Mark Corbett

9.1k citations

72 papers · 2.5k indexed · h-index 24

Impact in

Genetics top 2%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Pediatrics, Perinatology and Child Health top 2%
- Birth, Development, and Health

Papers in ⓘ

Otorhinolaryngology 7
- Sinusitis and nasal conditions 7
Immunology and Allergy 9
- Allergic Rhinitis and Sensitization 7

Co-authors: Jozef Gécz (36 shared papers)Tod Fullston (2 shared papers)Julie A. Owens (2 shared papers)Michelle Lane (2 shared papers)Cheryl Shoubridge (3 shared papers)Nicole O. Palmer (1 shared paper)Megan Mitchell (1 shared paper)Miles J. De Blasio (1 shared paper)
Journals: Human Molecular Genetics (6 papers)European Journal of Human Genetics (5 papers)npj Genomic Medicine (4 papers)The American Journal of Human Genetics (3 papers)Epilepsia (2 papers)
Partner nations: Australia United Kingdom United States

In The Last Decade

Mark Corbett

64 papers receiving 2.4k citations

Peers

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-authors

The 25 scholars most cited alongside Mark Corbett, 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 Mark Corbett Line = papers co-authored together Mark Corbett links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 72 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Paternal obesity initiates metabolic disturbances in two generations of mice with incomplete penetrance to the F ₂ generation and alters the transcriptional profile of testis and sperm microRNA content The FASEB Journal ·Tod Fullston, Edward Teague, Nicole O. Palmer, Miles J. De Blasio, Megan Mitchell, Mark Corbett, Cristin G. Print, Julie A. Owens, Michelle Lane	2013	438
2	Identification of a MicroRNA that Activates Gene Expression by Repressing Nonsense-Mediated RNA Decay Molecular Cell ·Ivone Bruno, Rachid Karam, Lulu Huang, Anjana Bhardwaj, Chih H. Lou, Eleen Y. Shum, Hye-Won Song, Mark Corbett, Wesley D. Gifford, Jozef Gécz, Samuel L. Pfaff, Miles Wilkinson	2011	230
3	Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy Molecular Psychiatry ·G. McMichael, Matthew N. Bainbridge, Eric Haan, Mark Corbett, Alison Gardner, Suzanna Thompson, Bregje W.M. van Bon, Clare L. van Eyk, J. L. BROADBENT, Chandra A. Reynolds, Michael O’Callaghan, Lam Son Nguyen, David L. Adelson, Remo Russo, Shalini N. Jhangiani, HarshaVardhan Doddapaneni, Donna M. Muzny, Richard A. Gibbs, Jozef Gécz, Alastair H. MacLennan	2015	147
4	The genetic landscape of intellectual disability arising from chromosome X Trends in Genetics ·Jozef Gécz, Cheryl Shoubridge, Mark Corbett	2009	138
5	A systematic review of photodynamic therapy in the treatment of pre-cancerous skin conditions, Barrett’s oesophagus and cancers of the biliary tract, brain, head and neck, lung, oesophagus and skin Health Technology Assessment ·Debra Fayter, Mark Corbett, Morag Heirs, D.C. Fox, Alison Eastwood	2010	108
6	A Focal Epilepsy and Intellectual Disability Syndrome Is Due to a Mutation in TBC1D24 The American Journal of Human Genetics ·Mark Corbett, Melanie Bahlo, Lachlan A. Jolly, Zaid Afawi, Alison Gardner, Karen Oliver, Stanley Tan, A. Kirtland Coffey, John C. Mulley, Leanne M. Dibbens, Simri Walid, Adel Shalata, Sara Kivity, Graeme D. Jackson, Samuel F. Berkovic, Jozef Gécz	2010	87
7	A Mutation in the Golgi Qb-SNARE Gene GOSR2 Causes Progressive Myoclonus Epilepsy with Early Ataxia The American Journal of Human Genetics ·Mark Corbett, Michael Schwake, Melanie Bahlo, Leanne M. Dibbens, Meng Lin, Luke C. Gandolfo, Danya F. Vears, John D. O’Sullivan, Thomas Robertson, Marta A. Bayly, Alison Gardner, Annemarie Vlaar, Georg Christoph Korenke, Bastiaan R. Bloem, I.F.M. de Coo, Judith M.A. Verhagen, Anna‐Elina Lehesjoki, Jozef Gécz, Samuel F. Berkovic	2011	84
8	A mutation in alpha-tropomyosinslow affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy Human Molecular Genetics ·Mark Corbett	2001	77
9	A ubiquitin-dependent signalling axis specific for ALKBH-mediated DNA dealkylation repair Nature ·Joshua R. Brickner, Jennifer M. Soll, Patrick M. Lombardi, Cathrine Broberg Vågbø, Miranda C. Mudge, Clément Oyeniran, Renana Rabe, Jessica Jackson, Meagan E. Sullender, Elyse Blazosky, Andrea K. Byrum, Yu Zhao, Mark Corbett, Jozef Gécz, Michael Field, Alessandro Vindigni, Geir Slupphaug, Cynthia Wolberger, Nima Mosammaparast	2017	76
10	A Noncoding, Regulatory Mutation Implicates HCFC1 in Nonsyndromic Intellectual Disability The American Journal of Human Genetics ·Lingli Huang, Lachlan A. Jolly, Saffron A.G. Willis‐Owen, Alison Gardner, Raman Kumar, Evelyn Douglas, Cheryl Shoubridge, Dagmar Wieczorek, Andreas Tzschach, Monika Cohen, Anna Hackett, Michael Field, Guy Froyen, Hao Hu, Stefan A. Haas, Hans‐Hilger Ropers, Vera M. Kalscheuer, Mark Corbett, Jozef Gécz	2012	73
11	DominantKCNA2mutation causes episodic ataxia and pharmacoresponsive epilepsy Neurology ·Mark Corbett, Susannah T. Bellows, Melody Li, Renée Carroll, Silvana Micallef, Gemma L. Carvill, Candace T. Myers, Katherine B. Howell, Snezana Maljevic, Holger Lerche, Elena V. Gazina, Heather C. Mefford, Melanie Bahlo, Samuel F. Berkovic, Steven Petrou, Ingrid E. Scheffer, Jozef Gécz	2016	67
12	Paternal under-nutrition programs metabolic syndrome in offspring which can be reversed by antioxidant/vitamin food fortification in fathers Scientific Reports ·Nicole O. McPherson, Tod Fullston, Wan Xian Kang, Lauren Sandeman, Mark Corbett, Julie A. Owens, Michelle Lane	2016	57
13	Complex Interplay Between Determinants of Pacing and Performance During 20-km Cycle Time Trials International Journal of Sports Physiology and Performance ·Andrew Renfree, Julia West, Mark Corbett, Clare Rhoden, Alan St Clair Gibson	2012	56
14	Interchromosomal Insertional Translocation at Xq26.3 AltersSOX3Expression in an Individual With XX Male Sex Reversal The Journal of Clinical Endocrinology & Metabolism ·Bryan P. Haines, James Hughes, Mark Corbett, Marie Shaw, Josie Innes, Leena Patel, Jozef Gécz, Jill Clayton‐Smith, Paul Q. Thomas	2015	50
15	Substrate promiscuity of cytochrome P450 RhF Catalysis Science & Technology ·Elaine O’Reilly, Mark Corbett, Shahed Hussain, Paul P. Kelly, Dominique Richardson, Sabine L. Flitsch, Nicholas J. Turner	2013	48
16	An αtropomyosin mutation alters dimer preference in nemaline myopathy Annals of Neurology ·Mark Corbett, P. Anthony Akkari, Ana Domazetovska, Sandra T. Cooper, Kathryn N. North, Nigel G. Laing, Peter W. Gunning, Edna C. Hardeman	2004	44
17	Skeletal muscle repair in a mouse model of nemaline myopathy Human Molecular Genetics ·Despina Sanoudou, Mark Corbett, Mei Han, Majid Ghoddusi, Mai-Anh T. Nguyen, Nicole Vlahovich, Edna C. Hardeman, Alan H. Beggs	2006	41
18	Expanding the molecular basis and phenotypic spectrum of X-linked Joubert syndrome associated with OFD1 mutations European Journal of Human Genetics ·Michael Field, Ingrid E. Scheffer, Deepak Gill, Meredith Wilson, Louise Christie, Marie Shaw, Alison Gardner, Georgie C. Glubb, Lynne Hobson, Mark Corbett, Kathryn Friend, Saffron A.G. Willis‐Owen, Jozef Gécz	2012	41
19	PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering Epilepsy Neurobiology of Disease ·Claire C. Homan, Stephen Pederson, Thu-Hien To, Chuan Tan, Sandra Piltz, Mark Corbett, Ernst J. Wolvetang, Paul Q. Thomas, Lachlan A. Jolly, Jozef Gécz	2018	40
20	A novel X-linked trichothiodystrophy associated with a nonsense mutation in RNF113A Journal of Medical Genetics ·Mark Corbett, Tracy Dudding‐Byth, Patricia Crock, Elena Botta, Louise Christie, Tiziana Nardò, Giuseppina Caligiuri, Lynne Hobson, Jackie Boyle, Albert Mansour, Kathryn Friend, Joanna Crawford, Graeme D. Jackson, Lucianne Vandeleur, Anna Hackett, Patrick Tarpey, Michael R. Stratton, Gillian Turner, Jozef Gécz, Michael Field	2015	40

About Mark Corbett

Mark Corbett is a scholar working on Otorhinolaryngology, Immunology and Allergy, Genetics, Psychiatry and Mental health and Genetics, having authored 72 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (19 papers), Genomics and Rare Diseases (10 papers), Allergic Rhinitis and Sensitization (7 papers), RNA Research and Splicing (7 papers), Genomic variations and chromosomal abnormalities (7 papers), Sinusitis and nasal conditions (7 papers), Glycogen Storage Diseases and Myoclonus (7 papers) and Neurogenetic and Muscular Disorders Research (6 papers). The work is most often cited by research in Genetics (715 citations), Pediatrics, Perinatology and Child Health (428 citations), Molecular Biology (1.4k citations), Psychiatry and Mental health (253 citations) and Genetics (154 citations). Mark Corbett has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Jozef Gécz, Tod Fullston, Julie A. Owens, Michelle Lane, Cheryl Shoubridge, Nicole O. Palmer, Megan Mitchell, Miles J. De Blasio, Edward Teague and Cristin G. Print. Their work appears in journals such as Human Molecular Genetics, European Journal of Human Genetics, npj Genomic Medicine, The American Journal of Human Genetics and Epilepsia.

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.

Explore authors with similar magnitude of impact