Mark Corbett

9.1k total citations
72 papers, 2.5k citations indexed

About

Mark Corbett is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Mark Corbett has authored 72 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Genetics, 28 papers in Molecular Biology and 10 papers in Psychiatry and Mental health. Recurrent topics in Mark Corbett's work include Genetics and Neurodevelopmental Disorders (19 papers), Genomics and Rare Diseases (10 papers) and Allergic Rhinitis and Sensitization (7 papers). Mark Corbett is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), Genomics and Rare Diseases (10 papers) and Allergic Rhinitis and Sensitization (7 papers). Mark Corbett collaborates with scholars based in Australia, United Kingdom and United States. Mark Corbett's co-authors include Jozef Gécz, Julie A. Owens, Tod Fullston, Michelle Lane, Cheryl Shoubridge, Megan Mitchell, Cristin G. Print, Nicole O. Palmer, Edward Teague and Miles J. De Blasio and has published in prestigious journals such as Nature, Molecular Cell and PLoS ONE.

In The Last Decade

Mark Corbett

64 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark Corbett Australia 24 1.4k 715 428 253 190 72 2.5k
Elena Rossi Italy 37 1.4k 1.0× 1.2k 1.6× 505 1.2× 182 0.7× 142 0.7× 141 3.9k
Bregje W.M. van Bon Netherlands 19 1.3k 1.0× 1.7k 2.4× 404 0.9× 146 0.6× 185 1.0× 43 2.9k
Knut Brockmann Germany 35 1.8k 1.4× 877 1.2× 410 1.0× 229 0.9× 136 0.7× 135 3.9k
Bronwyn Kerr United Kingdom 32 1.6k 1.2× 1.3k 1.8× 399 0.9× 127 0.5× 128 0.7× 67 3.2k
Kathleen Freson Belgium 34 1.3k 0.9× 705 1.0× 435 1.0× 105 0.4× 147 0.8× 143 3.6k
Jillian S. Parboosingh Canada 29 936 0.7× 617 0.9× 306 0.7× 87 0.3× 142 0.7× 85 2.0k
Susan Moore United Kingdom 20 873 0.6× 716 1.0× 297 0.7× 177 0.7× 89 0.5× 30 2.0k
Luis A. Pérez‐Jurado Spain 36 1.6k 1.2× 1.5k 2.0× 365 0.9× 104 0.4× 222 1.2× 105 3.5k
A. Micheil Innes Canada 33 2.0k 1.5× 1.1k 1.5× 531 1.2× 120 0.5× 184 1.0× 113 3.5k
Jong‐Hee Chae South Korea 33 1.4k 1.1× 699 1.0× 504 1.2× 857 3.4× 106 0.6× 258 3.6k

Countries citing papers authored by Mark Corbett

Since Specialization
Citations

This map shows the geographic impact of Mark Corbett'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 Mark Corbett with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Corbett more than expected).

Fields of papers citing papers by Mark Corbett

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark Corbett. 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 Mark Corbett. The network helps show where Mark Corbett may publish in the future.

Co-authorship network of co-authors of Mark Corbett

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Corbett. A scholar is included among the top collaborators of Mark Corbett 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 Mark Corbett. Mark Corbett 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.
Neveling, Kornelia, Michael D. Gallagher, Joyce Lee, et al.. (2025). Optical genome mapping enables accurate testing of large repeat expansions. Genome Research. 35(4). 810–823. 2 indexed citations
2.
Soler, Zachary M., Zara M. Patel, Joaquim Mullol, et al.. (2024). Association Between Smell Loss, Disease Burden, and Dupilumab Efficacy in Chronic Rhinosinusitis with Nasal Polyps. American Journal of Rhinology and Allergy. 39(1). 6–12. 2 indexed citations
3.
Alshawsh, Mohammed Abdullah, Melissa Wake, Jozef Gécz, et al.. (2024). Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns. Epigenomics. 16(18). 1203–1214. 2 indexed citations
4.
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Corbett, Mark, Christel Depienne, Liana Veneziano, et al.. (2023). Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansions. Epilepsia. 64(S1). S14–S21. 11 indexed citations
7.
Kuot, Abraham, Mark Corbett, Richard Mills, et al.. (2021). Differential gene expression analysis of corneal endothelium indicates involvement of phagocytic activity in Fuchs’ endothelial corneal dystrophy. Experimental Eye Research. 210. 108692–108692. 5 indexed citations
8.
Hu, Jinghua, Lily R. Qiu, Gerardo Zapata, et al.. (2021). Transgenic mice with an R342X mutation in Phf6 display clinical features of Börjeson–Forssman–Lehmann Syndrome. Human Molecular Genetics. 30(7). 575–594. 7 indexed citations
9.
Bennett, Mark F., Karen Oliver, Brigid M. Regan, et al.. (2020). Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian families. European Journal of Human Genetics. 28(7). 973–978. 22 indexed citations
10.
Mol, Ben W., Jozef Gécz, Alastair H. MacLennan, et al.. (2020). Definition and diagnosis of cerebral palsy in genetic studies: a systematic review. Developmental Medicine & Child Neurology. 62(9). 1024–1030. 28 indexed citations
11.
Sun, Jingjing, Shuo Yang, Xiaocui Zhang, et al.. (2020). Chromatin-Binding Protein PHF6 Regulates Activity-Dependent Transcriptional Networks to Promote Hunger Response. Cell Reports. 30(11). 3717–3728.e6. 6 indexed citations
12.
Corbett, Mark, Clare L. van Eyk, Dani L. Webber, et al.. (2018). Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy. npj Genomic Medicine. 3(1). 33–33. 27 indexed citations
13.
Carroll, Renée, Raman Kumar, Marie Shaw, et al.. (2017). Variant in the X-chromosome spliceosomal gene GPKOW causes male-lethal microcephaly with intrauterine growth restriction. European Journal of Human Genetics. 25(9). 1078–1082. 6 indexed citations
14.
Corbett, Mark, Samantha J. Turner, Alison Gardner, et al.. (2017). Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations. European Journal of Medical Genetics. 60(8). 437–443. 8 indexed citations
15.
Kumar, Raman, Thuong Ha, Duyen Pham, et al.. (2016). A non-coding variant in the 5ʹ UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability. European Journal of Human Genetics. 24(11). 1612–1616. 8 indexed citations
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17.
Renfree, Andrew, et al.. (2012). Complex Interplay Between Determinants of Pacing and Performance During 20-km Cycle Time Trials. International Journal of Sports Physiology and Performance. 7(2). 121–129. 56 indexed citations
18.
Huang, Lingli, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, et al.. (2012). A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability. The American Journal of Human Genetics. 91(4). 694–702. 73 indexed citations
19.
Voss, Anne K., Caitlin Collin, Cheryl Shoubridge, et al.. (2007). Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson–Forssman–Lehmann Syndrome of intellectual disability and obesity. Gene Expression Patterns. 7(8). 858–871. 37 indexed citations
20.
Corbett, Mark, P. Anthony Akkari, Ana Domazetovska, et al.. (2004). An αtropomyosin mutation alters dimer preference in nemaline myopathy. Annals of Neurology. 57(1). 42–49. 44 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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