Franck De Graeve

2.0k total citations
11 papers, 481 citations indexed

About

Franck De Graeve is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Franck De Graeve has authored 11 papers receiving a total of 481 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Surgery and 6 papers in Molecular Biology. Recurrent topics in Franck De Graeve's work include Pancreatic function and diabetes (7 papers), Diabetes and associated disorders (3 papers) and Diet, Metabolism, and Disease (3 papers). Franck De Graeve is often cited by papers focused on Pancreatic function and diabetes (7 papers), Diabetes and associated disorders (3 papers) and Diet, Metabolism, and Disease (3 papers). Franck De Graeve collaborates with scholars based in France, United Kingdom and Germany. Franck De Graeve's co-authors include Philippe Froguel, Martine Vaxillaire, Olivier Sand, Amélie Bonnefond, Emmanuelle Durand, Julien Philippe, Jérôme Delplanque, Beverley Balkau, Michel Marre and David Meyre and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Diabetes Care.

In The Last Decade

Franck De Graeve

11 papers receiving 474 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Franck De Graeve France 9 309 271 203 134 44 11 481
Noèlia Téllez Spain 15 219 0.7× 326 1.2× 131 0.6× 202 1.5× 51 1.2× 23 522
Lars Selander Sweden 7 200 0.6× 369 1.4× 242 1.2× 148 1.1× 36 0.8× 7 494
Sarah Bocchini Italy 9 243 0.8× 115 0.4× 129 0.6× 47 0.4× 39 0.9× 25 385
Wilfred Ip Canada 11 116 0.4× 237 0.9× 312 1.5× 159 1.2× 47 1.1× 12 511
Nicholas Bhagroo United States 9 139 0.4× 257 0.9× 120 0.6× 163 1.2× 37 0.8× 11 400
Martina Škopková Slovakia 12 192 0.6× 210 0.8× 171 0.8× 135 1.0× 77 1.8× 31 438
Don Fleenor United States 9 124 0.4× 179 0.7× 133 0.7× 242 1.8× 125 2.8× 10 528
Lauren Gianniny United States 4 381 1.2× 200 0.7× 274 1.3× 175 1.3× 42 1.0× 4 598
Johanne H. Ellenbroek Netherlands 12 152 0.5× 280 1.0× 209 1.0× 258 1.9× 157 3.6× 12 576
Claire Cheyssac Switzerland 6 113 0.4× 175 0.6× 172 0.8× 74 0.6× 31 0.7× 6 300

Countries citing papers authored by Franck De Graeve

Since Specialization
Citations

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

Fields of papers citing papers by Franck De Graeve

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Franck De Graeve. 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 Franck De Graeve. The network helps show where Franck De Graeve may publish in the future.

Co-authorship network of co-authors of Franck De Graeve

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

All Works

11 of 11 papers shown
1.
Bonnefond, Amélie, Julien Philippe, Emmanuel Vaillant, et al.. (2017). A novel NEUROG3 mutation in neonatal diabetes associated with a neuro‐intestinal syndrome. Pediatric Diabetes. 19(3). 381–387. 15 indexed citations
2.
Foucan, L., Laurent Larifla, Emmanuelle Durand, et al.. (2017). High Prevalence of Rare Monogenic Forms of Obesity in Obese Guadeloupean Afro-Caribbean Children. The Journal of Clinical Endocrinology & Metabolism. 103(2). 539–545. 24 indexed citations
3.
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
4.
Philippe, Julien, Pieter Stijnen, David Meyre, et al.. (2014). A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity. International Journal of Obesity. 39(2). 295–302. 47 indexed citations
5.
Bonnefond, Amélie, Julien Philippe, Emmanuelle Durand, et al.. (2013). Highly Sensitive Diagnosis of 43 Monogenic Forms of Diabetes or Obesity Through One-Step PCR-Based Enrichment in Combination With Next-Generation Sequencing. Diabetes Care. 37(2). 460–467. 50 indexed citations
6.
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
7.
Bonnefond, Amélie, Emmanuelle Durand, Olivier Sand, et al.. (2010). Molecular Diagnosis of Neonatal Diabetes Mellitus Using Next-Generation Sequencing of the Whole Exome. PLoS ONE. 5(10). e13630–e13630. 86 indexed citations
8.
Choquet, Hélène, Yann Labrune, Franck De Graeve, et al.. (2010). Lack of Association of CD36 SNPs With Early Onset Obesity: A Meta‐Analysis in 9,973 European Subjects. Obesity. 19(4). 833–839. 18 indexed citations
9.
Cauchi, Stéphane, Christine Proença, Hélène Choquet, et al.. (2008). Analysis of novel risk loci for type 2 diabetes in a general French population: the D.E.S.I.R. study. Journal of Molecular Medicine. 86(3). 341–348. 65 indexed citations
10.
Bouatia‐Naji, Nabila, Franck De Graeve, Günter Brönner, et al.. (2008). INS VNTR Is Not Associated With Childhood Obesity in 1,023 Families: A Family‐based Study. Obesity. 16(6). 1471–1475. 7 indexed citations
11.
Héroum, C., et al.. (2006). Une cause rare d’embolie cérébrale : la cardiopathie amyloïde. Revue Neurologique. 162(11). 1128–1130. 3 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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