JACK M. RARY
Impact in
- Cancer Research top 5%
- Carcinogens and Genotoxicity Assessment
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 15
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
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- Carcinogens and Genotoxicity Assessment 6
- Co-authors
- Kirby D. Smith (1 shared paper)W. Roy Breg (1 shared paper)Samuel H. Boyer (1 shared paper)S S Wachtel (1 shared paper)O. J. Miller (1 shared paper)Louis M. Kunkel (1 shared paper)Digamber S. Borgaonkar (1 shared paper)Raymond R. Tice (3 shared papers)
- Journals
- Journal of Heredity (7 papers)Mutation research. Fundamental and molecular mechanisms of mutagenesis (4 papers)Clinical Genetics (2 papers)Human Genetics (1 paper)International Journal of Gynecology & Obstetrics (1 paper)
- Partner nations
- United States
In The Last Decade
JACK M. RARY
26 papers receiving 1.9k citations
JACK M. RARY's Hit Papers
Peers
Comparison fields: 5 of 115
- Cancer Research 434
- Genetics 539
- Hematology 189
- Molecular Biology 1.1k
- Genetics 120
Countries citing papers authored by JACK M. RARY
This map shows the geographic impact of JACK M. RARY'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 JACK M. RARY with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites JACK M. RARY more than expected).
Fields of papers citing papers by JACK M. RARY
This network shows the impact of papers produced by JACK M. RARY. 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 JACK M. RARY. The network helps show where JACK M. RARY may publish in the future.
Co-authors
The 25 scholars most cited alongside JACK M. RARY, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants. Hit paper breakdown → | 1977 | 1291 |
| 2 | 1976 | 204 | |
| 3 | 1979 | 66 | |
| 4 | 1979 | 66 | |
| 5 | 1966 | 60 | |
| 6 | 1978 | 53 | |
| 7 | 1985 | 50 | |
| 8 | 1985 | 33 | |
| 9 | 1975 | 27 | |
| 10 | 1974 | 26 | |
| 11 | 1979 | 21 | |
| 12 | 1986 | 21 | |
| 13 | 1978 | 15 | |
| 14 | 1968 | 15 | |
| 15 | 1977 | 15 | |
| 16 | 1977 | 14 | |
| 17 | 1979 | 12 | |
| 18 | 1976 | 11 | |
| 19 | 1983 | 8 | |
| 20 | 1974 | 8 |
About JACK M. RARY
JACK M. RARY is a scholar working on Genetics, Cancer Research, Pediatrics, Perinatology and Child Health, Molecular Biology and Plant Science, having authored 27 papers that have together received 2.0k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (8 papers), Genomic variations and chromosomal abnormalities (8 papers), Carcinogens and Genotoxicity Assessment (6 papers), Prenatal Screening and Diagnostics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Chromosomal and Genetic Variations (4 papers), Acute Lymphoblastic Leukemia research (3 papers) and Sexual Differentiation and Disorders (3 papers). The work is most often cited by research in Cancer Research (434 citations), Genetics (539 citations), Hematology (189 citations), Molecular Biology (1.1k citations) and Genetics (120 citations). JACK M. RARY has collaborated with scholars based in United States. Frequent co-authors include Kirby D. Smith, W. Roy Breg, Samuel H. Boyer, S S Wachtel, O. J. Miller, Louis M. Kunkel, Digamber S. Borgaonkar, Raymond R. Tice, Edward L. Schneider and Michael A. Bender. Their work appears in journals such as Journal of Heredity, Mutation research. Fundamental and molecular mechanisms of mutagenesis, Clinical Genetics, Human Genetics and International Journal of Gynecology & Obstetrics.
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.