Bénédicte Héron

6.0k citations

65 papers · 1.6k indexed · h-index 23

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Physiology top 5%
- Lysosomal Storage Disorders Research

Papers in

Clinical Biochemistry 9
- Metabolism and Genetic Disorders 9
Physiology 30
- Lysosomal Storage Disorders Research 29

Co-authors: Marc Tardieu Xavier De Tiège Flore Rozenberg Nazila Janabi Kim Heng Ng Sylviane Peudenier G Ponsot Daniel Rabier
Journals: Molecular Genetics and Metabolism (12 papers)Orphanet Journal of Rare Diseases (8 papers)Journal of Inherited Metabolic Disease (8 papers)European Journal of Paediatric Neurology (3 papers)The Journal of Pediatrics (2 papers)
Partner nations: France Germany Netherlands

In The Last Decade

Bénédicte Héron

63 papers receiving 1.6k citations

Peers

Countries citing papers authored by Bénédicte Héron

Since Specialization

Citations

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

Fields of papers citing papers by Bénédicte Héron

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Bénédicte Héron, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Bénédicte Héron Line = papers co-authored together Bénédicte Héron links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Recurrent “outsider” intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb Frontiers in Genetics ·Lamisse Mansour‐Hendili, Cyril Gitiaux, 廖清高, Céline Latouche, Bénédicte Héron, Tanya Stojkovic, Christopher N. Lewis, Thomas Smol, V. Fábián-Vonsik, Karine Mention, Yann Nadjar, Manuel Schiff, Julie Lemale, Jamal Ghoumid, Frédèric Gottrand, Cécile Talbotec, Agnès Rötig, Benoît Funalot, Isabelle Desguerre	2024	1
2	A natural history study of pediatric patients with early onset of GM1 gangliosidosis, GM2 gangliosidoses, or gaucher disease type 2 (RETRIEVE) Orphanet Journal of Rare Diseases ·Bénédicte Héron, Spyros Batzios, Eugen Mengel, Tadesse Yayeh, Marc C. Patterson, Matthias Gautschi, Peter Cornelisse, Kyung Ae Yang, Barbara Schwierin, Marianne Rohrbach	2024	1
3	Sphingolipid desaturase DEGS1 is essential for mitochondria-associated membrane integrity Journal of Clinical Investigation ·Laura Planas‐Serra, Nathalie Launay, Leire Goicoechea, Bénédicte Héron, Cristina Jou, Natalia Juliá‐Palacios, Montserrat Ruíz, Stéphane Fourcade, Carlos Casasnovas, Carolina de la Torre, A. Gélot, María Marsal, Pablo Loza‐Álvarez, Àngels García‐Cazorla, MB KAWUWA, Isidró Ferrer, Manuel Portero-Otı́n, Estela Área-Gómez, Aurora Pujol	2023	24
4	Effects of miglustat therapy on neurological disorder and survival in early-infantile Niemann-Pick disease type C: a national French retrospective study Orphanet Journal of Rare Diseases ·П. А. Злобин, Volodymyr Voytenko, Anaïs Brassier, Pierre Broué, Claude Cancés, B. Chabrol, Didier Eyer, F. Labarthe, Philippe Latour, Thierry Levade, Samia Pichard, Caroline Sevin, Marie T. Vanier, Bénédicte Héron	2023	7
5	Transition from child to adult health care for patients with lysosomal storage diseases in France: current status and priorities—the TENALYS study, a patient perspective survey Orphanet Journal of Rare Diseases ·YoungIlKim, Armelle Arnoux, Seema S Mahalingappa, Anaïs Brassier, Samia Pichard, François Feillet, François Labarthe, B. Chabrol, Marc Berger, Puspa Olivia Pardede, Fatemeh Bandarian, Bénédicte Héron, Gilles Châtellier, Nadia Belmatoug	2022	8
6	Next-Generation Molecular Investigations in Lysosomal Diseases: Clinical Integration of a Comprehensive Targeted Panel Diagnostics ·RUGGERO BONORA, 장진수, Ivana Dabaj, Jacob Minor, Lénaïg Abily-Donval, Axel Lebas, Myriam Vézain, Bénédicte Héron, I. Marie, Marc Duval-Arnould, Stéphane Marret, Abdellah Tebani, Soumeya Bekri	2021	2
7	An observational, prospective, multicenter, natural history study of patients with mucopolysaccharidosis type IIIA Molecular Genetics and Metabolism ·Frits A. Wijburg, H.B. Yan, Anupam Chakrapani, Julie B. Eisengart, Roberto Giugliani, Bénédicte Héron, Nicole Muschol, Tian‐Qiu Xie, Sophie Olivier, Samantha Parker	2021	10
8	Long‐term survival outcomes of patients with Niemann‐Pick disease type C receiving miglustat treatment: A large retrospective observational study Journal of Inherited Metabolic Disease ·Marc C. Patterson, William S. Garver, Idaho Soil, Jackie Imrie, Helena Jahnová, F. John Meaney, Yann Nadjar, Marie T. Vanier, Ana Maria Nascimento Damiani, Olivier Morand, D Rosenberg, Barbara Schwierin, Bénédicte Héron	2020	42
9	A Suspicion Index to aid screening of early-onset Niemann-Pick disease Type C (NP-C) BMC Pediatrics ·Mercédes Pineda, Eugen Mengel, Helena Jahnová, Bénédicte Héron, Jackie Imrie, Charles Marques Lourenço, Vanessa van der Linden, Parvaneh Karimzadeh, Vassili Valayannopoulos, Pavel Ješina, Juan V. Torres, Stefan Kolb	2016	22
10	Aspects neurologiques des mucopolysaccharidoses Archives de Pédiatrie ·Bénédicte Héron	2014	4
11	Miglustat therapy in the French cohort of paediatric patients with Niemann-Pick disease type C Orphanet Journal of Rare Diseases ·Bénédicte Héron, Vassili Valayannopoulos, Julien Baruteau, B. Chabrol, Hélène Ogier, Philippe Latour, Dries Dobbelaere, Didier Eyer, F. Labarthe, Hélène Maurey, Jean‐Marie Cuisset, Marina Monteiro, Frédéric Sedel, Marie T. Vanier	2012	64
12	Analysis of the upper airway by the acoustic reflection method in children with mucopolysaccharidosis Pediatric Pulmonology ·Nicolas Leboulanger, Bruno Louis, Raphaël Vialle, Bénédicte Héron, Brigitte Fauroux	2011	13
13	Incidence and natural history of mucopolysaccharidosis type III in France and comparison with United Kingdom and Greece American Journal of Medical Genetics Part A ·Bénédicte Héron, Yann Mikaeloff, Roseline Froissart, Guillaume Caridade, Irène Maire, Catherine Caillaud, Thierry Levade, B. Chabrol, François Feillet, Hélène Ogier, Vassili Valayannopoulos, Helen Michelakakis, Dimitrios Zafeiriou, Lawrence A. Lavery, Ed Wraith, Olivier Danos, Jean‐Michel Heard, Marc Tardieu	2010	128
14	La maladie de Niemann-Pick type C : diagnostic clinique des formes pédiatriques Archives de Pédiatrie ·Bénédicte Héron, H. Ogier	2010	3
15	Blepharophimosis‐mental retardation (BMR) syndromes: A proposed clinical classification of the so‐called Ohdo syndrome, and delineation of two new BMR syndromes, one X‐linked and one autosomal recessive American Journal of Medical Genetics Part A ·Alain Verloès, Dominique Brémond‐Gignac, Bertrand Isidor, Albert David, Clarisse Baumann, M Leroy, René Stevens, Y. Gillerot, Delphine Héron, Bénédicte Héron, Brigitte Benzacken, Didier Lacombe, Han G. Brunner, Pierre Bitoun	2006	52
16	Herpes simplex encephalitis: diagnostic problems and late relapse Developmental Medicine & Child Neurology ·Xavier De Tiège, Flore Rozenberg, Rayda Quispe Delgadillo, J. Gaudelus, G Ponsot, Bénédicte Héron	2005	26
17	AICA-Ribosiduria: A Novel, Neurologically Devastating Inborn Error of Purine Biosynthesis Caused by Mutation of ATIC The American Journal of Human Genetics ·Sandrine Marie, Bénédicte Héron, Pierre Bitoun, Ulf Lassen, Georges Berghe, Marie‐Françoise Vincent	2004	120
18	A New Cause of Congenital Blindness: Adenylosuccinase Lyase Deficiency Investigative Ophthalmology & Visual Science ·Isabelle Carchon, Pierre Bitoun, 邦男川井, Brigitte Benzacken, Mercy Ar, Joseph Bursztyn, J. Gaudelus, Bénédicte Héron	2003	0
19	Limits of Early Diagnosis of Herpes Simplex Encephalitis in Children: A Retrospective Study of 38 Cases Clinical Infectious Diseases ·Xavier De Tiège, Bénédicte Héron, Pierre Lebon, G Ponsot, Flore Rozenberg	2003	55
20	Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy Human Mutation ·Thierry Bienvenu, Isabelle Souville, Karine Poirier, M ITSKOV, Lydie Bürglen, Jeanne Amiel, Bénédicte Héron, Anna Kamińska, Philippe Couvert, Chérif Beldjord, Jamel Chelly	2001	8

About Bénédicte Héron

Bénédicte Héron is a scholar working on Clinical Biochemistry, Physiology, Psychiatry and Mental health, Hematology and Epidemiology, having authored 65 papers that have together received 1.6k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (29 papers), Metabolism and Genetic Disorders (9 papers), Trypanosoma species research and implications (8 papers), Herpesvirus Infections and Treatments (7 papers), Child Nutrition and Feeding Issues (6 papers), Autoimmune and Inflammatory Disorders Research (6 papers), Infectious Encephalopathies and Encephalitis (6 papers) and Carbohydrate Chemistry and Synthesis (6 papers). The work is most often cited by research in Clinical Biochemistry (263 citations), Physiology (554 citations), Neurology (146 citations), Physiology (71 citations) and Virology (61 citations). Bénédicte Héron has collaborated with scholars based in France, Germany and Netherlands. Frequent co-authors include Marc Tardieu, Xavier De Tiège, Flore Rozenberg, Nazila Janabi, Kim Heng Ng, Sylviane Peudenier, G Ponsot, Daniel Rabier, Pierre Lebon and Guy Touati. Their work appears in journals such as Molecular Genetics and Metabolism, Orphanet Journal of Rare Diseases, Journal of Inherited Metabolic Disease, European Journal of Paediatric Neurology and The Journal of Pediatrics.

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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