Deborah M. Lambert
- Genetics top 2%
- Molecular Biology
- Pharmacology top 5%
- Pediatrics, Perinatology and Child Health top 5%
- Physiology
- Co-authors
- Daniel N. MurphyValérie Serrière-LanneauYann Le CamAnnie OlryStéphanie Nguengang WakapCharlotte RodwellAna RathGeoffray Labar
- Topics
- BRCA gene mutations in cancer (12 papers)Genomics and Rare Diseases (10 papers)Metabolism and Genetic Disorders (8 papers)
In The Last Decade
Deborah M. Lambert
48 papers receiving 1.7k citations
Hit Papers
Peers
Comparison fields: 5 of 125
- Genetics 730
- Molecular Biology 486
- Pharmacology 294
- Pediatrics, Perinatology and Child Health 202
- Physiology 165
Countries citing papers authored by Deborah M. Lambert
This map shows the geographic impact of Deborah M. Lambert'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 Deborah M. Lambert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Deborah M. Lambert more than expected).
Fields of papers citing papers by Deborah M. Lambert
This network shows the impact of papers produced by Deborah M. Lambert. 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 Deborah M. Lambert. The network helps show where Deborah M. Lambert may publish in the future.
Co-authorship network of co-authors of Deborah M. Lambert
This figure shows the co-authorship network connecting the top 25 collaborators of Deborah M. Lambert. A scholar is included among the top collaborators of Deborah M. Lambert 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 Deborah M. Lambert. Deborah M. Lambert 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 | 2 | |
| 3 | 0 | |
| 4 | 4 | |
| 5 | 8 | |
| 6 | 24 | |
| 7 | 3 | |
| 8 | 2 | |
| 9 | 18 | |
| 10 | 10 | |
| 11 | 3 | |
| 12 | 1 | |
| 13 | 22 | |
| 14 | 26 | |
| 15 | 21 | |
| 16 | 77 | |
| 17 | 37 | |
| 18 | 16 | |
| 19 | 60 | |
| 20 | [Ectodermal anhidrotic dysplasia (author's transl)]. | 0 |
About Deborah M. Lambert
Deborah M. Lambert is a scholar working on Clinical Biochemistry, Genetics and Pediatrics, Perinatology and Child Health, having authored 52 papers that have together received 1.8k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (12 papers), Genomics and Rare Diseases (10 papers) and Metabolism and Genetic Disorders (8 papers). The work is most often cited by research in Genetics (730 citations), Clinical Biochemistry (162 citations) and Pharmacology (294 citations). Deborah M. Lambert has collaborated with scholars based in Ireland, Canada and Belgium. Frequent co-authors include Daniel N. Murphy, Valérie Serrière-Lanneau, Yann Le Cam, Annie Olry, Stéphanie Nguengang Wakap, Charlotte Rodwell, Ana Rath, Geoffray Labar, Eileen P. Treacy and Johan Wouters. Their work appears in journals such as British Journal of Pharmacology, The Journal of Pediatrics and Epilepsia.
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.