Val Davison
Impact in
- Genetics top 10%
- Glioma Diagnosis and Treatment
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
-
- Renal and related cancers 2
- Congenital heart defects research 2
- Epigenetics and DNA Methylation 1
- Genetics 4
- Genomic variations and chromosomal abnormalities 4
- Co-authors
- Dominic McMullan (3 shared papers)Sara Dyer (3 shared papers)Richard G. Grundy (2 shared papers)Pramila Ramani (2 shared papers)David W. Ellison (1 shared paper)Paul Davies (1 shared paper)Lisa Cooper‐Charles (1 shared paper)Jenny Morton (1 shared paper)
- Journals
- European Journal of Cancer (2 papers)European Journal of Human Genetics (1 paper)American Journal Of Pathology (1 paper)Biochemical Society Transactions (1 paper)Genes Chromosomes and Cancer (1 paper)
- Partner nations
- United KingdomGermanySpain
In The Last Decade
Val Davison
10 papers receiving 371 citations
Peers
Comparison fields: 5 of 55
- Genetics 107
- Genetics 121
- Cancer Research 46
- Neurology 43
- Molecular Biology 179
Countries citing papers authored by Val Davison
This map shows the geographic impact of Val Davison'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 Val Davison with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Val Davison more than expected).
Fields of papers citing papers by Val Davison
This network shows the impact of papers produced by Val Davison. 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 Val Davison. The network helps show where Val Davison may publish in the future.
Co-authors
The 25 scholars most cited alongside Val Davison, 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 | 2002 | 119 | |
| 2 | 2009 | 96 | |
| 3 | 2011 | 66 | |
| 4 | 2010 | 58 | |
| 5 | 2007 | 29 | |
| 6 | 2007 | 27 | |
| 7 | 2007 | 13 | |
| 8 | 2006 | 3 | |
| 9 | 1996 | 3 | |
| 10 | 2001 | 1 |
About Val Davison
Val Davison is a scholar working on Molecular Biology, Genetics, Neurology, Pediatrics, Perinatology and Child Health and Plant Science, having authored 10 papers that have together received 415 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Chromosomal and Genetic Variations (2 papers), Renal and related cancers (2 papers), Congenital heart defects research (2 papers), Neuroblastoma Research and Treatments (2 papers), Autism Spectrum Disorder Research (1 paper), Fetal and Pediatric Neurological Disorders (1 paper) and Epigenetics and DNA Methylation (1 paper). The work is most often cited by research in Genetics (107 citations), Genetics (121 citations), Cancer Research (46 citations), Neurology (43 citations) and Molecular Biology (179 citations). Val Davison has collaborated with scholars based in United Kingdom, Germany and Spain. Frequent co-authors include Dominic McMullan, Sara Dyer, Richard G. Grundy, Pramila Ramani, David W. Ellison, Paul Davies, Lisa Cooper‐Charles, Jenny Morton, Chirag Patel and Eamonn R. Maher. Their work appears in journals such as European Journal of Cancer, European Journal of Human Genetics, American Journal Of Pathology, Biochemical Society Transactions and Genes Chromosomes and Cancer.
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.