Shay Tzur
Impact in
- Nephrology top 0.5%
- Renal Diseases and Glomerulopathies
- Chronic Kidney Disease and Diabetes
- Genetics top 5%
- Forensic and Genetic Research
- Chronic Lymphocytic Leukemia Research
- Genetic diversity and population structure
- Race, Genetics, and Society
- Genetic Associations and Epidemiology
Papers in
-
- Mitochondrial Function and Pathology 5
- RNA and protein synthesis mechanisms 5
- Genetics 16
- Chronic Lymphocytic Leukemia Research 6
- Forensic and Genetic Research 5
- Genetic diversity and population structure 4
- Co-authors
- Saharon Rosset (15 shared papers)Karl Skorecki (13 shared papers)Walter G. Wasser (9 shared papers)Doron M. Behar (6 shared papers)Doron M. Behar (13 shared papers)Guennady Yudkovsky (3 shared papers)Revital Shemer (3 shared papers)Sara Selig (2 shared papers)
- Journals
- Genetics Research (3 papers)European Journal of Human Genetics (3 papers)The Journal of Clinical Endocrinology & Metabolism (3 papers)Human Mutation (3 papers)PLoS ONE (3 papers)
- Partner nations
- IsraelUnited StatesEstonia
In The Last Decade
Shay Tzur
44 papers receiving 2.1k citations
Shay Tzur's Hit Papers
Peers
Comparison fields: 5 of 130
- Nephrology 715
- Genetics 337
- Genetics 812
- Archeology 20
- Transplantation 49
Countries citing papers authored by Shay Tzur
This map shows the geographic impact of Shay Tzur'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 Shay Tzur with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shay Tzur more than expected).
Fields of papers citing papers by Shay Tzur
This network shows the impact of papers produced by Shay Tzur. 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 Shay Tzur. The network helps show where Shay Tzur may publish in the future.
Co-authors
The 25 scholars most cited alongside Shay Tzur, 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 | Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene Hit paper breakdown → | 2010 | 451 |
| 2 | 2008 | 295 | |
| 3 | 2006 | 118 | |
| 4 | 2014 | 116 | |
| 5 | 2007 | 98 | |
| 6 | 2008 | 88 | |
| 7 | 2011 | 84 | |
| 8 | 2013 | 71 | |
| 9 | 2019 | 70 | |
| 10 | 2012 | 69 | |
| 11 | 2010 | 64 | |
| 12 | 2017 | 63 | |
| 13 | 2011 | 56 | |
| 14 | 2011 | 56 | |
| 15 | 2013 | 47 | |
| 16 | 2016 | 40 | |
| 17 | 2012 | 39 | |
| 18 | 2016 | 33 | |
| 19 | 2013 | 24 | |
| 20 | 2015 | 24 |
About Shay Tzur
Shay Tzur is a scholar working on Molecular Biology, Genetics, Nephrology, Genetics and Cardiology and Cardiovascular Medicine, having authored 44 papers that have together received 2.2k indexed citations. Recurring topics across this work include Renal Diseases and Glomerulopathies (8 papers), Chronic Lymphocytic Leukemia Research (6 papers), Forensic and Genetic Research (5 papers), Mitochondrial Function and Pathology (5 papers), RNA and protein synthesis mechanisms (5 papers), Cardiomyopathy and Myosin Studies (4 papers), Genetic diversity and population structure (4 papers) and Chronic Kidney Disease and Diabetes (4 papers). The work is most often cited by research in Nephrology (715 citations), Genetics (337 citations), Genetics (812 citations), Archeology (20 citations) and Transplantation (49 citations). Shay Tzur has collaborated with scholars based in Israel, United States and Estonia. Frequent co-authors include Saharon Rosset, Karl Skorecki, Walter G. Wasser, Doron M. Behar, Doron M. Behar, Guennady Yudkovsky, Revital Shemer, Sara Selig, Neil Bradman and Endashaw Bekele. Their work appears in journals such as Genetics Research, European Journal of Human Genetics, The Journal of Clinical Endocrinology & Metabolism, Human Mutation and PLoS ONE.
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.