John MacMillan
Impact in
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- Genetic Neurodegenerative Diseases
- Neuroscience and Neuropharmacology Research
- Neurology top 2%
- Neurological disorders and treatments
Papers in
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- Genetic Neurodegenerative Diseases 8
- Hereditary Neurological Disorders 2
-
- Migraine and Headache Studies 9
- Co-authors
- Lyn R. Griffiths (10 shared papers)Rod A. Lea (8 shared papers)Duncan J. Shaw (1 shared paper)Iain Fenton (1 shared paper)Marcy E. MacDonald (1 shared paper)Jeremy P. Cheadle (1 shared paper)L. Lazarou (1 shared paper)Russell G. Snell (1 shared paper)
- Journals
- Human Mutation (3 papers)Neurogenetics (2 papers)Nature Genetics (2 papers)Clinical Genetics (2 papers)BMC Medicine (1 paper)
- Partner nations
- AustraliaNew ZealandUnited States
In The Last Decade
John MacMillan
27 papers receiving 1.8k citations
John MacMillan's Hit Papers
Peers
Comparison fields: 5 of 88
- Cellular and Molecular Neuroscience 888
- Neurology 398
- Psychiatry and Mental health 283
- Developmental Neuroscience 55
- Molecular Biology 965
Countries citing papers authored by John MacMillan
This map shows the geographic impact of John MacMillan'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 MacMillan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John MacMillan more than expected).
Fields of papers citing papers by John MacMillan
This network shows the impact of papers produced by John MacMillan. 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 MacMillan. The network helps show where John MacMillan may publish in the future.
Co-authors
The 25 scholars most cited alongside John MacMillan, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease Hit paper breakdown → | 1993 | 592 |
| 2 | 1998 | 389 | |
| 3 | 1999 | 117 | |
| 4 | 1996 | 108 | |
| 5 | 2004 | 104 | |
| 6 | 2004 | 92 | |
| 7 | 2005 | 69 | |
| 8 | 2015 | 50 | |
| 9 | 2000 | 46 | |
| 10 | 1994 | 31 | |
| 11 | 2014 | 31 | |
| 12 | 2000 | 30 | |
| 13 | 2009 | 27 | |
| 14 | 1999 | 25 | |
| 15 | 2002 | 24 | |
| 16 | 2002 | 23 | |
| 17 | 2014 | 21 | |
| 18 | 2005 | 14 | |
| 19 | 2005 | 12 | |
| 20 | 1992 | 11 |
About John MacMillan
John MacMillan is a scholar working on Cellular and Molecular Neuroscience, Psychiatry and Mental health, Molecular Biology, Neurology and Pulmonary and Respiratory Medicine, having authored 27 papers that have together received 1.9k indexed citations. Recurring topics across this work include Migraine and Headache Studies (9 papers), Genetic Neurodegenerative Diseases (8 papers), Pediatric Hepatobiliary Diseases and Treatments (3 papers), Gallbladder and Bile Duct Disorders (3 papers), Mitochondrial Function and Pathology (3 papers), Folate and B Vitamins Research (2 papers), DNA Repair Mechanisms (2 papers) and Hereditary Neurological Disorders (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (888 citations), Neurology (398 citations), Psychiatry and Mental health (283 citations), Developmental Neuroscience (55 citations) and Molecular Biology (965 citations). John MacMillan has collaborated with scholars based in Australia, New Zealand and United States. Frequent co-authors include Lyn R. Griffiths, Rod A. Lea, Duncan J. Shaw, Iain Fenton, Marcy E. MacDonald, Jeremy P. Cheadle, L. Lazarou, Russell G. Snell, Peter J. Davies and Peter S. Harper. Their work appears in journals such as Human Mutation, Neurogenetics, Nature Genetics, Clinical Genetics and BMC 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.