Natalie Canham
- Co-authors
- Matthew E. HurlesSusan HolderRichard J. EllisJodi M. LestnerJames FloydSahar MansourHelen V. FirthHayley Archer
- Topics
- Genomics and Rare Diseases (4 papers)Genomic variations and chromosomal abnormalities (4 papers)Metabolism and Genetic Disorders (3 papers)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Natalie Canham
19 papers receiving 352 citations
Peers
Comparison fields: 5 of 52
- Genetics 198
- Molecular Biology 158
- Surgery 93
- Cancer Research 77
- Endocrinology, Diabetes and Metabolism 76
Countries citing papers authored by Natalie Canham
This map shows the geographic impact of Natalie Canham'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 Natalie Canham with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Natalie Canham more than expected).
Fields of papers citing papers by Natalie Canham
This network shows the impact of papers produced by Natalie Canham. 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 Natalie Canham. The network helps show where Natalie Canham may publish in the future.
Co-authorship network of co-authors of Natalie Canham
This figure shows the co-authorship network connecting the top 25 collaborators of Natalie Canham. A scholar is included among the top collaborators of Natalie Canham 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 Natalie Canham. Natalie Canham is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 6 | |
| 3 | 9 | |
| 4 | 12 | |
| 5 | 9 | |
| 6 | 16 | |
| 7 | 35 | |
| 8 | 3 | |
| 9 | 89 | |
| 10 | 3 | |
| 11 | 27 | |
| 12 | 54 | |
| 13 | 7 | |
| 14 | 60 | |
| 15 | 24 | |
| 16 | 1 | |
| 17 | 5 | |
| 18 | 4 | |
| 19 | 21 | |
| 20 | 3 |
About Natalie Canham
Natalie Canham is a scholar working on Clinical Biochemistry, Genetics and Pharmacy, having authored 20 papers that have together received 388 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Metabolism and Genetic Disorders (3 papers). The work is most often cited by research in Genetics (198 citations), Cancer Research (77 citations) and Endocrinology, Diabetes and Metabolism (76 citations). Natalie Canham has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Matthew E. Hurles, Susan Holder, Richard J. Ellis, Jodi M. Lestner, James Floyd, Sahar Mansour, Helen V. Firth, Hayley Archer, Keren Carss and Anna Hackett. Their work appears in journals such as Brain, The Journal of Clinical Endocrinology & Metabolism and Genome Research.
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.