediatric Neurological Disorders (3 papers), Genetic and Kidney Cyst Diseases (3 papers), RNA regulation and disease (3 papers), Connective tissue disorders research (3 papers), Craniofacial Disorders and Treatments (3 papers), Renal and related cancers (2 papers), interferon and immune responses (2 papers) and Wnt/β-catenin signaling in development and cancer (2 papers). The work is most often cited by research in Genetics (205 citations), Developmental Biology (15 citations), Molecular Biology (175 citations), Genetics (21 citations) and Rheumatology (25 citations). A Baxová has collaborated with scholars based in Czechia, Australia and Slovakia. Frequent co-authors include Štěpán Kutílek, Andrew O.M. Wilkie, Gillian Morriss‐Kay, Steven A. Wall, Chong Ae Kim, Lampros A. Mavrogiannis, K. Kozlowski, J Zeman, Pavel Calda and Jitka Štekrová. Their work appears in journals such as The Journal of Dermatology, Gene, Journal of Child Neurology, BMC Nephrology and Brain and Development.
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.