Karine Hovanes
- Molecular Biology top 10%
- Immunology top 5%
- Neurology top 2%
- Genetics top 5%
- Pediatrics, Perinatology and Child Health top 5%
- Co-authors
- Marian L. WatermanJuha PalonevaRandall F. HolcombeTatjana MilovanovićJoan MarshAndrea SalmaggiGrant P. ChristmanYrjö T. Konttinen
- Topics
- Genomic variations and chromosomal abnormalities (9 papers)Prenatal Screening and Diagnostics (7 papers)Wnt/β-catenin signaling in development and cancer (4 papers)
- Cited by
- NeurologyImmunologyGenetics
- Partner nations
- United StatesCanadaFinland
In The Last Decade
Karine Hovanes
27 papers receiving 1.9k citations
Hit Papers
Peers
Comparison fields: 5 of 94
- Molecular Biology 978
- Immunology 517
- Neurology 447
- Genetics 444
- Pediatrics, Perinatology and Child Health 262
Countries citing papers authored by Karine Hovanes
This map shows the geographic impact of Karine Hovanes'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 Karine Hovanes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karine Hovanes more than expected).
Fields of papers citing papers by Karine Hovanes
This network shows the impact of papers produced by Karine Hovanes. 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 Karine Hovanes. The network helps show where Karine Hovanes may publish in the future.
Co-authorship network of co-authors of Karine Hovanes
This figure shows the co-authorship network connecting the top 25 collaborators of Karine Hovanes. A scholar is included among the top collaborators of Karine Hovanes 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 Karine Hovanes. Karine Hovanes is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 21 | |
| 2 | 53 | |
| 3 | 62 | |
| 4 | 3 | |
| 5 | 120 | |
| 6 | 6 | |
| 7 | 16 | |
| 8 | 80 | |
| 9 | 12 | |
| 10 | 10 | |
| 11 | 36 | |
| 12 | 41 | |
| 13 | 91 | |
| 14 | 67 | |
| 15 | Mutations in Two Genes Encoding Different Subunits of a Receptor Signaling Complex Result in an Identical Disease Phenotypebreakdown → | 522 |
| 16 | 84 | |
| 17 | 68 | |
| 18 | 133 | |
| 19 | 3 | |
| 20 | 22 |
About Karine Hovanes
Karine Hovanes is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Immunology, having authored 28 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (7 papers) and Wnt/β-catenin signaling in development and cancer (4 papers). The work is most often cited by research in Neurology (447 citations), Immunology (517 citations) and Genetics (444 citations). Karine Hovanes has collaborated with scholars based in United States, Canada and Finland. Frequent co-authors include Marian L. Waterman, Juha Paloneva, Randall F. Holcombe, Tatjana Milovanović, Joan Marsh, Andrea Salmaggi, Grant P. Christman, Yrjö T. Konttinen, Rolf Adolfsson and Leena Peltonen. Their work appears in journals such as Nucleic Acids Research, Journal of Biological Chemistry and Nature Genetics.
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.