James German
Impact in
- Cancer Research top 0.5%
- Carcinogens and Genotoxicity Assessment
- Molecular Biology top 0.5%
- DNA Repair Mechanisms
- Genomics and Chromatin Dynamics
- CRISPR and Genetic Engineering
- DNA and Nucleic Acid Chemistry
Papers in
-
- DNA Repair Mechanisms 34
- Sexual Differentiation and Disorders 13
- CRISPR and Genetic Engineering 11
- Genomics and Chromatin Dynamics 8
- Genetics 36
- Genomic variations and chromosomal abnormalities 16
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 14
- Co-authors
- R. S. K. Chaganti (10 shared papers)Nathan A. Ellis (12 shared papers)S. A. Schonberg (1 shared paper)Joanna Groden (8 shared papers)David C. Bloom (6 shared papers)Maria Proytcheva (6 shared papers)Joel E. Straughen (4 shared papers)David Lennon (2 shared papers)
- Journals
- Clinical Genetics (10 papers)Human Genetics (7 papers)Science (7 papers)Chromosoma (7 papers)Nature (5 papers)
- Partner nations
- United StatesUnited KingdomGermany
In The Last Decade
James German
118 papers receiving 7.9k citations
James German's Hit Papers
Peers
Comparison fields: 5 of 144
- Cancer Research 1.9k
- Molecular Biology 6.2k
- Genetics 2.1k
- Aging 92
- Hematology 506
Countries citing papers authored by James German
This map shows the geographic impact of James German'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 James German with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James German more than expected).
Fields of papers citing papers by James German
This network shows the impact of papers produced by James German. 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 James German. The network helps show where James German may publish in the future.
Co-authors
The 25 scholars most cited alongside James German, 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 118 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Bloom's syndrome gene product is homologous to RecQ helicases Hit paper breakdown → | 1995 | 1195 |
| 2 | A Manyfold Increase in Sister Chromatid Exchanges in Bloom's Syndrome Lymphocytes Hit paper breakdown → | 1974 | 845 |
| 3 | 1993 | 487 | |
| 4 | 1969 | 435 | |
| 5 | 1995 | 300 | |
| 6 | Chromosome mutation and neoplasia | 1983 | 275 |
| 7 | Chromosomal Breakage in a Rare and Probably Genetically Determined Syndrome of Man Hit paper breakdown → | 1965 | 262 |
| 8 | 1997 | 246 | |
| 9 | 2000 | 200 | |
| 10 | 1964 | 180 | |
| 11 | 2002 | 173 | |
| 12 | 1964 | 168 | |
| 13 | 1962 | 166 | |
| 14 | 2007 | 158 | |
| 15 | 1987 | 141 | |
| 16 | 2004 | 138 | |
| 17 | 1970 | 135 | |
| 18 | 1974 | 129 | |
| 19 | 1962 | 123 | |
| 20 | 1974 | 113 |
About James German
James German is a scholar working on Molecular Biology, Genetics, Plant Science, Cancer Research and Pediatrics, Perinatology and Child Health, having authored 118 papers that have together received 8.8k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (34 papers), Genomic variations and chromosomal abnormalities (16 papers), Chromosomal and Genetic Variations (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Sexual Differentiation and Disorders (13 papers), Carcinogens and Genotoxicity Assessment (12 papers), CRISPR and Genetic Engineering (11 papers) and Genomics and Chromatin Dynamics (8 papers). The work is most often cited by research in Cancer Research (1.9k citations), Molecular Biology (6.2k citations), Genetics (2.1k citations), Aging (92 citations) and Hematology (506 citations). James German has collaborated with scholars based in United States, United Kingdom and Germany. Frequent co-authors include R. S. K. Chaganti, Nathan A. Ellis, S. A. Schonberg, Joanna Groden, David C. Bloom, Maria Proytcheva, Joel E. Straughen, David Lennon, Eberhard Passarge and James D. Regan. Their work appears in journals such as Clinical Genetics, Human Genetics, Science, Chromosoma and Nature.
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.