John Melnyk
- Co-authors
- Ernest C. AdamsRobert M. McAllisterMurray B. GardnerJerry Z. FinklesteinMiriam G. WilsonFrederick HechtRobert S. SparkesJ W Towner
- Topics
- Genomic variations and chromosomal abnormalities (5 papers)Prenatal Screening and Diagnostics (4 papers)Chromosomal and Genetic Variations (3 papers)
- Partner nations
- United StatesCanada
In The Last Decade
John Melnyk
26 papers receiving 720 citations
Peers
Comparison fields: 5 of 102
- Genetics 373
- Molecular Biology 356
- Plant Science 112
- Oncology 94
- Pulmonary and Respiratory Medicine 73
Countries citing papers authored by John Melnyk
This map shows the geographic impact of John Melnyk'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 John Melnyk with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John Melnyk more than expected).
Fields of papers citing papers by John Melnyk
This network shows the impact of papers produced by John Melnyk. 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 John Melnyk. The network helps show where John Melnyk may publish in the future.
Co-authorship network of co-authors of John Melnyk
This figure shows the co-authorship network connecting the top 25 collaborators of John Melnyk. A scholar is included among the top collaborators of John Melnyk based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with John Melnyk. John Melnyk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 3 | |
| 3 | An Automated System for Chromosome Analysis | 8 |
| 4 | Computer-assisted karyotyping. | 5 |
| 5 | 4 | |
| 6 | 27 | |
| 7 | Experience with cytogenetic analysis in a reference laboratory. | 0 |
| 8 | 19 | |
| 9 | 20 | |
| 10 | 282 | |
| 11 | 8 | |
| 12 | 42 | |
| 13 | 23 | |
| 14 | Translocation-normal mosaicism in D1 trisomy. | 13 |
| 15 | 11 | |
| 16 | 49 | |
| 17 | 94 | |
| 18 | 8 | |
| 19 | 5 | |
| 20 | 10 |
About John Melnyk
John Melnyk is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Genetics, having authored 28 papers that have together received 842 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (5 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Developmental Biology (31 citations), Genetics (373 citations) and Molecular Biology (356 citations). John Melnyk has collaborated with scholars based in United States and Canada. Frequent co-authors include Ernest C. Adams, Robert M. McAllister, Murray B. Gardner, Jerry Z. Finklestein, Miriam G. Wilson, Frederick Hecht, Robert S. Sparkes, J W Towner, Benjamin Goldberg and Irene A. Uchida. Their work appears in journals such as Nature, Science and New England Journal of Medicine.
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.