Vincent Vatin

13.4k total citations
35 papers, 2.2k citations indexed

About

Vincent Vatin is a scholar working on Molecular Biology, Endocrine and Autonomic Systems and Physiology. According to data from OpenAlex, Vincent Vatin has authored 35 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 12 papers in Endocrine and Autonomic Systems and 11 papers in Physiology. Recurrent topics in Vincent Vatin's work include Regulation of Appetite and Obesity (12 papers), Adipose Tissue and Metabolism (10 papers) and Biochemical Analysis and Sensing Techniques (9 papers). Vincent Vatin is often cited by papers focused on Regulation of Appetite and Obesity (12 papers), Adipose Tissue and Metabolism (10 papers) and Biochemical Analysis and Sensing Techniques (9 papers). Vincent Vatin collaborates with scholars based in France, United Kingdom and United States. Vincent Vatin's co-authors include Philippe Froguel, Stephen Eyre, Christian Dina, Cécile Lecœur, Beverley Balkau, Emmanuelle Durand, Stephan Francke, Emmanuel Vaillant, Fritz Horber and Jérôme Delplanque and has published in prestigious journals such as Nature Genetics, PLoS ONE and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Vincent Vatin

35 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vincent Vatin France 24 760 667 652 635 567 35 2.2k
Cécile Lecœur France 23 655 0.9× 501 0.8× 679 1.0× 742 1.2× 496 0.9× 41 2.2k
Béatrice Dubern France 22 347 0.5× 746 1.1× 332 0.5× 437 0.7× 303 0.5× 58 1.6k
Hideo Makimura United States 24 236 0.3× 514 0.8× 479 0.7× 668 1.1× 161 0.3× 43 1.8k
Philippe Boutin France 24 634 0.8× 261 0.4× 726 1.1× 492 0.8× 625 1.1× 39 1.8k
Bethany P. Cummings United States 28 181 0.2× 192 0.3× 645 1.0× 926 1.5× 678 1.2× 63 2.1k
René Pecquery France 21 203 0.3× 441 0.7× 430 0.7× 660 1.0× 78 0.1× 34 1.8k
Katie C. Coate United States 17 231 0.3× 145 0.2× 1.1k 1.7× 636 1.0× 413 0.7× 37 2.1k
Cármen Garcés Spain 22 195 0.3× 182 0.3× 382 0.6× 403 0.6× 235 0.4× 106 1.8k
Jesse Roth United States 17 193 0.3× 145 0.2× 602 0.9× 566 0.9× 272 0.5× 32 1.5k
Mary F. Feitosa United States 21 370 0.5× 106 0.2× 269 0.4× 314 0.5× 139 0.2× 95 1.5k

Countries citing papers authored by Vincent Vatin

Since Specialization
Citations

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

Fields of papers citing papers by Vincent Vatin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vincent Vatin

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent Vatin. A scholar is included among the top collaborators of Vincent Vatin 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 Vincent Vatin. Vincent Vatin 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.
Rouskas, Konstantinos, Stephen Eyre, Fanny Stutzmann, et al.. (2012). Loss‐of‐Function Mutations in MC4R Are Very Rare in the Greek Severely Obese Adult Population. Obesity. 20(11). 2278–2282. 16 indexed citations
2.
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
3.
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
4.
Creemers, John W.M., Hélène Choquet, Pieter Stijnen, et al.. (2011). Heterozygous Mutations Causing Partial Prohormone Convertase 1 Deficiency Contribute to Human Obesity. Diabetes. 61(2). 383–390. 82 indexed citations
5.
Walley, Andrew J., Peter Jacobson, Mario Falchi, et al.. (2011). Differential coexpression analysis of obesity-associated networks in human subcutaneous adipose tissue. International Journal of Obesity. 36(1). 137–147. 36 indexed citations
6.
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
7.
Ghoussaini, Maya, Fanny Stutzmann, Cyril Couturier, et al.. (2010). Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population. Obesity. 18(8). 1670–1675. 14 indexed citations
8.
Ennafaa, Hajer, et al.. (2010). Study of TNFα -308G/A and IL6 -174G/C polymorphisms in type 2 diabetes and obesity risk in the Tunisian population. Clinical Biochemistry. 43(6). 549–552. 43 indexed citations
9.
Gueorguiev, Maria, Cécile Lecœur, Stephen Eyre, et al.. (2009). Association Studies on Ghrelin and Ghrelin Receptor Gene Polymorphisms With Obesity. Obesity. 17(4). 745–754. 57 indexed citations
10.
Blakemore, Alexandra I. F., Stephen Eyre, Jérôme Delplanque, et al.. (2009). A Rare Variant in the Visfatin Gene (NAMPT/PBEF1) Is Associated With Protection From Obesity. Obesity. 17(8). 1549–1553. 56 indexed citations
11.
Achhab, Youness El, Stephen Eyre, Nabila Bouatia‐Naji, et al.. (2008). Association of the ENPP1 K121Q polymorphism with type 2 diabetes and obesity in the Moroccan population. Diabetes & Metabolism. 35(1). 37–42. 24 indexed citations
12.
Gueorguiev, Maria, Cécile Lecœur, Michael Benzinou, et al.. (2008). A Genetic Study of the Ghrelin and Growth Hormone Secretagogue Receptor (GHSR) Genes and Stature. Annals of Human Genetics. 73(1). 1–9. 19 indexed citations
13.
Eyre, Stephen, Hassen Kamoun, Hajer Ennafaa, et al.. (2008). Effect of ENPP1/PC-1-K121Q and PPARγ-Pro12Ala polymorphisms on the genetic susceptibility to T2D in the Tunisian population. Diabetes Research and Clinical Practice. 81(3). 278–283. 31 indexed citations
14.
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
15.
Stutzmann, Fanny, Vincent Vatin, Stéphane Cauchi, et al.. (2007). Non-synonymous polymorphisms in melanocortin-4 receptor protect against obesity: the two facets of a Janus obesity gene. Human Molecular Genetics. 16(15). 1837–1844. 143 indexed citations
16.
Eyre, Stephen, Nabila Bouatia‐Naji, Vincent Vatin, et al.. (2007). ENPP1 K121Q polymorphism and obesity, hyperglycaemia and type 2 diabetes in the prospective DESIR Study. Diabetologia. 50(10). 2090–2096. 40 indexed citations
17.
Bouatia‐Naji, Nabila, Vincent Vatin, Cécile Lecœur, et al.. (2007). Secretory granule neuroendocrine protein 1 (SGNE1) genetic variation and glucose intolerance in severe childhood and adult obesity. BMC Medical Genetics. 8(1). 44–44. 8 indexed citations
18.
Grasberger, Helmut, Martine Vaxillaire, Silvana Pannain, et al.. (2005). Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1. Human Genetics. 118(3-4). 348–355. 13 indexed citations
19.
Leprêtre, Frédéric, Corinne Lacquemant, Vincent Vatin, et al.. (2004). Genetic study of the CD36 gene In a French diabetic population. Diabetes & Metabolism. 30(5). 459–463. 35 indexed citations
20.
Hager, Jörg, Christian Dina, Stephan Francke, et al.. (1998). A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10. Nature Genetics. 20(3). 304–308. 292 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 Cécile Lecœur Breakdown of academic impact, for papers by Béatrice Dubern Breakdown of academic impact, for papers by Hideo Makimura Breakdown of academic impact, for papers by Philippe Boutin Breakdown of academic impact, for papers by Bethany P. Cummings Breakdown of academic impact, for papers by René Pecquery Breakdown of academic impact, for papers by Katie C. Coate Breakdown of academic impact, for papers by Cármen Garcés Breakdown of academic impact, for papers by Jesse Roth Breakdown of academic impact, for papers by Mary F. Feitosa
Rankless by CCL
2026