Laurence Perrin

3.4k total citations
28 papers, 366 citations indexed

About

Laurence Perrin is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Laurence Perrin has authored 28 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Genetics and 10 papers in Surgery. Recurrent topics in Laurence Perrin's work include Congenital Diaphragmatic Hernia Studies (4 papers), Congenital heart defects research (3 papers) and Renal Diseases and Glomerulopathies (3 papers). Laurence Perrin is often cited by papers focused on Congenital Diaphragmatic Hernia Studies (4 papers), Congenital heart defects research (3 papers) and Renal Diseases and Glomerulopathies (3 papers). Laurence Perrin collaborates with scholars based in France, Germany and Netherlands. Laurence Perrin's co-authors include Alain Verloès, Azzedine Aboura, A Bensman, Georges Deschênes, Tim Ulinski, Séverine Drunat, Virginie Lambert, Corinne Guitton, Isabelle Koné‐Paut and Tú-Anh Tran and has published in prestigious journals such as The EMBO Journal, Brain and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Laurence Perrin

27 papers receiving 345 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Laurence Perrin France 10 149 141 67 57 33 28 366
Marion Gérard‐Blanluet France 13 158 1.1× 200 1.4× 61 0.9× 23 0.4× 33 1.0× 24 399
Luciano Abreu Brito Brazil 14 400 2.7× 232 1.6× 56 0.8× 54 0.9× 39 1.2× 19 574
Ye Jee Shim South Korea 9 100 0.7× 144 1.0× 115 1.7× 29 0.5× 11 0.3× 49 422
Yoshiko Hirano Japan 12 136 0.9× 143 1.0× 36 0.5× 49 0.9× 11 0.3× 27 430
Cecilie F. Rustad Norway 11 116 0.8× 210 1.5× 37 0.6× 80 1.4× 84 2.5× 18 491
Virginia Fano Argentina 15 395 2.7× 206 1.5× 83 1.2× 93 1.6× 62 1.9× 55 634
Magdalena Badura‐Stronka Poland 12 141 0.9× 183 1.3× 77 1.1× 22 0.4× 22 0.7× 32 357
Claire Gerber United States 11 71 0.5× 133 0.9× 27 0.4× 24 0.4× 21 0.6× 17 400
Haruhiko Isotani Japan 9 67 0.4× 183 1.3× 56 0.8× 42 0.7× 12 0.4× 24 363
Tetsuya Oishi Japan 10 40 0.3× 105 0.7× 41 0.6× 48 0.8× 35 1.1× 33 420

Countries citing papers authored by Laurence Perrin

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Laurence Perrin

This figure shows the co-authorship network connecting the top 25 collaborators of Laurence Perrin. A scholar is included among the top collaborators of Laurence Perrin 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 Laurence Perrin. Laurence Perrin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Kovermann, Peter, Allan Bayat, Christina Fenger, et al.. (2025). The severity of SLC1A2-associated neurodevelopmental disorders correlates with transporter dysfunction. EBioMedicine. 114. 105648–105648. 3 indexed citations
2.
Wischmeijer, Anita, Laurence Perrin, Duccio Maria Cordelli, et al.. (2024). Olfactory bulb anomalies in KBG syndrome mouse model and patients. BMC Medicine. 22(1). 158–158. 2 indexed citations
3.
Breton, Sylvain, Marie‐Liesse Piketty, Alexandra Afenjar, et al.. (2022). SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients. Orphanet Journal of Rare Diseases. 17(1). 100–100. 10 indexed citations
4.
Dobritzsch, Doreen, Judith Meijer, Rutger Meinsma, et al.. (2022). β-Ureidopropionase deficiency due to novel and rare UPB1 mutations affecting pre-mRNA splicing and protein structural integrity and catalytic activity. Molecular Genetics and Metabolism. 136(3). 177–185. 6 indexed citations
5.
6.
Bertacchi, Michele, Agnès Loubat, Frédéric Tran Mau‐Them, et al.. (2020). NR2F1 regulates regional progenitor dynamics in the mouse neocortex and cortical gyrification in BBSOAS patients. The EMBO Journal. 39(13). e104163–e104163. 42 indexed citations
7.
Bruel, Ange‐Line, Jonathan Lévy, Narcisse Elenga, et al.. (2018). INTU‐related oral‐facial‐digital syndrome type VI: A confirmatory report. Clinical Genetics. 93(6). 1205–1209. 6 indexed citations
8.
Marcellus, Charles de, et al.. (2018). Severe neonatal hypertension revealing arterial tortuosity syndrome. Kidney International. 93(2). 526–526. 4 indexed citations
9.
Ageeli, Essam Al, Séverine Drunat, Catherine Delanöe, et al.. (2013). Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases. European Journal of Medical Genetics. 57(1). 5–14. 67 indexed citations
10.
Perrin, Laurence, Odile Fenneteau, Brice Ilharreborde, et al.. (2012). A new lysosomal storage disorder resembling Morquio syndrome in sibs. European Journal of Medical Genetics. 55(3). 157–162. 1 indexed citations
11.
Dupont, Céline, Fabien Guimiot, Laurence Perrin, et al.. (2011). 3D position of pericentromeric heterochromatin within the nucleus of a patient with ICF syndrome. Clinical Genetics. 82(2). 187–192. 9 indexed citations
12.
Manouvrier, Sylvie, Fabienne Escande, Sandrine Passemard, et al.. (2011). A familial syndromal form of omphalocele. European Journal of Medical Genetics. 54(3). 337–340. 2 indexed citations
13.
Osimani, Sara, Isabelle Husson, Sandrine Passemard, et al.. (2010). Craniosynostosis: A rare complication of pycnodysostosis. European Journal of Medical Genetics. 53(2). 89–92. 20 indexed citations
14.
Schiff, Manuel, Andrée Delahaye‐Duriez, Joris Andrieux, et al.. (2010). Further delineation of the 17p13.3 microdeletion involving YWHAE but distal to PAFAH1B1: Four additional patients. European Journal of Medical Genetics. 53(5). 303–308. 34 indexed citations
15.
Verloès, Alain, et al.. (2010). Congenital absence of the left pericardium and diaphragmatic defect in sibs. European Journal of Medical Genetics. 53(3). 133–135. 6 indexed citations
16.
Perrin, Laurence, Alexia Letierce, Corinne Guitton, et al.. (2009). Comparative study of complete versus incomplete Kawasaki disease in 59 pediatric patients. Joint Bone Spine. 76(5). 481–485. 35 indexed citations
17.
Ulinski, Tim, Laurence Perrin, Vincent Guigonis, et al.. (2007). Remission of steroid- and CyA-resistant nephrotic syndrome using multiple drug immunosuppression. Pediatric Nephrology. 22(10). 1723–1726. 3 indexed citations
18.
Perrin, Laurence, et al.. (2005). Acute pancreatitis in paediatric systemic lupus erythematosus. Acta Paediatrica. 95(1). 121–124. 14 indexed citations
19.
Zuck, Thomas F., Patricia M. Carey, J Burckhardt, et al.. (1990). Autologous Transfusion Practice Controversies about Current Fashions and Real Needs. Vox Sanguinis. 58(3). 234–253. 24 indexed citations
20.
Lambert, P.H., et al.. (1984). Recent Advances in Systemic Lupus Erythematosus. Medical Entomology and Zoology. 1 indexed citations

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.

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