Ruth Voss
Impact in
- Genetics top 5%
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
Papers in
-
- Prenatal Screening and Diagnostics 8
- Genetics 11
- Genomic variations and chromosomal abnormalities 5
- Chronic Lymphocytic Leukemia Research 4
- Co-authors
- E. Solomon (2 shared papers)A.J. Jeffreys (1 shared paper)Ishwar Patel (1 shared paper)Frances C. Lucibello (1 shared paper)Victoria L. Hall (1 shared paper)Jeremy R. Jass (1 shared paper)Walter Fred Bodmer (1 shared paper)S.H. Rider (1 shared paper)
- Journals
- Nature (3 papers)British Journal of Haematology (2 papers)Prenatal Diagnosis (2 papers)Leukemia Research (2 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- IsraelUnited StatesGermany
In The Last Decade
Ruth Voss
37 papers receiving 1.3k citations
Ruth Voss's Hit Papers
Peers
Comparison fields: 5 of 88
- Genetics 578
- Cancer Research 262
- Pathology and Forensic Medicine 311
- Oncology 331
- Pediatrics, Perinatology and Child Health 199
Countries citing papers authored by Ruth Voss
This map shows the geographic impact of Ruth Voss'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 Ruth Voss with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruth Voss more than expected).
Fields of papers citing papers by Ruth Voss
This network shows the impact of papers produced by Ruth Voss. 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 Ruth Voss. The network helps show where Ruth Voss may publish in the future.
Co-authors
The 25 scholars most cited alongside Ruth Voss, 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 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Chromosome 5 allele loss in human colorectal carcinomas Hit paper breakdown → | 1987 | 495 |
| 2 | 1989 | 193 | |
| 3 | 1983 | 158 | |
| 4 | 1983 | 96 | |
| 5 | 1982 | 72 | |
| 6 | 2008 | 44 | |
| 7 | 1982 | 41 | |
| 8 | 1976 | 40 | |
| 9 | 1980 | 39 | |
| 10 | 1980 | 34 | |
| 11 | 1987 | 33 | |
| 12 | Ultrastructural, cell membrane, and cytogenetic characteristics of B-cell leukemia, a murine model of chronic lymphocytic leukemia. | 1981 | 26 |
| 13 | 1989 | 26 | |
| 14 | 1983 | 25 | |
| 15 | 1982 | 24 | |
| 16 | Increased level of bleomycin-induced chromosome breakage in ataxia telangiectasia skin fibroblasts. | 1983 | 19 |
| 17 | 1981 | 19 | |
| 18 | 1983 | 16 | |
| 19 | 1975 | 15 | |
| 20 | 1989 | 14 |
About Ruth Voss
Ruth Voss is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Genetics, Hematology and Cancer Research, having authored 39 papers that have together received 1.5k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (5 papers), DNA Repair Mechanisms (5 papers), Chronic Lymphocytic Leukemia Research (4 papers), Carcinogens and Genotoxicity Assessment (3 papers), Glycosylation and Glycoproteins Research (3 papers), Chromosomal and Genetic Variations (3 papers) and Cancer Genomics and Diagnostics (2 papers). The work is most often cited by research in Genetics (578 citations), Cancer Research (262 citations), Pathology and Forensic Medicine (311 citations), Oncology (331 citations) and Pediatrics, Perinatology and Child Health (199 citations). Ruth Voss has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include E. Solomon, A.J. Jeffreys, Ishwar Patel, Frances C. Lucibello, Victoria L. Hall, Jeremy R. Jass, Walter Fred Bodmer, S.H. Rider, George S. Banting and Denise Sheer. Their work appears in journals such as Nature, British Journal of Haematology, Prenatal Diagnosis, Leukemia Research and Journal of Medical 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.