Ulrike Laß
Impact in
- Genetics top 5%
- Glioma Diagnosis and Treatment
- Mesenchymal stem cell research
-
- MicroRNA in disease regulation
- Cancer Genomics and Diagnostics
Papers in
-
- Epigenetics and DNA Methylation 4
- Hedgehog Signaling Pathway Studies 2
- RNA Research and Splicing 2
- Genetics 8
- Glioma Diagnosis and Treatment 7
- Co-authors
- Wolf Mueller (18 shared papers)Andreas von Deimling (13 shared papers)M Reichenberger (6 shared papers)Christian Hartmann (4 shared papers)Günter Germann (6 shared papers)Uwe Leimer (5 shared papers)Sina Heimer (5 shared papers)Martha Maria Gebhard (3 shared papers)
- Journals
- Brain Pathology (3 papers)Clinical Cancer Research (1 paper)Injury (1 paper)Acta Neuropathologica (1 paper)PLoS ONE (1 paper)
- Partner nations
- GermanyUnited StatesCanada
In The Last Decade
Ulrike Laß
19 papers receiving 450 citations
Peers
Comparison fields: 5 of 50
- Genetics 177
- Cancer Research 83
- Rehabilitation 29
- Molecular Biology 181
- Developmental Neuroscience 9
Countries citing papers authored by Ulrike Laß
This map shows the geographic impact of Ulrike Laß'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 Ulrike Laß with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ulrike Laß more than expected).
Fields of papers citing papers by Ulrike Laß
This network shows the impact of papers produced by Ulrike Laß. 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 Ulrike Laß. The network helps show where Ulrike Laß may publish in the future.
Co-authors
The 25 scholars most cited alongside Ulrike Laß, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 50 | |
| 2 | 2005 | 44 | |
| 3 | 2008 | 43 | |
| 4 | 2012 | 42 | |
| 5 | 2009 | 41 | |
| 6 | 2015 | 34 | |
| 7 | 2011 | 30 | |
| 8 | 2004 | 26 | |
| 9 | 2011 | 23 | |
| 10 | 2012 | 22 | |
| 11 | 2001 | 20 | |
| 12 | Somatic mutations in peroxisome proliferator-activated receptor-gamma are rare events in human cancer cells. | 2004 | 19 |
| 13 | 2012 | 17 | |
| 14 | 2003 | 10 | |
| 15 | 2005 | 9 | |
| 16 | 2007 | 9 | |
| 17 | 2003 | 8 | |
| 18 | 2013 | 7 | |
| 19 | 2012 | 2 | |
| 20 | Frequent epigenetic silencing of NPTXII and AREG in glioblastomas | 2007 | 0 |
About Ulrike Laß
Ulrike Laß is a scholar working on Molecular Biology, Genetics, Surgery, Oncology and Cancer Research, having authored 20 papers that have together received 456 indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (7 papers), Epigenetics and DNA Methylation (4 papers), Cancer-related molecular mechanisms research (3 papers), Wound Healing and Treatments (2 papers), Cancer-related Molecular Pathways (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Reconstructive Surgery and Microvascular Techniques (2 papers) and RNA Research and Splicing (2 papers). The work is most often cited by research in Genetics (177 citations), Cancer Research (83 citations), Rehabilitation (29 citations), Molecular Biology (181 citations) and Developmental Neuroscience (9 citations). Ulrike Laß has collaborated with scholars based in Germany, United States and Canada. Frequent co-authors include Wolf Mueller, Andreas von Deimling, M Reichenberger, Christian Hartmann, Günter Germann, Uwe Leimer, Sina Heimer, Martha Maria Gebhard, Suzanne Kamel‐Reid and Christel Herold‐Mende. Their work appears in journals such as Brain Pathology, Clinical Cancer Research, Injury, Acta Neuropathologica 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.