Peter C. Corry
Impact in
- Developmental Neuroscience top 2%
- Neurogenesis and neuroplasticity mechanisms
- Virology top 5%
- HIV Research and Treatment
Papers in
-
- Fetal and Pediatric Neurological Disorders 6
- Genetics 7
- Genomics and Rare Diseases 7
- Genetics and Neurodevelopmental Disorders 3
- Co-authors
- Christopher Geoffrey Woods (4 shared papers)Yasmin Abdul Rashid (3 shared papers)Hussain Jafri (3 shared papers)Gulshan Karbani (3 shared papers)Kelly Springell (3 shared papers)Emma Roberts (3 shared papers)Jacquelyn Bond (2 shared papers)Daniel J. Hampshire (2 shared papers)
- Journals
- The American Journal of Human Genetics (6 papers)Nature Genetics (3 papers)The Lancet (1 paper)Molecular Genetics and Metabolism (1 paper)Public Health Genomics (1 paper)
- Partner nations
- United KingdomAustraliaUnited States
In The Last Decade
Peter C. Corry
22 papers receiving 3.2k citations
Peter C. Corry's Hit Papers
Peers
Comparison fields: 5 of 94
- Developmental Neuroscience 242
- Virology 210
- Immunology 911
- Pediatrics, Perinatology and Child Health 479
- Clinical Biochemistry 113
Countries citing papers authored by Peter C. Corry
This map shows the geographic impact of Peter C. 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 C. 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 C. Corry more than expected).
Fields of papers citing papers by Peter C. Corry
This network shows the impact of papers produced by Peter C. 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 C. Corry. The network helps show where Peter C. Corry may publish in the future.
Co-authors
The 25 scholars most cited alongside Peter C. Corry, 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 22 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus Hit paper breakdown → | 2006 | 779 |
| 2 | 2009 | 610 | |
| 3 | 2005 | 467 | |
| 4 | 2007 | 376 | |
| 5 | 2013 | 189 | |
| 6 | 2003 | 147 | |
| 7 | 2009 | 145 | |
| 8 | 1998 | 138 | |
| 9 | 2000 | 93 | |
| 10 | 2000 | 71 | |
| 11 | 2001 | 66 | |
| 12 | 1997 | 44 | |
| 13 | 2000 | 42 | |
| 14 | 2015 | 41 | |
| 15 | 2014 | 30 | |
| 16 | 2002 | 29 | |
| 17 | 2004 | 25 | |
| 18 | 2012 | 24 | |
| 19 | 2017 | 20 | |
| 20 | 2014 | 9 |
About Peter C. Corry
Peter C. Corry is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Psychiatry and Mental health, Immunology and Developmental Neuroscience, having authored 22 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Fetal and Pediatric Neurological Disorders (6 papers), interferon and immune responses (4 papers), Cerebral Palsy and Movement Disorders (4 papers), Inflammasome and immune disorders (3 papers), Congenital Anomalies and Fetal Surgery (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Lysosomal Storage Disorders Research (2 papers). The work is most often cited by research in Developmental Neuroscience (242 citations), Virology (210 citations), Immunology (911 citations), Pediatrics, Perinatology and Child Health (479 citations) and Clinical Biochemistry (113 citations). Peter C. Corry has collaborated with scholars based in United Kingdom, Australia and United States. Frequent co-authors include Christopher Geoffrey Woods, Yasmin Abdul Rashid, Hussain Jafri, Gulshan Karbani, Kelly Springell, Emma Roberts, Jacquelyn Bond, Daniel J. Hampshire, Christopher A. Walsh and Sheila Scott. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, The Lancet, Molecular Genetics and Metabolism and Public Health Genomics.
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.