David Markie

6.5k total citations
55 papers, 1.4k citations indexed

About

David Markie is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, David Markie has authored 55 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 14 papers in Genetics and 10 papers in Pathology and Forensic Medicine. Recurrent topics in David Markie's work include Genetic factors in colorectal cancer (10 papers), Fungal and yeast genetics research (7 papers) and Connective tissue disorders research (6 papers). David Markie is often cited by papers focused on Genetic factors in colorectal cancer (10 papers), Fungal and yeast genetics research (7 papers) and Connective tissue disorders research (6 papers). David Markie collaborates with scholars based in New Zealand, United Kingdom and Australia. David Markie's co-authors include Walter F. Bodmer, Ian Tomlinson, Anna‐Maria Björkqvist, Reijo Salovaara, Darryl Shibata, Heikki Järvinen, Lauri A. Aaltonen, Sakari Knuutila, Albert de la Chapelle and Pertti Sistonen and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

David Markie

54 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
David Markie New Zealand 21 704 495 301 295 194 55 1.4k
Joseph R. Podojil United States 28 606 0.9× 318 0.6× 205 0.7× 420 1.4× 124 0.6× 55 2.4k
W Lütz United States 17 738 1.0× 555 1.1× 229 0.8× 245 0.8× 99 0.5× 24 1.8k
Gemma M. Dingjan Netherlands 26 716 1.0× 228 0.5× 177 0.6× 286 1.0× 97 0.5× 37 2.1k
Giuseppe Ragona Italy 21 753 1.1× 205 0.4× 80 0.3× 555 1.9× 162 0.8× 58 1.6k
Frances A. Lemckert Australia 21 753 1.1× 121 0.2× 310 1.0× 166 0.6× 111 0.6× 27 1.9k
B Bödey United States 26 866 1.2× 66 0.1× 407 1.4× 654 2.2× 267 1.4× 93 2.0k
William B. Solomon United States 13 1.2k 1.7× 128 0.3× 387 1.3× 132 0.4× 111 0.6× 32 1.7k
Lesley Vanes United Kingdom 21 897 1.3× 91 0.2× 390 1.3× 219 0.7× 114 0.6× 26 2.2k
Claire Usal France 30 914 1.3× 97 0.2× 427 1.4× 210 0.7× 103 0.5× 67 2.7k
Sulman Basit Saudi Arabia 21 931 1.3× 159 0.3× 520 1.7× 113 0.4× 75 0.4× 134 1.9k

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-authorship network of co-authors of David Markie

This figure shows the co-authorship network connecting the top 25 collaborators of David Markie. A scholar is included among the top collaborators of David Markie based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with David Markie. David Markie is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Franz, Elizabeth A., et al.. (2024). Aberrant connectivity of the lateralized readiness system in non-syndromic congenital mirror movements. Clinical Neurophysiology. 167. 61–73.
2.
Cadzow, Murray, David Markie, Amanda Phipps‐Green, et al.. (2020). Trans-ancestral dissection of urate- and gout-associated major loci SLC2A9 and ABCG2 reveals primate-specific regulatory effects. Journal of Human Genetics. 66(2). 161–169. 9 indexed citations
3.
Hunter, Matthew F., Sixto García‐Miñáur, Francesca Sperotto, et al.. (2020). Wilms tumor in patients with osteopathia striata with cranial sclerosis. European Journal of Human Genetics. 29(3). 396–401. 10 indexed citations
4.
Stapleton, Rachel, Tim Morgan, Ian Hayes, et al.. (2018). A pilot study of exome sequencing in a diverse New Zealand cohort with undiagnosed disorders and cancer. Journal of the Royal Society of New Zealand. 48(4). 262–279. 3 indexed citations
5.
Cameron‐Christie, Sophia, Andrew Gray, Rick M. Tankard, et al.. (2018). Genetic investigation into an increased susceptibility to biliary atresia in an extended New Zealand Māori family. BMC Medical Genomics. 11(1). 121–121. 7 indexed citations
6.
O’Neill, Adam C., Christina Kyrousi, Richard J. Leventer, et al.. (2018). A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration. Cell Reports. 25(10). 2729–2741.e6. 34 indexed citations
7.
Oliver, Verity F., Murray Cadzow, Bernhard Steger, et al.. (2016). A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions. Ophthalmology. 123(4). 709–722. 33 indexed citations
8.
O’Neill, Adam C., Sophia Cameron‐Christie, Tim Morgan, et al.. (2015). Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome. The American Journal of Human Genetics. 96(4). 623–630. 54 indexed citations
9.
Markie, David, et al.. (2011). Cholecystokinin system genes: Associations with panic and other psychiatric disorders. Journal of Affective Disorders. 136(3). 902–908. 16 indexed citations
10.
Mizumoto, Shuji, Shuhei Yamada, Tim Morgan, et al.. (2008). Spondyloepiphyseal dysplasia, Omani type: Further definition of the phenotype. American Journal of Medical Genetics Part A. 146A(18). 2376–2384. 37 indexed citations
11.
Markie, David, et al.. (2004). The Telomere Repeat Binding Protein Trf1 Interacts with the Spindle Checkpoint Protein Mad1 and Nek2 Mitotic Kinase. Cell Cycle. 4(1). 121–124. 23 indexed citations
12.
Markie, David & Jiannis Ragoussis. (2003). Genomic Reconstruction by Mitotic Recombination of YACs. Humana Press eBooks. 54. 217–230. 1 indexed citations
13.
Bevan, Steve, K Woodford-Richens, Paul Rozen, et al.. (1999). Screening SMAD1 , SMAD2 , SMAD3 , and SMAD5 for germline mutations in juvenile polyposis syndrome. Gut. 45(3). 406–408. 45 indexed citations
14.
Houlston, Richard S., Steve Bevan, Alison C. Williams, et al.. (1998). Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases. Human Molecular Genetics. 7(12). 1907–1912. 96 indexed citations
15.
Hemminki, Akseli, Ian Tomlinson, David Markie, et al.. (1997). Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis. Nature Genetics. 15(1). 87–90. 380 indexed citations
16.
Markie, David, Susan Huson, E. J. Maher, et al.. (1996). A pericentric inversion of chromosome six in a patient with Peutz-Jeghers' syndrome and the use of FISH to localise the breakpoints on a genetic map. Human Genetics. 98(2). 125–128. 26 indexed citations
17.
Markie, David. (1996). A simple assay for optimizing yeast-mammalian cell fusion conditions. Molecular Biotechnology. 6(2). 99–104. 6 indexed citations
18.
Ragoussis, Jiannis, John Trowsdale, & David Markie. (1992). Mitotic recombination of yeast artificial chromosomes. Nucleic Acids Research. 20(12). 3135–3138. 11 indexed citations
19.
Parry, Pauline, David Markie, Eric R. Fearon, et al.. (1991). PCR-based detection of two MspI Polymorphic sites at D18S8. Nucleic Acids Research. 19(24). 6983–6983. 12 indexed citations
20.
Bicknell, David, David Markie, Nigel K. Spurr, & Walter F. Bodmer. (1991). The human chromosome content in human × rodent somatic cell hybrids analyzed by a screening technique using Alu PCR. Genomics. 10(1). 186–192. 8 indexed citations

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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