Annabelle Chaussenot

2.6k total citations
35 papers, 870 citations indexed

About

Annabelle Chaussenot is a scholar working on Molecular Biology, Clinical Biochemistry and Neurology. According to data from OpenAlex, Annabelle Chaussenot has authored 35 papers receiving a total of 870 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 5 papers in Neurology. Recurrent topics in Annabelle Chaussenot's work include Mitochondrial Function and Pathology (21 papers), Metabolism and Genetic Disorders (12 papers) and ATP Synthase and ATPases Research (10 papers). Annabelle Chaussenot is often cited by papers focused on Mitochondrial Function and Pathology (21 papers), Metabolism and Genetic Disorders (12 papers) and ATP Synthase and ATPases Research (10 papers). Annabelle Chaussenot collaborates with scholars based in France, United Kingdom and Denmark. Annabelle Chaussenot's co-authors include Véronique Paquis‐Flucklinger, Cécile Rouzier, Sylvie Bannwarth, Konstantina Fragaki, B. Chabrol, Samira Ait-El-Mkadem, Vincent Procaccio, Jean Pouget, Valérie Serre and Annie Verschueren and has published in prestigious journals such as Brain, Annals of Neurology and Human Molecular Genetics.

In The Last Decade

Annabelle Chaussenot

33 papers receiving 860 citations

Peers

Annabelle Chaussenot

CMN

PHYSI

Pengfei Lin China

Ginat Narkis Israel

Emil Ylikallio Finland

Sonia Ciarmatori Germany

Anna Ardissone Italy

Edoardo Malfatti France

Chandree L. Beaulieu Canada

Sarah B. Mueller United States

Chiara Aiello Italy

Michiel Krols Belgium

Pengfei Lin China

Annabelle Chaussenot

445 ×0.7

124 ×0.6

105 ×0.6

169 ×1.2

CMN

88 ×0.8

PHYSI

Citations per year, relative to Annabelle Chaussenot Annabelle Chaussenot (= 1×) peers Pengfei Lin

Countries citing papers authored by Annabelle Chaussenot

Since Specialization

Citations

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

Fields of papers citing papers by Annabelle Chaussenot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annabelle Chaussenot

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

Chaussenot, Annabelle, Xavier Ayrignac, Nicolas Chatron, et al.. (2024). Loss of heterozygosity in CCM2 cDNA revealing a structural variant causing multiple cerebral cavernous malformations. European Journal of Human Genetics. 32(7). 876–878. 2 indexed citations

Plutino, Morgane, Perrine Charles, Jean‐Philippe Azulay, et al.. (2023). A Case Report of SYNE1 Deficiency-Mimicking Mitochondrial Disease and the Value of Pangenomic Investigations. Genes. 14(12). 2154–2154. 1 indexed citations

Kaphan, Elsa, Konstantina Fragaki, Annabelle Chaussenot, et al.. (2022). Splicing variants in NARS2 are associated with milder phenotypes and intra-familial variability. European Journal of Medical Genetics. 65(12). 104643–104643. 3 indexed citations

Chaussenot, Annabelle, Gérard Besson, Foudil Lamari, et al.. (2019). Cholic acid as a treatment for cerebrotendinous xanthomatosis in adults. Journal of Neurology. 266(8). 2043–2050. 30 indexed citations

Fragaki, Konstantina, Annabelle Chaussenot, Valérie Serre, et al.. (2019). A novel variant m.8561C>T in the overlapping region of MT-ATP6 and MT-ATP8 in a child with early-onset severe neurological signs. Molecular Genetics and Metabolism Reports. 21. 100543–100543. 12 indexed citations

Plutino, Morgane, Annabelle Chaussenot, Cécile Rouzier, et al.. (2018). Targeted next generation sequencing with an extended gene panel does not impact variant detection in mitochondrial diseases. BMC Medical Genetics. 19(1). 57–57. 19 indexed citations

Stojkovic, Tanya, Amandine Boyer, Nathalie Martini, et al.. (2018). Molecular diagnosis of inherited peripheral neuropathies by targeted next-generation sequencing: molecular spectrum delineation. BMJ Open. 8(10). e021632–e021632. 40 indexed citations

Rouzier, Cécile, David Moore, Cécile Delorme, et al.. (2017). A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions. Human Molecular Genetics. 26(9). 1599–1611. 52 indexed citations

Fragaki, Konstantina, Annabelle Chaussenot, Jean‐François Benoist, et al.. (2016). Coenzyme Q10 defects may be associated with a deficiency of Q10-independent mitochondrial respiratory chain complexes. Biological Research. 49(1). 4–4. 16 indexed citations

10.

Lebrun‐Frénay, Christine, Mikaël Cohen, Annabelle Chaussenot, Lydiane Mondot, & S. Chanalet. (2014). A Prospective Study of Patients with Brain MRI Showing Incidental T2 Hyperintensities Addressed as Multiple Sclerosis: a Lot of Work to do Before Treating. Neurology and Therapy. 3(2). 123–132. 18 indexed citations

11.

Chaussenot, Annabelle, Isabelle Le Ber, Samira Ait-El-Mkadem, et al.. (2014). Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients. Neurobiology of Aging. 35(12). 2884.e1–2884.e4. 68 indexed citations

12.

Chaussenot, Annabelle & Véronique Paquis‐Flucklinger. (2014). An overview of neurological and neuromuscular signs in mitochondrial diseases. Revue Neurologique. 170(5). 323–338. 6 indexed citations

13.

Rouzier, Cécile, Annabelle Chaussenot, Valérie Serre, et al.. (2013). Quantitative multiplex PCR of short fluorescent fragments for the detection of large intragenic POLG rearrangements in a large French cohort. European Journal of Human Genetics. 22(4). 542–550. 28 indexed citations

14.

Ribière, Catherine, Annabelle Chaussenot, Véronique Paquis‐Flucklinger, et al.. (2013). Troubles vésicosphinctériens au cours du syndrome de Wolfram. Progrès en Urologie. 23(8). 519–523. 6 indexed citations

15.

Fragaki, Konstantina, Aline Cano, Jean‐François Benoist, et al.. (2011). Fatal heart failure associated with CoQ10 and multiple OXPHOS deficiency in a child with propionic acidemia. Mitochondrion. 11(3). 533–536. 31 indexed citations

16.

Rouzier, Cécile, Sylvie Bannwarth, Annabelle Chaussenot, et al.. (2011). The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype. Brain. 135(1). 23–34. 176 indexed citations

17.

Chaussenot, Annabelle, Sylvie Bannwarth, Cécile Rouzier, et al.. (2010). Neurologic features and genotype‐phenotype correlation in Wolfram syndrome. Annals of Neurology. 69(3). 501–508. 98 indexed citations

18.

Rouzier, Cécile, Konstantina Fragaki, Valérie Serre, et al.. (2010). The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 protein. Journal of Medical Genetics. 47(10). 670–676. 37 indexed citations

19.

Chaussenot, Annabelle, et al.. (2008). Ataxie cérébelleuse tardive due à la prémutation de l’X fragile. Revue Neurologique. 164(11). 957–963. 1 indexed citations

20.

Chaussenot, Annabelle, et al.. (2007). Neurosarcoïdose et mycophénolate mofétil. Revue Neurologique. 163(4). 471–475. 20 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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