Hélène Puccio

6.3k total citations · 1 hit paper
62 papers, 4.7k citations indexed

About

Hélène Puccio is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cell Biology. According to data from OpenAlex, Hélène Puccio has authored 62 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 57 papers in Molecular Biology, 46 papers in Cellular and Molecular Neuroscience and 18 papers in Cell Biology. Recurrent topics in Hélène Puccio's work include Mitochondrial Function and Pathology (47 papers), Genetic Neurodegenerative Diseases (46 papers) and Endoplasmic Reticulum Stress and Disease (16 papers). Hélène Puccio is often cited by papers focused on Mitochondrial Function and Pathology (47 papers), Genetic Neurodegenerative Diseases (46 papers) and Endoplasmic Reticulum Stress and Disease (16 papers). Hélène Puccio collaborates with scholars based in France, United States and Germany. Hélène Puccio's co-authors include Alain Martelli, Laurence Reutenauer, Louis M. Kunkel, Michel Kœnig, Stéphane Schmucker, Delphine Simon, Marie Wattenhofer‐Donzé, Pierre Rustin, Annalisa Pastore and Mireille Cossée and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Hélène Puccio

61 papers receiving 4.6k 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.

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits

2001 588 citations Hélène Puccio, Mireille Cossée et al. profile →

Peers

Countries citing papers authored by Hélène Puccio

Since Specialization

Citations

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

Fields of papers citing papers by Hélène Puccio

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hélène Puccio

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

#	Work	Indexed citations
1	Autosomal Recessive Cerebellar Ataxias: Translating Genes to Therapies 2025 ·Annals of Neurology ·Brent L. Fogel, Thomas Klopstock, David R. Lynch, Francesca Maltecca, Mayank Verma, (unknown), Frances M. Platt, (unknown), Hélène Puccio, Andreas Roos, Matthis Synofzik	1
2	Muscle mTOR controls iron homeostasis and ferritinophagy via NRF2, HIFs and AKT/PKB signaling pathways 2025 ·Cellular and Molecular Life Sciences ·Agnès Conjard‐Duplany, (unknown), Aline Lamboux, (unknown), (unknown), Vincent Moncollin, (unknown), (unknown), Hélène Puccio, Pascal Leblanc, Bruno Galy, Vincent Balter, Laurent Schaeffer, Yann‐Gaël Gangloff	1
3	Omaveloxolone: a groundbreaking milestone as the first FDA-approved drug for Friedreich ataxia 2024 ·Trends in Molecular Medicine ·Federica Pilotto, (unknown), Hélène Puccio	41
4	Hereditary Ataxias: From Bench to Clinic, Where Do We Stand? 2024 ·Cells ·Federica Pilotto, (unknown), Hélène Puccio	7
5	Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy 2022 ·Brain ·Arnaud Jacquier, (unknown), Fanny Fontaine, (unknown), Nicolas Lacoste, (unknown), Valérie Risson, (unknown), (unknown), Thomas Simonet, Philippe Latour, Tanya Stojkovic, Juliette Piard, (unknown), Gaëtan Lesca, Françoise Bouhour, Stéphane Allouche, Hélène Puccio, Antoine Pégat, Laurent Schaeffer	11
6	ISCA1 is essential for mitochondrial Fe4S4 biogenesis in vivo 2017 ·Nature Communications ·(unknown), Sandrine Ollagnier de Choudens, Marjorie Fournier, (unknown), (unknown), Martin Clémancey, Geneviève Blondin, Stéphane Schmucker, (unknown), Amélie Weiss, Pascale Koebel, Nadia Messaddeq, Hélène Puccio, Alain Martelli	82
7	Mammalian Fe–S cluster biogenesis and its implication in disease 2014 ·Biochimie ·(unknown), Hélène Puccio	83
8	Dysregulation of cellular iron metabolism in Friedreich ataxia: from primary iron-sulfur cluster deficit to mitochondrial iron accumulation 2014 ·Frontiers in Pharmacology ·Alain Martelli, Hélène Puccio	106
9	Vers une thérapie génique pour la cardiomyopathie associée à l’ataxie de Friedreich 2014 ·médecine/sciences ·Brahim Belbellaa, Hélène Puccio	1
10	An Overview of Current Mouse Models Recapitulating Coenzyme Q<sub>10</sub> Deficiency Syndrome 2014 ·Molecular Syndromology ·Floriana Licitra, Hélène Puccio	15
11	The molecular genetics of coenzyme Q biosynthesis in health and disease 2013 ·Biochimie ·Leila Laredj, Floriana Licitra, Hélène Puccio	58
12	Multicellular models of Friedreich ataxia 2009 ·Journal of Neurology ·Hélène Puccio	33
13	Frataxin deficiency causes upregulation of mitochondrial Lon and ClpP proteases and severe loss of mitochondrial Fe–S proteins 2009 ·FEBS Journal ·Blanche Guillon, Anne‐Laure Bulteau, Marie Wattenhofer‐Donzé, Stéphane Schmucker, Bertrand Friguet, Hélène Puccio, Jean‐Claude Drapier, Cécile Bouton	68
14	Advancements in the pathophysiology of Friedreich’s Ataxia and new prospects for treatments 2007 ·Molecular Genetics and Metabolism ·(unknown), (unknown), Robert D. Wells, Tracey A. Rouault, Michio Hirano, David R. Lynch, Martin B. Delatycki, Robert B. Wilson, Grazia Isaya, Hélène Puccio	57
15	Targeted disruption of hepatic frataxin expression causes impaired mitochondrial function, decreased life span and tumor growth in mice 2005 ·Human Molecular Genetics ·René Thierbach, Tim J. Schulz, Frank Isken, Anja Voigt, (unknown), (unknown), Jürgen‐Christoph von Kleist-Retzow, Rudolf J. Wiesner, Mark A. Magnuson, Hélène Puccio, Andreas Pfeiffer, Pablo Steinberg, Michael Ristow	109
16	Frataxin deficiency alters heme pathway transcripts and decreases mitochondrial heme metabolites in mammalian cells 2005 ·Human Molecular Genetics ·Robert Schoenfeld, Eleonora Napoli, Alice Wong, (unknown), Laurence Reutenauer, Dexter Morin, Alan R. Buckpitt, Franco Taroni, Bo Lönnerdal, Michael Ristow, Hélène Puccio, Gino Cortopassi	92
17	Frataxin deficiency in pancreatic islets causes diabetes due to loss of β cell mass 2003 ·Journal of Clinical Investigation ·Michael Ristow, Hindrik Mulder, (unknown), Tim J. Schulz, (unknown), Anja Krause, Malin Fex, Hélène Puccio, Jörg Müller, Frank Isken, Joachim Spranger, Dirk Müller‐Wieland, Mark A. Magnuson, Matthias Möhlig, Michel Kœnig, Andreas Pfeiffer	107
18	Frataxin deficiency in pancreatic islets causes diabetes due to loss of β cell mass 2003 ·Journal of Clinical Investigation ·Michael Ristow, Hindrik Mulder, (unknown), Tim J. Schulz, (unknown), Anja Krause, Malin Fex, Hélène Puccio, Jörg Müller, Frank Isken, Joachim Spranger, Dirk Müller‐Wieland, Mark A. Magnuson, Matthias Möhlig, Michel Kœnig, Andreas Pfeiffer	7
19	Friedreich ataxia: a paradigm for mitochondrial diseases 2002 ·Current Opinion in Genetics & Development ·Hélène Puccio, M. Kœnig	90
20	Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesis 2001 ·Neurogenetics ·Mark A. Pook, Sahar Al‐Mahdawi, Christopher J. Carroll, Mireille Cossée, Hélène Puccio, Lorraine Lawrence, Peter Clark, Margaret B. Lowrie, Jane L. Bradley, Jonathan M. Cooper, M. Kœnig, Susan Chamberlain	58

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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