S. Gerken
Impact in
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- Carcinogens and Genotoxicity Assessment
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- Multiple Sclerosis Research Studies
Papers in
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- DNA Repair Mechanisms 2
- RNA modifications and cancer 2
- RNA and protein synthesis mechanisms 2
- RNA Research and Splicing 1
- Viral Infectious Diseases and Gene Expression in Insects 1
- Genetics 4
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 1
- Co-authors
- Stuart M. Arfin (2 shared papers)Jeffrey D. McDonald (1 shared paper)Rebecca White (3 shared papers)Dan Fults (1 shared paper)L. Chessa (1 shared paper)Norisada Matsunami (1 shared paper)Shubhada Chiplunkar (1 shared paper)Teresa Liang (1 shared paper)
- Journals
- Journal of Biological Chemistry (2 papers)Human Molecular Genetics (1 paper)The Lancet (1 paper)PubMed (5 papers)Cytogenetics and Cell Genetics (1 paper)
- Partner nations
- United StatesPolandNetherlands
In The Last Decade
S. Gerken
10 papers receiving 336 citations
Peers
Comparison fields: 5 of 50
- Cancer Research 59
- Pathology and Forensic Medicine 70
- Genetics 39
- Genetics 103
- Molecular Biology 228
Countries citing papers authored by S. Gerken
This map shows the geographic impact of S. Gerken'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. Gerken with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Gerken more than expected).
Fields of papers citing papers by S. Gerken
This network shows the impact of papers produced by S. Gerken. 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. Gerken. The network helps show where S. Gerken may publish in the future.
Co-authors
The 25 scholars most cited alongside S. Gerken, 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 | Localization of an ataxia-telangiectasia gene to an approximately 500-kb interval on chromosome 11q23.1: linkage analysis of 176 families by an international consortium. | 1995 | 69 |
| 2 | 1993 | 59 | |
| 3 | 1995 | 58 | |
| 4 | Correlation of chromosome 17p loss with clinical outcome in medulloblastoma. | 1996 | 49 |
| 5 | A strategy for constructing high-resolution genetic maps of the human genome: a genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels. | 1995 | 29 |
| 6 | Report and abstracts of the second international workshop on human chromosome 18 mapping. Doorwerth, the Netherlands, July 19-20, 1993. | 1994 | 27 |
| 7 | 1984 | 27 | |
| 8 | 1984 | 23 | |
| 9 | Breakpoint analysis: precise localization of genetic markers by means of nonstatistical computation using relatively few genotypes. | 1995 | 9 |
| 10 | 2008 | 2 |
About S. Gerken
S. Gerken is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Rheumatology and Genetics, having authored 10 papers that have together received 352 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), DNA Repair Mechanisms (2 papers), Genetic Neurodegenerative Diseases (2 papers), RNA modifications and cancer (2 papers), RNA and protein synthesis mechanisms (2 papers), RNA Research and Splicing (1 paper), Viral Infectious Diseases and Gene Expression in Insects (1 paper) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Cancer Research (59 citations), Pathology and Forensic Medicine (70 citations), Genetics (39 citations), Genetics (103 citations) and Molecular Biology (228 citations). S. Gerken has collaborated with scholars based in United States, Poland and Netherlands. Frequent co-authors include Stuart M. Arfin, Jeffrey D. McDonald, Rebecca White, Dan Fults, L. Chessa, Norisada Matsunami, Shubhada Chiplunkar, Teresa Liang, A L Børresen and Aravinda Chakravarti. Their work appears in journals such as Journal of Biological Chemistry, Human Molecular Genetics, The Lancet, PubMed and Cytogenetics and Cell 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.