Emine İkbal Atlı
Impact in
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- Glioma Diagnosis and Treatment
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
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- Multiple Myeloma Research and Treatments
Papers in
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- Congenital heart defects research 4
- Cancer-related gene regulation 3
- Genetics 17
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 5
- Genomics and Rare Diseases 4
- Glioma Diagnosis and Treatment 3
- Co-authors
- Hakan Gürkan (42 shared papers)Rasime Kalkan (9 shared papers)Selma Demır (34 shared papers)Mehmet Baysal (2 shared papers)Ahmet Muzaffer Demir (4 shared papers)Hilmi Tozkır (4 shared papers)Sevilhan Artan (2 shared papers)Alı Arslantaş (2 shared papers)
- Journals
- Scientific Reports (1 paper)Journal of Clinical Investigation (1 paper)The Journal of Maternal-Fetal & Neonatal Medicine (1 paper)Gene (1 paper)Critical Reviews in Eukaryotic Gene Expression (1 paper)
- Partner nations
- TürkiyeCyprusUnited States
In The Last Decade
Emine İkbal Atlı
40 papers receiving 206 citations
Peers
Comparison fields: 5 of 44
- Genetics 51
- Hematology 51
- Cancer Research 33
- Molecular Biology 119
- Genetics 46
Countries citing papers authored by Emine İkbal Atlı
This map shows the geographic impact of Emine İkbal Atlı'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 Emine İkbal Atlı with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emine İkbal Atlı more than expected).
Fields of papers citing papers by Emine İkbal Atlı
This network shows the impact of papers produced by Emine İkbal Atlı. 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 Emine İkbal Atlı. The network helps show where Emine İkbal Atlı may publish in the future.
Co-authors
The 25 scholars most cited alongside Emine İkbal Atlı, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 38 | |
| 2 | 2014 | 19 | |
| 3 | 2016 | 16 | |
| 4 | 2020 | 15 | |
| 5 | 2017 | 13 | |
| 6 | 2020 | 10 | |
| 7 | 2021 | 8 | |
| 8 | 2017 | 8 | |
| 9 | 2021 | 7 | |
| 10 | 2021 | 7 | |
| 11 | 2019 | 7 | |
| 12 | 2021 | 6 | |
| 13 | 2020 | 6 | |
| 14 | 2020 | 5 | |
| 15 | 2022 | 5 | |
| 16 | 2018 | 4 | |
| 17 | 2020 | 3 | |
| 18 | 2016 | 3 | |
| 19 | 2017 | 3 | |
| 20 | 2019 | 3 |
About Emine İkbal Atlı
Emine İkbal Atlı is a scholar working on Molecular Biology, Genetics, Genetics, Surgery and Pediatrics, Perinatology and Child Health, having authored 48 papers that have together received 212 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), Congenital heart defects research (4 papers), Genomics and Rare Diseases (4 papers), Cancer-related gene regulation (3 papers), Glioma Diagnosis and Treatment (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Genetics (51 citations), Hematology (51 citations), Cancer Research (33 citations), Molecular Biology (119 citations) and Genetics (46 citations). Emine İkbal Atlı has collaborated with scholars based in Türkiye, Cyprus and United States. Frequent co-authors include Hakan Gürkan, Rasime Kalkan, Selma Demır, Mehmet Baysal, Ahmet Muzaffer Demir, Hilmi Tozkır, Sevilhan Artan, Alı Arslantaş, İşık Görker and Füsun Varol. Their work appears in journals such as Scientific Reports, Journal of Clinical Investigation, The Journal of Maternal-Fetal & Neonatal Medicine, Gene and Critical Reviews in Eukaryotic Gene Expression.
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.