Markus Stümm
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
-
- Prenatal Screening and Diagnostics 32
- Genetics 41
- Genomic variations and chromosomal abnormalities 31
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 7
- Genomics and Rare Diseases 3
- Co-authors
- Raymonda Varon (8 shared papers)Krystyńa Chrzańowska (7 shared papers)Karen M. Cerosaletti (2 shared papers)Richard A. Gatti (2 shared papers)PATRICK J. CONCANNON (2 shared papers)Karl Sperling (4 shared papers)André Reis (4 shared papers)Peter F. Wieacker (26 shared papers)
- Journals
- Prenatal Diagnosis (11 papers)Cytogenetic and Genome Research (8 papers)European Journal of Pediatrics (4 papers)Journal of Medical Genetics (3 papers)Human Genetics (3 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Markus Stümm
85 papers receiving 4k citations
Markus Stümm's Hit Papers
Peers
Comparison fields: 5 of 103
- Genetics 1.2k
- Pediatrics, Perinatology and Child Health 482
- Molecular Biology 1.8k
- Cellular and Molecular Neuroscience 298
- Immunology 347
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 92 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 | 879 |
| 2 | 2001 | 447 | |
| 3 | 1998 | 374 | |
| 4 | 2010 | 202 | |
| 5 | 2009 | 200 | |
| 6 | 2003 | 159 | |
| 7 | 2003 | 144 | |
| 8 | 2002 | 113 | |
| 9 | 2004 | 110 | |
| 10 | 2000 | 105 | |
| 11 | The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. | 1997 | 96 |
| 12 | 2014 | 92 | |
| 13 | 1999 | 72 | |
| 14 | 2002 | 69 | |
| 15 | Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defects. | 2000 | 59 |
| 16 | 2001 | 57 | |
| 17 | 2000 | 56 | |
| 18 | 2015 | 53 | |
| 19 | 1995 | 49 | |
| 20 | 2002 | 47 |
About Markus Stümm
Markus Stümm is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Developmental Biology and Immunology, having authored 92 papers that have together received 4.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (32 papers), Genomic variations and chromosomal abnormalities (31 papers), DNA Repair Mechanisms (20 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (7 papers), Immunodeficiency and Autoimmune Disorders (4 papers), Genomics and Rare Diseases (3 papers), Congenital limb and hand anomalies (3 papers) and Acute Myeloid Leukemia Research (2 papers). The work is most often cited by research in Genetics (1.2k citations), Pediatrics, Perinatology and Child Health (482 citations), Molecular Biology (1.8k citations), Cellular and Molecular Neuroscience (298 citations) and Immunology (347 citations). Markus Stümm has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Raymonda Varon, Krystyńa Chrzańowska, Karen M. Cerosaletti, Richard A. Gatti, PATRICK J. CONCANNON, Karl Sperling, André Reis, Peter F. Wieacker, Kathrin Saar and E Seemanová. Their work appears in journals such as Prenatal Diagnosis, Cytogenetic and Genome Research, European Journal of Pediatrics, Journal of Medical Genetics and 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.