Christine Barnérias

4.9k total citations
73 papers, 1.4k citations indexed

About

Christine Barnérias is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Christine Barnérias has authored 73 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 26 papers in Genetics and 16 papers in Surgery. Recurrent topics in Christine Barnérias's work include Neurogenetic and Muscular Disorders Research (25 papers), Congenital Anomalies and Fetal Surgery (12 papers) and Metabolism and Genetic Disorders (8 papers). Christine Barnérias is often cited by papers focused on Neurogenetic and Muscular Disorders Research (25 papers), Congenital Anomalies and Fetal Surgery (12 papers) and Metabolism and Genetic Disorders (8 papers). Christine Barnérias collaborates with scholars based in France, Italy and Chile. Christine Barnérias's co-authors include Isabelle Desguerre, Rima Nabbout, Pascale de Lonlay, Nathalie Boddaert, Cyril Gitiaux, Jean‐Marie Saudubray, Nadia Bahi‐Buisson, Olivier Dulac, C. Marsac and M. Brivet and has published in prestigious journals such as Neurology, PEDIATRICS and Journal of Clinical Microbiology.

In The Last Decade

Christine Barnérias

68 papers receiving 1.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Christine Barnérias France 20 704 283 236 203 193 73 1.4k
Göknur Haliloğlu Türkiye 23 922 1.3× 259 0.9× 183 0.8× 110 0.5× 236 1.2× 116 1.7k
Denise Cassandrini Italy 23 735 1.0× 176 0.6× 228 1.0× 99 0.5× 132 0.7× 62 1.3k
Esther Leshinsky‐Silver Israel 25 928 1.3× 522 1.8× 287 1.2× 171 0.8× 71 0.4× 76 1.7k
Bruno Maranda Canada 23 714 1.0× 394 1.4× 260 1.1× 93 0.5× 93 0.5× 57 1.4k
Gerald Pfeffer Canada 22 1.2k 1.7× 160 0.6× 449 1.9× 140 0.7× 191 1.0× 75 1.9k
Nancy D. Leslie United States 18 929 1.3× 261 0.9× 401 1.7× 100 0.5× 172 0.9× 37 1.7k
Philippe Latour France 28 733 1.0× 137 0.5× 99 0.4× 180 0.9× 118 0.6× 103 2.5k
Andreas Hahn Germany 21 680 1.0× 183 0.6× 54 0.2× 130 0.6× 224 1.2× 93 1.3k
Patricia Dickson United States 23 415 0.6× 291 1.0× 85 0.4× 426 2.1× 144 0.7× 109 1.9k
Marc Engelen Netherlands 28 1.9k 2.7× 240 0.8× 832 3.5× 133 0.7× 185 1.0× 97 2.6k

Countries citing papers authored by Christine Barnérias

Since Specialization
Citations

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

Fields of papers citing papers by Christine Barnérias

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christine Barnérias

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

All Works

20 of 20 papers shown
1.
Degrelle, Séverine A., Brigitte Bader‐Meunier, Christine Barnérias, et al.. (2025). Muscle Spatial Transcriptomic Reveals Heterogeneous Profiles in Juvenile Dermatomyositis and Persistence of Abnormal Signature After Remission. Cells. 14(12). 939–939.
2.
Barrois, Rémi, Lucie Griffon, Christine Barnérias, et al.. (2024). Polysomnography findings and respiratory muscle function in infants with early onset spinal muscular atrophy after gene replacement as monotherapy: A prospective study. Sleep Medicine. 119. 335–341. 1 indexed citations
3.
Barnérias, Christine, Mehrdad A. Estiar, Claire Ewenczyk, et al.. (2024). From spastic paraplegia to infantile neurodegenerative disorder: Expanding the phenotypic spectrum associated with biallelic SPAST variants. European Journal of Neurology. 32(1). e70025–e70025. 2 indexed citations
4.
Barrois, Rémi, et al.. (2023). Correlations between clinical motor scores and CMAP in patients with type 2 spinal muscular amyotrophy treated with nusinersen. Archives de Pédiatrie. 31(1). 26–31. 3 indexed citations
5.
Taglietti, Valentina, Kaouthar Kefi, Cyril Gitiaux, et al.. (2023). Myopathologic trajectory in Duchenne muscular dystrophy (DMD) reveals lack of regeneration due to senescence in satellite cells. Acta Neuropathologica Communications. 11(1). 167–167. 24 indexed citations
6.
Brassier, Anaïs, Samia Pichard, Manuel Schiff, et al.. (2023). Motor outcomes in patients with infantile and juvenile Pompe disease: Lessons from neurophysiological findings. Molecular Genetics and Metabolism. 139(4). 107650–107650. 1 indexed citations
7.
Castiglioni, Claudia, François Feillet, Christine Barnérias, et al.. (2020). Expanding the phenotype of X‐linked SSR4–CDG: Connective tissue implications. Human Mutation. 42(2). 142–149. 13 indexed citations
8.
Barnérias, Christine, Christine Bodemer, Isabelle Desguerre, et al.. (2020). From Diagnosis to Prognosis: Revisiting the Meaning of Muscle ISG15 Overexpression in Juvenile Inflammatory Myopathies. Arthritis & Rheumatology. 73(6). 1044–1052. 14 indexed citations
9.
Ropars, Juliette, et al.. (2020). Multidisciplinary approach and psychosocial management of spinal muscular atrophy (SMA). Archives de Pédiatrie. 27(7). 7S45–7S49. 12 indexed citations
10.
Ropars, Juliette, Christine Barnérias, Marie Hully, et al.. (2019). Thoracic circumference: A new outcome measure in spinal muscular atrophy type 1?. Neuromuscular Disorders. 29(6). 415–421. 7 indexed citations
11.
Chareyre, Judith, Marie Hully, H Simonnet, et al.. (2017). Acute axonal neuropathy subtype of Guillain Barré syndrome in a French pediatric series: Adequate follow-up may require repetitive electrophysiological studies. European Journal of Paediatric Neurology. 21(6). 891–897. 5 indexed citations
12.
Griffon, Lucie, Alessandro Amaddeo, Guillaume Mortamet, et al.. (2016). Sleep study as a diagnostic tool for unexplained respiratory failure in infants hospitalized in the PICU. Journal of Critical Care. 42. 317–323. 8 indexed citations
13.
Gitiaux, Cyril, Nicole Chémaly, Susana Quijano-Roy, et al.. (2016). Motor neuropathy contributes to crouching in patients with Dravet syndrome. Neurology. 87(3). 277–281. 31 indexed citations
14.
Tauziède‐Espariat, Arnault, A. Maues de Paula, Mélanie Pagès, et al.. (2015). Primary Leptomeningeal Gliomatosis in Children and Adults. Neurosurgery. 78(3). 343–352. 9 indexed citations
15.
Barcia, Giulia, Nicole Chémaly, Stéphanie Gobin, et al.. (2013). Early epileptic encephalopathies associated with STXBP1 mutations: Could we better delineate the phenotype?. European Journal of Medical Genetics. 57(1). 15–20. 42 indexed citations
16.
Barcia, Giulia, Christine Barnérias, Marlène Rio, et al.. (2013). A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiency. European Journal of Medical Genetics. 56(12). 683–685. 9 indexed citations
17.
Assouline, Zahra, Marguerite Jambou, Marlène Rio, et al.. (2012). A constant and similar assembly defect of mitochondrial respiratory chain complex I allows rapid identification of NDUFS4 mutations in patients with Leigh syndrome. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(6). 1062–1069. 44 indexed citations
18.
Bader‐Meunier, Brigitte, Dominique Monnet, Christine Barnérias, et al.. (2012). Thrombotic Microangiopathy and Purtscher-like Retinopathy as a Rare Presentation of Juvenile Dermatomyositis. PEDIATRICS. 129(3). e821–e824. 15 indexed citations
19.
Barnérias, Christine, Jean‐Marie Saudubray, Guy Touati, et al.. (2009). Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis. Developmental Medicine & Child Neurology. 52(2). e1–9. 119 indexed citations
20.
Barnérias, Christine, Irina Giurgea, Lucie Hertz‐Pannier, et al.. (2006). Respiratory chain deficiency in a female with Aicardi-Goutières syndrome. Developmental Medicine & Child Neurology. 48(3). 227–230. 12 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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