Emmanuel Richard

1.9k total citations · 1 hit paper
57 papers, 1.2k citations indexed

About

Emmanuel Richard is a scholar working on Molecular Biology, Physiology and Genetics. According to data from OpenAlex, Emmanuel Richard has authored 57 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Molecular Biology, 13 papers in Physiology and 12 papers in Genetics. Recurrent topics in Emmanuel Richard's work include Porphyrin Metabolism and Disorders (16 papers), Virus-based gene therapy research (11 papers) and CRISPR and Genetic Engineering (9 papers). Emmanuel Richard is often cited by papers focused on Porphyrin Metabolism and Disorders (16 papers), Virus-based gene therapy research (11 papers) and CRISPR and Genetic Engineering (9 papers). Emmanuel Richard collaborates with scholars based in France, United States and Spain. Emmanuel Richard's co-authors include François Moreau‐Gaudry, Cécile Ged, Magalie Lalanne, Hubert de Verneuil, Jean‐Marc Blouin, Catherine Caillaud, Gaëlle Douillard‐Guilloux, Aurélie Bedel, Isabelle Lamrissi‐Garcia and Sandrine Dabernat and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Blood.

In The Last Decade

Emmanuel Richard

54 papers receiving 1.2k 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.

CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations

2019 310 citations Grégoire Cullot, Julian Boutin et al. Nature Communications profile →

Peers

Emmanuel Richard

GENET

PHYSI

PPCH

PRM

Nancy Wu United States

Nicolás Montalbetti United States

Diana Hernandez United Kingdom

Zae Young Ryoo South Korea

Julie R. Jones United States

Troels Marstrand Denmark

Maria Cristina Antal France

Michela Galdieri Italy

Julien Avérous France

Elı́zabeth Pintado Spain

Nancy Wu United States

Emmanuel Richard

1.3k ×1.5

469 ×1.8

GENET

124 ×0.6

PHYSI

34 ×0.3

PPCH

66 ×0.6

PRM

Citations per year, relative to Emmanuel Richard Emmanuel Richard (= 1×) peers Nancy Wu

Countries citing papers authored by Emmanuel Richard

Since Specialization

Citations

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

Fields of papers citing papers by Emmanuel Richard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emmanuel Richard

This figure shows the co-authorship network connecting the top 25 collaborators of Emmanuel Richard. A scholar is included among the top collaborators of Emmanuel Richard 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 Emmanuel Richard. Emmanuel Richard 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

Mercié, P., Étienne Rivière, Noémie Gensous, et al.. (2025). Place de la chitotriosidase au sein des biomarqueurs sériques de la sarcoïdose : une revue narrative de la littérature. La Revue de Médecine Interne. 46(9). 517–528.

Ged, Cécile, Audrey Petit, Aïcha Salhi, et al.. (2024). Severe Perinatal Presentations of Günther’s Disease: Series of 20 Cases and Perspectives. Life. 14(1). 130–130. 1 indexed citations

Redonnet‐Vernhet, Isabelle, P. Mercié, Jean‐Marc Blouin, et al.. (2024). Preventing hyperhomocysteinemia using vitamin B6 supplementation in Givosiran-treated acute intermittent porphyria: Highlights from a case report and brief literature review. Molecular Genetics and Metabolism Reports. 39. 101076–101076.

Helbling, Jean‐Christophe, Serge Alfos, Mathieu Di Miceli, et al.. (2023). Impact of dietary vitamin A on striatal function in adult rats. The FASEB Journal. 37(8). e23037–e23037.

Cullot, Grégoire, Julian Boutin, David Cappellen, et al.. (2023). Cell cycle arrest and p53 prevent ON-target megabase-scale rearrangements induced by CRISPR-Cas9. Nature Communications. 14(1). 4072–4072. 16 indexed citations

Estrade, V., Michel Daudon, Emmanuel Richard, et al.. (2021). Towards automatic recognition of pure and mixed stones using intra‐operative endoscopic digital images. British Journal of Urology. 129(2). 234–242. 23 indexed citations

Blouin, Jean‐Marc, Cécile Ged, Ganeko Bernardo‐Seisdedos, et al.. (2021). Identification of novel UROS mutations in a patient with congenital erythropoietic porphyria and efficient treatment by phlebotomy. Molecular Genetics and Metabolism Reports. 27. 100722–100722. 9 indexed citations

Alfos, Serge, Fabien Dumetz, Jean‐Christophe Helbling, et al.. (2020). Dietary vitamin A supplementation prevents early obesogenic diet-induced microbiota, neuronal and cognitive alterations. International Journal of Obesity. 45(3). 588–598. 25 indexed citations

Toutain, Jérôme, Julian Boutin, Samuel Amintas, et al.. (2020). Mutation-Specific Guide RNA for Compound Heterozygous Porphyria On-target Scarless Correction by CRISPR/Cas9 in Stem Cells. Stem Cell Reports. 15(3). 677–693. 4 indexed citations

10.

Blouin, Jean‐Marc, Magalie Lalanne, Lamia Azzi‐Martin, et al.. (2019). Targeted gene therapy in human-induced pluripotent stem cells from a patient with primary hyperoxaluria type 1 using CRISPR/Cas9 technology. Biochemical and Biophysical Research Communications. 517(4). 677–683. 22 indexed citations

11.

Blouin, Jean‐Marc, Ganeko Bernardo‐Seisdedos, Cécile Ged, et al.. (2017). Missense UROS mutations causing congenital erythropoietic porphyria reduce UROS homeostasis that can be rescued by proteasome inhibition. Human Molecular Genetics. 26(8). 1565–1576. 19 indexed citations

12.

Minni, Amandine, Serge Alfos, Pascale Roux, et al.. (2014). Vitamin A status regulates glucocorticoid availability in Wistar rats: consequences on cognitive functions and hippocampal neurogenesis?. Frontiers in Behavioral Neuroscience. 8. 20–20. 31 indexed citations

13.

Bedel, Aurélie, Jean‐Max Pasquet, Éric Lippert, et al.. (2013). Variable Behavior of iPSCs Derived from CML Patients for Response to TKI and Hematopoietic Differentiation. PLoS ONE. 8(8). e71596–e71596. 24 indexed citations

14.

Touyarot, Katia, Pascale Roux, Serge Alfos, et al.. (2013). A Mid-Life Vitamin A Supplementation Prevents Age-Related Spatial Memory Deficits and Hippocampal Neurogenesis Alterations through CRABP-I. PLoS ONE. 8(8). e72101–e72101. 35 indexed citations

15.

Bedel, Aurélie, Veronique Guyonnet‐Dupérat, Éric Lippert, et al.. (2012). Metabolic Correction of Congenital Erythropoietic Porphyria with iPSCs Free of Reprogramming Factors. The American Journal of Human Genetics. 91(1). 109–121. 17 indexed citations

16.

Richard, Élodie, Magalie Lalanne, Isabelle Lamrissi‐Garcia, et al.. (2010). Modeling of congenital erythropoietic porphyria by RNA interference: a new tool for preclinical gene therapy evaluation. The Journal of Gene Medicine. 12(8). 637–646. 6 indexed citations

17.

Douillard‐Guilloux, Gaëlle, Nina Raben, Shoichi Takikita, et al.. (2009). Restoration of muscle functionality by genetic suppression of glycogen synthesis in a murine model of Pompe disease. Human Molecular Genetics. 19(4). 684–696. 49 indexed citations

18.

Douillard‐Guilloux, Gaëlle, et al.. (2009). Partial phenotypic correction and immune tolerance induction to enzyme replacement therapy after hematopoietic stem cell gene transfer of α‐glucosidase in Pompe disease. The Journal of Gene Medicine. 11(4). 279–287. 31 indexed citations

19.

Richard, Emmanuel, Élodie Richard, Cécile Ged, François Moreau‐Gaudry, & Hubert de Verneuil. (2008). Erythropoietic Porphyrias: Animal Models and Update in Gene-Based Therapies. Current Gene Therapy. 8(3). 176–186. 21 indexed citations

20.

Richard, Emmanuel, Manuel Méndez, Frédéric Mazurier, et al.. (2001). Gene Therapy of a Mouse Model of Protoporphyria with a Self-Inactivating Erythroid-Specific Lentiviral Vector without Preselection. Molecular Therapy. 4(4). 331–338. 49 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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