Michael R. Speicher
- Cancer Research top 0.05%
- Cancer Genomics and Diagnostics 56
- Oncology top 0.2%
- Cancer Cells and Metastasis 15
- Genetics top 0.2%
- Genomic variations and chromosomal abnormalities 68
- Molecular Biology top 0.2%
- Genomics and Chromatin Dynamics 26
- Single-cell and spatial transcriptomics 13
- Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer 19
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- Chromosomal and Genetic Variations 38
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- Prenatal Screening and Diagnostics 15
- Co-authors
- Ellen HeitzerDavid C. WardJochen B. GeiglAnna C. ObenaufKlaus PantelStephen Gwyn BallardThomas CremerCharles E. S. Roberts
- Cited by
- Cancer ResearchOncologyGenetics
- Partner nations
- GermanyAustriaUnited States
In The Last Decade
Michael R. Speicher
174 papers receiving 18.7k citations
Hit Papers
Peers
Comparison fields: 5 of 180
- Cancer Research 6.5k
- Oncology 5.7k
- Genetics 4.2k
- Molecular Biology 10.0k
- Pathology and Forensic Medicine 1.8k
Countries citing papers authored by Michael R. Speicher
This map shows the geographic impact of Michael R. Speicher'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 Michael R. Speicher with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael R. Speicher more than expected).
Fields of papers citing papers by Michael R. Speicher
This network shows the impact of papers produced by Michael R. Speicher. 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 Michael R. Speicher. The network helps show where Michael R. Speicher may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Michael R. Speicher, 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 | 2024 | 0 | |
| 2 | 2023 | 1 | |
| 3 | Biallelic BUB1 mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation | 2022 | 15 |
| 4 | 2022 | 80 | |
| 5 | 2021 | 45 | |
| 6 | 2021 | 22 | |
| 7 | 2021 | 12 | |
| 8 | 2020 | 164 | |
| 9 | 2020 | 3 | |
| 10 | 2020 | 23 | |
| 11 | 2020 | 28 | |
| 12 | 2019 | 10 | |
| 13 | 2018 | 46 | |
| 14 | 2017 | 39 | |
| 15 | 2016 | 110 | |
| 16 | 2016 | 280 | |
| 17 | 2013 | 159 | |
| 18 | 2013 | 403 | |
| 19 | 2006 | 49 | |
| 20 | 2004 | 64 |
About Michael R. Speicher
Michael R. Speicher is a scholar working on Cancer Research, Genetics and Oncology, having authored 177 papers that have together received 19.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (68 papers), Cancer Genomics and Diagnostics (56 papers), Chromosomal and Genetic Variations (38 papers), Genomics and Chromatin Dynamics (26 papers), Genetic factors in colorectal cancer (19 papers), Prenatal Screening and Diagnostics (15 papers), Cancer Cells and Metastasis (15 papers) and Single-cell and spatial transcriptomics (13 papers). The work is most often cited by research in Cancer Research (6.5k citations), Oncology (5.7k citations) and Genetics (4.2k citations). Michael R. Speicher has collaborated with scholars based in Germany, Austria and United States. Frequent co-authors include Ellen Heitzer, David C. Ward, Jochen B. Geigl, Anna C. Obenauf, Klaus Pantel, Stephen Gwyn Ballard, Thomas Cremer, Charles E. S. Roberts, Imran S. Haque and Zlatko Trajanoski. Their work appears in journals such as Nature, New England Journal of Medicine and Cell.
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.