Emmanuelle Durand

8.5k total citations · 2 hit papers
39 papers, 2.8k citations indexed

About

Emmanuelle Durand is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Emmanuelle Durand has authored 39 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 16 papers in Molecular Biology and 11 papers in Surgery. Recurrent topics in Emmanuelle Durand's work include Pancreatic function and diabetes (11 papers), Genetic Associations and Epidemiology (8 papers) and Epigenetics and DNA Methylation (6 papers). Emmanuelle Durand is often cited by papers focused on Pancreatic function and diabetes (11 papers), Genetic Associations and Epidemiology (8 papers) and Epigenetics and DNA Methylation (6 papers). Emmanuelle Durand collaborates with scholars based in France, United Kingdom and Pakistan. Emmanuelle Durand's co-authors include Philippe Froguel, Serge Herçberg, Christian Vaisse, Karine Clément, Cécile Lecœur, Christian Dina, Stephan Francke, Sophie Gallina, Nathalie Vionnet and Frédéric Leprêtre and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Emmanuelle Durand

39 papers receiving 2.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Melanocortin-4 receptor mutations are a frequent and heterogeneous cause of morbid obesity

2000 661 citations Emmanuelle Durand, Serge Herçberg et al. profile →
Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24

2000 576 citations Nathalie Vionnet, El Habib Hani et al. The American Journal of Human Genetics profile →

Peers

Emmanuelle Durand

GENET

EAS

PHYSI

SURGE

Michael K. Badman United States

Benjamin Challis United Kingdom

Tsuyoshi Monden Japan

Rima Boyadjian United States

Françoise Assimacopoulos‐Jeannet Switzerland

Louise Sanders United Kingdom

Kentaro Yamada Japan

Catherine Le Stunff France

Gregory Collier Australia

José Córdoba‐Chacón United States

Michael K. Badman United States

Emmanuelle Durand

2.6k ×2.8

514 ×0.6

GENET

694 ×0.8

EAS

1.3k ×1.7

PHYSI

1000 ×1.7

SURGE

Citations per year, relative to Emmanuelle Durand Emmanuelle Durand (= 1×) peers Michael K. Badman

Countries citing papers authored by Emmanuelle Durand

Since Specialization

Citations

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

Fields of papers citing papers by Emmanuelle Durand

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanuelle Durand

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Durand, Emmanuelle. (2023). Se forger une place à Beyrouth. SPIRE - Sciences Po Institutional REpository. N° 4(2). 43–66. 2 indexed citations

Yao, Xi, Frédérik Oger, Mehdi Derhourhi, et al.. (2023). Knocking Down CDKN2A in 3D hiPSC-Derived Brown Adipose Progenitors Potentiates Differentiation, Oxidative Metabolism and Browning Process. Cells. 12(6). 870–870. 3 indexed citations

Brasselet, Camille, Damien Metz, Fausto Biancari, et al.. (2022). Transfemoral versus transcarotid access for transcatheter aortic valve replacement. JTCVS Techniques. 15. 46–53. 5 indexed citations

Rabhi, Nabil, Emmanuelle Durand, François Pattou, et al.. (2022). Glucose Regulates m6A Methylation of RNA in Pancreatic Islets. Cells. 11(2). 291–291. 22 indexed citations

Coppin, Lucie, Arnaud Jannin, Emilie Ait‐Yahya, et al.. (2020). Galectin-3 modulates epithelial cell adaptation to stress at the ER-mitochondria interface. Cell Death and Disease. 11(5). 360–360. 24 indexed citations

Rabhi, Nabil, Sarah Anissa Hannou, Xi Yao, et al.. (2017). Cdkn2a deficiency promotes adipose tissue browning. Molecular Metabolism. 8. 65–76. 32 indexed citations

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

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

Oger, Frédérik, Julie Dubois‐Chevalier, Céline Gheeraert, et al.. (2013). Peroxisome Proliferator-activated Receptor γ Regulates Genes Involved in Insulin/Insulin-like Growth Factor Signaling and Lipid Metabolism during Adipogenesis through Functionally Distinct Enhancer Classes. Journal of Biological Chemistry. 289(2). 708–722. 40 indexed citations

10.

Boëlle, Pierre‐Yves, Maria Antonietta D’Agostino, J.-F. Vibert, et al.. (2013). Influence of Environmental Factors on Disease Activity in Spondyloarthritis: A Prospective Cohort Study. The Journal of Rheumatology. 40(4). 469–475. 11 indexed citations

11.

Sérandour, Aurélien A., Stéphane Avner, Frédérik Oger, et al.. (2012). Dynamic hydroxymethylation of deoxyribonucleic acid marks differentiation-associated enhancers. Nucleic Acids Research. 40(17). 8255–8265. 149 indexed citations

12.

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

13.

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

14.

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

15.

Cauchi, Stéphane, Fanny Stutzmann, Christine Cavalcanti-Proença, et al.. (2009). Combined effects of MC4R and FTO common genetic variants on obesity in European general populations. Journal of Molecular Medicine. 87(5). 537–546. 128 indexed citations

16.

Cauchi, Stéphane, I. Byrjalsen, Emmanuelle Durand, M.A. Karsdal, & Philippe Froguel. (2009). PLCL1 rs7595412 variation is not associated with hip bone size variation in postmenopausal Danish women. BMC Medical Genetics. 10(1). 145–145. 2 indexed citations

17.

Stutzmann, Fanny, Stéphane Cauchi, Emmanuelle Durand, et al.. (2009). Common genetic variation near MC4R is associated with eating behaviour patterns in European populations. International Journal of Obesity. 33(3). 373–378. 81 indexed citations

18.

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

19.

Cauchi, Stéphane, Stephen Eyre, Hélène Choquet, et al.. (2007). TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population. BMC Medical Genetics. 8(1). 37–37. 15 indexed citations

20.

Vionnet, Nathalie, El Habib Hani, S. Dupont, et al.. (2000). Genomewide Search for Type 2 Diabetes–Susceptibility Genes in French Whites: Evidence for a Novel Susceptibility Locus for Early-Onset Diabetes on Chromosome 3q27-qter and Independent Replication of a Type 2–Diabetes Locus on Chromosome 1q21–q24. The American Journal of Human Genetics. 67(6). 1470–1480. 576 indexed citations breakdown →

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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