Markus Stümm
Impact in
- Cancer Research top 2%
- Carcinogens and Genotoxicity Assessment
- Molecular Biology top 2%
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- Genomics and Chromatin Dynamics
Papers in
-
- Prenatal Screening and Diagnostics 38
- Fetal and Pediatric Neurological Disorders 9
- Genetics 37
- Genomic variations and chromosomal abnormalities 29
- Co-authors
- Raymonda Varon (7 shared papers)Krystyńa Chrzańowska (6 shared papers)Karen Cerosaletti (2 shared papers)Patrick Concannon (2 shared papers)Richard A. Gatti (2 shared papers)Karl Sperling (4 shared papers)André Reis (3 shared papers)Kathrin Saar (3 shared papers)
- Journals
- Prenatal Diagnosis (10 papers)Cytogenetic and Genome Research (7 papers)European Journal of Pediatrics (4 papers)Human Genetics (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Markus Stümm
78 papers receiving 3.5k citations
Markus Stümm's Hit Papers
Peers
Comparison fields: 5 of 112
- Cancer Research 728
- Molecular Biology 2.5k
- Genetics 929
- Cell Biology 437
- Oncology 651
Countries citing papers authored by Markus Stümm
This map shows the geographic impact of Markus Stümm'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 Markus Stümm with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Markus Stümm more than expected).
Fields of papers citing papers by Markus Stümm
This network shows the impact of papers produced by Markus Stümm. 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 Markus Stümm. The network helps show where Markus Stümm may publish in the future.
Co-authors
The 25 scholars most cited alongside Markus Stümm, 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 86 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome Hit paper breakdown → | 1998 | 873 |
| 2 | 2001 | 435 | |
| 3 | 1998 | 373 | |
| 4 | 2009 | 203 | |
| 5 | 2010 | 190 | |
| 6 | 2003 | 160 | |
| 7 | 2002 | 108 | |
| 8 | 2004 | 105 | |
| 9 | 2000 | 104 | |
| 10 | 2014 | 90 | |
| 11 | The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. | 1997 | 90 |
| 12 | 2002 | 70 | |
| 13 | 1999 | 69 | |
| 14 | Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects. | 2000 | 60 |
| 15 | 2001 | 55 | |
| 16 | 1995 | 48 | |
| 17 | The differential expression of proinflammatory cytokines IL-6, IL-8 and TNF-alpha in renal cell carcinoma. | 1999 | 42 |
| 18 | 2013 | 33 | |
| 19 | 2001 | 31 | |
| 20 | 2003 | 31 |
About Markus Stümm
Markus Stümm is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Plant Science and Cancer Research, having authored 86 papers that have together received 3.8k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (38 papers), Genomic variations and chromosomal abnormalities (29 papers), DNA Repair Mechanisms (19 papers), Chromosomal and Genetic Variations (15 papers), Carcinogens and Genotoxicity Assessment (14 papers), Fetal and Pediatric Neurological Disorders (9 papers), Cancer-related Molecular Pathways (6 papers) and Renal and related cancers (5 papers). The work is most often cited by research in Cancer Research (728 citations), Molecular Biology (2.5k citations), Genetics (929 citations), Cell Biology (437 citations) and Oncology (651 citations). Markus Stümm has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Raymonda Varon, Krystyńa Chrzańowska, Karen Cerosaletti, Patrick Concannon, Richard A. Gatti, Karl Sperling, André Reis, Kathrin Saar, E Seemanová and Peter Wieacker. Their work appears in journals such as Prenatal Diagnosis, Cytogenetic and Genome Research, European Journal of Pediatrics, Human Genetics and European Journal of Human Genetics.
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.