Emmanuelle Masson

2.9k total citations
49 papers, 914 citations indexed

About

Emmanuelle Masson is a scholar working on Surgery, Oncology and Molecular Biology. According to data from OpenAlex, Emmanuelle Masson has authored 49 papers receiving a total of 914 indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Surgery, 25 papers in Oncology and 11 papers in Molecular Biology. Recurrent topics in Emmanuelle Masson's work include Pancreatitis Pathology and Treatment (33 papers), Pancreatic and Hepatic Oncology Research (22 papers) and Pancreatic function and diabetes (13 papers). Emmanuelle Masson is often cited by papers focused on Pancreatitis Pathology and Treatment (33 papers), Pancreatic and Hepatic Oncology Research (22 papers) and Pancreatic function and diabetes (13 papers). Emmanuelle Masson collaborates with scholars based in France, United Kingdom and China. Emmanuelle Masson's co-authors include Jian‐Min Chen, Claude Férec, Cédric Le Maréchal, D.N. Cooper, Philippe Ruszniewski, Philippe Lévy, Virginie Scotet, Fréderic Morel, M.‐P. Audrézet and Claude Férec and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and PLoS ONE.

In The Last Decade

Emmanuelle Masson

46 papers receiving 906 citations

Peers

Emmanuelle Masson

SURGE

ONCOL

GENET

EPIDE

Kei Shiraishi Japan

Sota Kodama Japan

Serge Garbay France

Stuti G. Shroff United States

B. Lee United States

Hans‐Peter Bruch Germany

Giuseppe Leoncini Italy

Jiun‐Yi Hsia Taiwan

Yann‐Jang Chen Taiwan

M Hisanaga Japan

Kei Shiraishi Japan

Emmanuelle Masson

233 ×0.4

SURGE

268 ×0.6

ONCOL

185 ×1.0

GENET

215 ×1.3

72 ×1.1

EPIDE

Citations per year, relative to Emmanuelle Masson Emmanuelle Masson (= 1×) peers Kei Shiraishi

Countries citing papers authored by Emmanuelle Masson

Since Specialization

Citations

This map shows the geographic impact of Emmanuelle Masson'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 Emmanuelle Masson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emmanuelle Masson more than expected).

Fields of papers citing papers by Emmanuelle Masson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emmanuelle Masson. 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 Emmanuelle Masson. The network helps show where Emmanuelle Masson may publish in the future.

Co-authorship network of co-authors of Emmanuelle Masson

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

All Works

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20 of 20 papers shown

Xiao, Xunjun, Mark E. Lowe, Bálint Erőss, et al.. (2024). Carboxyl ester lipase hybrid 1 (CEL-HYB1) haplotypes confer varying risk for chronic pancreatitis. Scientific Reports. 14(1). 30965–30965.

Masson, Emmanuelle, et al.. (2024). Alu insertion-mediated dsRNA structure formation with pre-existing Alu elements as a disease-causing mechanism. The American Journal of Human Genetics. 111(10). 2176–2189. 4 indexed citations

Wu, Hao, Jin‐Huan Lin, Xin‐Ying Tang, et al.. (2024). Combining full-length gene assay and SpliceAI to interpret the splicing impact of all possible SPINK1 coding variants. Human Genomics. 18(1). 21–21. 4 indexed citations

Masson, Emmanuelle, et al.. (2024). Diagnostic yield of repeat genetic testing in idiopathic chronic pancreatitis. Clinics and Research in Hepatology and Gastroenterology. 48(6). 102346–102346.

Wang, Yuan‐Chen, Emmanuelle Masson, Yahui Wang, et al.. (2024). SEC16A Variants Predispose to Chronic Pancreatitis by Impairing ER‐to‐Golgi Transport and Inducing ER Stress. Advanced Science. 11(38). e2402550–e2402550. 3 indexed citations

Masson, Emmanuelle, Jian‐Min Chen, Claude Férec, et al.. (2023). Genetic and functional analysis of chymotrypsin-like protease (CTRL) in chronic pancreatitis. Pancreatology. 23(8). 957–963. 2 indexed citations

Zhang, Guofu, Qi Yang, Gang Li, et al.. (2023). Frameshift coding sequence variants in the LPL gene: identification of two novel events and exploration of the genotype–phenotype relationship for variants reported to date. Lipids in Health and Disease. 22(1). 128–128. 7 indexed citations

Zou, Wen‐Bin, D.N. Cooper, Emmanuelle Masson, et al.. (2022). Trypsinogen (PRSS1 and PRSS2) gene dosage correlates with pancreatitis risk across genetic and transgenic studies: a systematic review and re-analysis. Human Genetics. 141(8). 1327–1338. 8 indexed citations

Masson, Emmanuelle, Wen‐Bin Zou, Emmanuelle Génin, et al.. (2022). Expanding ACMG variant classification guidelines into a general framework. Human Genomics. 16(1). 31–31. 41 indexed citations

10.

Canaff, Lucie, Emmanuelle Masson, Jian‐Min Chen, et al.. (2021). The three common polymorphisms p.A986S, p.R990G and p.Q1011E in the calcium sensing receptor (CASR) are not associated with chronic pancreatitis. Pancreatology. 21(7). 1299–1304. 3 indexed citations

11.

Lin, Jin‐Huan, Emmanuelle Masson, Arnaud Boulling, et al.. (2020). 5′ splice site GC>GT and GT>GC variants differ markedly in terms of their functionality and pathogenicity. Human Mutation. 41(8). 1358–1364. 5 indexed citations

12.

Génin, Emmanuelle, et al.. (2020). Role of the Common PRSS1-PRSS2 Haplotype in Alcoholic and Non-Alcoholic Chronic Pancreatitis: Meta- and Re-Analyses. Genes. 11(11). 1349–1349. 7 indexed citations

13.

Chen, Jian‐Min, Jin‐Huan Lin, Emmanuelle Masson, et al.. (2020). The Experimentally Obtained Functional Impact Assessments of 5' Splice Site GT>GC Variants Differ Markedly from Those Predicted. Current Genomics. 21(1). 56–66. 13 indexed citations

14.

Tang, Xin‐Ying, Jin‐Huan Lin, Wen‐Bin Zou, et al.. (2019). Toward a clinical diagnostic pipeline for SPINK1 intronic variants. Human Genomics. 13(1). 8–8. 9 indexed citations

15.

Müller, Nelly, Ioannis Sarantitis, Marie Rouanet, et al.. (2019). Natural history of SPINK1 germline mutation related-pancreatitis. EBioMedicine. 48. 581–591. 45 indexed citations

16.

Woerd, Wendy L. van der, Stan F.J. van de Graaf, Claude Férec, et al.. (2013). Mutational Analysis of ATP8B1 in Patients with Chronic Pancreatitis. PLoS ONE. 8(11). e80553–e80553. 8 indexed citations

17.

Boulling, Arnaud, Heiko Witt, Giriraj R. Chandak, et al.. (2011). Assessing the pathological relevance of SPINK1 promoter variants. European Journal of Human Genetics. 19(10). 1066–1073. 16 indexed citations

18.

Masson, Emmanuelle, Cédric Le Maréchal, Richard Delcenserie, Jian‐Min Chen, & Claude Férec. (2008). Hereditary pancreatitis caused by a double gain-of-function trypsinogen mutation. Human Genetics. 123(5). 521–529. 34 indexed citations

19.

Masson, Emmanuelle, Cédric Le Maréchal, Giriraj R. Chandak, et al.. (2007). Trypsinogen Copy Number Mutations in Patients With Idiopathic Chronic Pancreatitis. Clinical Gastroenterology and Hepatology. 6(1). 82–88. 54 indexed citations

20.

Chen, Jian‐Min, Emmanuelle Masson, Milan Maçek, et al.. (2007). Detection of two Alu insertions in the CFTR gene. Journal of Cystic Fibrosis. 7(1). 37–43. 27 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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