Patrick MacLeod
Impact in
-
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
Papers in
-
- Mitochondrial Function and Pathology 11
- DNA Repair Mechanisms 5
- RNA regulation and disease 5
-
- Genetic Neurodegenerative Diseases 18
- Co-authors
- Raquel Seruca (3 shared papers)Charles E. Jackson (2 shared papers)Carlos Caldas (3 shared papers)David G. Huntsman (3 shared papers)J. Tapio Pantzar (2 shared papers)Barbara McGillivray (3 shared papers)Henry G. Dunn (3 shared papers)Fátima Carneiro (2 shared papers)
- Journals
- Neurology (5 papers)Human Genetics (4 papers)Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques (4 papers)Journal of the Neurological Sciences (4 papers)Journal of Inherited Metabolic Disease (2 papers)
- Partner nations
- CanadaUnited StatesPortugal
In The Last Decade
Patrick MacLeod
72 papers receiving 3.0k citations
Peers
Comparison fields: 5 of 117
- Cellular and Molecular Neuroscience 614
- Genetics 863
- Pathology and Forensic Medicine 347
- Pediatrics, Perinatology and Child Health 331
- Molecular Biology 1.2k
Countries citing papers authored by Patrick MacLeod
This map shows the geographic impact of Patrick MacLeod'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 Patrick MacLeod with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick MacLeod more than expected).
Fields of papers citing papers by Patrick MacLeod
This network shows the impact of papers produced by Patrick MacLeod. 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 Patrick MacLeod. The network helps show where Patrick MacLeod may publish in the future.
Co-authors
The 25 scholars most cited alongside Patrick MacLeod, 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 74 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 283 | |
| 2 | 1993 | 282 | |
| 3 | Identification of germ-line E-cadherin mutations in gastric cancer families of European origin. | 1998 | 245 |
| 4 | 1997 | 209 | |
| 5 | 1992 | 180 | |
| 6 | 2006 | 142 | |
| 7 | 2013 | 128 | |
| 8 | 1990 | 124 | |
| 9 | 1979 | 97 | |
| 10 | 1970 | 85 | |
| 11 | 2001 | 83 | |
| 12 | 1983 | 76 | |
| 13 | 2009 | 73 | |
| 14 | 2007 | 72 | |
| 15 | 2001 | 49 | |
| 16 | 1981 | 47 | |
| 17 | 1996 | 45 | |
| 18 | 1995 | 44 | |
| 19 | A familial factor independent of CAG repeat length influences age at onset of Machado-Joseph disease. | 1996 | 42 |
| 20 | 1985 | 41 |
About Patrick MacLeod
Patrick MacLeod is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Neurology and Physiology, having authored 74 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (18 papers), Mitochondrial Function and Pathology (11 papers), Genetics and Neurodevelopmental Disorders (9 papers), Lysosomal Storage Disorders Research (8 papers), DNA Repair Mechanisms (5 papers), RNA regulation and disease (5 papers), Folate and B Vitamins Research (5 papers) and Metabolism and Genetic Disorders (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (614 citations), Genetics (863 citations), Pathology and Forensic Medicine (347 citations), Pediatrics, Perinatology and Child Health (331 citations) and Molecular Biology (1.2k citations). Patrick MacLeod has collaborated with scholars based in Canada, United States and Portugal. Frequent co-authors include Raquel Seruca, Charles E. Jackson, Carlos Caldas, David G. Huntsman, J. Tapio Pantzar, Barbara McGillivray, Henry G. Dunn, Fátima Carneiro, Raymond Maung and Kristin G. Monaghan. Their work appears in journals such as Neurology, Human Genetics, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, Journal of the Neurological Sciences and Journal of Inherited Metabolic Disease.
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.