Deborah M. Lambert
Impact in
- Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders
- Genetics top 5%
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 20
- Genomics and Rare Diseases 9
- BRCA gene mutations in cancer 5
- Digestive system and related health 2
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- Cannabis and Cannabinoid Research 8
- Pharmacogenetics and Drug Metabolism 3
- Co-authors
- Daniel N. Murphy (3 shared papers)Ana Rath (2 shared papers)Charlotte Rodwell (1 shared paper)Valérie Serrière-Lanneau (1 shared paper)Annie Olry (1 shared paper)Stéphanie Nguengang Wakap (1 shared paper)Yann Le Cam (1 shared paper)Geoffray Labar (3 shared papers)
In The Last Decade
Deborah M. Lambert
40 papers receiving 1.7k citations
Deborah M. Lambert's Hit Papers
Peers
Comparison fields: 5 of 120
- Clinical Biochemistry 149
- Genetics 625
- Pharmacology 289
- Toxicology 39
- Biochemistry 84
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-authors
The 25 scholars most cited alongside Deborah M. Lambert, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Estimating cumulative point prevalence of rare diseases: analysis of the Orphanet database Hit paper breakdown → | 2019 | 895 |
| 2 | 2010 | 86 | |
| 3 | 2009 | 85 | |
| 4 | 2006 | 78 | |
| 5 | 2005 | 63 | |
| 6 | 1999 | 60 | |
| 7 | 2007 | 58 | |
| 8 | 1998 | 51 | |
| 9 | 2001 | 37 | |
| 10 | 2008 | 26 | |
| 11 | 2022 | 26 | |
| 12 | 1997 | 24 | |
| 13 | 2008 | 23 | |
| 14 | 2007 | 21 | |
| 15 | 2020 | 19 | |
| 16 | 2005 | 18 | |
| 17 | 2020 | 18 | |
| 18 | 2021 | 16 | |
| 19 | 2000 | 16 | |
| 20 | 1993 | 11 |
About Deborah M. Lambert
Deborah M. Lambert is a scholar working on Genetics, Pharmacology, Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 44 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Cannabis and Cannabinoid Research (8 papers), Metabolism and Genetic Disorders (6 papers), BRCA gene mutations in cancer (5 papers), Pharmacogenetics and Drug Metabolism (3 papers), Digestive system and related health (2 papers), Prenatal Screening and Diagnostics (2 papers) and Pancreatic function and diabetes (2 papers). The work is most often cited by research in Clinical Biochemistry (149 citations), Genetics (625 citations), Pharmacology (289 citations), Toxicology (39 citations) and Biochemistry (84 citations). Deborah M. Lambert has collaborated with scholars based in Ireland, Belgium and Canada. Frequent co-authors include Daniel N. Murphy, Ana Rath, Charlotte Rodwell, Valérie Serrière-Lanneau, Annie Olry, Stéphanie Nguengang Wakap, Yann Le Cam, Geoffray Labar, Eileen P. Treacy and Johan Wouters. Their work appears in journals such as European Journal of Human Genetics, British Journal of Pharmacology, Current Medicinal Chemistry, The Journal of Pediatrics and Orphanet Journal of Rare Diseases.
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.