Frances Elmslie
- Molecular Biology
- Genetics
- Cellular and Molecular Neuroscience
- Endocrinology, Diabetes and Metabolism
- Pediatrics, Perinatology and Child Health
- Co-authors
- Sahar MansourIan WalpoleNicola FouldsElaine HughesSonia BertrandJ R TrounceOrtrud K. SteinleinThomas Sander
- Topics
- Genomics and Rare Diseases (2 papers)BRCA gene mutations in cancer (2 papers)Neuroscience and Neuropharmacology Research (2 papers)
- Journals
- Nature CommunicationsSHILAP Revista de lepidopterologíaHuman Molecular Genetics
- Partner nations
- United KingdomFranceUnited States
In The Last Decade
Frances Elmslie
15 papers receiving 287 citations
Peers
Comparison fields: 5 of 59
- Molecular Biology 117
- Genetics 99
- Cellular and Molecular Neuroscience 67
- Endocrinology, Diabetes and Metabolism 50
- Pediatrics, Perinatology and Child Health 43
Countries citing papers authored by Frances Elmslie
This map shows the geographic impact of Frances Elmslie'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 Frances Elmslie with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Frances Elmslie more than expected).
Fields of papers citing papers by Frances Elmslie
This network shows the impact of papers produced by Frances Elmslie. 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 Frances Elmslie. The network helps show where Frances Elmslie may publish in the future.
Co-authorship network of co-authors of Frances Elmslie
This figure shows the co-authorship network connecting the top 25 collaborators of Frances Elmslie. A scholar is included among the top collaborators of Frances Elmslie 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 Frances Elmslie. Frances Elmslie is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 2 | |
| 2 | 3 | |
| 3 | 9 | |
| 4 | 13 | |
| 5 | 29 | |
| 6 | 14 | |
| 7 | 4 | |
| 8 | De novo, heterozygous missense variants in YWHAG as a novel cause of developmental and epileptic encephalopathy | 1 |
| 9 | 21 | |
| 10 | 14 | |
| 11 | 17 | |
| 12 | 7 | |
| 13 | 0 | |
| 14 | 76 | |
| 15 | 70 | |
| 16 | 11 |
About Frances Elmslie
Frances Elmslie is a scholar working on Clinical Biochemistry, Genetics and Nephrology, having authored 16 papers that have together received 291 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (2 papers), BRCA gene mutations in cancer (2 papers) and Neuroscience and Neuropharmacology Research (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (67 citations), Genetics (99 citations) and Endocrinology, Diabetes and Metabolism (50 citations). Frances Elmslie has collaborated with scholars based in United Kingdom, France and United States. Frequent co-authors include Sahar Mansour, Ian Walpole, Nicola Foulds, Elaine Hughes, Sonia Bertrand, J R Trounce, Ortrud K. Steinlein, Thomas Sander, Daniel Bertrand and Mark Gardiner. Their work appears in journals such as Nature Communications, SHILAP Revista de lepidopterología and Human Molecular 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.