John MacPherson
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research
Papers in
- Genetics 10
- Genetics and Neurodevelopmental Disorders 9
- Genomic variations and chromosomal abnormalities 5
- Genetic Associations and Epidemiology 2
- Genomics and Rare Diseases 1
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
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- Congenital heart defects research 2
- Co-authors
- Newton E. Morton (6 shared papers)Anna Murray (6 shared papers)P. A. Jacobs (3 shared papers)N R Dennis (4 shared papers)Gerard Conway (1 shared paper)C.E. Bennett (1 shared paper)David L. Nelson (2 shared papers)Kay E. Davies (2 shared papers)
- Journals
- Annals of Human Genetics (3 papers)Journal of Medical Genetics (3 papers)Proceedings of the National Academy of Sciences (2 papers)Human Molecular Genetics (2 papers)Human Reproduction (1 paper)
- Partner nations
- United KingdomUnited StatesIndia
In The Last Decade
John MacPherson
13 papers receiving 408 citations
Peers
Comparison fields: 5 of 35
- Genetics 342
- Cognitive Neuroscience 163
- Cellular and Molecular Neuroscience 64
- Molecular Biology 209
- Neurology 17
Countries citing papers authored by John MacPherson
This map shows the geographic impact of John MacPherson'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 MacPherson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John MacPherson more than expected).
Fields of papers citing papers by John MacPherson
This network shows the impact of papers produced by John MacPherson. 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 MacPherson. The network helps show where John MacPherson may publish in the future.
Co-authors
The 25 scholars most cited alongside John MacPherson, 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 | 1992 | 88 | |
| 2 | 1997 | 65 | |
| 3 | 2010 | 62 | |
| 4 | 1998 | 61 | |
| 5 | 1993 | 54 | |
| 6 | 1995 | 21 | |
| 7 | 1996 | 20 | |
| 8 | 1992 | 17 | |
| 9 | 1998 | 15 | |
| 10 | 1995 | 9 | |
| 11 | 2001 | 4 | |
| 12 | 2000 | 1 | |
| 13 | 2009 | 1 |
About John MacPherson
John MacPherson is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Cellular and Molecular Neuroscience and Neurology, having authored 13 papers that have together received 418 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (5 papers), Autism Spectrum Disorder Research (4 papers), Genetic Neurodegenerative Diseases (3 papers), Congenital heart defects research (2 papers), Genetic Associations and Epidemiology (2 papers), Genomics and Rare Diseases (1 paper) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Genetics (342 citations), Cognitive Neuroscience (163 citations), Cellular and Molecular Neuroscience (64 citations), Molecular Biology (209 citations) and Neurology (17 citations). John MacPherson has collaborated with scholars based in United Kingdom, United States and India. Frequent co-authors include Newton E. Morton, Anna Murray, P. A. Jacobs, N R Dennis, Gerard Conway, C.E. Bennett, David L. Nelson, Kay E. Davies, Mark C. Hirst and P.A. Jacobs. Their work appears in journals such as Annals of Human Genetics, Journal of Medical Genetics, Proceedings of the National Academy of Sciences, Human Molecular Genetics and Human Reproduction.
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.