Avni Santani
- Genetics top 5%
- Molecular Biology
- Cancer Research
- Cellular and Molecular Neuroscience
- Pulmonary and Respiratory Medicine
- Co-authors
- Madhuri HegdeCatherine A. StolleBirgit FunkeElaine H. ZackaiTerje RaudseppBhanu P. ChowdharyKristin McDonald GibsonMatthew S. Lebo
- Topics
- Genomics and Rare Diseases (14 papers)Genomic variations and chromosomal abnormalities (10 papers)Cancer Genomics and Diagnostics (5 papers)
- Journals
- Proceedings of the National Academy of SciencesPLoS ONEThe American Journal of Human Genetics
- Partner nations
- United StatesUnited KingdomAustria
In The Last Decade
Avni Santani
37 papers receiving 767 citations
Peers
Comparison fields: 5 of 75
- Genetics 439
- Molecular Biology 405
- Cancer Research 110
- Cellular and Molecular Neuroscience 93
- Pulmonary and Respiratory Medicine 69
Countries citing papers authored by Avni Santani
This map shows the geographic impact of Avni Santani'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 Avni Santani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Avni Santani more than expected).
Fields of papers citing papers by Avni Santani
This network shows the impact of papers produced by Avni Santani. 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 Avni Santani. The network helps show where Avni Santani may publish in the future.
Co-authorship network of co-authors of Avni Santani
This figure shows the co-authorship network connecting the top 25 collaborators of Avni Santani. A scholar is included among the top collaborators of Avni Santani 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 Avni Santani. Avni Santani 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 | 2 | |
| 3 | 6 | |
| 4 | 4 | |
| 5 | 1 | |
| 6 | 13 | |
| 7 | 10 | |
| 8 | 17 | |
| 9 | 27 | |
| 10 | 34 | |
| 11 | 14 | |
| 12 | 22 | |
| 13 | 129 | |
| 14 | 23 | |
| 15 | 1 | |
| 16 | 5 | |
| 17 | 48 | |
| 18 | 80 | |
| 19 | 1 | |
| 20 | 22 |
About Avni Santani
Avni Santani is a scholar working on Genetics, Cancer Research and Clinical Biochemistry, having authored 39 papers that have together received 781 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (10 papers) and Cancer Genomics and Diagnostics (5 papers). The work is most often cited by research in Genetics (439 citations), Cancer Research (110 citations) and Molecular Biology (405 citations). Avni Santani has collaborated with scholars based in United States, United Kingdom and Austria. Frequent co-authors include Madhuri Hegde, Catherine A. Stolle, Birgit Funke, Elaine H. Zackai, Terje Raudsepp, Bhanu P. Chowdhary, Kristin McDonald Gibson, Matthew S. Lebo, Ryan J. Schmidt and Diana Mandelker. Their work appears in journals such as Proceedings of the National Academy of Sciences, PLoS ONE and The American Journal of 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.