Mark A Corbett

9k citations

100 papers · 7k · 2 hit papers · h-index 43

Impact in

Psychiatry and Mental health top 1%
- Epilepsy research and treatment
- Cerebral Palsy and Movement Disorders
Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities

Papers in

Genetics 57
- Genetics and Neurodevelopmental Disorders 37
- Genomics and Rare Diseases 27
- Genomic variations and chromosomal abnormalities 5
Psychiatry and Mental health 37
- Epilepsy research and treatment 25
- Cerebral Palsy and Movement Disorders 12

Co-authors: Jozef Gécz (37 shared papers)Michelle Lane (2 shared papers)Tod Fullston (2 shared papers)Nicole Olivia McPherson (2 shared papers)Julie A. Owens (2 shared papers)Cheryl Shoubridge (3 shared papers)Megan Mitchell (1 shared paper)Edward Teague (1 shared paper)
Journals: The American Journal of Human Genetics (15 papers)Human Molecular Genetics (9 papers)Nature Genetics (6 papers)European Journal of Human Genetics (6 papers)npj Genomic Medicine (5 papers)
Partner nations: Australia United States United Kingdom

In The Last Decade

Mark A Corbett

97 papers receiving 6.8k citations

Mark A Corbett's Hit Papers

align trajectories log scale

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 2013 · 494 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2013 The FASEB Journal
2009 Nature Genetics

Peers

Countries citing papers authored by Mark A Corbett

Since Specialization

Citations

This map shows the geographic impact of Mark A 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 A 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 A Corbett more than expected).

Fields of papers citing papers by Mark A Corbett

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mark A 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 A Corbett Line = papers co-authored together Mark A 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 100 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation Nature Genetics ·Patrick S. Tarpey, Raffaella Smith, Erin Pleasance, Annabel C. Whibley, Sarah Edkins, Claire W. Hardy, Sarah O’Meara, Calli Latimer Hit paper breakdown →	2009	505
2	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 Olivia McPherson, Miles J. De Blasio, Megan Mitchell, Mark A Corbett, Cristin Gregor Print, Julie A. Owens Hit paper breakdown →	2013	494
3	X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment Nature Genetics ·Leanne M. Dibbens, Patrick S. Tarpey, Kim Hynes, Marta A. Bayly, Ingrid Eileen Scheffer, Raffaella Smith, Jamee M. Bomar, Edwina Sutton	2008	354
4	Mutations in DEPDC5 cause familial focal epilepsy with variable foci Nature Genetics ·Leanne M. Dibbens, Boukje de Vries, Simona Donatello, Sarah E. Heron, Bree L. Hodgson, Satyan Chintawar, Douglas Ewan Crompton, James Nicholas Hughes	2013	285
5	Large deletions induced by Cas9 cleavage Nature ·Fatwa Adikusuma, Sandra Piltz, Mark A Corbett, Michelle E. Turvey, Shaun R. McColl, Karla J. Helbig, Michael R. Beard, James Hughes	2018	280
6	X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes Molecular Psychiatry ·Hao Hu, Stefan A. Haas, Jamel Chelly, Hilde Van Esch, Martine Raynaud, Arjan P.M. de Brouwer, Stefanie Weinert, Guy Froyen	2015	245
7	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 A Corbett	2011	244
8	Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation Nature Genetics ·Patrick S. Tarpey, Frances Lucy Raymond, Lam Son Nguyen, Jayson D. Rodriguez, Anna Hackett, Lucianne Vandeleur, Raffaella Smith, Cheryl Shoubridge	2007	230
9	De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies The American Journal of Human Genetics ·Mark A Corbett, Jozef Gécz, David John Coman, Sophie Calvert, Tally Lerman‐Sagie, Patrick Cossette, Evan E. Eichler, Michael R. Johnson	2016	227
10	PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome The American Journal of Human Genetics ·Sarah E. Heron, Bronwyn E. Grinton, Sara Kivity, Zaid Afawi, Sameer M. Zuberi, James Nicholas Hughes, Clair Pridmore, Bree L. Hodgson	2012	222
11	Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation The American Journal of Human Genetics ·Guy Froyen, Mark A Corbett, Joke Vandewalle, Irma E. Järvelä, Owen Lawrence, Cliff J. Meldrum, Marijke Bauters, Karen Govaerts	2008	179
12	Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy Molecular Psychiatry ·G. McMichael, Matthew Neil Bainbridge, Eric Haan, Mark A Corbett, Alison E. Gardner, Suzanna C. Thompson, Bregje W.M. van Bon, Clare L. van Eyk	2015	177
13	The genetic landscape of intellectual disability arising from chromosome X Trends in Genetics ·Jozef Gécz, Cheryl Shoubridge, Mark A Corbett	2009	159
14	Targeted Next‐Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability Human Mutation ·Detelina Grozeva, Keren Carss, Olivera Spasić-Bošković, María‐Isabel Tejada, Jozef Gécz, Marie A Shaw, Mark A Corbett, Eric Haan	2015	148
15	Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3 Nature Communications ·Rahel T. Florian, Florian Kraft, Elsa Leitão, Sabine Kaya, Stephan Klebe, Éloi Magnin, Anne‐Fleur van Rootselaar, Julien Buratti	2019	123
16	Mutations disrupting neuritogenesis genes confer risk for cerebral palsy Nature Genetics ·Sheng Chih Jin, Sara A. Lewis, Somayeh Bakhtiari, Xue Qiang Zeng, Michael C. Sierant, Sheetal Shetty, Sandra M. Nordlie, Aureliane Elie	2020	123
17	De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias The American Journal of Human Genetics ·Katherine L. Helbig, Robert J. Lauerer, Jacqueline C Bahr, Ivana Assis Souza, Candace T. Myers, Niklas Schwarz, María A. Gandini, Sun Huang	2018	109
18	TBC1D24 genotype–phenotype correlation Neurology ·Simona Balestrini, Mathieu Milh, Claudia Castiglioni T, Kevin Lüthy, Mattéa J. Finelli, Patrik Verstreken, Aaron L. Cardon, Barbara Gnidovec Stražišar	2016	108
19	Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2 Nature Communications ·Mark A Corbett, Thessa Kroes, Liana Veneziano, Mark F. Bennett, Rahel T. Florian, Amy Schneider, Antonietta Coppola, Laura Licchetta	2019	106
20	Transcriptome profiling of UPF3B/NMD-deficient lymphoblastoid cells from patients with various forms of intellectual disability Molecular Psychiatry ·Lam Son Nguyen, Lachlan A. Jolly, Cheryl Shoubridge, Wai-Kin Chan, Lulu Huang, Frédéric Laumonnier, Martine Raynaud, Anna Hackett	2011	104

About Mark A Corbett

Mark A Corbett is a scholar working on Genetics, Psychiatry and Mental health, Pediatrics, Perinatology and Child Health, Molecular Biology and Cellular and Molecular Neuroscience, having authored 100 papers that have together received 7k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (37 papers), Genomics and Rare Diseases (27 papers), Epilepsy research and treatment (25 papers), Cerebral Palsy and Movement Disorders (12 papers), RNA Research and Splicing (9 papers), Fetal and Pediatric Neurological Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Muscle Physiology and Disorders (5 papers). The work is most often cited by research in Psychiatry and Mental health (1.8k citations), Genetics (2.5k citations), Developmental Neuroscience (125 citations), Pediatrics, Perinatology and Child Health (469 citations) and Molecular Biology (2k citations). Mark A Corbett has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Jozef Gécz, Michelle Lane, Tod Fullston, Nicole Olivia McPherson, Julie A. Owens, Cheryl Shoubridge, Megan Mitchell, Edward Teague, Cristin Gregor Print and Miles J. De Blasio. Their work appears in journals such as The American Journal of Human Genetics, Human Molecular Genetics, Nature Genetics, European Journal of Human Genetics and npj Genomic Medicine.

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

Mark A Corbett

Impact in

Papers in i

In The Last Decade

Mark A Corbett

Mark A Corbett's Hit Papers

Peers

Countries citing papers authored by Mark A Corbett

Fields of papers citing papers by Mark A Corbett

All Works

About Mark A Corbett

Explore authors with similar magnitude of impact

Papers in