M. Ray
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 19
- Genomic variations and chromosomal abnormalities 13
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Chronic Lymphocytic Leukemia Research 4
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- Prenatal Screening and Diagnostics 7
- Co-authors
- JOHN L. HAMERTON (13 shared papers)Shelley D. Smith (1 shared paper)Albert E. Chudley (2 shared papers)Jodi F. Abbott (1 shared paper)Irene A. Uchida (3 shared papers)PHYLLIS J. McALPINE (5 shared papers)Sérgio D.J. Pena (1 shared paper)T. V. N. Persaud (3 shared papers)
- Journals
- Human Genetics (5 papers)Clinical Genetics (3 papers)Journal of Medical Genetics (3 papers)Nature (2 papers)Cancer Letters (2 papers)
- Partner nations
- CanadaUnited States
In The Last Decade
M. Ray
32 papers receiving 987 citations
M. Ray's Hit Papers
Peers
Comparison fields: 5 of 80
- Genetics 731
- Pediatrics, Perinatology and Child Health 369
- Developmental Biology 39
- Plant Science 286
- Reproductive Medicine 51
Countries citing papers authored by M. Ray
This map shows the geographic impact of M. Ray'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 M. Ray with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Ray more than expected).
Fields of papers citing papers by M. Ray
This network shows the impact of papers produced by M. Ray. 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 M. Ray. The network helps show where M. Ray may publish in the future.
Co-authors
The 25 scholars most cited alongside M. Ray, 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 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A cytogenetic survey of 14,069 newborn infants Hit paper breakdown → | 1975 | 496 |
| 2 | 1974 | 96 | |
| 3 | Chromosome studies in a neonatal population. | 1972 | 95 |
| 4 | Familial occurrence of trisomy 22. | 1968 | 45 |
| 5 | 1992 | 45 | |
| 6 | 1977 | 42 | |
| 7 | 1982 | 31 | |
| 8 | 1978 | 31 | |
| 9 | 1987 | 29 | |
| 10 | 1972 | 27 | |
| 11 | 1976 | 21 | |
| 12 | 1979 | 21 | |
| 13 | 1984 | 17 | |
| 14 | 1970 | 17 | |
| 15 | 1987 | 14 | |
| 16 | Methylmercury toxicity: in vivo evaluation of teratogenesis and cytogenetic changes. | 1983 | 13 |
| 17 | 1969 | 13 | |
| 18 | 1989 | 12 | |
| 19 | The pathologic findings of the fetal membranes in very prolonged amniotic fluid leakage. | 1986 | 12 |
| 20 | 1964 | 11 |
About M. Ray
M. Ray is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Genetics and Health, Toxicology and Mutagenesis, having authored 36 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (7 papers), Genomics and Chromatin Dynamics (7 papers), Chromosomal and Genetic Variations (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Chronic Lymphocytic Leukemia Research (4 papers), Mercury impact and mitigation studies (3 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). The work is most often cited by research in Genetics (731 citations), Pediatrics, Perinatology and Child Health (369 citations), Developmental Biology (39 citations), Plant Science (286 citations) and Reproductive Medicine (51 citations). M. Ray has collaborated with scholars based in Canada and United States. Frequent co-authors include JOHN L. HAMERTON, Shelley D. Smith, Albert E. Chudley, Jodi F. Abbott, Irene A. Uchida, PHYLLIS J. McALPINE, Sérgio D.J. Pena, T. V. N. Persaud, Alasdair G. W. Hunter and Cheryl R. Greenberg. Their work appears in journals such as Human Genetics, Clinical Genetics, Journal of Medical Genetics, Nature and Cancer Letters.
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.