J.L. Hamerton
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic diversity and population structure
- Animal Genetics and Reproduction
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 60
- Genomic variations and chromosomal abnormalities 28
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 18
- Genetics and Neurodevelopmental Disorders 8
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- Prenatal Screening and Diagnostics 19
J.L. Hamerton
131 papers receiving 4.5k citations
Hit Papers
Peers
Comparison fields: 5 of 151
- Genetics 2.8k
- Pediatrics, Perinatology and Child Health 1.0k
- Developmental Biology 91
- Hematology 414
- Plant Science 1.3k
Countries citing papers authored by J.L. Hamerton
This map shows the geographic impact of J.L. Hamerton'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.L. Hamerton with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites J.L. Hamerton more than expected).
Fields of papers citing papers by J.L. Hamerton
This network shows the impact of papers produced by J.L. Hamerton. 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.L. Hamerton. The network helps show where J.L. Hamerton may publish in the future.
Co-authorship network
The 25 scholars most cited alongside J.L. Hamerton, 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 | 1994 | 2 | |
| 2 | 1993 | 2 | |
| 3 | Children and young adults with sex chromosome aneuploidy : follow-up, clinical, and molecular studies : proceedings of the 5th International Workshop on Sex Chromosome Anomalies held at Minaki, Ontario, Canada, June 7-10, 1989 | 1991 | 4 |
| 4 | The cytogenetics of mammalian autosomal rearrangements. | 1989 | 28 |
| 5 | 1988 | 29 | |
| 6 | 1986 | 16 | |
| 7 | 1980 | 13 | |
| 8 | Antenatal diagnosis of neural tube defects in Canada: extension of a collaborative study. | 1979 | 4 |
| 9 | Human gene mapping 4 : Winnipeg conference (1977), fourth International Workshop on Human Gene Mapping | 1978 | 4 |
| 10 | 1978 | 4 | |
| 11 | Human cytogenetics : general cytogenetics | 1971 | 8 |
| 12 | 1969 | 1 | |
| 13 | 1968 | 8 | |
| 14 | 1965 | 28 | |
| 15 | 1963 | 42 | |
| 16 | 1963 | 47 | |
| 17 | 1961 | 84 | |
| 18 | 1961 | 49 | |
| 19 | 1958 | 6 | |
| 20 | 1956 | 5 |
About J.L. Hamerton
J.L. Hamerton is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Clinical Biochemistry and Developmental Biology, having authored 134 papers that have together received 5.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (28 papers), Prenatal Screening and Diagnostics (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers), Genomics and Chromatin Dynamics (14 papers), Chromosomal and Genetic Variations (12 papers), Sexual Differentiation and Disorders (11 papers), DNA Repair Mechanisms (8 papers) and Genetics and Neurodevelopmental Disorders (8 papers). The work is most often cited by research in Genetics (2.8k citations), Pediatrics, Perinatology and Child Health (1.0k citations), Developmental Biology (91 citations), Hematology (414 citations) and Plant Science (1.3k citations). J.L. Hamerton has collaborated with scholars based in Canada, United Kingdom and United States. Frequent co-authors include C. E. Ford, M. Ray, J. F. Loutit, David W. Barnes, S. D. Smith, F. Giannelli, P. E. Polani, Jane Evans, Ross T. A. MacGillivray and P.J. McAlpine. Their work appears in journals such as Cytogenetic and Genome Research, Nature, Journal of Medical Genetics, Human Genetics and Prenatal Diagnosis.
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.