Giulia Barcia

3.4k total citations
56 papers, 1.3k citations indexed

About

Giulia Barcia is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Giulia Barcia has authored 56 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 20 papers in Genetics and 14 papers in Psychiatry and Mental health. Recurrent topics in Giulia Barcia's work include Mitochondrial Function and Pathology (16 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Epilepsy research and treatment (12 papers). Giulia Barcia is often cited by papers focused on Mitochondrial Function and Pathology (16 papers), Genetics and Neurodevelopmental Disorders (14 papers) and Epilepsy research and treatment (12 papers). Giulia Barcia collaborates with scholars based in France, United States and Italy. Giulia Barcia's co-authors include Rima Nabbout, Olivier Dulac, Isabelle Desguerre, Nathalie Boddaert, Arnold Münnich, Nicole Chémaly, Laurence Colleaux, Leonard K. Kaczmarek, Jack Kronengold and Anna Kamińska and has published in prestigious journals such as Nature Genetics, Neurology and Journal of Neurophysiology.

In The Last Decade

Giulia Barcia

53 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giulia Barcia France 17 583 539 501 292 221 56 1.3k
Tiziana Pisano Italy 17 420 0.7× 537 1.0× 448 0.9× 286 1.0× 248 1.1× 49 1.1k
Bobby P.C. Koeleman Netherlands 23 482 0.8× 819 1.5× 547 1.1× 368 1.3× 315 1.4× 48 1.4k
Amy McTague United Kingdom 16 344 0.6× 640 1.2× 653 1.3× 223 0.8× 275 1.2× 32 1.2k
Katherine L. Helbig United States 20 641 1.1× 411 0.8× 1.1k 2.1× 232 0.8× 145 0.7× 42 1.6k
Zaid Afawi Israel 17 442 0.8× 449 0.8× 441 0.9× 266 0.9× 90 0.4× 27 1.1k
Marina Trivisano Italy 25 460 0.8× 875 1.6× 644 1.3× 307 1.1× 406 1.8× 104 1.7k
Dorothée Ville France 20 355 0.6× 367 0.7× 559 1.1× 172 0.6× 230 1.0× 56 1.2k
Xinhua Bao China 24 1.1k 1.9× 388 0.7× 864 1.7× 363 1.2× 148 0.7× 130 2.0k
Ikuyo Inoue Japan 10 576 1.0× 512 0.9× 324 0.6× 527 1.8× 100 0.5× 19 1.1k
G Kurlemann Germany 17 399 0.7× 626 1.2× 250 0.5× 306 1.0× 250 1.1× 40 1.4k

Countries citing papers authored by Giulia Barcia

Since Specialization
Citations

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

Fields of papers citing papers by Giulia Barcia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giulia Barcia

This figure shows the co-authorship network connecting the top 25 collaborators of Giulia Barcia. A scholar is included among the top collaborators of Giulia Barcia 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 Giulia Barcia. Giulia Barcia 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.
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.
2.
Roux, Charles‐Joris, Marie Hully, Agnès Rötig, et al.. (2024). Polyradiculoneuritis on MRI. Neurology. 102(11). e209356–e209356.
3.
Nabbout, Rima, Mélodie Aubart, Giulia Barcia, et al.. (2024). Transition from pediatric to adult care system in patients with complex epilepsies: Necker model for transition evaluated on 70 consecutive patients. Epilepsia. 66(1). 134–147. 5 indexed citations
4.
Bui, Mai Thao, Gorka Fernández‐Eulate, Teresinha Evangelista, et al.. (2024). Relevance of muscle biopsies in the neonatal and early infantile period: a 52 years retrospective study in the gene-sequencing era. Acta Neuropathologica Communications. 12(1). 191–191. 1 indexed citations
5.
Grévent, D., Mélodie Aubart, Manoëlle Kossorotoff, et al.. (2023). Clinical and radiological description of 120 pediatric stroke‐like episodes. European Journal of Neurology. 30(7). 2051–2061. 2 indexed citations
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.
McTague, Amy, Andreas Brunklaus, Giulia Barcia, et al.. (2022). Defining causal variants in rare epilepsies: an essential team effort between biomedical scientists, geneticists and epileptologists. European Journal of Medical Genetics. 65(7). 104531–104531. 3 indexed citations
8.
Breton, Sylvain, Marie‐Liesse Piketty, Alexandra Afenjar, et al.. (2022). SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients. Orphanet Journal of Rare Diseases. 17(1). 100–100. 10 indexed citations
9.
Patat, Olivier, Sandra Whalen, Lionel Arnaud, et al.. (2021). Patients with KCNH1 -related intellectual disability without distinctive features of Zimmermann-Laband/Temple-Baraitser syndrome. Journal of Medical Genetics. 59(5). 505–510. 8 indexed citations
10.
Ruzzenente, Benedetta, Charles‐Joris Roux, Giulia Barcia, et al.. (2021). Cerebral blood flow and acute episodes of Leigh syndrome in neurometabolic disorders. Developmental Medicine & Child Neurology. 63(6). 705–711. 4 indexed citations
11.
Rötig, Agnès, Charles‐Joris Roux, R. Lévy, et al.. (2020). Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?. Journal of Medical Genetics. 59(2). 204–208. 5 indexed citations
12.
Barcia, Giulia, Marlène Rio, Zahra Assouline, et al.. (2020). Novel FARS2 variants in patients with early onset encephalopathy with or without epilepsy associated with long survival. European Journal of Human Genetics. 29(3). 533–538. 8 indexed citations
13.
Steffann, Julie, Sophie Monnot, Zahra Assouline, et al.. (2020). A retrospective study on the efficacy of prenatal diagnosis for pregnancies at risk of mitochondrial DNA disorders. Genetics in Medicine. 23(4). 720–731. 9 indexed citations
14.
Grévent, D., Marlène Rio, Isabelle Desguerre, et al.. (2018). High predictive value of brain MRI imaging in primary mitochondrial respiratory chain deficiency. Journal of Medical Genetics. 55(6). 378–383. 12 indexed citations
15.
Fleming, Matthew R., Maile R. Brown, Jack Kronengold, et al.. (2016). Stimulation of Slack K+ Channels Alters Mass at the Plasma Membrane by Triggering Dissociation of a Phosphatase-Regulatory Complex. Cell Reports. 16(9). 2281–2288. 31 indexed citations
16.
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
17.
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
18.
Barcia, Giulia, Matthew R. Fleming, Valeswara‐Rao Gazula, et al.. (2012). De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy. Nature Genetics. 44(11). 1255–1259. 335 indexed citations
19.
Cordelli, Duccio Maria, Riccardo Masetti, Bruno De Bernardi, et al.. (2011). Status epilepticus as a main manifestation of posterior reversible encephalopathy syndrome after pediatric hematopoietic stem cell transplantation. Pediatric Blood & Cancer. 58(5). 785–790. 43 indexed citations
20.
Parmeggiani, Antonia, Giulia Barcia, Annio Posar, et al.. (2010). Epilepsy and EEG paroxysmal abnormalities in autism spectrum disorders. Brain and Development. 32(9). 783–789. 91 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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