Marie Hully

2.3k total citations
34 papers, 591 citations indexed

About

Marie Hully is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Marie Hully has authored 34 papers receiving a total of 591 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 8 papers in Neurology and 6 papers in Genetics. Recurrent topics in Marie Hully's work include Mitochondrial Function and Pathology (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Microtubule and mitosis dynamics (4 papers). Marie Hully is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Microtubule and mitosis dynamics (4 papers). Marie Hully collaborates with scholars based in France, United Kingdom and United States. Marie Hully's co-authors include Nathalie Boddaert, Nadia Bahi‐Buisson, Isabelle Desguerre, Jamel Chelly, Franck J. Fourniol, Caroline Elie, Isabelle Souville, Chérif Beldjord, Karine Poirier and Rima Nabbout and has published in prestigious journals such as Brain, Neurology and Clinical Neurophysiology.

In The Last Decade

Marie Hully

28 papers receiving 582 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marie Hully France 11 226 165 149 129 106 34 591
Karine Lascelles United Kingdom 16 295 1.3× 137 0.8× 183 1.2× 126 1.0× 136 1.3× 25 858
Naomi Hino‐Fukuyo Japan 17 454 2.0× 107 0.6× 137 0.9× 168 1.3× 91 0.9× 59 901
A. Mrabet Tunisia 12 184 0.8× 143 0.9× 128 0.9× 122 0.9× 179 1.7× 59 716
Rosario Domingo‐Jiménez Spain 14 224 1.0× 77 0.5× 145 1.0× 70 0.5× 92 0.9× 48 648
Ichiro Kuki Japan 13 203 0.9× 106 0.6× 143 1.0× 32 0.2× 107 1.0× 87 675
Shin Okazaki Japan 12 243 1.1× 66 0.4× 160 1.1× 34 0.3× 112 1.1× 79 620
R. Gaggero Italy 16 162 0.7× 199 1.2× 227 1.5× 64 0.5× 153 1.4× 33 715
Sylvie Joriot France 10 219 1.0× 93 0.6× 185 1.2× 101 0.8× 45 0.4× 27 509
D Fontan France 14 271 1.2× 181 1.1× 152 1.0× 56 0.4× 149 1.4× 43 719
Yoshiteru Azuma Japan 13 168 0.7× 62 0.4× 67 0.4× 49 0.4× 33 0.3× 34 464

Countries citing papers authored by Marie Hully

Since Specialization
Citations

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

Fields of papers citing papers by Marie Hully

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marie Hully

This figure shows the co-authorship network connecting the top 25 collaborators of Marie Hully. A scholar is included among the top collaborators of Marie Hully 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 Marie Hully. Marie Hully 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.
Bélot, Alexandre, Odile Boespflug‐Tanguy, Guilaine Boursier, et al.. (2025). French protocol for diagnosis and management of type 1 interferonopathies. La Revue de Médecine Interne. 46(6). 320–340.
2.
Barcia, Giulia, Marlène Rio, Cyril Gitiaux, et al.. (2024). Exploring the clinical spectrum of CNTNAP2-related neurodevelopmental disorders: A case series and a literature appraisal. European Journal of Medical Genetics. 72. 104979–104979.
3.
Villagrán‐García, Macarena, Marie Bénaiteau, Antonio Farina, et al.. (2024). Specific clinical and radiological characteristics of anti-NMDA receptor autoimmune encephalitis following herpes encephalitis. Journal of Neurology. 271(10). 6692–6701. 4 indexed citations
4.
Roux, Charles‐Joris, Marie Hully, Agnès Rötig, et al.. (2024). Polyradiculoneuritis on MRI. Neurology. 102(11). e209356–e209356.
5.
Bernheim, Susannah M., et al.. (2024). Abnormal movements following heart surgery: A series of pediatric post-pump chorea. Archives of cardiovascular diseases. 117(8-9). S234–S234.
6.
Zanin, Sofia, Anne Guimier, Marie Hully, et al.. (2023). Novel ELAC2 Mutations in Individuals Presenting with Variably Severe Neurological Disease in the Presence or Absence of Cardiomyopathy. Life. 13(2). 445–445. 4 indexed citations
7.
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
8.
Lebigot, Élise, Marie Hully, Larbi Amazit, et al.. (2020). Expanding the phenotype of mitochondrial disease: Novel pathogenic variant in ISCA1 leading to instability of the iron-sulfur cluster in the protein. Mitochondrion. 52. 75–82. 6 indexed citations
9.
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
10.
Toulouse, Joseph, Marie Hully, David Brossier, et al.. (2018). The role of the neuropediatrician in pediatric intensive care unit: Diagnosis, therapeutics and major participation in collaborative multidisciplinary deliberations about life-sustaining treatments’ withdrawal. European Journal of Paediatric Neurology. 23(1). 171–180. 2 indexed citations
11.
Cavallin, Mara, Marie Hully, Nathalie Boddaert, et al.. (2018). TLE1, a key player in neurogenesis, a new candidate gene for autosomal recessive postnatal microcephaly. European Journal of Medical Genetics. 61(12). 729–732. 7 indexed citations
12.
Gitiaux, Cyril, Anna Kamińska, Nathalie Boddaert, et al.. (2018). PLA2G6-associated neurodegeneration: Lessons from neurophysiological findings. European Journal of Paediatric Neurology. 22(5). 854–861. 6 indexed citations
13.
Eisermann, Monika, H Simonnet, Marie Hully, et al.. (2017). Unilateral predominance of abnormal movements: A characteristic feature of the pediatric anti-NMDA receptor encephalitis?. Epilepsy & Behavior Case Reports. 7. 42–44. 3 indexed citations
14.
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
15.
Hully, Marie, Juliette Ropars, Laurence Hubert, et al.. (2016). Mosaicism in ATP1A3-related disorders: not just a theoretical risk. Neurogenetics. 18(1). 23–28. 24 indexed citations
16.
Liso, Paola De, Nicole Chémaly, Jacques Laschet, et al.. (2016). Patients with dravet syndrome in the era of stiripentol: A French cohort cross-sectional study. Epilepsy Research. 125. 42–46. 47 indexed citations
17.
Bahi‐Buisson, Nadia, Karine Poirier, Franck J. Fourniol, et al.. (2014). The wide spectrum of tubulinopathies: what are the key features for the diagnosis?. Brain. 137(6). 1676–1700. 190 indexed citations
18.
Desguerre, I., Marie Hully, Marlène Rio, & Rima Nabbout. (2014). Mitochondrial disorders and epilepsy. Revue Neurologique. 170(5). 375–380. 11 indexed citations
19.
Gitiaux, Cyril, Marie Hully, Andoni Echaniz‐Laguna, et al.. (2014). Progressive demyelinating neuropathy correlates with clinical severity in Cockayne syndrome. Clinical Neurophysiology. 126(7). 1435–1439. 12 indexed citations
20.
Bahi‐Buisson, Nadia, Isabelle Souville, Franck J. Fourniol, et al.. (2013). New insights into genotype–phenotype correlations for the doublecortin-related lissencephaly spectrum. Brain. 136(1). 223–244. 74 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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