M. Ray
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 11
- Genomic variations and chromosomal abnormalities 9
- Chronic Lymphocytic Leukemia Research 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
-
- Carcinogens and Genotoxicity Assessment 4
- Co-authors
- JOHN L. HAMERTON (13 shared papers)Shelley D. Smith (1 shared paper)Albert E. Chudley (2 shared papers)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)Cheryl R. Greenberg (2 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
31 papers receiving 962 citations
M. Ray's Hit Papers
Peers
Comparison fields: 5 of 45
- Genetics 497
- Pediatrics, Perinatology and Child Health 105
- Transplantation 13
- Cancer Research 30
- Reproductive Medicine 22
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 35 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 | 494 |
| 2 | 1974 | 97 | |
| 3 | Chromosome studies in a neonatal population. | 1972 | 93 |
| 4 | Familial occurrence of trisomy 22. | 1968 | 44 |
| 5 | 1992 | 42 | |
| 6 | 1977 | 41 | |
| 7 | 1978 | 31 | |
| 8 | 1982 | 31 | |
| 9 | 1987 | 29 | |
| 10 | 1972 | 27 | |
| 11 | 1979 | 21 | |
| 12 | 1976 | 19 | |
| 13 | 1970 | 17 | |
| 14 | 1984 | 17 | |
| 15 | 1987 | 15 | |
| 16 | 1969 | 13 | |
| 17 | Methylmercury toxicity: in vivo evaluation of teratogenesis and cytogenetic changes. | 1983 | 13 |
| 18 | 1989 | 12 | |
| 19 | 1964 | 11 | |
| 20 | 1990 | 10 |
About M. Ray
M. Ray is a scholar working on Genetics, Cancer Research, Genetics, Transplantation and Pediatrics, Perinatology and Child Health, having authored 35 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Carcinogens and Genotoxicity Assessment (4 papers), Chronic Lymphocytic Leukemia Research (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Down syndrome and intellectual disability research (1 paper), Chronic Myeloid Leukemia Treatments (1 paper), Prenatal Screening and Diagnostics (1 paper) and Immunodeficiency and Autoimmune Disorders (1 paper). The work is most often cited by research in Genetics (497 citations), Pediatrics, Perinatology and Child Health (105 citations), Transplantation (13 citations), Cancer Research (30 citations) and Reproductive Medicine (22 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, Irene A. Uchida, PHYLLIS J. McALPINE, Sérgio D.J. Pena, T. V. N. Persaud, Cheryl R. Greenberg, Alasdair G. W. Hunter and Jane Alison Evans. 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.