Nahid Tayebi
Impact in
- Cell Biology top 0.5%
- Cellular transport and secretion
- Physiology top 0.5%
- Lysosomal Storage Disorders Research
Papers in
- Physiology 67
- Lysosomal Storage Disorders Research 67
- Cell Biology 47
- Cellular transport and secretion 47
- Co-authors
- Ellen Sidransky (69 shared papers)Barbara Stubblefield (23 shared papers)Joseph K. Park (10 shared papers)M. Javad Aman (2 shared papers)Eduard Orviský (8 shared papers)Warren J. Leonard (2 shared papers)Deborah L. Stone (7 shared papers)Victor Madike (5 shared papers)
- Journals
- Molecular Genetics and Metabolism (19 papers)Human Mutation (5 papers)Blood Cells Molecules and Diseases (3 papers)European Journal of Human Genetics (2 papers)Movement Disorders (2 papers)
- Partner nations
- United StatesIsraelNetherlands
In The Last Decade
Nahid Tayebi
72 papers receiving 4.0k citations
Nahid Tayebi's Hit Papers
Peers
Comparison fields: 5 of 100
- Cell Biology 1.8k
- Physiology 2.6k
- Neurology 921
- Physiology 170
- Immunology 691
Countries citing papers authored by Nahid Tayebi
This map shows the geographic impact of Nahid Tayebi'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 Nahid Tayebi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nahid Tayebi more than expected).
Fields of papers citing papers by Nahid Tayebi
This network shows the impact of papers produced by Nahid Tayebi. 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 Nahid Tayebi. The network helps show where Nahid Tayebi may publish in the future.
Co-authors
The 25 scholars most cited alongside Nahid Tayebi, 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 74 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutation of Jak3 in a Patient with SCID: Essential Role of Jak3 in Lymphoid Development Hit paper breakdown → | 1995 | 641 |
| 2 | Reduced glucocerebrosidase is associated with increased α-synuclein in sporadic Parkinson’s disease Hit paper breakdown → | 2014 | 382 |
| 3 | 1996 | 252 | |
| 4 | 2003 | 244 | |
| 5 | 2000 | 226 | |
| 6 | 2000 | 170 | |
| 7 | 2001 | 163 | |
| 8 | 2002 | 155 | |
| 9 | 1998 | 140 | |
| 10 | 2003 | 116 | |
| 11 | 2014 | 97 | |
| 12 | 2012 | 95 | |
| 13 | 2003 | 84 | |
| 14 | 2003 | 71 | |
| 15 | 2011 | 68 | |
| 16 | 2013 | 68 | |
| 17 | 2011 | 61 | |
| 18 | 2010 | 58 | |
| 19 | 2018 | 56 | |
| 20 | 2010 | 54 |
About Nahid Tayebi
Nahid Tayebi is a scholar working on Physiology, Cell Biology, Molecular Biology, Organic Chemistry and Neurology, having authored 74 papers that have together received 4.1k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (67 papers), Cellular transport and secretion (47 papers), Carbohydrate Chemistry and Synthesis (21 papers), Glycosylation and Glycoproteins Research (19 papers), Parkinson's Disease Mechanisms and Treatments (14 papers), Studies on Chitinases and Chitosanases (7 papers), Glycogen Storage Diseases and Myoclonus (4 papers) and CRISPR and Genetic Engineering (3 papers). The work is most often cited by research in Cell Biology (1.8k citations), Physiology (2.6k citations), Neurology (921 citations), Physiology (170 citations) and Immunology (691 citations). Nahid Tayebi has collaborated with scholars based in United States, Israel and Netherlands. Frequent co-authors include Ellen Sidransky, Barbara Stubblefield, Joseph K. Park, M. Javad Aman, Eduard Orviský, Warren J. Leonard, Deborah L. Stone, Victor Madike, Sarah M. Russell and Joseph L. Roberts. Their work appears in journals such as Molecular Genetics and Metabolism, Human Mutation, Blood Cells Molecules and Diseases, European Journal of Human Genetics and Movement Disorders.
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.