Ronnie Wright
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
- Genetic Associations and Epidemiology
-
- CRISPR and Genetic Engineering
- Congenital heart defects research
Papers in
- Genetics 12
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- BRCA gene mutations in cancer 2
- Animal Genetics and Reproduction 1
-
- Congenital heart defects research 2
- Glycosylation and Glycoproteins Research 1
- Co-authors
- Julija Pavaine (2 shared papers)Pauline Hensman (1 shared paper)Alexander A. Broomfield (1 shared paper)Helen Prunty (1 shared paper)Simon Allan Jones (1 shared paper)Philip A. Lewis (1 shared paper)Kay Poulton (1 shared paper)Marcus Lowe (1 shared paper)
- Journals
- Genetics in Medicine (3 papers)Journal of Medical Genetics (2 papers)Neuromuscular Disorders (1 paper)The American Journal of Human Genetics (1 paper)Theriogenology (1 paper)
- Partner nations
- United KingdomUnited StatesNetherlands
In The Last Decade
Ronnie Wright
18 papers receiving 810 citations
Ronnie Wright's Hit Papers
Peers
Comparison fields: 5 of 76
- Genetics 448
- Molecular Biology 336
- Immunology 77
- Cognitive Neuroscience 66
- Genetics 34
Countries citing papers authored by Ronnie Wright
This map shows the geographic impact of Ronnie Wright'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 Ronnie Wright with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ronnie Wright more than expected).
Fields of papers citing papers by Ronnie Wright
This network shows the impact of papers produced by Ronnie Wright. 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 Ronnie Wright. The network helps show where Ronnie Wright may publish in the future.
Co-authors
The 25 scholars most cited alongside Ronnie Wright, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | Evidence for 28 genetic disorders discovered by combining healthcare and research data Hit paper breakdown → | 2020 | 402 |
| 2 | 2019 | 94 | |
| 3 | 2015 | 80 | |
| 4 | 2016 | 46 | |
| 5 | 2021 | 42 | |
| 6 | 2017 | 37 | |
| 7 | 2017 | 26 | |
| 8 | 2017 | 26 | |
| 9 | 2021 | 25 | |
| 10 | 2020 | 15 | |
| 11 | 2021 | 8 | |
| 12 | 2021 | 7 | |
| 13 | 2021 | 7 | |
| 14 | 2022 | 5 | |
| 15 | 2023 | 5 | |
| 16 | 2000 | 3 | |
| 17 | 2024 | 1 | |
| 18 | 2019 | 1 | |
| 19 | 2025 | 0 |
About Ronnie Wright
Ronnie Wright is a scholar working on Genetics, Molecular Biology, Otorhinolaryngology, Physiology and Immunology and Allergy, having authored 19 papers that have together received 830 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (2 papers), BRCA gene mutations in cancer (2 papers), Animal Genetics and Reproduction (1 paper), Glycogen Storage Diseases and Myoclonus (1 paper) and Glycosylation and Glycoproteins Research (1 paper). The work is most often cited by research in Genetics (448 citations), Molecular Biology (336 citations), Immunology (77 citations), Cognitive Neuroscience (66 citations) and Genetics (34 citations). Ronnie Wright has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Julija Pavaine, Pauline Hensman, Alexander A. Broomfield, Helen Prunty, Simon Allan Jones, Philip A. Lewis, Kay Poulton, Marcus Lowe, Despina Soteriou and Lisa M. Grady. Their work appears in journals such as Genetics in Medicine, Journal of Medical Genetics, Neuromuscular Disorders, The American Journal of Human Genetics and Theriogenology.
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.