Henriett Pikó
- Molecular Biology
- Genetics
- Pediatrics, Perinatology and Child Health
- Cardiology and Cardiovascular Medicine
- Public Health, Environmental and Occupational Health
- Co-authors
- Veronika KarcagiArtúr BekeGyörgy FeketeIrén HaltrichJudit PásztiBéla NagyÁgnes HerczegfalviJános P. Kósa
- Topics
- Genomic variations and chromosomal abnormalities (8 papers)Genetics and Neurodevelopmental Disorders (5 papers)Muscle Physiology and Disorders (4 papers)
In The Last Decade
Henriett Pikó
24 papers receiving 151 citations
Peers
Comparison fields: 5 of 54
- Molecular Biology 63
- Genetics 52
- Pediatrics, Perinatology and Child Health 21
- Cardiology and Cardiovascular Medicine 17
- Public Health, Environmental and Occupational Health 15
Countries citing papers authored by Henriett Pikó
This map shows the geographic impact of Henriett Pikó'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 Henriett Pikó with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Henriett Pikó more than expected).
Fields of papers citing papers by Henriett Pikó
This network shows the impact of papers produced by Henriett Pikó. 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 Henriett Pikó. The network helps show where Henriett Pikó may publish in the future.
Co-authorship network of co-authors of Henriett Pikó
This figure shows the co-authorship network connecting the top 25 collaborators of Henriett Pikó. A scholar is included among the top collaborators of Henriett Pikó 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 Henriett Pikó. Henriett Pikó is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 0 | |
| 3 | 4 | |
| 4 | 3 | |
| 5 | 1 | |
| 6 | 15 | |
| 7 | 6 | |
| 8 | 2 | |
| 9 | 1 | |
| 10 | 5 | |
| 11 | 8 | |
| 12 | 9 | |
| 13 | 3 | |
| 14 | 1 | |
| 15 | 5 | |
| 16 | 6 | |
| 17 | 17 | |
| 18 | 19 | |
| 19 | [Screening for hereditary neuromuscular disorders with molecular genetic methods in the Roma population of Hungary]. | 2 |
| 20 | 19 |
About Henriett Pikó
Henriett Pikó is a scholar working on Anatomy, Genetics and Molecular Biology, having authored 28 papers that have together received 153 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Muscle Physiology and Disorders (4 papers). The work is most often cited by research in Molecular Medicine (10 citations), Endocrinology (10 citations) and Genetics (52 citations). Henriett Pikó has collaborated with scholars based in Hungary, Portugal and Germany. Frequent co-authors include Veronika Karcagi, Artúr Beke, György Fekete, Irén Haltrich, Judit Pászti, Béla Nagy, Ágnes Herczegfalvi, János P. Kósa, Noémi Nógrády and Zoltán Bán. Their work appears in journals such as International Journal of Molecular Sciences, Modern Pathology and Clinical Chemistry and Laboratory Medicine (CCLM).
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.