Thomas Ried
Impact in
- Geriatrics and Gerontology top 0.2%
- Sirtuins and Resveratrol in Medicine
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 102
- Genomic variations and chromosomal abnormalities 86
-
- Cancer Genomics and Diagnostics 40
- Co-authors
- Evelin Schröck (38 shared papers)Michael J. Difilippantonio (31 shared papers)Stanislas du Manoir (18 shared papers)Hesed M. Padilla‐Nash (44 shared papers)Anthony J. Wynshaw-Boris (10 shared papers)Gert Auer (39 shared papers)André Nussenzweig (10 shared papers)Marek Liyanage (9 shared papers)
- Journals
- Genes Chromosomes and Cancer (26 papers)Oncogene (16 papers)Cancer Research (12 papers)Proceedings of the National Academy of Sciences (11 papers)Blood (9 papers)
- Partner nations
- United StatesGermanySweden
In The Last Decade
Thomas Ried
342 papers receiving 25.4k citations
Thomas Ried's Hit Papers
Peers
Comparison fields: 5 of 158
- Geriatrics and Gerontology 975
- Cancer Research 2.7k
- Genetics 4.9k
- Molecular Biology 9.2k
- Oncology 2.9k
Countries citing papers authored by Thomas Ried
This map shows the geographic impact of Thomas Ried'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 Thomas Ried with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Thomas Ried more than expected).
Fields of papers citing papers by Thomas Ried
This network shows the impact of papers produced by Thomas Ried. 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 Thomas Ried. The network helps show where Thomas Ried may publish in the future.
Co-authors
The 25 scholars most cited alongside Thomas Ried, 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 346 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Multicolor Spectral Karyotyping of Human Chromosomes Hit paper breakdown → | 1996 | 1450 |
| 2 | Atm-Deficient Mice: A Paradigm of Ataxia Telangiectasia Hit paper breakdown → | 1996 | 1267 |
| 3 | SIRT6 is a histone H3 lysine 9 deacetylase that modulates telomeric chromatin Hit paper breakdown → | 2008 | 927 |
| 4 | 2008 | 684 | |
| 5 | 1999 | 639 | |
| 6 | 2004 | 572 | |
| 7 | Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3 Hit paper breakdown → | 1997 | 565 |
| 8 | 2005 | 495 | |
| 9 | 2000 | 471 | |
| 10 | 2003 | 465 | |
| 11 | 2001 | 437 | |
| 12 | 2007 | 411 | |
| 13 | 1996 | 404 | |
| 14 | 1998 | 334 | |
| 15 | 1992 | 329 | |
| 16 | 1997 | 300 | |
| 17 | 1998 | 288 | |
| 18 | 2000 | 278 | |
| 19 | 1995 | 274 | |
| 20 | Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping. | 1999 | 256 |
About Thomas Ried
Thomas Ried is a scholar working on Genetics, Cancer Research, Oncology, Pathology and Forensic Medicine and Molecular Biology, having authored 346 papers that have together received 26.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (86 papers), Cancer Genomics and Diagnostics (40 papers), DNA Repair Mechanisms (29 papers), Genomics and Chromatin Dynamics (26 papers), Microtubule and mitosis dynamics (25 papers), Genetic factors in colorectal cancer (19 papers), Cancer-related Molecular Pathways (16 papers) and Cervical Cancer and HPV Research (13 papers). The work is most often cited by research in Geriatrics and Gerontology (975 citations), Cancer Research (2.7k citations), Genetics (4.9k citations), Molecular Biology (9.2k citations) and Oncology (2.9k citations). Thomas Ried has collaborated with scholars based in United States, Germany and Sweden. Frequent co-authors include Evelin Schröck, Michael J. Difilippantonio, Stanislas du Manoir, Hesed M. Padilla‐Nash, Anthony J. Wynshaw-Boris, Gert Auer, André Nussenzweig, Marek Liyanage, Chu‐Xia Deng and Carrolee Barlow. Their work appears in journals such as Genes Chromosomes and Cancer, Oncogene, Cancer Research, Proceedings of the National Academy of Sciences and Blood.
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.