S. Adolph
Impact in
- Genetics top 5%
- Genetic Mapping and Diversity in Plants and Animals
- Genetic diversity and population structure
- Genomic variations and chromosomal abnormalities
- Hematology top 10%
Papers in
-
- Genomics and Chromatin Dynamics 11
- DNA Repair Mechanisms 6
- DNA and Nucleic Acid Chemistry 4
- Congenital heart defects research 3
- Genetics 17
- Genomic variations and chromosomal abnormalities 7
- Genetic diversity and population structure 6
- Co-authors
- H. Hameister (24 shared papers)Jan Klein (3 shared papers)Rolf Müller (3 shared papers)A. Sewing (1 shared paper)Anja Wimmel (1 shared paper)Frances C. Lucibello (1 shared paper)Carl L. Schildkraut (3 shared papers)Christophe Cordevant (1 shared paper)
- Journals
- Chromosoma (6 papers)Human Genetics (5 papers)Genetics Research (2 papers)Nucleic Acids Research (2 papers)Molecular and Cellular Biology (2 papers)
- Partner nations
- GermanyFranceUnited States
In The Last Decade
S. Adolph
41 papers receiving 906 citations
Peers
Comparison fields: 5 of 88
- Genetics 314
- Hematology 79
- Molecular Biology 481
- Oceanography 82
- Oncology 149
Countries citing papers authored by S. Adolph
This map shows the geographic impact of S. Adolph'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 S. Adolph with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Adolph more than expected).
Fields of papers citing papers by S. Adolph
This network shows the impact of papers produced by S. Adolph. 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 S. Adolph. The network helps show where S. Adolph may publish in the future.
Co-authors
The 25 scholars most cited alongside S. Adolph, 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 45 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 119 | |
| 2 | Inducible acceleration of G1 progression through tetracycline-regulated expression of human cyclin E. | 1994 | 114 |
| 3 | 1981 | 56 | |
| 4 | 1989 | 51 | |
| 5 | 1989 | 48 | |
| 6 | 2006 | 46 | |
| 7 | 1987 | 45 | |
| 8 | 1990 | 45 | |
| 9 | 1992 | 39 | |
| 10 | 1984 | 37 | |
| 11 | 1983 | 34 | |
| 12 | 1985 | 30 | |
| 13 | 1988 | 30 | |
| 14 | 1993 | 24 | |
| 15 | 1990 | 23 | |
| 16 | 1989 | 23 | |
| 17 | 1988 | 20 | |
| 18 | Amplification and rearrangement of c-myc in radiation-induced murine osteosarcomas. | 1990 | 18 |
| 19 | 1985 | 16 | |
| 20 | The Southwestern Ontario Joint Replacement Pilot Project: electronic point-of-care data collection. Southwestern Ontario Study Group. | 2001 | 15 |
About S. Adolph
S. Adolph is a scholar working on Molecular Biology, Genetics, Plant Science, Oncology and Pathology and Forensic Medicine, having authored 45 papers that have together received 939 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (11 papers), Chromosomal and Genetic Variations (10 papers), Genomic variations and chromosomal abnormalities (7 papers), DNA Repair Mechanisms (6 papers), Genetic diversity and population structure (6 papers), Lymphoma Diagnosis and Treatment (5 papers), DNA and Nucleic Acid Chemistry (4 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Genetics (314 citations), Hematology (79 citations), Molecular Biology (481 citations), Oceanography (82 citations) and Oncology (149 citations). S. Adolph has collaborated with scholars based in Germany, France and United States. Frequent co-authors include H. Hameister, Jan Klein, Rolf Müller, A. Sewing, Anja Wimmel, Frances C. Lucibello, Carl L. Schildkraut, Christophe Cordevant, Anne Cueff and S. A. Poulet. Their work appears in journals such as Chromosoma, Human Genetics, Genetics Research, Nucleic Acids Research and Molecular and Cellular Biology.
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.