A Baxová

800 citations
40 papers · 416 · h-index 10

Impact in

  • Genetics top 10%
    • Craniofacial Disorders and Treatments
    • Connective tissue disorders research
    • Cleft Lip and Palate Research
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

Papers in

    • Connective tissue disorders research 4
    • Genetic and Kidney Cyst Diseases 3
    • Craniofacial Disorders and Treatments 3
    • Genetics and Neurodevelopmental Disorders 3
    • RNA regulation and disease 3
    • Renal and related cancers 3

A Baxová

37 papers receiving 414 citations

Peers

A Baxová
Comparison fields: 5 of 71
  • Developmental Biology 21
  • Genetics 246
  • Molecular Biology 243
  • Cell Biology 49
  • Genetics 26
Replace Maria Luigia Cavaliere with:
Maria Luigia Cavaliere Italy
Maria Rosaria Piemontese Italy
Wolfram Heinritz Germany
Wim Brussel Netherlands
Andreas Hehr Germany
Piergiorgio Franceschini Italy
Nina Bögershausen Germany
Olivier Pichon France
Natalie C. Butterfield Australia
Satoshi Ishikiriyama Japan
A Baxová relative to Maria Luigia Cavaliere Italy Maria Luigia Cavaliere's profile →
Citations per field
00.5×1.5×
Maria Luigia Cavaliere · 1×
Citations per year

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-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.

Border = papers with A Baxová Line = papers co-authored together A Baxová links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 40 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2001109
2 200984
3 201136
4
FGFR2 gene mutation (Tyr375Cys) in a new case of Beare-Stevenson syndrome.
199823
5 200719
6 201415
7 199412
8 199811
9 20099
10 19979
11 20188
12
X-linked dominant chondrodysplasia punctata (CDPX2): multisystemic impact of the defect in cholesterol biosynthesis.
20077
13 20186
14 20206
15 20166
16 19976
17 20155
18 20114
19 19944
20 19973

About A Baxová

A Baxová is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 40 papers that have together received 416 indexed citations. Recurring topics across this work include Connective tissue disorders research (4 papers), Genetic and Kidney Cyst Diseases (3 papers), RNA regulation and disease (3 papers), Fetal and Pediatric Neurological Disorders (3 papers), Renal and related cancers (3 papers), Craniofacial Disorders and Treatments (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Medical Imaging and Pathology Studies (2 papers). The work is most often cited by research in Developmental Biology (21 citations), Genetics (246 citations), Molecular Biology (243 citations), Cell Biology (49 citations) and Genetics (26 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, Chong Ae Kim, Steven A. Wall, Lampros A. Mavrogiannis, K. Kozlowski, J Zeman, Pavel Calda and Tiong Yang Tan. Their work appears in journals such as The American Journal of Human Genetics, Gene, Nature Genetics, Pharmacogenomics and BMC Nephrology.

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.

Explore authors with similar magnitude of impact