Stéphane Lobbens

20.5k total citations
29 papers, 1.3k citations indexed

About

Stéphane Lobbens is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Stéphane Lobbens has authored 29 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 13 papers in Molecular Biology and 10 papers in Epidemiology. Recurrent topics in Stéphane Lobbens's work include Pancreatic function and diabetes (8 papers), Genetic Associations and Epidemiology (7 papers) and Adipokines, Inflammation, and Metabolic Diseases (7 papers). Stéphane Lobbens is often cited by papers focused on Pancreatic function and diabetes (8 papers), Genetic Associations and Epidemiology (7 papers) and Adipokines, Inflammation, and Metabolic Diseases (7 papers). Stéphane Lobbens collaborates with scholars based in France, United Kingdom and Italy. Stéphane Lobbens's co-authors include Philippe Froguel, Christian Dina, Stephen Eyre, Amélie Bonnefond, Jacques Weill, G. Charpentier, Philipp E. Scherer, Karine Clément, Beverley Balkau and Michel Marre and has published in prestigious journals such as Nature Genetics, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Stéphane Lobbens

29 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stéphane Lobbens France 21 460 423 413 377 226 29 1.3k
Momoko Horikoshi Japan 17 494 1.1× 565 1.3× 368 0.9× 453 1.2× 185 0.8× 25 1.5k
Sandra D. O’Dell United Kingdom 20 430 0.9× 200 0.5× 311 0.8× 349 0.9× 146 0.6× 46 1.2k
Catherine Le Stunff France 19 416 0.9× 219 0.5× 482 1.2× 325 0.9× 213 0.9× 48 1.4k
Běla Bendlová Czechia 26 436 0.9× 277 0.7× 354 0.9× 406 1.1× 378 1.7× 118 2.1k
Eva Sjölin Sweden 13 386 0.8× 414 1.0× 642 1.6× 131 0.3× 94 0.4× 15 1.1k
Marina T. DiStefano United States 13 500 1.1× 190 0.4× 243 0.6× 567 1.5× 114 0.5× 27 1.4k
Josef Včelák Czechia 22 295 0.6× 141 0.3× 207 0.5× 270 0.7× 202 0.9× 81 1.3k
Ichiro Yokota Japan 24 716 1.6× 255 0.6× 475 1.2× 245 0.6× 204 0.9× 92 2.0k
Andrew Whatmore United Kingdom 20 278 0.6× 150 0.4× 244 0.6× 231 0.6× 82 0.4× 51 1.1k
Min Jin Go South Korea 18 315 0.7× 111 0.3× 150 0.4× 340 0.9× 151 0.7× 34 1.1k

Countries citing papers authored by Stéphane Lobbens

Since Specialization
Citations

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

Fields of papers citing papers by Stéphane Lobbens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stéphane Lobbens

This figure shows the co-authorship network connecting the top 25 collaborators of Stéphane Lobbens. A scholar is included among the top collaborators of Stéphane Lobbens 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 Stéphane Lobbens. Stéphane Lobbens 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.
Canouil, Mickaël, Amna Khamis, Elina Keikkala, et al.. (2021). Epigenome-Wide Association Study Reveals Methylation Loci Associated With Offspring Gestational Diabetes Mellitus Exposure and Maternal Methylome. Diabetes Care. 44(9). 1992–1999. 21 indexed citations
2.
Khamis, Amna, Raphaël Boutry, Mickaël Canouil, et al.. (2020). Histone deacetylase 9 promoter hypomethylation associated with adipocyte dysfunction is a statin-related metabolic effect. Clinical Epigenetics. 12(1). 68–68. 12 indexed citations
3.
Huyvaert, Marlène, Mickaël Canouil, Cécile Lecœur, et al.. (2019). The expression of genes in top obesity-associated loci is enriched in insula and substantia nigra brain regions involved in addiction and reward. International Journal of Obesity. 44(2). 539–543. 40 indexed citations
4.
Morandi, Anita, Amélie Bonnefond, Stéphane Lobbens, et al.. (2016). Associations Between Type 2 Diabetes-Related Genetic Scores and Metabolic Traits, in Obese and Normal-Weight Youths. The Journal of Clinical Endocrinology & Metabolism. 101(11). 4244–4250. 12 indexed citations
5.
Morandi, Anita, Amélie Bonnefond, Stéphane Lobbens, et al.. (2015). A girl with incomplete Prader–Willi syndrome and negative MS‐PCR, found to have mosaic maternal UPD‐15 at SNP array. American Journal of Medical Genetics Part A. 167(11). 2720–2726. 21 indexed citations
6.
Bouckenooghe, Thomas, Jérôme Delplanque, Elodie Eury, et al.. (2014). Placental antiangiogenic prolactin fragments are increased in human and rat maternal diabetes. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(9). 1783–1793. 14 indexed citations
7.
Vaxillaire, Martine, Loïc Yengo, Stéphane Lobbens, et al.. (2014). Type 2 diabetes-related genetic risk scores associated with variations in fasting plasma glucose and development of impaired glucose homeostasis in the prospective DESIR study. Diabetologia. 57(8). 1601–1610. 35 indexed citations
8.
Makki, Kassem, Solenne Taront, Olivier Molendi‐Coste, et al.. (2014). Beneficial Metabolic Effects of Rapamycin Are Associated with Enhanced Regulatory Cells in Diet-Induced Obese Mice. PLoS ONE. 9(4). e92684–e92684. 57 indexed citations
9.
Bonnefond, Amélie, Boris Skrobek, Stéphane Lobbens, et al.. (2013). Association between large detectable clonal mosaicism and type 2 diabetes with vascular complications. Nature Genetics. 45(9). 1040–1043. 102 indexed citations
10.
Bonnefond, Amélie, Nabila Bouatia‐Naji, James K. Oeser, et al.. (2013). Multiple functional polymorphisms in the G6PC2 gene contribute to the association with higher fasting plasma glucose levels. Diabetologia. 56(6). 1306–1316. 27 indexed citations
11.
Robiou-du-Pont, Sébastien, Loïc Yengo, Emmanuel Vaillant, et al.. (2013). Common variants near BDNF and SH2B1 show nominal evidence of association with snacking behavior in European populations. Journal of Molecular Medicine. 91(9). 1109–1115. 4 indexed citations
12.
Bonnefond, Amélie, Emmanuel Vaillant, Julien Philippe, et al.. (2013). Transcription factor gene MNX1 is a novel cause of permanent neonatal diabetes in a consanguineous family. Diabetes & Metabolism. 39(3). 276–280. 38 indexed citations
13.
Morandi, Anita, Stephen Eyre, Stéphane Lobbens, et al.. (2012). Estimation of Newborn Risk for Child or Adolescent Obesity: Lessons from Longitudinal Birth Cohorts. PLoS ONE. 7(11). e49919–e49919. 81 indexed citations
14.
Rouskas, Konstantinos, Anastasia Kouvatsi, Konstantinos Paletas, et al.. (2011). Common Variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population. Obesity. 20(2). 389–395. 50 indexed citations
15.
Vasseur, Francis, Mouna Barat‐Houari, Stéphane Lobbens, et al.. (2010). Concordance of two multiple analytical approaches demonstrate that interaction between BMI and ADIPOQ haplotypes is a determinant of LDL cholesterol in a general French population. Journal of Human Genetics. 55(4). 227–231. 3 indexed citations
16.
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
17.
Morandi, Anita, Claudio Maffeis, Stéphane Lobbens, et al.. (2009). Early Detrimental Metabolic Outcomes of rs17300539‐A Allele of ADIPOQ Gene Despite Higher Adiponectinemia. Obesity. 18(7). 1469–1473. 17 indexed citations
18.
Benzinou, Michael, Jean-Claude Chèvre, Kirsten Ward, et al.. (2008). Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations. Human Molecular Genetics. 17(13). 1916–1921. 87 indexed citations
19.
Ghoussaini, Maya, Stephen Eyre, Stéphane Lobbens, et al.. (2005). Implication of the Pro12Ala polymorphism of the PPAR-gamma 2gene in type 2 diabetes and obesity in the French population. BMC Medical Genetics. 6(1). 11–11. 91 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Momoko Horikoshi Breakdown of academic impact, for papers by Sandra D. O’Dell Breakdown of academic impact, for papers by Catherine Le Stunff Breakdown of academic impact, for papers by Běla Bendlová Breakdown of academic impact, for papers by Eva Sjölin Breakdown of academic impact, for papers by Marina T. DiStefano Breakdown of academic impact, for papers by Josef Včelák Breakdown of academic impact, for papers by Ichiro Yokota Breakdown of academic impact, for papers by Andrew Whatmore Breakdown of academic impact, for papers by Min Jin Go
Rankless by CCL
2026