Natalie Canham
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 10
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 3
- Genomics and Rare Diseases 3
- Connective tissue disorders research 2
- Co-authors
- Matthew E. Hurles (2 shared papers)Richard J. Ellis (2 shared papers)Susan Holder (3 shared papers)Jodi M. Lestner (1 shared paper)Anna Hackett (1 shared paper)Soo‐Mi Park (1 shared paper)Helen V. Firth (1 shared paper)Detelina Grozeva (1 shared paper)
- Journals
- European Journal of Medical Genetics (3 papers)Journal of Child Neurology (1 paper)BMC Medical Genomics (1 paper)The Journal of Clinical Endocrinology & Metabolism (1 paper)Ultrasound in Obstetrics and Gynecology (1 paper)
- Partner nations
- United KingdomUnited StatesAustralia
In The Last Decade
Natalie Canham
19 papers receiving 355 citations
Peers
Comparison fields: 5 of 50
- Genetics 174
- Cancer Research 56
- Endocrinology, Diabetes and Metabolism 59
- Surgery 81
- Molecular Biology 136
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-authors
The 25 scholars most cited alongside Natalie Canham, 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 | 89 | |
| 2 | 2013 | 60 | |
| 3 | 2013 | 54 | |
| 4 | 2016 | 35 | |
| 5 | 2014 | 27 | |
| 6 | 2012 | 24 | |
| 7 | 2007 | 21 | |
| 8 | 2016 | 17 | |
| 9 | 2020 | 12 | |
| 10 | 2020 | 10 | |
| 11 | 2018 | 9 | |
| 12 | 2022 | 7 | |
| 13 | 2013 | 7 | |
| 14 | 2009 | 5 | |
| 15 | 2008 | 4 | |
| 16 | 2015 | 3 | |
| 17 | 2006 | 3 | |
| 18 | 2014 | 3 | |
| 19 | 2009 | 1 | |
| 20 | 2024 | 0 |
About Natalie Canham
Natalie Canham is a scholar working on Genetics, Molecular Biology, Surgery, Pathology and Forensic Medicine and Pulmonary and Respiratory Medicine, having authored 20 papers that have together received 391 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (3 papers), Metabolism and Genetic Disorders (2 papers), Connective tissue disorders research (2 papers), Epilepsy research and treatment (2 papers), Genetic factors in colorectal cancer (2 papers) and Adrenal and Paraganglionic Tumors (2 papers). The work is most often cited by research in Genetics (174 citations), Cancer Research (56 citations), Endocrinology, Diabetes and Metabolism (59 citations), Surgery (81 citations) and Molecular Biology (136 citations). Natalie Canham has collaborated with scholars based in United Kingdom, United States and Australia. Frequent co-authors include Matthew E. Hurles, Richard J. Ellis, Susan Holder, Jodi M. Lestner, Anna Hackett, Soo‐Mi Park, Helen V. Firth, Detelina Grozeva, Sahar Mansour and Michael Parker. Their work appears in journals such as European Journal of Medical Genetics, Journal of Child Neurology, BMC Medical Genomics, The Journal of Clinical Endocrinology & Metabolism and Ultrasound in Obstetrics and Gynecology.
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.