Bernhard Payer
Impact in
- Cell Biology top 2%
- Hippo pathway signaling and YAP/TAZ
- Molecular Biology top 2%
- Pluripotent Stem Cells Research
- Epigenetics and DNA Methylation
- CRISPR and Genetic Engineering
- Genomics and Chromatin Dynamics
- Renal and related cancers
Papers in
- Genetics 19
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 14
- Genetics and Neurodevelopmental Disorders 7
-
- CRISPR and Genetic Engineering 14
- Pluripotent Stem Cells Research 12
- Epigenetics and DNA Methylation 12
- Genomics and Chromatin Dynamics 9
- Renal and related cancers 7
- RNA Research and Splicing 6
- Co-authors
- Jeannie T. Lee (15 shared papers)Mitinori Saitou (9 shared papers)M. Azim Surani (6 shared papers)Sheila C. Barton (4 shared papers)Yasuhide Ohinata (3 shared papers)Dónal O’Carroll (3 shared papers)Mitsue Sano (1 shared paper)Yukiko Ono (1 shared paper)
- Journals
- Proceedings of the National Academy of Sciences (4 papers)Genetics (2 papers)Molecular Cell (2 papers)RNA Biology (1 paper)Developmental Biology (1 paper)
- Partner nations
- United StatesSpainUnited Kingdom
In The Last Decade
Bernhard Payer
36 papers receiving 4.1k citations
Bernhard Payer's Hit Papers
Peers
Comparison fields: 5 of 110
- Cell Biology 829
- Molecular Biology 3.1k
- Genetics 1.2k
- Aging 64
- Cancer Research 413
Countries citing papers authored by Bernhard Payer
This map shows the geographic impact of Bernhard Payer'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 Bernhard Payer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernhard Payer more than expected).
Fields of papers citing papers by Bernhard Payer
This network shows the impact of papers produced by Bernhard Payer. 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 Bernhard Payer. The network helps show where Bernhard Payer may publish in the future.
Co-authors
The 25 scholars most cited alongside Bernhard Payer, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Blimp1 is a critical determinant of the germ cell lineage in mice Hit paper breakdown → | 2005 | 850 |
| 2 | Mst1 and Mst2 Maintain Hepatocyte Quiescence and Suppress Hepatocellular Carcinoma Development through Inactivation of the Yap1 Oncogene Hit paper breakdown → | 2009 | 774 |
| 3 | 2008 | 391 | |
| 4 | 2015 | 384 | |
| 5 | 2003 | 323 | |
| 6 | 2003 | 168 | |
| 7 | 2012 | 136 | |
| 8 | 2006 | 129 | |
| 9 | 2016 | 115 | |
| 10 | 2010 | 98 | |
| 11 | 2013 | 90 | |
| 12 | 2002 | 88 | |
| 13 | 2021 | 76 | |
| 14 | 2003 | 75 | |
| 15 | 2005 | 62 | |
| 16 | 2017 | 57 | |
| 17 | 2011 | 48 | |
| 18 | 2015 | 38 | |
| 19 | 2016 | 37 | |
| 20 | 2021 | 34 |
About Bernhard Payer
Bernhard Payer is a scholar working on Genetics, Molecular Biology, Aging, Developmental Neuroscience and Hematology, having authored 38 papers that have together received 4.2k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), CRISPR and Genetic Engineering (14 papers), Pluripotent Stem Cells Research (12 papers), Epigenetics and DNA Methylation (12 papers), Genomics and Chromatin Dynamics (9 papers), Renal and related cancers (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and RNA Research and Splicing (6 papers). The work is most often cited by research in Cell Biology (829 citations), Molecular Biology (3.1k citations), Genetics (1.2k citations), Aging (64 citations) and Cancer Research (413 citations). Bernhard Payer has collaborated with scholars based in United States, Spain and United Kingdom. Frequent co-authors include Jeannie T. Lee, Mitinori Saitou, M. Azim Surani, Sheila C. Barton, Yasuhide Ohinata, Dónal O’Carroll, Mitsue Sano, Yukiko Ono, Tetyana V. Obukhanych and Alexander Tarakhovsky. Their work appears in journals such as Proceedings of the National Academy of Sciences, Genetics, Molecular Cell, RNA Biology and Developmental Biology.
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.