Fanny Mochel

9.8k total citations · 1 hit paper
123 papers, 4.1k citations indexed

About

Fanny Mochel is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Fanny Mochel has authored 123 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 44 papers in Cellular and Molecular Neuroscience and 38 papers in Clinical Biochemistry. Recurrent topics in Fanny Mochel's work include Mitochondrial Function and Pathology (39 papers), Metabolism and Genetic Disorders (38 papers) and Genetic Neurodegenerative Diseases (34 papers). Fanny Mochel is often cited by papers focused on Mitochondrial Function and Pathology (39 papers), Metabolism and Genetic Disorders (38 papers) and Genetic Neurodegenerative Diseases (34 papers). Fanny Mochel collaborates with scholars based in France, United States and Netherlands. Fanny Mochel's co-authors include Alexandra Dürr, Ronald G. Haller, Isaac Adanyeguh, Raphael Schiffmann, Jean‐Marie Saudubray, Foudil Lamari, Charles R. Roe, Romain Valabrègue, Emmanuel Roze and Pierre-Gilles Henry and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Neuron.

In The Last Decade

Fanny Mochel

121 papers receiving 4.0k 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.

Promoting the clearance of neurotoxic proteins in neurodegenerative disorders of ageing

2018 394 citations Fanny Mochel et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Fanny Mochel France	35	2.3k	1.2k	815	722	702	123	4.1k
Raffaele Lodi Italy	47	3.2k 1.4×	1.6k 1.3×	688 0.8×	1.5k 2.1×	639 0.9×	231	6.5k
Barbara Garavaglia Italy	36	2.0k 0.9×	815 0.7×	501 0.6×	998 1.4×	1.4k 2.0×	152	4.0k
Charalampos Tzoulis Norway	31	1.8k 0.8×	656 0.5×	429 0.5×	896 1.2×	751 1.1×	95	3.0k
Stefan Vielhaber Germany	45	2.1k 0.9×	1.4k 1.1×	1.3k 1.6×	2.7k 3.8×	481 0.7×	166	5.8k
Rudy Van Coster Belgium	39	3.7k 1.6×	665 0.5×	345 0.4×	473 0.7×	1.4k 1.9×	156	5.5k
Gráinne S. Gorman United Kingdom	33	3.8k 1.7×	633 0.5×	409 0.5×	599 0.8×	2.0k 2.8×	118	5.0k
Thomas Klopstock Germany	46	5.1k 2.2×	1.8k 1.4×	860 1.1×	1.3k 1.9×	1.7k 2.4×	198	7.7k
Tiziana Granata Italy	39	1.5k 0.7×	2.0k 1.6×	411 0.5×	703 1.0×	330 0.5×	142	5.9k
Caroline Graff Sweden	40	3.1k 1.4×	883 0.7×	3.2k 3.9×	730 1.0×	476 0.7×	159	6.5k
Hoon‐Chul Kang South Korea	44	2.5k 1.1×	1.0k 0.8×	1.9k 2.3×	333 0.5×	1.5k 2.2×	237	6.6k

Countries citing papers authored by Fanny Mochel

Since Specialization

Citations

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

Fields of papers citing papers by Fanny Mochel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fanny Mochel

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

Langeveld, Mirjam, Sandra Sirrs, Timothy Fazio, et al.. (2025). Screening for Life: Perspectives From Adult Metabolic Specialists on Newborn Screening for Inherited Metabolic Diseases. Journal of Inherited Metabolic Disease. 48(4). e70057–e70057. 1 indexed citations

Semeraro, Michaëla, Fabienne Marquant, Laurence Robel, et al.. (2025). Allopurinol Treatment Improves Cognitive Skills, Adaptive Behavior, and Biochemical Markers in Young Patients With Adenylosuccinate Lyase Deficiency. Journal of Inherited Metabolic Disease. 48(6). e70092–e70092. 1 indexed citations

Sevin, Caroline & Fanny Mochel. (2024). Hematopoietic stem cell transplantation in leukodystrophies. Handbook of clinical neurology. 204. 355–366. 2 indexed citations

Charif, Majida, Arnaud Chevrollier, Naïg Guéguen, et al.. (2022). Next-Generation Sequencing Identifies Novel PMPCA Variants in Patients with Late-Onset Dominant Optic Atrophy. Genes. 13(7). 1202–1202. 1 indexed citations

Lejeune, François‐Xavier, Farid Ichou, Benoît Colsch, et al.. (2022). A Multimodal Omics Exploration of the Motor and Non-Motor Symptoms of Parkinson’s Disease. SHILAP Revista de lepidopterología. 2(1). 97–112. 3 indexed citations

Wiehler, Antonius, Francesca Branzoli, Isaac Adanyeguh, Fanny Mochel, & Mathias Pessiglione. (2022). A neuro-metabolic account of why daylong cognitive work alters the control of economic decisions. Current Biology. 32(16). 3564–3575.e5. 79 indexed citations

Wilson, Jenny L., Allison Gregory, Manju A. Kurian, et al.. (2021). Consensus clinical management guideline for beta‐propeller protein‐associated neurodegeneration. Developmental Medicine & Child Neurology. 63(12). 1402–1409. 23 indexed citations

Doummar, Diane, Thierry Bienvenu, Perrine Charles, et al.. (2021). Tremor-like subcortical myoclonus in STXBP1 encephalopathy. European Journal of Paediatric Neurology. 34. 62–66. 4 indexed citations

Keren, Boris, et al.. (2021). Dysfunctional Homozygous VRK1-D263G Variant Impairs the Assembly of Cajal Bodies and DNA Damage Response in Hereditary Spastic Paraplegia. Neurology Genetics. 7(5). e624–e624. 5 indexed citations

10.

Stelten, Bianca M. L., Maria Teresa Dotti, Aad Verrips, et al.. (2021). Expert opinion on diagnosing, treating and managing patients with cerebrotendinous xanthomatosis (CTX): a modified Delphi study. Orphanet Journal of Rare Diseases. 16(1). 353–353. 26 indexed citations

11.

Laemmle, Alexander, André Schaller, Andrea Felser, et al.. (2021). Triheptanoin – Novel therapeutic approach for the ultra-rare disease mitochondrial malate dehydrogenase deficiency. Molecular Genetics and Metabolism Reports. 29. 100814–100814. 12 indexed citations

12.

Arystarkhova, Elena, Ihtsham Haq, Fanny Mochel, et al.. (2019). Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition. Neurobiology of Disease. 132. 104577–104577. 28 indexed citations

13.

Masingue, Marion, Isaac Adanyeguh, Maya Tchikviladzé, et al.. (2018). Quantitative neuroimaging biomarkers in a series of 20 adult patients with POLG mutations. Mitochondrion. 45. 22–28. 6 indexed citations

14.

Chabrol, B., Pierre Broué, D. Dobbelaere, et al.. (2018). Transition from pediatric to adult care in adolescents with hereditary metabolic diseases: Specific guidelines from the French network for rare inherited metabolic diseases (G2M). Archives de Pédiatrie. 25(5). 344–349. 15 indexed citations

15.

Mochel, Fanny & Ronald G. Haller. (2016). Myopathy with Deficiency of ISCU. 7 indexed citations

16.

Mochel, Fanny. (2015). Outline of metabolic diseases in adult neurology. Revue Neurologique. 171(6-7). 531–538. 1 indexed citations

17.

Mochel, Fanny, Dinesh K. Deelchand, Daisy Rinaldi, et al.. (2012). Abnormal response to cortical activation in early stages of Huntington disease. Movement Disorders. 27(7). 907–910. 39 indexed citations

18.

Mochel, Fanny, Catherine Sarret, Éléonore Eymard-Pierre, et al.. (2010). Elevated CSF N-acetylaspartylglutamate suggests specific molecular diagnostic abnormalities in patients with white matter diseases. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802(11). 1112–1117. 15 indexed citations

19.

Engelke, Udo F. H., Fokje Zijlstra, Fanny Mochel, et al.. (2010). Mitochondrial involvement and erythronic acid as a novel biomarker in transaldolase deficiency. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802(11). 1028–1035. 34 indexed citations

20.

Mochel, Fanny, Abdelhamid Slama, Guy Touati, et al.. (2005). Respiratory Chain Defects May Present Only with Hypoglycemia. The Journal of Clinical Endocrinology & Metabolism. 90(6). 3780–3785. 23 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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