J.M. Rary
- Cancer Research top 5%
- Carcinogens and Genotoxicity Assessment 6
- Genetics top 5%
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetics and Neurodevelopmental Disorders 3
- Hematology top 5%
- Molecular Biology top 10%
- DNA Repair Mechanisms 7
- Genetics top 10%
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetics and Neurodevelopmental Disorders 3
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- Prenatal Screening and Diagnostics 5
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- Acute Lymphoblastic Leukemia research 3
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- Chromosomal and Genetic Variations 3
- Co-authors
- Louis M. KunkelKirby D. SmithS S WachtelSamuel H. BoyerW. Roy BregDigamber S. BorgaonkarO. J. MillerRaymond R. Tice
- Cited by
- Cancer ResearchGeneticsHematology
- Journals
- Journal of Heredity (7 papers)Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis (4 papers)Cytogenetic and Genome Research (2 papers)
- Partner nations
- United States
In The Last Decade
J.M. Rary
25 papers receiving 1.8k citations
Hit Papers
Peers
Comparison fields: 5 of 115
- Cancer Research 426
- Genetics 537
- Hematology 191
- Molecular Biology 1.1k
- Genetics 122
Countries citing papers authored by J.M. Rary
This map shows the geographic impact of J.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 J.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 J.M. Rary more than expected).
Fields of papers citing papers by J.M. Rary
This network shows the impact of papers produced by J.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 J.M. Rary. The network helps show where J.M. Rary may publish in the future.
Co-authorship network
The 25 scholars most cited alongside J.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
| # | Work | ||
|---|---|---|---|
| 1 | 1985 | 30 | |
| 2 | 1985 | 51 | |
| 3 | 1985 | 3 | |
| 4 | 1983 | 8 | |
| 5 | 1982 | 4 | |
| 6 | 1979 | 60 | |
| 7 | 1979 | 65 | |
| 8 | The fallability of X-chromatin as a screening test for anomalies of the X chromosome. | 1978 | 3 |
| 9 | 1978 | 52 | |
| 10 | 1977 | 5 | |
| 11 | 1977 | 15 | |
| 12 | 1977 | 13 | |
| 13 | Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.breakdown → | 1977 | 1270 |
| 14 | 1976 | 11 | |
| 15 | 1976 | 192 | |
| 16 | 1975 | 25 | |
| 17 | 1974 | 25 | |
| 18 | 1974 | 6 | |
| 19 | 1968 | 15 | |
| 20 | 1966 | 54 |
About J.M. Rary
J.M. Rary is a scholar working on Genetics, Developmental Biology, Cancer Research, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 25 papers that have together received 2.0k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), DNA Repair Mechanisms (7 papers), Carcinogens and Genotoxicity Assessment (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Prenatal Screening and Diagnostics (5 papers), Acute Lymphoblastic Leukemia research (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Cancer Research (426 citations), Genetics (537 citations), Hematology (191 citations), Molecular Biology (1.1k citations) and Genetics (122 citations). J.M. Rary has collaborated with scholars based in United States. Frequent co-authors include Louis M. Kunkel, Kirby D. Smith, S S Wachtel, Samuel H. Boyer, W. Roy Breg, Digamber S. Borgaonkar, O. J. Miller, Raymond R. Tice, Edward L. Schneider and M. A. Bender. Their work appears in journals such as Journal of Heredity, Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, Cytogenetic and Genome Research, Clinical Genetics and Proceedings of the National Academy of Sciences.
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.