David Markie
Impact in
- Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
-
- Fungal and yeast genetics research 7
- CRISPR and Genetic Engineering 6
- Bone Metabolism and Diseases 5
-
- Genetic factors in colorectal cancer 13
- Co-authors
- Walter Fred Bodmer (11 shared papers)Stephen P. Robertson (19 shared papers)Ian Tomlinson (1 shared paper)Anna‐Maria Björkqvist (1 shared paper)Reijo Salovaara (1 shared paper)Albert de la Chapelle (1 shared paper)Heikki Järvinen (1 shared paper)Lauri A. Aaltonen (1 shared paper)
- Journals
- The American Journal of Human Genetics (7 papers)Nucleic Acids Research (5 papers)Journal of Bacteriology (3 papers)Nature Genetics (3 papers)Genomics (2 papers)
- Partner nations
- New ZealandUnited KingdomUnited States
In The Last Decade
David Markie
69 papers receiving 5.1k citations
David Markie's Hit Papers
Peers
Comparison fields: 5 of 123
- Pathology and Forensic Medicine 1.6k
- Cancer Research 614
- Physiology 191
- Oncology 943
- Cell Biology 585
Countries citing papers authored by David Markie
This map shows the geographic impact of David Markie'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 David Markie with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Markie more than expected).
Fields of papers citing papers by David Markie
This network shows the impact of papers produced by David Markie. 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 David Markie. The network helps show where David Markie may publish in the future.
Co-authors
The 25 scholars most cited alongside David Markie, 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 72 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A serine/threonine kinase gene defective in Peutz–Jeghers syndrome Hit paper breakdown → | 1998 | 1301 |
| 2 | Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis Hit paper breakdown → | 1997 | 1273 |
| 3 | 1997 | 401 | |
| 4 | 2013 | 218 | |
| 5 | 2001 | 197 | |
| 6 | 2009 | 190 | |
| 7 | 1998 | 123 | |
| 8 | 2000 | 102 | |
| 9 | 1998 | 78 | |
| 10 | 2017 | 78 | |
| 11 | Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome. | 1997 | 75 |
| 12 | 2015 | 68 | |
| 13 | 1985 | 67 | |
| 14 | 2017 | 58 | |
| 15 | Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q. | 1996 | 54 |
| 16 | 1982 | 53 | |
| 17 | 2016 | 52 | |
| 18 | 1999 | 50 | |
| 19 | 2017 | 48 | |
| 20 | 2008 | 45 |
About David Markie
David Markie is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Genetics, Cancer Research and Cell Biology, having authored 72 papers that have together received 5.3k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (13 papers), Fungal and yeast genetics research (7 papers), Cancer Genomics and Diagnostics (6 papers), Genomics and Rare Diseases (6 papers), CRISPR and Genetic Engineering (6 papers), Connective tissue disorders research (6 papers), Bone Metabolism and Diseases (5 papers) and Microtubule and mitosis dynamics (5 papers). The work is most often cited by research in Pathology and Forensic Medicine (1.6k citations), Cancer Research (614 citations), Physiology (191 citations), Oncology (943 citations) and Cell Biology (585 citations). David Markie has collaborated with scholars based in New Zealand, United Kingdom and United States. Frequent co-authors include Walter Fred Bodmer, Stephen P. Robertson, Ian Tomlinson, Anna‐Maria Björkqvist, Reijo Salovaara, Albert de la Chapelle, Heikki Järvinen, Lauri A. Aaltonen, Darryl K. Shibata and Sakari Knuutila. Their work appears in journals such as The American Journal of Human Genetics, Nucleic Acids Research, Journal of Bacteriology, Nature Genetics and Genomics.
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.