Peter Corry

4.0k citations

18 papers · 1.3k indexed · h-index 15

Impact in

Cell Biology top 2%
- Microtubule and mitosis dynamics
Developmental Neuroscience top 5%
- Neurogenesis and neuroplasticity mechanisms

Papers in ⓘ

Genetics 9
- Genomics and Rare Diseases 4
- Hemoglobinopathies and Related Disorders 2
- Cleft Lip and Palate Research 2
Cell Biology 5
- Microtubule and mitosis dynamics 4

Co-authors: C. Geoffrey Woods (4 shared papers)Yasmin Abdul Rashid (3 shared papers)Gulshan Karbani (3 shared papers)Hussain Jafri (3 shared papers)Emma Roberts (3 shared papers)Kelly Springell (3 shared papers)Daniel J. Hampshire (2 shared papers)Christopher A. Walsh (2 shared papers)
Journals: The American Journal of Human Genetics (4 papers)Public Health Genomics (1 paper)Nature Genetics (1 paper)European Journal of Human Genetics (1 paper)BMJ Paediatrics Open (1 paper)
Partner nations: United Kingdom United States Australia

In The Last Decade

Peter Corry

18 papers receiving 1.3k citations

Peers

Countries citing papers authored by Peter Corry

Since Specialization

Citations

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

Fields of papers citing papers by Peter Corry

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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18 of 18 papers shown

#	Work
1	A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size Nature Genetics ·Jacquelyn Bond, Emma Roberts, Kelly Springell, Sophia Lizarraga, Sheila Scott, J. William Higgins, Daniel J. Hampshire, Ewan E. Morrison, Gabriella F Leal, Elias O. Silva, Suzana M R Costa, Diana Baralle, Michela Raponi, Gulshan Karbani, Yasmin Abdul Rashid, Hussain Jafri, Christopher Bennett, Peter Corry, Christopher A. Walsh, C. Geoffrey Woods	2005	423
2	Risk factors for congenital anomaly in a multiethnic birth cohort: an analysis of the Born in Bradford study The Lancet ·Eamonn Sheridan, John Wright, Neil Small, Peter Corry, Sam Oddie, Catherine Whibley, Emily Petherick, Teena Malik, Nicole Pawson, Patricia A. McKinney, Roger Parslow	2013	145
3	Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size The American Journal of Human Genetics ·Jacquelyn Bond, Sheila Scott, Daniel J. Hampshire, Kelly Springell, Peter Corry, Marc Abramowicz, Ganeshwaran H. Mochida, Raoul C. M. Hennekam, Eamonn R. Maher, Jean‐Pierre Fryns, Abdulrahman Alswaid, Hussain Jafri, Yasmin Abdul Rashid, Ammar F. Mubaidin, Christopher A. Walsh, Emma Roberts, C. Geoffrey Woods	2003	133
4	Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia The American Journal of Human Genetics ·Mohammad Reza Abdollahi, Ewan E. Morrison, Tamara Sirey, Zoltán Molnár, Bruce E. Hayward, Ian Carr, Kelly Springell, C. Geoff Woods, Mushtaq Ahmed, Louise Hattingh, Peter Corry, Daniela T. Pilz, Neil Stoodley, Yanick J. Crow, Graham R. Taylor, David T. Bonthron, Eamonn Sheridan	2009	122
5	Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter The American Journal of Human Genetics ·Andrew P. Jackson, Duncan P. McHale, David A. Campbell, Hussain Jafri, Yasmin Abdul Rashid, Jovaria Mannan, Gulshan Karbani, Peter Corry, Malcolm I. Levene, Robert F. Mueller, A.F. Markham, Nicholas Lench, C. Geoffrey Woods	1998	117
6	A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34 The American Journal of Human Genetics ·Leanne Moynihan, Andrew P. Jackson, Emma Roberts, Gulshan Karbani, Ian Lewis, Peter Corry, G Turner, Robert F. Mueller, Nicholas Lench, C. Geoffrey Woods	2000	81
7	Compound heterozygosity and nonsense mutations in the α1-subunit of the inhibitory glycine receptor in hyperekplexia Human Genetics ·Mark I. Rees, T. Lewis, Behnaz Vafa, Colin D. Ferrie, Peter Corry, F. Muntoni, Heinz Jungbluth, John B.P. Stephenson, Mike Kerr, Russell G. Snell, Peter R. Schofield, Michael J. Owen	2001	64
8	Prevalence and type of cerebral palsy in a British ethnic community: the role of consanguinity Developmental Medicine & Child Neurology ·Gyan Sinha, Peter Corry, D. Subesinghe, Jennifer Wild, Malcolm I. Levene	1997	42
9	A gene for ataxic cerebral palsy maps to chromosome 9p12–q12 European Journal of Human Genetics ·DP McHale, Andrew P. Jackson, Donald Campbell, MI Levene, Peter Corry, CG Woods, Nicholas Lench, Mueller Rf, AF Markham	2000	38
10	Addressing key issues in the consanguinity-related risk of autosomal recessive disorders in consanguineous communities: lessons from a qualitative study of British Pakistanis Journal of Community Genetics ·Aliya Darr, Neil Small, Waqar Ahmad, Karl Atkin, Peter Corry, B. Modell	2015	31
11	Consanguinity and Prevalence Patterns of Inherited Disease in the UK Pakistani Community Human Heredity ·Peter Corry	2014	28
12	Intellectual Disability and Cerebral Palsy in a UK Community Public Health Genomics ·Peter Corry	2002	27
13	Examining the family-centred approach to genetic testing and counselling among UK Pakistanis: a community perspective Journal of Community Genetics ·Aliya Darr, Neil Small, Waqar Ahmad, Karl Atkin, Peter Corry, J W Benson, Richard E. Morton, B. Modell	2012	19
14	Juvenile Sandhoff disease—Nine new cases and a review of the literature Journal of Inherited Metabolic Disease ·Christian J. Hendriksz, Peter Corry, J. E. Wraith, G. T. N. Besley, Alan Cooper, C. D. Ferrie	2004	19
15	Improving case ascertainment of congenital anomalies: findings from a prospective birth cohort with detailed primary care record linkage BMJ Paediatrics Open ·Chrissy Bishop, Neil Small, Dan Mason, Peter Corry, John Wright, Roger Parslow, A.H. Bittles, Eamonn Sheridan	2017	15
16	Risk Factors for Congenital Anomaly in a Multiethnic Birth Cohort Obstetrical & Gynecological Survey ·Eamonn Sheridan, John Wright, Neil Small, Peter Corry, Sam Oddie, Catherine Whibley, Emily Petherick, Teena Malik, Nicole Pawson, Patricia A. McKinney, Roger Parslow	2014	9
17	A novel HEXB mutation and its structural effects in juvenile Sandhoff disease Molecular Genetics and Metabolism ·S.Z. Wang, María Begoña Cachón-González, Penelope E. Stein, Robin Lachmann, Peter Corry, J. E. Wraith, Timothy M. Cox	2008	3
18	Incidence of Cerebral Palsy in Yorkshire by ethnicity and area deprivation White Rose Research Online (University of Leeds, The University of Sheffield, University of York) ·PD Norman, Roger Parslow, Peter Corry, P A McKinney, Lorna Fraser	2013	1

About Peter Corry

Peter Corry is a scholar working on Genetics, Cell Biology, Pediatrics, Perinatology and Child Health, Genetics and Clinical Biochemistry, having authored 18 papers that have together received 1.3k indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (4 papers), Microtubule and mitosis dynamics (4 papers), Genomics and Rare Diseases (4 papers), Hemoglobinopathies and Related Disorders (2 papers), Cleft Lip and Palate Research (2 papers), Lysosomal Storage Disorders Research (2 papers), Cerebral Palsy and Movement Disorders (2 papers) and Mitochondrial Function and Pathology (2 papers). The work is most often cited by research in Cell Biology (498 citations), Developmental Neuroscience (104 citations), Genetics (471 citations), Pediatrics, Perinatology and Child Health (228 citations) and Genetics (115 citations). Peter Corry has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include C. Geoffrey Woods, Yasmin Abdul Rashid, Gulshan Karbani, Hussain Jafri, Emma Roberts, Kelly Springell, Daniel J. Hampshire, Christopher A. Walsh, Jacquelyn Bond and Ewan E. Morrison. Their work appears in journals such as The American Journal of Human Genetics, Public Health Genomics, Nature Genetics, European Journal of Human Genetics and BMJ Paediatrics Open.

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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