Ralf Werner
Impact in
- Nephrology top 5%
- Parathyroid Disorders and Treatments
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
-
- Sexual Differentiation and Disorders 47
- Genetics 21
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genetic Syndromes and Imprinting 7
- Genomics and Rare Diseases 4
- Co-authors
- Olaf Hiort (57 shared papers)Paul‐Martin Holterhus (26 shared papers)Dagmar Struve (10 shared papers)Susanne Thiele (7 shared papers)Lutz Wünsch (8 shared papers)Ulla Döhnert (5 shared papers)Ieuan A. Hughes (3 shared papers)Trevor Bunch (2 shared papers)
- Journals
- Sexual Development (13 papers)The Journal of Clinical Endocrinology & Metabolism (8 papers)PLoS ONE (4 papers)European Journal of Endocrinology (3 papers)Human Mutation (3 papers)
- Partner nations
- GermanyUnited StatesBrazil
In The Last Decade
Ralf Werner
74 papers receiving 1.8k citations
Peers
Comparison fields: 5 of 97
- Nephrology 204
- Genetics 526
- Molecular Biology 1k
- Reproductive Medicine 98
- Endocrinology, Diabetes and Metabolism 132
Countries citing papers authored by Ralf Werner
This map shows the geographic impact of Ralf Werner'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 Ralf Werner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ralf Werner more than expected).
Fields of papers citing papers by Ralf Werner
This network shows the impact of papers produced by Ralf Werner. 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 Ralf Werner. The network helps show where Ralf Werner may publish in the future.
Co-authors
The 25 scholars most cited alongside Ralf Werner, 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 76 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 109 | |
| 2 | 2014 | 107 | |
| 3 | 2005 | 104 | |
| 4 | 2012 | 101 | |
| 5 | 2015 | 66 | |
| 6 | 2011 | 60 | |
| 7 | 2015 | 57 | |
| 8 | 2016 | 57 | |
| 9 | 2015 | 52 | |
| 10 | 2011 | 50 | |
| 11 | 2006 | 49 | |
| 12 | 2014 | 46 | |
| 13 | 2016 | 44 | |
| 14 | 2017 | 44 | |
| 15 | 2013 | 43 | |
| 16 | 1998 | 40 | |
| 17 | 2006 | 39 | |
| 18 | 1997 | 38 | |
| 19 | 2015 | 38 | |
| 20 | 2018 | 37 |
About Ralf Werner
Ralf Werner is a scholar working on Molecular Biology, Genetics, Nephrology, Urology and Endocrinology, Diabetes and Metabolism, having authored 76 papers that have together received 1.9k indexed citations. Recurring topics across this work include Sexual Differentiation and Disorders (47 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Genetic Syndromes and Imprinting (7 papers), Parathyroid Disorders and Treatments (5 papers), Prostate Cancer Treatment and Research (4 papers), Genomics and Rare Diseases (4 papers), Hormonal and reproductive studies (3 papers) and Plant Virus Research Studies (3 papers). The work is most often cited by research in Nephrology (204 citations), Genetics (526 citations), Molecular Biology (1k citations), Reproductive Medicine (98 citations) and Endocrinology, Diabetes and Metabolism (132 citations). Ralf Werner has collaborated with scholars based in Germany, United States and Brazil. Frequent co-authors include Olaf Hiort, Paul‐Martin Holterhus, Dagmar Struve, Susanne Thiele, Lutz Wünsch, Ulla Döhnert, Ieuan A. Hughes, Trevor Bunch, Wiebke Birnbaum and Louise Marshall. Their work appears in journals such as Sexual Development, The Journal of Clinical Endocrinology & Metabolism, PLoS ONE, European Journal of Endocrinology and Human Mutation.
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.