Julitta de Bellescize

2.8k total citations
31 papers, 714 citations indexed

About

Julitta de Bellescize is a scholar working on Genetics, Psychiatry and Mental health and Cognitive Neuroscience. According to data from OpenAlex, Julitta de Bellescize has authored 31 papers receiving a total of 714 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 12 papers in Psychiatry and Mental health and 9 papers in Cognitive Neuroscience. Recurrent topics in Julitta de Bellescize's work include Epilepsy research and treatment (12 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (8 papers). Julitta de Bellescize is often cited by papers focused on Epilepsy research and treatment (12 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (8 papers). Julitta de Bellescize collaborates with scholars based in France, United States and Switzerland. Julitta de Bellescize's co-authors include Alexis Arzimanoglou, Gaëtan Lesca, Philippe Ryvlin, Damien Sanlaville, Nadia Boutry‐Kryza, Karine Ostrowsky‐Coste, Audrey Labalme, Patrick Edery, Vania Herbillon and Alexandra Montavont and has published in prestigious journals such as Brain, Epilepsia and Human Brain Mapping.

In The Last Decade

Julitta de Bellescize

29 papers receiving 705 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Julitta de Bellescize France	14	332	274	273	168	158	31	714
Luca De Palma Italy	19	374 1.1×	220 0.8×	268 1.0×	157 0.9×	146 0.9×	64	901
Guohe Tan China	9	188 0.6×	331 1.2×	72 0.3×	140 0.8×	270 1.7×	22	659
Carmela Scuderi Italy	13	120 0.4×	187 0.7×	186 0.7×	51 0.3×	146 0.9×	34	473
Hiroki Kitaura Japan	16	117 0.4×	111 0.4×	123 0.5×	243 1.4×	312 2.0×	35	703
SakkuBai Naidu United States	15	92 0.3×	643 2.3×	354 1.3×	87 0.5×	483 3.1×	18	991
Aurélie Méneret France	14	178 0.5×	131 0.5×	45 0.2×	195 1.2×	159 1.0×	46	704
Seth Dobrin United States	8	80 0.2×	441 1.6×	239 0.9×	89 0.5×	372 2.4×	15	789
Sakkubai Naidu United States	18	88 0.3×	1.0k 3.8×	665 2.4×	123 0.7×	731 4.6×	25	1.3k
Lyudmila Georgieva United Kingdom	10	146 0.4×	670 2.4×	131 0.5×	122 0.7×	516 3.3×	15	1.0k
S. Naidu United States	11	73 0.2×	462 1.7×	385 1.4×	42 0.3×	374 2.4×	15	734

Countries citing papers authored by Julitta de Bellescize

Since Specialization

Citations

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

Fields of papers citing papers by Julitta de Bellescize

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julitta de Bellescize. 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 Julitta de Bellescize. The network helps show where Julitta de Bellescize may publish in the future.

Co-authorship network of co-authors of Julitta de Bellescize

This figure shows the co-authorship network connecting the top 25 collaborators of Julitta de Bellescize. A scholar is included among the top collaborators of Julitta de Bellescize 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 Julitta de Bellescize. Julitta de Bellescize 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

Bouet, Romain, Julien Jung, Jean-Philippe Lachaux, et al.. (2025). Early age at seizure onset is a risk factor for attention deficit hyperactivity disorder in children with epilepsy. Epilepsy & Behavior. 173. 110577–110577.

Faure‐Conter, Cécile, et al.. (2023). Antiseizure effect of MEK inhibitor in a child with neurofibromatosis type 1—Developmental and epileptic encephalopathy and optic pathway glioma. Epileptic Disorders. 26(1). 133–138. 3 indexed citations

Putois, Benjamin, Vania Herbillon, Carlo Cottone, et al.. (2022). Sleep disorders and ADHD symptoms in children and adolescents with typical absence seizures: An observational study. Epilepsy & Behavior. 128. 108513–108513. 6 indexed citations

Bellescize, Julitta de, et al.. (2021). Epileptic phenotype in late-onset hyperinsulinemic hypoglycemia successfully treated by diazoxide. Journal of Pediatric Endocrinology and Metabolism. 34(5). 667–673. 3 indexed citations

Rudolf, Gabrielle, Julitta de Bellescize, Anne de Saint Martin, et al.. (2020). Exome sequencing in 57 patients with self-limited focal epilepsies of childhood with typical or atypical presentations suggests novel candidate genes. European Journal of Paediatric Neurology. 27. 104–110. 11 indexed citations

Ciumas, Carolina, Alexandra Montavont, Agathe Laurent, et al.. (2020). Neural correlates of verbal working memory in children with epilepsy with centro-temporal spikes. NeuroImage Clinical. 28. 102392–102392. 7 indexed citations

Jung, Julien, Romain Bouet, Daniel Gérard, et al.. (2019). BLAST paradigm: A new test to assess brief attentional fluctuations in children with epilepsy, ADHD, and normally developing children. Epilepsy & Behavior. 99. 106470–106470. 4 indexed citations

Panagiotakaki, Eleni, Julitta de Bellescize, Hélène Catenoix, et al.. (2018). SEEG in ... Family. Neuropediatrics. 49(S 01). S1–S12.

Bellescize, Julitta de, Marianne Till, V. Flurin, et al.. (2018). Electrical status epilepticus in sleep, a constitutive feature of Christianson syndrome?. European Journal of Paediatric Neurology. 22(6). 1124–1132. 10 indexed citations

10.

Pons, Linda, Gaëtan Lesca, Damien Sanlaville, et al.. (2018). Neonatal tremor episodes and hyperekplexia‐like presentation at onset in a child with SCN8A developmental and epileptic encephalopathy. Epileptic Disorders. 20(4). 289–294. 9 indexed citations

11.

Herbillon, Vania, Marcela Perrone‐Bertolotti, & Julitta de Bellescize. (2016). Impacts cognitifs des anomalies paroxystiques intercritiques chez l’enfant épileptique : aspects EEG et neuropsychologiques, présentation d’un test cognitif synchronisé à l’EEG. Neurophysiologie Clinique. 46(3). 225–226. 1 indexed citations

12.

Alfaiz, Ali Abdullah, Verena Müller, Nadia Boutry‐Kryza, et al.. (2015). West syndrome caused by homozygous variant in the evolutionary conserved gene encoding the mitochondrial elongation factor GUF1. European Journal of Human Genetics. 24(7). 1001–1008. 13 indexed citations

13.

Dimassi, Sarra, Thomas Simonet, Audrey Jalabert, et al.. (2015). Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA. PubMed. 7. 19–25. 19 indexed citations

14.

Poulat, Anne‐Lise, Dorothée Ville, Julitta de Bellescize, et al.. (2015). Homozygous TBC1D24 mutation in two siblings with familial infantile myoclonic epilepsy (FIME) and moderate intellectual disability. Epilepsy Research. 111. 72–77. 13 indexed citations

15.

Ciumas, Carolina, Vania Herbillon, Agathe Laurent, et al.. (2014). White matter development in children with benign childhood epilepsy with centro-temporal spikes. Brain. 137(4). 1095–1106. 72 indexed citations

16.

Boutry‐Kryza, Nadia, Audrey Labalme, Dorothée Ville, et al.. (2014). Molecular characterization of a cohort of 73 patients with infantile spasms syndrome. European Journal of Medical Genetics. 58(2). 51–58. 51 indexed citations

17.

Bedoin, Nathalie, et al.. (2011). Atypical hemispheric asymmetries for the processing of phonological features in children with rolandic epilepsy. Epilepsy & Behavior. 21(1). 42–51. 25 indexed citations

18.

Ville, Dorothée, Julitta de Bellescize, Hervé Testard, et al.. (2009). Ring 14 chromosome presenting as early‐onset isolated partial epilepsy. Developmental Medicine & Child Neurology. 51(11). 917–922. 14 indexed citations

19.

Bellescize, Julitta de, E Chabrol, Nathalie André‐Obadia, et al.. (2009). A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodes. Epilepsy Research. 85(1). 118–122. 16 indexed citations

20.

Morlet, Thierry, et al.. (2000). Effect of sleep stages on synchronized spontaneous otoacoustic emissions in pre-term neonates. Clinical Neurophysiology. 111(8). 1498–1504. 5 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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