Christopher Wragg
Impact in
Papers in
- Genetics 9
- Glioma Diagnosis and Treatment 9
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 3
-
- Acute Myeloid Leukemia Research 2
- Co-authors
- Kathreena Mary Kurian (9 shared papers)Claire Faulkner (8 shared papers)Paul White (3 shared papers)Harry R. Haynes (2 shared papers)Julian P. T. Higgins (6 shared papers)Sarah Jefferies (6 shared papers)Alexandra McAleenan (6 shared papers)Sarah Dawson (6 shared papers)
- Journals
- Cochrane Database of Systematic Reviews (4 papers)The American Journal of Human Genetics (4 papers)Blood (2 papers)Journal of Medical Genetics (2 papers)British Journal of Haematology (2 papers)
- Partner nations
- United KingdomGermanyUnited States
In The Last Decade
Christopher Wragg
23 papers receiving 1.4k citations
Christopher Wragg's Hit Papers
Peers
Comparison fields: 5 of 72
- Genetics 180
- Neurology 173
- Pathology and Forensic Medicine 209
- Genetics 325
- Developmental Biology 20
Countries citing papers authored by Christopher Wragg
This map shows the geographic impact of Christopher Wragg'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 Christopher Wragg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Christopher Wragg more than expected).
Fields of papers citing papers by Christopher Wragg
This network shows the impact of papers produced by Christopher Wragg. 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 Christopher Wragg. The network helps show where Christopher Wragg may publish in the future.
Co-authors
The 25 scholars most cited alongside Christopher Wragg, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Effect of remote ischaemic conditioning on clinical outcomes in patients with acute myocardial infarction (CONDI-2/ERIC-PPCI): a single-blind randomised controlled trial Hit paper breakdown → | 2019 | 269 |
| 2 | 2017 | 213 | |
| 3 | 2016 | 190 | |
| 4 | 2017 | 113 | |
| 5 | 2016 | 102 | |
| 6 | 2018 | 95 | |
| 7 | 2014 | 65 | |
| 8 | 2019 | 63 | |
| 9 | 2021 | 52 | |
| 10 | 2014 | 51 | |
| 11 | 2015 | 49 | |
| 12 | 2019 | 49 | |
| 13 | 2021 | 32 | |
| 14 | 2021 | 18 | |
| 15 | 2023 | 16 | |
| 16 | 2022 | 15 | |
| 17 | 2019 | 9 | |
| 18 | 2019 | 7 | |
| 19 | 2019 | 6 | |
| 20 | 2022 | 4 |
About Christopher Wragg
Christopher Wragg is a scholar working on Genetics, Genetics, Hematology, Psychiatry and Mental health and Developmental Biology, having authored 24 papers that have together received 1.4k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (9 papers), Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (3 papers), Epilepsy research and treatment (2 papers), Acute Myeloid Leukemia Research (2 papers), Acute Lymphoblastic Leukemia research (2 papers), Epigenetics and DNA Methylation (1 paper) and Congenital limb and hand anomalies (1 paper). The work is most often cited by research in Genetics (180 citations), Neurology (173 citations), Pathology and Forensic Medicine (209 citations), Genetics (325 citations) and Developmental Biology (20 citations). Christopher Wragg has collaborated with scholars based in United Kingdom, Germany and United States. Frequent co-authors include Kathreena Mary Kurian, Claire Faulkner, Paul White, Harry R. Haynes, Julian P. T. Higgins, Sarah Jefferies, Alexandra McAleenan, Sarah Dawson, Sebastian Brandner and Lena Schmidt. Their work appears in journals such as Cochrane Database of Systematic Reviews, The American Journal of Human Genetics, Blood, Journal of Medical Genetics and British Journal of Haematology.
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.