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

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

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20 of 20 papers shown

#	Title	Journal	Authors	Indexed citations
1	Se forger une place à Beyrouth	SPIRE - Sciences Po Institutional REpository	Emmanuelle Durand	2
2	Knocking Down CDKN2A in 3D hiPSC-Derived Brown Adipose Progenitors Potentiates Differentiation, Oxidative Metabolism and Browning Process	Cells	Xi Yao, Frédérik Oger et al.	3
3	Transfemoral versus transcarotid access for transcatheter aortic valve replacement	JTCVS Techniques	Camille Brasselet, Damien Metz et al.	5
4	Glucose Regulates m6A Methylation of RNA in Pancreatic Islets	Cells	Nabil Rabhi, Emmanuelle Durand et al.	22
5	Galectin-3 modulates epithelial cell adaptation to stress at the ER-mitochondria interface	Cell Death and Disease	Lucie Coppin, Arnaud Jannin et al.	24
6	Cdkn2a deficiency promotes adipose tissue browning	Molecular Metabolism	Nabil Rabhi, Sarah Anissa Hannou et al.	32
7	High Prevalence of Rare Monogenic Forms of Obesity in Obese Guadeloupean Afro-Caribbean Children	The Journal of Clinical Endocrinology & Metabolism	L. Foucan, Laurent Larifla et al.	24
8	What Is the Best NGS Enrichment Method for the Molecular Diagnosis of Monogenic Diabetes and Obesity?	PLoS ONE	Julien Philippe, Mehdi Derhourhi et al.	13
9	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	Frédérik Oger, Julie Dubois‐Chevalier et al.	40
10	Influence of Environmental Factors on Disease Activity in Spondyloarthritis: A Prospective Cohort Study	The Journal of Rheumatology	Pierre‐Yves Boëlle, Maria Antonietta D’Agostino et al.	11
11	Dynamic hydroxymethylation of deoxyribonucleic acid marks differentiation-associated enhancers	Nucleic Acids Research	Aurélien A. Sérandour, Stéphane Avner et al.	149
12	Whole-Exome Sequencing and High Throughput Genotyping Identified KCNJ11 as the Thirteenth MODY Gene	PLoS ONE	Amélie Bonnefond, Julien Philippe et al.	153
13	Common Variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 Show Evidence of Association With Adult Obesity in the Greek Population	Obesity	Konstantinos Rouskas, Anastasia Kouvatsi et al.	50
14	Analysis of the SIM1 Contribution to Polygenic Obesity in the French Population	Obesity	Maya Ghoussaini, Fanny Stutzmann et al.	14
15	Combined effects of MC4R and FTO common genetic variants on obesity in European general populations	Journal of Molecular Medicine	Stéphane Cauchi, Fanny Stutzmann et al.	128
16	PLCL1 rs7595412 variation is not associated with hip bone size variation in postmenopausal Danish women	BMC Medical Genetics	Stéphane Cauchi, I. Byrjalsen et al.	2
17	Common genetic variation near MC4R is associated with eating behaviour patterns in European populations	International Journal of Obesity	Fanny Stutzmann, Stéphane Cauchi et al.	81
18	INS VNTR Is Not Associated With Childhood Obesity in 1,023 Families: A Family‐based Study	Obesity	Nabila Bouatia‐Naji, Franck De Graeve et al.	7
19	TCF7L2 rs7903146 variant does not associate with smallness for gestational age in the French population	BMC Medical Genetics	Stéphane Cauchi, Stephen Eyre et al.	15
20	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 breakdown →	The American Journal of Human Genetics	Nathalie Vionnet, El Habib Hani et al.	576

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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