Mark Einon
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Associations and Epidemiology
-
- Congenital heart defects research
Papers in
- Genetics 3
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 2
- BRCA gene mutations in cancer 1
-
- Viral Infections and Immunology Research 2
- Co-authors
- Valentina Escott‐Price (3 shared papers)Elliott Rees (3 shared papers)George Kirov (3 shared papers)Kimberley Kendall (3 shared papers)Michael O’Donovan (3 shared papers)James Walters (2 shared papers)Michael J. Owen (2 shared papers)David Owen (2 shared papers)
- Partner nations
- United Kingdom
In The Last Decade
Mark Einon
3 papers receiving 241 citations
Peers
Comparison fields: 5 of 35
- Genetics 206
- Molecular Biology 125
- Pediatrics, Perinatology and Child Health 31
- Developmental Neuroscience 6
- Cognitive Neuroscience 25
Countries citing papers authored by Mark Einon
This map shows the geographic impact of Mark Einon'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 Mark Einon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Einon more than expected).
Fields of papers citing papers by Mark Einon
This network shows the impact of papers produced by Mark Einon. 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 Mark Einon. The network helps show where Mark Einon may publish in the future.
Co-authors
The 14 scholars most cited alongside Mark Einon, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
About Mark Einon
Mark Einon is a scholar working on Genetics, Cardiology and Cardiovascular Medicine, Molecular Biology, Infectious Diseases and Organic Chemistry, having authored 3 papers that have together received 242 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Viral Infections and Immunology Research (2 papers), Genomics and Rare Diseases (2 papers), Congenital heart defects research (1 paper) and BRCA gene mutations in cancer (1 paper). The work is most often cited by research in Genetics (206 citations), Molecular Biology (125 citations), Pediatrics, Perinatology and Child Health (31 citations), Developmental Neuroscience (6 citations) and Cognitive Neuroscience (25 citations). Mark Einon has collaborated with scholars based in United Kingdom. Frequent co-authors include Valentina Escott‐Price, Elliott Rees, George Kirov, Kimberley Kendall, Michael O’Donovan, James Walters, Michael J. Owen, David Owen, Rhys H. Thomas and Jonathan Hewitt. Their work appears in journals such as Biological Psychiatry, Journal of Medical Genetics and BMC 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.