Aurélie Dechaume

2.6k total citations
25 papers, 1.1k citations indexed

About

Aurélie Dechaume is a scholar working on Surgery, Genetics and Molecular Biology. According to data from OpenAlex, Aurélie Dechaume has authored 25 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Surgery, 16 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Aurélie Dechaume's work include Pancreatic function and diabetes (16 papers), Diabetes and associated disorders (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Aurélie Dechaume is often cited by papers focused on Pancreatic function and diabetes (16 papers), Diabetes and associated disorders (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Aurélie Dechaume collaborates with scholars based in France, United Kingdom and Denmark. Aurélie Dechaume's co-authors include Philippe Froguel, Martine Vaxillaire, Michel Marre, Amélie Bonnefond, Beverley Balkau, Michel Polak, G. Charpentier, Jean Tichet, Christine Cavalcanti-Proença and Julien Philippe and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Diabetes Care.

In The Last Decade

Aurélie Dechaume

25 papers receiving 1.1k citations

Peers

Aurélie Dechaume
Rohit B. Sharma United States
Manju Surana United States
Kerstin Kirchhoff Germany
Daniel U. Rabin United States
Jean‐Valéry Turatsinze Belgium
Mark Lipsett Canada
Jeffrey C. Raum United States
Brenda Strutt Canada
Ilham Kharroubi Belgium
Lars Hansen Denmark
Rohit B. Sharma United States
Aurélie Dechaume
Citations per year, relative to Aurélie Dechaume Aurélie Dechaume (= 1×) peers Rohit B. Sharma

Countries citing papers authored by Aurélie Dechaume

Since Specialization
Citations

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

Fields of papers citing papers by Aurélie Dechaume

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aurélie Dechaume

This figure shows the co-authorship network connecting the top 25 collaborators of Aurélie Dechaume. A scholar is included among the top collaborators of Aurélie Dechaume 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 Aurélie Dechaume. Aurélie Dechaume 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.
Baron, Morgane, Emmanuel Vaillant, Aurélie Dechaume, et al.. (2024). Pathogenic, Total Loss-of-Function DYRK1B Variants Cause Monogenic Obesity Associated With Type 2 Diabetes. Diabetes Care. 47(3). 444–451. 6 indexed citations
2.
Kouidrat, Youssef, Martine Vaxillaire, Aurélie Dechaume, et al.. (2023). Dominant PDX1 deficiency causes highly penetrant diabetes at different ages, associated with obesity and exocrine pancreatic deficiency: Lessons for precision medicine. Diabetes & Metabolism. 50(1). 101507–101507. 3 indexed citations
3.
Boutry, Raphaël, Emmanuel Vaillant, Aurélie Dechaume, et al.. (2023). Pathogenic monoallelic variants in GLIS3 increase type 2 diabetes risk and identify a subgroup of patients sensitive to sulfonylureas. Diabetologia. 67(2). 327–332. 4 indexed citations
4.
Delemer, Brigitte, Christine Poitou, Martine Vaxillaire, et al.. (2023). Heterozygous pathogenic variants in POMC are not responsible for monogenic obesity: Implication for MC4R agonist use. Genetics in Medicine. 25(7). 100857–100857. 10 indexed citations
5.
Cornière, Nicolas, R. Brent Thomson, Bruno O. Villoutreix, et al.. (2022). Dominant negative mutation in oxalate transporter SLC26A6 associated with enteric hyperoxaluria and nephrolithiasis. Journal of Medical Genetics. 59(11). 1035–1043. 10 indexed citations
6.
Bonnefond, Amélie, Loïc Yengo, Aurélie Dechaume, et al.. (2017). Relationship between salivary/pancreatic amylase and body mass index: a systems biology approach. BMC Medicine. 15(1). 37–37. 47 indexed citations
7.
Philippe, Julien, Mehdi Derhourhi, Emmanuelle Durand, et al.. (2015). What Is the Best NGS Enrichment Method for the Molecular Diagnosis of Monogenic Diabetes and Obesity?. PLoS ONE. 10(11). e0143373–e0143373. 13 indexed citations
8.
Bonnefond, Amélie, Loïc Yengo, Marlène Huyvaert, et al.. (2014). Beneficial effect of a high number of copies of salivary amylase AMY1 gene on obesity risk in Mexican children. Diabetologia. 58(2). 290–294. 78 indexed citations
9.
Raimondo, Anne, Bruno Delobel, Bénédicte Duban‐Bedu, et al.. (2014). Identification of two novel loss-of-function SIM1 mutations in two overweight children with developmental delay. Obesity. 22(12). 2621–2624. 14 indexed citations
10.
Bonnefond, Amélie, Pierre‐Jean Saulnier, Maria G. Stathopoulou, et al.. (2013). What Is the Contribution of Two Genetic Variants Regulating VEGF Levels to Type 2 Diabetes Risk and to Microvascular Complications?. PLoS ONE. 8(2). e55921–e55921. 32 indexed citations
11.
Bonnefond, Amélie, Julien Philippe, Emmanuelle Durand, et al.. (2012). Whole-Exome Sequencing and High Throughput Genotyping Identified KCNJ11 as the Thirteenth MODY Gene. PLoS ONE. 7(6). e37423–e37423. 153 indexed citations
12.
Bonnefond, Amélie, Loïc Yengo, Julien Philippe, et al.. (2012). Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes. Diabetologia. 56(3). 492–496. 31 indexed citations
13.
Vaxillaire, Martine, Štěpánka Průhová, Aurélie Dechaume, et al.. (2011). Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations. Pediatric Diabetes. 12(3pt2). 266–269. 13 indexed citations
14.
Fukuda, Yu, Lydia Aguilar‐Bryan, Martine Vaxillaire, et al.. (2011). Conserved Intramolecular Disulfide Bond Is Critical to Trafficking and Fate of ATP-binding Cassette (ABC) Transporters ABCB6 and Sulfonylurea Receptor 1 (SUR1)/ABCC8. Journal of Biological Chemistry. 286(10). 8481–8492. 37 indexed citations
15.
Riveline, Jean‐Pierre, Yves Reznik, S. Fetita, et al.. (2011). Clinical and Metabolic Features of Adult-Onset Diabetes Caused by ABCC8 Mutations. Diabetes Care. 35(2). 248–251. 39 indexed citations
16.
Ezzidi, Intissar, Nabil Mtiraoui, Stéphane Cauchi, et al.. (2009). Contribution of type 2 diabetes associated loci in the Arabic population from Tunisia: a case-control study. BMC Medical Genetics. 10(1). 33–33. 68 indexed citations
17.
Vaxillaire, Martine, Aurélie Dechaume, Kanetee Busiah, et al.. (2007). New ABCC8 Mutations in Relapsing Neonatal Diabetes and Clinical Features. Diabetes. 56(6). 1737–1741. 63 indexed citations
18.
Cheyssac, Claire, Cécile Lecœur, Aurélie Dechaume, et al.. (2006). Analysis of common PTPN1gene variants in type 2 diabetes, obesity and associated phenotypes in the French population. BMC Medical Genetics. 7(1). 44–44. 40 indexed citations
19.
Vaxillaire, Martine, Aurélie Dechaume, Vincent Vatin, et al.. (2006). Genetic Analysis of ADIPOR1 and ADIPOR2 Candidate Polymorphisms for Type 2 Diabetes in the Caucasian Population. Diabetes. 55(3). 856–861. 56 indexed citations
20.
Vaxillaire, Martine, Christian Dina, Stéphane Lobbens, et al.. (2005). Effect of common polymorphisms in the HNF4? promoter on susceptibility to type 2 diabetes in the French Caucasian population. Diabetologia. 48(3). 440–444. 23 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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