Davut Pehli̇van
- Co-authors
- James R. LupskiClaudia M.B. CarvalhoRichard A. GibbsShalini N. JhangianiEnder KaracaZeynep Coban‐AkdemirDonna M. MuznyYavuz Bayram
- Topics
- Genetics and Neurodevelopmental Disorders (16 papers)Genomic variations and chromosomal abnormalities (12 papers)Genomics and Rare Diseases (10 papers)
- Partner nations
- United StatesTürkiyeKuwait
In The Last Decade
Davut Pehli̇van
53 papers receiving 1.0k citations
Hit Papers
Peers
Comparison fields: 5 of 94
- Molecular Biology 656
- Genetics 508
- Cellular and Molecular Neuroscience 117
- Plant Science 102
- Cell Biology 77
Countries citing papers authored by Davut Pehli̇van
This map shows the geographic impact of Davut Pehli̇van'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 Davut Pehli̇van with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Davut Pehli̇van more than expected).
Fields of papers citing papers by Davut Pehli̇van
This network shows the impact of papers produced by Davut Pehli̇van. 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 Davut Pehli̇van. The network helps show where Davut Pehli̇van may publish in the future.
Co-authorship network of co-authors of Davut Pehli̇van
This figure shows the co-authorship network connecting the top 25 collaborators of Davut Pehli̇van. A scholar is included among the top collaborators of Davut Pehli̇van 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 Davut Pehli̇van. Davut Pehli̇van 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 | Detection of mosaic and population-level structural variants with Sniffles2breakdown → | 118 |
| 4 | 3 | |
| 5 | 0 | |
| 6 | 2 | |
| 7 | 0 | |
| 8 | 3 | |
| 9 | 1 | |
| 10 | 6 | |
| 11 | 0 | |
| 12 | 7 | |
| 13 | 9 | |
| 14 | 0 | |
| 15 | 9 | |
| 16 | 60 | |
| 17 | 29 | |
| 18 | 2 | |
| 19 | 18 | |
| 20 | 46 |
About Davut Pehli̇van
Davut Pehli̇van is a scholar working on Genetics, Internal Medicine and Molecular Biology, having authored 62 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (16 papers), Genomic variations and chromosomal abnormalities (12 papers) and Genomics and Rare Diseases (10 papers). The work is most often cited by research in Genetics (508 citations), Molecular Biology (656 citations) and Cellular and Molecular Neuroscience (117 citations). Davut Pehli̇van has collaborated with scholars based in United States, Türkiye and Kuwait. Frequent co-authors include James R. Lupski, Claudia M.B. Carvalho, Richard A. Gibbs, Shalini N. Jhangiani, Ender Karaca, Zeynep Coban‐Akdemir, Donna M. Muzny, Yavuz Bayram, Ping Fang and Melissa B. Ramocki. Their work appears in journals such as Nucleic Acids Research, Nature Genetics and Nature Biotechnology.
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.