Tayfun Özçelık
Impact in
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- Circadian rhythm and melatonin
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
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- DNA Repair Mechanisms 4
- RNA Research and Splicing 3
- Epigenetics and DNA Methylation 3
- Genetics 22
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
- Genetics and Neurodevelopmental Disorders 4
- BRCA gene mutations in cancer 3
- Co-authors
- Uta Francke (10 shared papers)Onur Emre Onat (16 shared papers)Cemaliye Boylu Akyerli (8 shared papers)Philip M. Murphy (2 shared papers)Gökçe Törüner (5 shared papers)Elif Uz (7 shared papers)Patricia Murphy (1 shared paper)Alina Patke (1 shared paper)
- Journals
- Proceedings of the National Academy of Sciences (4 papers)European Journal of Human Genetics (3 papers)Nature Genetics (3 papers)PLoS ONE (2 papers)Clinical Reviews in Allergy & Immunology (2 papers)
- Partner nations
- TürkiyeUnited StatesUnited Kingdom
In The Last Decade
Tayfun Özçelık
58 papers receiving 3.1k citations
Peers
Comparison fields: 5 of 105
- Endocrine and Autonomic Systems 245
- Genetics 807
- Cellular and Molecular Neuroscience 519
- Aging 40
- Neurology 165
Countries citing papers authored by Tayfun Özçelık
This map shows the geographic impact of Tayfun Özçelık'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 Tayfun Özçelık with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tayfun Özçelık more than expected).
Fields of papers citing papers by Tayfun Özçelık
This network shows the impact of papers produced by Tayfun Özçelık. 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 Tayfun Özçelık. The network helps show where Tayfun Özçelık may publish in the future.
Co-authors
The 25 scholars most cited alongside Tayfun Özçelık, 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 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1992 | 337 | |
| 2 | 2017 | 256 | |
| 3 | 1992 | 213 | |
| 4 | 1993 | 201 | |
| 5 | 1992 | 178 | |
| 6 | 1990 | 137 | |
| 7 | 2005 | 124 | |
| 8 | 2012 | 102 | |
| 9 | 1995 | 98 | |
| 10 | 2014 | 95 | |
| 11 | 2006 | 90 | |
| 12 | 1992 | 90 | |
| 13 | 2002 | 78 | |
| 14 | 2008 | 73 | |
| 15 | 2009 | 73 | |
| 16 | 2001 | 71 | |
| 17 | 2002 | 67 | |
| 18 | 1992 | 60 | |
| 19 | 2021 | 53 | |
| 20 | 2011 | 53 |
About Tayfun Özçelık
Tayfun Özçelık is a scholar working on Molecular Biology, Genetics, Oncology, Pediatrics, Perinatology and Child Health and Surgery, having authored 59 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), DNA Repair Mechanisms (4 papers), Fetal and Pediatric Neurological Disorders (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), RNA Research and Splicing (3 papers), Epigenetics and DNA Methylation (3 papers), BRCA gene mutations in cancer (3 papers) and T-cell and B-cell Immunology (3 papers). The work is most often cited by research in Endocrine and Autonomic Systems (245 citations), Genetics (807 citations), Cellular and Molecular Neuroscience (519 citations), Aging (40 citations) and Neurology (165 citations). Tayfun Özçelık has collaborated with scholars based in Türkiye, United States and United Kingdom. Frequent co-authors include Uta Francke, Onur Emre Onat, Cemaliye Boylu Akyerli, Philip M. Murphy, Gökçe Törüner, Elif Uz, Patricia Murphy, Alina Patke, Michael W. Young and Béla Kosaras. Their work appears in journals such as Proceedings of the National Academy of Sciences, European Journal of Human Genetics, Nature Genetics, PLoS ONE and Clinical Reviews in Allergy & Immunology.
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.