Anna Wilsdon
Impact in
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- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Congenital heart defects research
- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
Papers in
- Genetics 5
- Genomic variations and chromosomal abnormalities 3
- Genetics and Neurodevelopmental Disorders 2
- Genomics and Rare Diseases 1
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- Congenital heart defects research 4
- RNA modifications and cancer 2
- Co-authors
- Tushar K. Ghosh (1 shared paper)J. David Brook (2 shared papers)Shelagh Joss (1 shared paper)Bertrand Isidor (1 shared paper)Toshiyuki Yamamoto (1 shared paper)Anna Erlandsson (1 shared paper)M Stefanova (1 shared paper)Keiko Shimojima (1 shared paper)
- Journals
- Journal of Anatomy (1 paper)Current topics in developmental biology (1 paper)Journal of Medical Genetics (1 paper)Advances in experimental medicine and biology (1 paper)Journal of Human Genetics (1 paper)
- Partner nations
- United KingdomSwedenGermany
In The Last Decade
Anna Wilsdon
5 papers receiving 63 citations
Peers
Comparison fields: 5 of 29
- Genetics 40
- Molecular Biology 42
- Pediatrics, Perinatology and Child Health 10
- Genetics 5
- Cellular and Molecular Neuroscience 5
Countries citing papers authored by Anna Wilsdon
This map shows the geographic impact of Anna Wilsdon'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 Anna Wilsdon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anna Wilsdon more than expected).
Fields of papers citing papers by Anna Wilsdon
This network shows the impact of papers produced by Anna Wilsdon. 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 Anna Wilsdon. The network helps show where Anna Wilsdon may publish in the future.
Co-authors
The 25 scholars most cited alongside Anna Wilsdon, 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 | 2014 | 38 | |
| 2 | 2016 | 31 | |
| 3 | 2023 | 4 | |
| 4 | 2013 | 2 | |
| 5 | 2024 | 1 | |
| 6 | 2024 | 0 |
About Anna Wilsdon
Anna Wilsdon is a scholar working on Genetics, Molecular Biology, Epidemiology, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 6 papers that have together received 76 indexed citations. Recurring topics across this work include Congenital heart defects research (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Congenital Heart Disease Studies (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), RNA modifications and cancer (2 papers), Immunodeficiency and Autoimmune Disorders (1 paper), Genomics and Rare Diseases (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (40 citations), Molecular Biology (42 citations), Pediatrics, Perinatology and Child Health (10 citations), Genetics (5 citations) and Cellular and Molecular Neuroscience (5 citations). Anna Wilsdon has collaborated with scholars based in United Kingdom, Sweden and Germany. Frequent co-authors include Tushar K. Ghosh, J. David Brook, Shelagh Joss, Bertrand Isidor, Toshiyuki Yamamoto, Anna Erlandsson, M Stefanova, Keiko Shimojima, Cédric Le Caignec and Noriko Sangu. Their work appears in journals such as Journal of Anatomy, Current topics in developmental biology, Journal of Medical Genetics, Advances in experimental medicine and biology and Journal of Human Genetics.
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.