Mark Corbett
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
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- Birth, Development, and Health
Papers in
- Genetics 28
- Genetics and Neurodevelopmental Disorders 19
- Genomics and Rare Diseases 10
- Genomic variations and chromosomal abnormalities 7
- Neurogenetic and Muscular Disorders Research 5
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- RNA Research and Splicing 6
- Co-authors
- Jozef Gécz (36 shared papers)Tod Fullston (2 shared papers)Michelle Lane (2 shared papers)Julie A. Owens (2 shared papers)Cheryl Shoubridge (3 shared papers)Cristin G. Print (1 shared paper)Nicole O. Palmer (1 shared paper)Megan Mitchell (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)Cochrane Database of Systematic Reviews (2 papers)
- Partner nations
- AustraliaUnited KingdomUnited States
In The Last Decade
Mark Corbett
65 papers receiving 2.6k citations
Mark Corbett's Hit Papers
Peers
Comparison fields: 5 of 115
- Genetics 663
- Pediatrics, Perinatology and Child Health 396
- Molecular Biology 1.3k
- Psychiatry and Mental health 220
- Reproductive Medicine 124
Countries citing papers authored by Mark Corbett
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
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.
All Works
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 Hit paper breakdown → | 2013 | 487 |
| 2 | 2011 | 239 | |
| 3 | 2015 | 158 | |
| 4 | 2009 | 146 | |
| 5 | 2010 | 116 | |
| 6 | 2011 | 88 | |
| 7 | 2010 | 88 | |
| 8 | 2017 | 82 | |
| 9 | 2001 | 80 | |
| 10 | 2012 | 75 | |
| 11 | 2016 | 70 | |
| 12 | 2016 | 60 | |
| 13 | 2012 | 57 | |
| 14 | 2015 | 57 | |
| 15 | 2004 | 55 | |
| 16 | 2013 | 48 | |
| 17 | 2006 | 46 | |
| 18 | 2015 | 42 | |
| 19 | 2012 | 42 | |
| 20 | 2018 | 41 |
About Mark Corbett
Mark Corbett is a scholar working on Genetics, Molecular Biology, Otorhinolaryngology, Rheumatology and Psychiatry and Mental health, having authored 72 papers that have together received 2.6k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (19 papers), Genomics and Rare Diseases (10 papers), Sinusitis and nasal conditions (7 papers), Genomic variations and chromosomal abnormalities (7 papers), RNA Research and Splicing (6 papers), Glycogen Storage Diseases and Myoclonus (6 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Genetic Neurodegenerative Diseases (5 papers). The work is most often cited by research in Genetics (663 citations), Pediatrics, Perinatology and Child Health (396 citations), Molecular Biology (1.3k citations), Psychiatry and Mental health (220 citations) and Reproductive Medicine (124 citations). Mark Corbett has collaborated with scholars based in Australia, United Kingdom and United States. Frequent co-authors include Jozef Gécz, Tod Fullston, Michelle Lane, Julie A. Owens, Cheryl Shoubridge, Cristin G. Print, Nicole O. Palmer, Megan Mitchell, Edward Teague and Miles J. De Blasio. 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 Cochrane Database of Systematic Reviews.
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.