Margaret Lever
- Genetics top 10%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 10%
- Endocrinology, Diabetes and Metabolism
- Pathology and Forensic Medicine
- Co-authors
- H. BullmanDeborah MackayI. Karen TempleEmma WakelingRebecca PooleSusan HolderDavid RobinsonMohnish Suri
- Topics
- Genetic Syndromes and Imprinting (9 papers)Epigenetics and DNA Methylation (9 papers)Prenatal Screening and Diagnostics (6 papers)
- Journals
- SHILAP Revista de lepidopterologíaThe Journal of Clinical Endocrinology & MetabolismDiabetes Care
- Partner nations
- United KingdomUnited StatesMalaysia
In The Last Decade
Margaret Lever
12 papers receiving 260 citations
Peers
Comparison fields: 5 of 36
- Genetics 246
- Molecular Biology 193
- Pediatrics, Perinatology and Child Health 153
- Endocrinology, Diabetes and Metabolism 17
- Pathology and Forensic Medicine 16
Countries citing papers authored by Margaret Lever
This map shows the geographic impact of Margaret Lever'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 Margaret Lever with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Margaret Lever more than expected).
Fields of papers citing papers by Margaret Lever
This network shows the impact of papers produced by Margaret Lever. 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 Margaret Lever. The network helps show where Margaret Lever may publish in the future.
Co-authorship network of co-authors of Margaret Lever
This figure shows the co-authorship network connecting the top 25 collaborators of Margaret Lever. A scholar is included among the top collaborators of Margaret Lever 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 Margaret Lever. Margaret Lever is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 7 | |
| 2 | 2 | |
| 3 | 16 | |
| 4 | 61 | |
| 5 | 1 | |
| 6 | 4 | |
| 7 | 4 | |
| 8 | 73 | |
| 9 | 3 | |
| 10 | 64 | |
| 11 | 1 | |
| 12 | 48 |
About Margaret Lever
Margaret Lever is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 12 papers that have together received 284 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (9 papers), Epigenetics and DNA Methylation (9 papers) and Prenatal Screening and Diagnostics (6 papers). The work is most often cited by research in Genetics (246 citations), Pediatrics, Perinatology and Child Health (153 citations) and Molecular Biology (193 citations). Margaret Lever has collaborated with scholars based in United Kingdom, United States and Malaysia. Frequent co-authors include H. Bullman, Deborah Mackay, I. Karen Temple, Emma Wakeling, Rebecca Poole, Susan Holder, David Robinson, Mohnish Suri, Justin H. Davies and Abhijit Dixit. Their work appears in journals such as SHILAP Revista de lepidopterología, The Journal of Clinical Endocrinology & Metabolism and Diabetes Care.
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.