Laurence Perrin
Impact in
-
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Diabetes and associated disorders
Papers in
- Co-authors
- Alain Verloès (7 shared papers)A Bensman (4 shared papers)Séverine Drunat (2 shared papers)Georges Deschênes (5 shared papers)Azzedine Aboura (3 shared papers)Tim Ulinski (4 shared papers)Tú-Anh Tran (2 shared papers)Alexia Letierce (2 shared papers)
- Journals
- European Journal of Medical Genetics (6 papers)Clinical Genetics (2 papers)Acta Paediatrica (2 papers)Nuclear Medicine Communications (1 paper)BMC Medicine (1 paper)
- Partner nations
- FranceGermanyUnited Kingdom
In The Last Decade
Laurence Perrin
27 papers receiving 354 citations
Peers
Comparison fields: 5 of 65
- Genetics 133
- Developmental Neuroscience 16
- Rheumatology 31
- Biochemistry 13
- Endocrinology, Diabetes and Metabolism 31
Countries citing papers authored by Laurence Perrin
This map shows the geographic impact of Laurence Perrin'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 Laurence Perrin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Laurence Perrin more than expected).
Fields of papers citing papers by Laurence Perrin
This network shows the impact of papers produced by Laurence Perrin. 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 Laurence Perrin. The network helps show where Laurence Perrin may publish in the future.
Co-authors
The 25 scholars most cited alongside Laurence Perrin, 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 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 68 | |
| 2 | 2020 | 43 | |
| 3 | 2006 | 36 | |
| 4 | 2009 | 35 | |
| 5 | 2010 | 35 | |
| 6 | 1990 | 24 | |
| 7 | 2010 | 21 | |
| 8 | 1966 | 19 | |
| 9 | 2005 | 14 | |
| 10 | 2021 | 11 | |
| 11 | 2022 | 10 | |
| 12 | 2011 | 9 | |
| 13 | 2018 | 6 | |
| 14 | 2022 | 6 | |
| 15 | 2010 | 6 | |
| 16 | 2018 | 5 | |
| 17 | 2023 | 4 | |
| 18 | 2025 | 4 | |
| 19 | 2009 | 3 | |
| 20 | 2007 | 3 |
About Laurence Perrin
Laurence Perrin is a scholar working on Surgery, Genetics, Molecular Biology, Pulmonary and Respiratory Medicine and Rheumatology, having authored 28 papers that have together received 375 indexed citations. Recurring topics across this work include Congenital Diaphragmatic Hernia Studies (4 papers), Craniofacial Disorders and Treatments (3 papers), Systemic Lupus Erythematosus Research (3 papers), Renal Diseases and Glomerulopathies (3 papers), Neonatal Respiratory Health Research (3 papers), Congenital heart defects research (2 papers), Kawasaki Disease and Coronary Complications (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (133 citations), Developmental Neuroscience (16 citations), Rheumatology (31 citations), Biochemistry (13 citations) and Endocrinology, Diabetes and Metabolism (31 citations). Laurence Perrin has collaborated with scholars based in France, Germany and United Kingdom. Frequent co-authors include Alain Verloès, A Bensman, Séverine Drunat, Georges Deschênes, Azzedine Aboura, Tim Ulinski, Tú-Anh Tran, Alexia Letierce, Isabelle Koné‐Paut and Yline Capri. Their work appears in journals such as European Journal of Medical Genetics, Clinical Genetics, Acta Paediatrica, Nuclear Medicine Communications and BMC Medicine.
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.