Peter Corry

4.0k total citations
18 papers, 1.3k citations indexed

About

Peter Corry is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Peter Corry has authored 18 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Peter Corry's work include Genomics and Rare Diseases (4 papers), Microtubule and mitosis dynamics (4 papers) and Prenatal Screening and Diagnostics (4 papers). Peter Corry is often cited by papers focused on Genomics and Rare Diseases (4 papers), Microtubule and mitosis dynamics (4 papers) and Prenatal Screening and Diagnostics (4 papers). Peter Corry collaborates with scholars based in United Kingdom, United States and Australia. Peter Corry's co-authors include C. Geoffrey Woods, Hussain Jafri, Yasmin Abdul Rashid, Gulshan Karbani, Emma Roberts, Kelly Springell, Daniel J. Hampshire, Christopher A. Walsh, Jacquelyn Bond and Ewan E. Morrison and has published in prestigious journals such as The Lancet, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Peter Corry

18 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter Corry United Kingdom 15 710 498 471 228 115 18 1.3k
Marie McDonald United States 19 749 1.1× 239 0.5× 1.1k 2.3× 188 0.8× 178 1.5× 45 1.7k
Yasmin Abdul Rashid Pakistan 15 1.3k 1.8× 688 1.4× 723 1.5× 180 0.8× 74 0.6× 49 1.9k
Renata Laxová United States 19 765 1.1× 171 0.3× 623 1.3× 289 1.3× 90 0.8× 53 1.6k
Alison Murdoch United Kingdom 30 1.7k 2.4× 389 0.8× 283 0.6× 691 3.0× 139 1.2× 79 3.3k
Ans M.W. van den Ouweland Netherlands 29 1.5k 2.1× 256 0.5× 1.7k 3.5× 325 1.4× 70 0.6× 74 3.4k
Manuela Volta Italy 13 1.5k 2.0× 104 0.2× 523 1.1× 256 1.1× 63 0.5× 16 1.9k
Petter Strømme Norway 28 1.2k 1.7× 182 0.4× 1.1k 2.4× 296 1.3× 86 0.7× 76 2.7k
Katrin Õunap Estonia 25 1.0k 1.4× 126 0.3× 857 1.8× 264 1.2× 48 0.4× 106 1.8k
C. Beldjord France 22 1.0k 1.5× 267 0.5× 887 1.9× 574 2.5× 690 6.0× 54 2.5k
Ragnheiður Fossdal Iceland 15 987 1.4× 130 0.3× 1.5k 3.2× 211 0.9× 37 0.3× 21 2.2k

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-authorship network of co-authors of Peter Corry

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Corry. A scholar is included among the top collaborators of Peter Corry 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 Peter Corry. Peter Corry is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Small, Neil, Dan Mason, Peter Corry, et al.. (2017). Improving case ascertainment of congenital anomalies: findings from a prospective birth cohort with detailed primary care record linkage. BMJ Paediatrics Open. 1(1). e000171–e000171. 15 indexed citations
2.
3.
Corry, Peter. (2014). Consanguinity and Prevalence Patterns of Inherited Disease in the UK Pakistani Community. Human Heredity. 77(1-4). 207–216. 28 indexed citations
4.
Sheridan, Eamonn, John Wright, Neil Small, et al.. (2014). Risk Factors for Congenital Anomaly in a Multiethnic Birth Cohort. Obstetrical & Gynecological Survey. 69(2). 75–77. 9 indexed citations
5.
Sheridan, Eamonn, John Wright, Neil Small, et al.. (2013). Risk factors for congenital anomaly in a multiethnic birth cohort: an analysis of the Born in Bradford study. The Lancet. 382(9901). 1350–1359. 145 indexed citations
6.
Parslow, Roger, et al.. (2013). 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). 1 indexed citations
7.
Small, Neil, Waqar Ahmad, Karl Atkin, et al.. (2012). Examining the family-centred approach to genetic testing and counselling among UK Pakistanis: a community perspective. Journal of Community Genetics. 4(1). 49–57. 19 indexed citations
8.
Abdollahi, Mohammad Reza, Ewan E. Morrison, Tamara Sirey, et al.. (2009). Mutation of the Variant α-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia. The American Journal of Human Genetics. 85(5). 737–744. 122 indexed citations
9.
Cachón-González, María Begoña, Penelope E. Stein, Robin Lachmann, et al.. (2008). A novel HEXB mutation and its structural effects in juvenile Sandhoff disease. Molecular Genetics and Metabolism. 95(4). 236–238. 3 indexed citations
10.
Bond, Jacquelyn, Emma Roberts, Kelly Springell, et al.. (2005). A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size. Nature Genetics. 37(4). 353–355. 423 indexed citations
11.
Hendriksz, Christian J., Peter Corry, J. E. Wraith, et al.. (2004). Juvenile Sandhoff disease—Nine new cases and a review of the literature. Journal of Inherited Metabolic Disease. 27(2). 241–249. 19 indexed citations
12.
Bond, Jacquelyn, Daniel J. Hampshire, Kelly Springell, et al.. (2003). Protein-Truncating Mutations in ASPM Cause Variable Reduction in Brain Size. The American Journal of Human Genetics. 73(5). 1170–1177. 133 indexed citations
13.
Corry, Peter. (2002). Intellectual Disability and Cerebral Palsy in a UK Community. Public Health Genomics. 5(3). 201–204. 27 indexed citations
14.
Rees, Mark I., T. Lewis, Colin D. Ferrie, et al.. (2001). Compound heterozygosity and nonsense mutations in the α1-subunit of the inhibitory glycine receptor in hyperekplexia. Human Genetics. 109(3). 267–270. 64 indexed citations
15.
Moynihan, Leanne, Andrew P. Jackson, Emma Roberts, et al.. (2000). A Third Novel Locus for Primary Autosomal Recessive Microcephaly Maps to Chromosome 9q34. The American Journal of Human Genetics. 66(2). 724–727. 81 indexed citations
16.
Jackson, Andrew P., et al.. (2000). A gene for ataxic cerebral palsy maps to chromosome 9p12–q12. European Journal of Human Genetics. 8(4). 267–272. 38 indexed citations
17.
Jackson, Andrew P., Duncan P. McHale, David A. Campbell, et al.. (1998). Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter. The American Journal of Human Genetics. 63(2). 541–546. 117 indexed citations
18.
Corry, Peter, et al.. (1997). Prevalence and type of cerebral palsy in a British ethnic community: the role of consanguinity. Developmental Medicine & Child Neurology. 39(4). 259–262. 42 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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