Patrick MacLeod
Impact in
-
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Genetics top 2%
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
Papers in
-
- Genetic Neurodegenerative Diseases 24
- Hereditary Neurological Disorders 6
- Genetics 24
- Genetics and Neurodevelopmental Disorders 9
- Genomic variations and chromosomal abnormalities 8
- Connective tissue disorders research 4
- Co-authors
- Raquel Seruca (3 shared papers)David D. Huntsman (3 shared papers)Carlos Caldas (3 shared papers)Charles E. Jackson (2 shared papers)J. Tapio Pantzar (2 shared papers)Barbara C. McGillivray (3 shared papers)Henry G. Dunn (3 shared papers)Fátima Carneiro (2 shared papers)
- Journals
- Neurology (6 papers)New England Journal of Medicine (4 papers)Clinical Genetics (4 papers)Journal of Medical Genetics (4 papers)Human Genetics (4 papers)
- Partner nations
- CanadaUnited StatesPortugal
In The Last Decade
Patrick MacLeod
85 papers receiving 4k citations
Peers
Comparison fields: 5 of 115
- Cellular and Molecular Neuroscience 803
- Genetics 1k
- Pathology and Forensic Medicine 452
- Pulmonary and Respiratory Medicine 812
- Clinical Biochemistry 120
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 88 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Familial gastric cancer: overview and guidelines for management. | 1999 | 408 |
| 2 | 2001 | 326 | |
| 3 | 1993 | 319 | |
| 4 | Identification of germ-line E-cadherin mutations in gastric cancer families of European origin. | 1998 | 274 |
| 5 | 1997 | 235 | |
| 6 | 1992 | 195 | |
| 7 | 2006 | 149 | |
| 8 | 2013 | 148 | |
| 9 | 1990 | 141 | |
| 10 | 2003 | 133 | |
| 11 | 1979 | 109 | |
| 12 | 1996 | 93 | |
| 13 | 2001 | 92 | |
| 14 | 1970 | 86 | |
| 15 | 1983 | 85 | |
| 16 | 2009 | 83 | |
| 17 | 2007 | 78 | |
| 18 | 1981 | 52 | |
| 19 | 2001 | 50 | |
| 20 | 1996 | 49 |
About Patrick MacLeod
Patrick MacLeod is a scholar working on Cellular and Molecular Neuroscience, Genetics, Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Physiology, having authored 88 papers that have together received 4.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (24 papers), Lysosomal Storage Disorders Research (9 papers), Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (8 papers), Hereditary Neurological Disorders (6 papers), Metabolism and Genetic Disorders (6 papers), Gastric Cancer Management and Outcomes (5 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (803 citations), Genetics (1k citations), Pathology and Forensic Medicine (452 citations), Pulmonary and Respiratory Medicine (812 citations) and Clinical Biochemistry (120 citations). Patrick MacLeod has collaborated with scholars based in Canada, United States and Portugal. Frequent co-authors include Raquel Seruca, David D. Huntsman, Carlos Caldas, Charles E. Jackson, J. Tapio Pantzar, Barbara C. McGillivray, Henry G. Dunn, Fátima Carneiro, Raymond Maung and Allen Hayashi. Their work appears in journals such as Neurology, New England Journal of Medicine, Clinical Genetics, Journal of Medical Genetics and Human Genetics.
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.