David Markie

6.6k citations
56 papers · 1.5k · h-index 22

Impact in

Papers in

    • Fungal and yeast genetics research 7
    • CRISPR and Genetic Engineering 6
    • Renal and related cancers 4
    • Connective tissue disorders research 4

David Markie

54 papers receiving 1.4k citations

Peers

David Markie
Comparison fields: 5 of 97
  • Pathology and Forensic Medicine 500
  • Cancer Research 171
  • Oncology 278
  • Genetics 298
  • Molecular Biology 682
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Paul T. Massa United States
Shuaiyao Lu China
Мikhail Pashenkov Russia
W Lütz United States
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Citations per field
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Citations per year

Countries citing papers authored by David Markie

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with David Markie Line = papers co-authored together David Markie links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 56 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1997395
2 1998106
3 198567
4 201558
5 198253
6
Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q.
199650
7 199947
8 200841
9 198640
10 201837
11 201635
12 201835
13 201131
14 201529
15 199626
16 198526
17 201825
18 200424
19 199322
20 201822

About David Markie

David Markie is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Cell Biology and Cancer Research, having authored 56 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (9 papers), Fungal and yeast genetics research (7 papers), CRISPR and Genetic Engineering (6 papers), Cancer Genomics and Diagnostics (5 papers), Antifungal resistance and susceptibility (5 papers), Microtubule and mitosis dynamics (4 papers), Renal and related cancers (4 papers) and Connective tissue disorders research (4 papers). The work is most often cited by research in Pathology and Forensic Medicine (500 citations), Cancer Research (171 citations), Oncology (278 citations), Genetics (298 citations) and Molecular Biology (682 citations). David Markie has collaborated with scholars based in New Zealand, United Kingdom and Australia. Frequent co-authors include Walter F. Bodmer, Lauri A. Aaltonen, Anna‐Maria Björkqvist, Heikki Järvinen, Reijo Salovaara, Sakari Knuutila, Ian Tomlinson, Darryl Shibata, Albert de la Chapelle and Pertti Sistonen. Their work appears in journals such as Nucleic Acids Research, Journal of Bacteriology, Genomics, European Journal of Human Genetics and The American Journal of 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.

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