Herbert Schulz
Impact in
- Aging top 1%
- Molecular Biology top 2%
- Pluripotent Stem Cells Research
- CRISPR and Genetic Engineering
- RNA Research and Splicing
Papers in
- Genetics 34
- Genetics and Neurodevelopmental Disorders 12
- Genomics and Rare Diseases 8
- Genomic variations and chromosomal abnormalities 6
-
- Pluripotent Stem Cells Research 17
- RNA Research and Splicing 7
- Renal and related cancers 6
- Co-authors
- Norbert Hübner (39 shared papers)Oliver Hummel (13 shared papers)Boctor Said (2 shared papers)Markus Wehland (27 shared papers)Daniela G. Grimm (29 shared papers)Manfred Infanger (20 shared papers)Anders Nykjær (2 shared papers)Thomas E. Willnow (2 shared papers)
- Journals
- International Journal of Molecular Sciences (11 papers)PLoS ONE (9 papers)Epilepsia (6 papers)Nature Genetics (6 papers)Hypertension (5 papers)
- Partner nations
- GermanyDenmarkUnited States
In The Last Decade
Herbert Schulz
148 papers receiving 9.0k citations
Herbert Schulz's Hit Papers
Peers
Comparison fields: 5 of 161
- Aging 229
- Molecular Biology 4.8k
- Genetics 1.8k
- Developmental Neuroscience 182
- Physiology 1.1k
Countries citing papers authored by Herbert Schulz
This map shows the geographic impact of Herbert Schulz'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 Herbert Schulz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Herbert Schulz more than expected).
Fields of papers citing papers by Herbert Schulz
This network shows the impact of papers produced by Herbert Schulz. 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 Herbert Schulz. The network helps show where Herbert Schulz may publish in the future.
Co-authors
The 25 scholars most cited alongside Herbert Schulz, 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 161 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genome sequence of the Brown Norway rat yields insights into mammalian evolution Hit paper breakdown → | 2004 | 1679 |
| 2 | RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing Hit paper breakdown → | 2012 | 470 |
| 3 | 2005 | 419 | |
| 4 | 2005 | 350 | |
| 5 | 2016 | 312 | |
| 6 | 2014 | 293 | |
| 7 | 2010 | 246 | |
| 8 | 2009 | 222 | |
| 9 | 2009 | 176 | |
| 10 | 2009 | 166 | |
| 11 | 2008 | 156 | |
| 12 | 2008 | 149 | |
| 13 | 2007 | 148 | |
| 14 | 2013 | 142 | |
| 15 | 2015 | 134 | |
| 16 | 2012 | 124 | |
| 17 | 2013 | 124 | |
| 18 | 2006 | 116 | |
| 19 | 2011 | 116 | |
| 20 | 1986 | 107 |
About Herbert Schulz
Herbert Schulz is a scholar working on Genetics, Molecular Biology, Physiology, Aging and Cancer Research, having authored 161 papers that have together received 9.3k indexed citations. Recurring topics across this work include Spaceflight effects on biology (24 papers), Pluripotent Stem Cells Research (17 papers), Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (8 papers), 3D Printing in Biomedical Research (7 papers), RNA Research and Splicing (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Renal and related cancers (6 papers). The work is most often cited by research in Aging (229 citations), Molecular Biology (4.8k citations), Genetics (1.8k citations), Developmental Neuroscience (182 citations) and Physiology (1.1k citations). Herbert Schulz has collaborated with scholars based in Germany, Denmark and United States. Frequent co-authors include Norbert Hübner, Oliver Hummel, Boctor Said, Markus Wehland, Daniela G. Grimm, Manfred Infanger, Anders Nykjær, Thomas E. Willnow, Thomas Kjærgaard Andreassen and Kathrin Saar. Their work appears in journals such as International Journal of Molecular Sciences, PLoS ONE, Epilepsia, Nature Genetics and Hypertension.
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.