Malcolm Parslow
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 19
- Genomic variations and chromosomal abnormalities 13
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Congenital Ear and Nasal Anomalies 3
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- Hedgehog Signaling Pathway Studies 2
- Genomics and Chromatin Dynamics 2
- Co-authors
- G.R. Sutherland (1 shared paper)Elizabeth Baker (1 shared paper)A. M. O. Veale (5 shared papers)Joe J. Hoo (3 shared papers)R. J. M. Gardner (1 shared paper)Patrick MacLeod (2 shared papers)Margherita Silengo (1 shared paper)R J Gardner (1 shared paper)
- Journals
- Human Genetics (6 papers)Clinical Genetics (3 papers)Journal of Medical Genetics (3 papers)Pathology (2 papers)Genome (1 paper)
- Partner nations
- New ZealandCanadaGermany
In The Last Decade
Malcolm Parslow
23 papers receiving 332 citations
Peers
Comparison fields: 5 of 63
- Genetics 286
- Developmental Biology 12
- Pediatrics, Perinatology and Child Health 96
- Plant Science 132
- Molecular Biology 146
Countries citing papers authored by Malcolm Parslow
This map shows the geographic impact of Malcolm Parslow'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 Malcolm Parslow with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Malcolm Parslow more than expected).
Fields of papers citing papers by Malcolm Parslow
This network shows the impact of papers produced by Malcolm Parslow. 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 Malcolm Parslow. The network helps show where Malcolm Parslow may publish in the future.
Co-authors
The 25 scholars most cited alongside Malcolm Parslow, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1985 | 79 | |
| 2 | 2003 | 32 | |
| 3 | 1981 | 31 | |
| 4 | 1974 | 27 | |
| 5 | 1990 | 26 | |
| 6 | 1979 | 25 | |
| 7 | 1986 | 24 | |
| 8 | 1979 | 20 | |
| 9 | 1986 | 19 | |
| 10 | 2009 | 14 | |
| 11 | 2008 | 14 | |
| 12 | 1972 | 14 | |
| 13 | 1980 | 9 | |
| 14 | 1974 | 9 | |
| 15 | 1979 | 7 | |
| 16 | 1973 | 6 | |
| 17 | 1979 | 5 | |
| 18 | 1977 | 4 | |
| 19 | 1983 | 3 | |
| 20 | 1980 | 2 |
About Malcolm Parslow
Malcolm Parslow is a scholar working on Genetics, Molecular Biology, Plant Science, Genetics and Cancer Research, having authored 24 papers that have together received 374 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Chromosomal and Genetic Variations (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Carcinogens and Genotoxicity Assessment (3 papers), Congenital Ear and Nasal Anomalies (3 papers), Hedgehog Signaling Pathway Studies (2 papers), Genomics and Chromatin Dynamics (2 papers) and Prenatal Screening and Diagnostics (2 papers). The work is most often cited by research in Genetics (286 citations), Developmental Biology (12 citations), Pediatrics, Perinatology and Child Health (96 citations), Plant Science (132 citations) and Molecular Biology (146 citations). Malcolm Parslow has collaborated with scholars based in New Zealand, Canada and Germany. Frequent co-authors include G.R. Sutherland, Elizabeth Baker, A. M. O. Veale, Joe J. Hoo, R. J. M. Gardner, Patrick MacLeod, Margherita Silengo, R J Gardner, William N. Hunter and Willard R. Centerwall. Their work appears in journals such as Human Genetics, Clinical Genetics, Journal of Medical Genetics, Pathology and Genome.
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.