Fulya Taylan
Impact in
- Genetics top 10%
- Connective tissue disorders research
- Genomics and Rare Diseases
- Dermatology top 10%
- Dermatology and Skin Diseases
Papers in
- Genetics 20
- Connective tissue disorders research 9
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 3
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- RNA modifications and cancer 3
- Co-authors
- Outi Mäkitie (13 shared papers)Ann Nordgren (21 shared papers)Anders Kämpe (7 shared papers)Magnus Nordenskjöld (12 shared papers)Alice Costantini (9 shared papers)Anna Lindstrand (9 shared papers)Riikka E. Mäkitie (3 shared papers)Giedré Grigelioniené (3 shared papers)
- Journals
- Clinical Genetics (3 papers)Journal of Medical Genetics (3 papers)Frontiers in Genetics (2 papers)Journal of Bone and Mineral Research (2 papers)Orphanet Journal of Rare Diseases (2 papers)
- Partner nations
- SwedenFinlandUnited States
In The Last Decade
Fulya Taylan
40 papers receiving 627 citations
Peers
Comparison fields: 5 of 73
- Genetics 253
- Dermatology 58
- Immunology and Allergy 39
- Cancer Research 79
- Rheumatology 78
Countries citing papers authored by Fulya Taylan
This map shows the geographic impact of Fulya Taylan'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 Fulya Taylan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fulya Taylan more than expected).
Fields of papers citing papers by Fulya Taylan
This network shows the impact of papers produced by Fulya Taylan. 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 Fulya Taylan. The network helps show where Fulya Taylan may publish in the future.
Co-authors
The 25 scholars most cited alongside Fulya Taylan, 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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 71 | |
| 2 | 2013 | 45 | |
| 3 | 2012 | 41 | |
| 4 | 2016 | 39 | |
| 5 | 2017 | 37 | |
| 6 | 2016 | 34 | |
| 7 | 2017 | 34 | |
| 8 | 2018 | 24 | |
| 9 | 2018 | 21 | |
| 10 | 2020 | 21 | |
| 11 | 2017 | 20 | |
| 12 | 2020 | 19 | |
| 13 | 2016 | 19 | |
| 14 | 2018 | 17 | |
| 15 | 2017 | 17 | |
| 16 | 2015 | 16 | |
| 17 | 2021 | 15 | |
| 18 | 2020 | 12 | |
| 19 | 2017 | 12 | |
| 20 | 2022 | 11 |
About Fulya Taylan
Fulya Taylan is a scholar working on Genetics, Molecular Biology, Oncology, Pathology and Forensic Medicine and Pulmonary and Respiratory Medicine, having authored 44 papers that have together received 631 indexed citations. Recurring topics across this work include Connective tissue disorders research (9 papers), Bone health and treatments (5 papers), Genomics and Rare Diseases (5 papers), Acute Lymphoblastic Leukemia research (4 papers), Acute Myeloid Leukemia Research (4 papers), Dermatology and Skin Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Genetics (253 citations), Dermatology (58 citations), Immunology and Allergy (39 citations), Cancer Research (79 citations) and Rheumatology (78 citations). Fulya Taylan has collaborated with scholars based in Sweden, Finland and United States. Frequent co-authors include Outi Mäkitie, Ann Nordgren, Anders Kämpe, Magnus Nordenskjöld, Alice Costantini, Anna Lindstrand, Riikka E. Mäkitie, Giedré Grigelioniené, Minna Pekkinen and Maria Bradley. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, Frontiers in Genetics, Journal of Bone and Mineral Research and Orphanet Journal of Rare Diseases.
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.