David Markie

6.5k citations

55 papers · 1.4k indexed · h-index 21

Impact in

Pathology and Forensic Medicine top 2%
- Genetic factors in colorectal cancer
Cancer Research top 10%
- Cancer Genomics and Diagnostics

Papers in ⓘ

Pathology and Forensic Medicine 10
- Genetic factors in colorectal cancer 10
Genetics 14
- Connective tissue disorders research 6

Co-authors: Walter F. Bodmer (11 shared papers)Sakari Knuutila (1 shared paper)Akseli Hemminki (1 shared paper)Anna‐Maria Björkqvist (1 shared paper)Darryl Shibata (1 shared paper)Pertti Sistonen (1 shared paper)Albert de la Chapelle (1 shared paper)Ian Tomlinson (1 shared paper)
Journals: Nucleic Acids Research (5 papers)Journal of Bacteriology (3 papers)European Journal of Human Genetics (2 papers)The American Journal of Human Genetics (2 papers)Genomics (2 papers)
Partner nations: New Zealand United Kingdom Australia

In The Last Decade

David Markie

54 papers receiving 1.3k citations

Peers

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

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20 of 20 papers shown

Showing the 20 most-cited of 55 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis Nature Genetics ·Akseli Hemminki, Ian Tomlinson, David Markie, Heikki Järvinen, Pertti Sistonen, Anna‐Maria Björkqvist, Sakari Knuutila, Reijo Salovaara, Walter F. Bodmer, Darryl Shibata, Albert de la Chapelle, Lauri A. Aaltonen	1997	380
2	Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases Human Molecular Genetics ·Richard S. Houlston, Steve Bevan, Alison C. Williams, Joanne Young, Malcolm G. Dunlop, Paul Rozen, Charis Eng, David Markie, K Woodford-Richens, Miguel A. Rodrı́guez-Bigas, Barbara Leggett, Kay Neale, R Phillips, E. Sheridan, Shirley Hodgson, Takeo Iwama∥, Diana Eccles, Walter F. Bodmer, I. Tomlinson	1998	96
3	Heat shock induces chromosome loss in the yeast Candida albicans Molecular and General Genetics MGG ·Craig Hilton, David Markie, Brain Corner, Erik H. A. Rikkerink, Russel Poulter	1985	61
4	Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome The American Journal of Human Genetics ·Kieran J. Bunn, Phil Daniel, Heleen S. Rösken, Adam C. O’Neill, Sophia Cameron‐Christie, Tim Morgan, Han G. Brunner, Angeline Lai, Henricus P. M. Kunst, David Markie, Stephen P. Robertson	2015	54
5	Recombination analysis of naturally diploid Candida albicans Journal of Bacteriology ·Russell T. M. Poulter, V. Hanrahan, Katie Jeffery, David Markie, M G Shepherd, P. A. Sullivan	1982	50
6	Genetic mapping of hereditary mixed polyposis syndrome to chromosome 6q. PubMed ·Hunu J W Thomas, S Whitelaw, Sally Cottrell, Victoria A. Murday, I. Tomlinson, David Markie, T. Alwyn Jones, D. Timothy Bishop, SV Hodgson, Denise Sheer, John Northover, I C Talbot, E. Solomon, Walter F. Bodmer	1996	46
7	Screening SMAD1 , SMAD2 , SMAD3 , and SMAD5 for germline mutations in juvenile polyposis syndrome Gut ·Steve Bevan, K Woodford-Richens, Paul Rozen, Charis Eng, Joanne Young, Malcolm G. Dunlop, Kay Neale, R Phillips, David Markie, Miguel A. Rodrı́guez-Bigas, Barbara Leggett, E. Sheridan, Shirley Hodgson, Takeo Iwama∥, Diana Eccles, Walter F. Bodmer, Richard S. Houlston, Ian Tomlinson	1999	45
8	Isolation and morphological characterization of a mycelial mutant of Candida albicans Journal of Bacteriology ·Michael J. Hubbard, David Markie, Russell T. M. Poulter	1986	38
9	Spondyloepiphyseal dysplasia, Omani type: Further definition of the phenotype American Journal of Medical Genetics Part A ·Mirjam H.H. van Roij, Shuji Mizumoto, Shuhei Yamada, Tim Morgan, Maria B. Tan-Sindhunata, Hanne Meijers‐Heijboer, J.I.L.M. Verbeke, David Markie, Kazuyuki Sugahara, Stephen P. Robertson	2008	37
10	A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration Cell Reports ·Adam C. O’Neill, Christina Kyrousi, Johannes Klaus, Richard J. Leventer, Edwin P. Kirk, Andrew E. Fry, Daniela T. Pilz, Tim Morgan, Zandra A. Jenkins, Micha Drukker, Samuel F. Berkovic, Ingrid E. Scheffer, Renzo Guerrini, David Markie, Magdalena Götz, Silvia Cappello, Stephen P. Robertson	2018	34
11	Germline mutations and somatic inactivation of TRIM28 in Wilms tumour PLoS Genetics ·Benjamin J. Halliday, Ryuji Fukuzawa, David Markie, Richard G. Grundy, Jackie L. Ludgate, Michael A. Black, Jane Skeen, Robert J. Weeks, Daniel Catchpoole, Aedan Roberts, Anthony E. Reeve, Ian M. Morison	2018	34
12	A COL17A1 Splice-Altering Mutation Is Prevalent in Inherited Recurrent Corneal Erosions Ophthalmology ·Verity F. Oliver, Katherine van Bysterveldt, Murray Cadzow, Bernhard Steger, Vito Romano, David Markie, Alex W. Hewitt, David A. Mackey, Colin E. Willoughby, Trevor Sherwin, Philip S. Crosier, Charles N. J. McGhee, Andrea L. Vincent	2016	33
13	Evidence of associations between bipolar disorder and the brain‐derived neurotrophic factor (BDNF) gene Bipolar Disorders ·Catherine Sears, David Markie, Robin J. Olds, Alison Fitches	2011	30
14	Congenital mirror movements: Phenotypes associated with DCC and RAD51 mutations Journal of the Neurological Sciences ·Elizabeth A. Franz, Rachel Chiaroni-Clarke, Stephanie Woodrow, Kelly A. Glendining, Christine L. Jasoni, Stephen P. Robertson, R. J McKinlay Gardner, David Markie	2015	28
15	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 ·David Markie, Susan Huson, E. J. Maher, Angela Davies, Ian Tomlinson, Walter F. Bodmer	1996	26
16	Mob2 Insufficiency Disrupts Neuronal Migration in the Developing Cortex Frontiers in Cellular Neuroscience ·Adam C. O’Neill, Christina Kyrousi, Melanie Einsiedler, Ingo Burtscher, Micha Drukker, David Markie, Edwin P. Kirk, Magdalena Götz, Stephen P. Robertson, Silvia Cappello	2018	24
17	Instability of Candida albicans hybrids Journal of Bacteriology ·W L Whelan, David Markie, K.G. Simpkin, R M Poulter	1985	24
18	The Telomere Repeat Binding Protein Trf1 Interacts with the Spindle Checkpoint Protein Mad1 and Nek2 Mitotic Kinase Cell Cycle ·Graham Prime, David Markie	2004	23
19	New vector for transfer of yeast artificial chromosomes to mammalian cells Somatic Cell and Molecular Genetics ·David Markie, Jiannis Ragoussis, Gabriele Senger, Andrew Rowan, David M. Sansom, John Trowsdale, Denise Sheer, Walter F. Bodmer	1993	22
20	Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3 The American Journal of Human Genetics ·Sophia Cameron‐Christie, Constance Wells, Marleen Simon, Marja W. Wessels, Candy Z.N. Tang, Wenhua Wei, Riku Takei, Coranne Aarts-Tesselaar, Sarah A. Sandaradura, David Sillence, Marie‐Pierre Cordier, Hermine E. Veenstra‐Knol, Matteo Cassina, Kathrin Ludwig, Eva Trevisson, Melanie Bahlo, David Markie, Zandra A. Jenkins, Stephen P. Robertson	2018	22

About David Markie

David Markie is a scholar working on Pathology and Forensic Medicine, Genetics, Molecular Biology, Developmental Neuroscience and Cancer Research, having authored 55 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (10 papers), Fungal and yeast genetics research (7 papers), CRISPR and Genetic Engineering (6 papers), Connective tissue disorders research (6 papers), Cancer Genomics and Diagnostics (5 papers), Antifungal resistance and susceptibility (5 papers), Wnt/β-catenin signaling in development and cancer (4 papers) and Microtubule and mitosis dynamics (4 papers). The work is most often cited by research in Pathology and Forensic Medicine (495 citations), Cancer Research (194 citations), Oncology (295 citations), Genetics (301 citations) and Molecular Biology (704 citations). David Markie has collaborated with scholars based in New Zealand, United Kingdom and Australia. Frequent co-authors include Walter F. Bodmer, Sakari Knuutila, Akseli Hemminki, Anna‐Maria Björkqvist, Darryl Shibata, Pertti Sistonen, Albert de la Chapelle, Ian Tomlinson, Heikki Järvinen and Reijo Salovaara. Their work appears in journals such as Nucleic Acids Research, Journal of Bacteriology, European Journal of Human Genetics, The American Journal of Human 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.

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