Anna Wilsdon

729 total citations
6 papers, 76 citations indexed

About

Anna Wilsdon is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Anna Wilsdon has authored 6 papers receiving a total of 76 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Epidemiology. Recurrent topics in Anna Wilsdon's work include Congenital heart defects research (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and RNA modifications and cancer (2 papers). Anna Wilsdon is often cited by papers focused on Congenital heart defects research (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and RNA modifications and cancer (2 papers). Anna Wilsdon collaborates with scholars based in United Kingdom, Sweden and Germany. Anna Wilsdon's co-authors include J. David Brook, Tushar K. Ghosh, Mohnish Suri, Shelagh Joss, Anna Erlandsson, Keiko Shimojima, Shino Shimada, Toshiyuki Yamamoto, Lena Samuelsson and Cédric Le Caignec and has published in prestigious journals such as Journal of Medical Genetics, Advances in experimental medicine and biology and Journal of Anatomy.

In The Last Decade

Anna Wilsdon

5 papers receiving 63 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Anna Wilsdon United Kingdom 3 42 40 10 10 5 6 76
Janet L. Goldstein United States 4 37 0.9× 57 1.4× 8 0.8× 9 0.9× 2 0.4× 4 110
Jin Fang Chai China 5 32 0.8× 27 0.7× 7 0.7× 10 1.0× 3 0.6× 13 72
Nobuhiko Okamoto Japan 4 35 0.8× 34 0.8× 8 0.8× 4 0.4× 5 1.0× 7 68
Paul R. Mark United States 7 70 1.7× 58 1.4× 14 1.4× 7 0.7× 5 1.0× 11 123
Marine Lebrun France 5 39 0.9× 46 1.1× 14 1.4× 12 1.2× 3 0.6× 9 78
Simon Zwolinski United Kingdom 4 27 0.6× 70 1.8× 12 1.2× 14 1.4× 9 1.8× 5 91
Elyse Mitchell United States 4 20 0.5× 45 1.1× 17 1.7× 11 1.1× 2 0.4× 5 65
Dagmar Huhle Germany 4 22 0.5× 22 0.6× 26 2.6× 5 0.5× 6 1.2× 5 48
Gaëlle Vieville France 6 63 1.5× 86 2.1× 18 1.8× 10 1.0× 11 2.2× 9 127
Olin Blodgett United States 2 54 1.3× 16 0.4× 3 0.3× 4 0.4× 3 0.6× 2 78

Countries citing papers authored by Anna Wilsdon

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Anna Wilsdon

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Wilsdon. A scholar is included among the top collaborators of Anna Wilsdon based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Anna Wilsdon. Anna Wilsdon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

6 of 6 papers shown
1.
Wilsdon, Anna, Frances Bu’Lock, Marc‐Phillip Hitz, et al.. (2024). Effect of deletion of the protein kinase PRKD1 on development of the mouse embryonic heart. Journal of Anatomy. 245(1). 70–83. 1 indexed citations
2.
Wilsdon, Anna & Siobhan Loughna. (2024). Human Genetics of Congenital Heart Defects. Advances in experimental medicine and biology. 1441. 57–75.
3.
Yu, Jing, Ana Lisa Taylor Tavares, Woolf T. Walker, et al.. (2023). Use of genome sequencing to hunt for cryptic second-hit variants: analysis of 31 cases recruited to the 100 000 Genomes Project. Journal of Medical Genetics. 60(12). 1235–1244. 4 indexed citations
4.
Ghosh, Tushar K., J. David Brook, & Anna Wilsdon. (2016). T-Box Genes in Human Development and Disease. Current topics in developmental biology. 122. 383–415. 31 indexed citations
5.
Yamamoto, Toshiyuki, Anna Wilsdon, Shelagh Joss, et al.. (2014). An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalities. Journal of Human Genetics. 59(6). 300–306. 38 indexed citations
6.
Wilsdon, Anna & Jacqueline Eason. (2013). Prenatal diagnosis of single gene disorders. Obstetrics Gynaecology & Reproductive Medicine. 23(1). 20–25. 2 indexed citations

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.

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