Z Gelman-Kohan
- Molecular Biology
- Clinical Biochemistry top 5%
- Genetics
- Pediatrics, Perinatology and Child Health
- Neurology
- Co-authors
- Orly ElpelegJan LoeffenW. RuitenbeekDiederik de BruijnEdwin C.M. MarimanJan SmeıtınkLambert van den HeuvelRoel Smeets
- Topics
- Genomic variations and chromosomal abnormalities (3 papers)Soft tissue tumor case studies (2 papers)Prenatal Screening and Diagnostics (2 papers)
- Partner nations
- IsraelNetherlands
In The Last Decade
Z Gelman-Kohan
12 papers receiving 361 citations
Peers
Comparison fields: 5 of 55
- Molecular Biology 264
- Clinical Biochemistry 149
- Genetics 54
- Pediatrics, Perinatology and Child Health 48
- Neurology 42
Countries citing papers authored by Z Gelman-Kohan
This map shows the geographic impact of Z Gelman-Kohan'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 Z Gelman-Kohan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Z Gelman-Kohan more than expected).
Fields of papers citing papers by Z Gelman-Kohan
This network shows the impact of papers produced by Z Gelman-Kohan. 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 Z Gelman-Kohan. The network helps show where Z Gelman-Kohan may publish in the future.
Co-authorship network of co-authors of Z Gelman-Kohan
This figure shows the co-authorship network connecting the top 25 collaborators of Z Gelman-Kohan. A scholar is included among the top collaborators of Z Gelman-Kohan 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 Z Gelman-Kohan. Z Gelman-Kohan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 19 | |
| 2 | 20 | |
| 3 | 6 | |
| 4 | 224 | |
| 5 | 7 | |
| 6 | H19 expression and tumorigenicity of choriocarcinoma derived cell lines. | 25 |
| 7 | 29 | |
| 8 | Ethnic distribution of the fragile X syndrome in Israel: evidence of founder chromosomes(?). | 3 |
| 9 | 6 | |
| 10 | [Huntington's disease: ethical aspects of presymptomatic testing]. | 1 |
| 11 | 14 | |
| 12 | 16 |
About Z Gelman-Kohan
Z Gelman-Kohan is a scholar working on Developmental Biology, Developmental Neuroscience and Genetics, having authored 12 papers that have together received 370 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Soft tissue tumor case studies (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Clinical Biochemistry (149 citations), Molecular Biology (264 citations) and Neurology (42 citations). Z Gelman-Kohan has collaborated with scholars based in Israel and Netherlands. Frequent co-authors include Orly Elpeleg, Jan Loeffen, W. Ruitenbeek, Diederik de Bruijn, Edwin C.M. Mariman, Jan Smeıtınk, Lambert van den Heuvel, Roel Smeets, Frans J.M. Trijbels and Juan Chemke. Their work appears in journals such as The American Journal of Human Genetics, Journal of Medical Genetics and Human 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.