Sımona Baldassari

1.1k total citations
22 papers, 399 citations indexed

About

Sımona Baldassari is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Sımona Baldassari has authored 22 papers receiving a total of 399 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 7 papers in Cellular and Molecular Neuroscience and 7 papers in Genetics. Recurrent topics in Sımona Baldassari's work include Pluripotent Stem Cells Research (5 papers), RNA regulation and disease (4 papers) and Genomics and Rare Diseases (3 papers). Sımona Baldassari is often cited by papers focused on Pluripotent Stem Cells Research (5 papers), RNA regulation and disease (4 papers) and Genomics and Rare Diseases (3 papers). Sımona Baldassari collaborates with scholars based in Italy, United States and Germany. Sımona Baldassari's co-authors include Federico Zara, Floriana Fruscione, Carlo Minetti, Elisabetta Gazzerro, Stefania Assereto, Fabio Benfenati, Anna Corradi, Ilaria Musante, Bruno Sterlini and Paolo Scudieri and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Nature Cell Biology.

In The Last Decade

Sımona Baldassari

21 papers receiving 399 citations

Peers

Sımona Baldassari

CMN

GENET

PMH

Eric Noé France

Suzanne F. C. Miller-Delaney Ireland

Filipa Franquinho Portugal

Susan van Erp Netherlands

Shahnawaz Khan United States

Bart Nieuwenhuis United Kingdom

Anna Oldenborg United States

Birgit H. Funke United States

Eleonora Di Gregorio Italy

Tarja Linnankivi Finland

Eric Noé France

Sımona Baldassari

168 ×0.7

83 ×0.9

CMN

119 ×1.3

GENET

63 ×0.8

76 ×1.4

PMH

Citations per year, relative to Sımona Baldassari Sımona Baldassari (= 1×) peers Eric Noé

Countries citing papers authored by Sımona Baldassari

Since Specialization

Citations

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

Fields of papers citing papers by Sımona Baldassari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sımona Baldassari

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

Conteduca, Giuseppina, Chiara Baldo, Renata Bocciardi, et al.. (2025). Derivation of the IGGi006-A stem cell line from a patient with CAPRIN1 haploinsufficiency. Stem Cell Research. 85. 103696–103696. 1 indexed citations

Loiacono, Fabrizio, Lorenzo Ferrando, Pierluigi Valente, et al.. (2025). Optimization of Transcription Factor-Driven Neuronal Differentiation from Human Induced Pluripotent Stem Cells for Disease Modelling and Drug Screening. Stem Cell Reviews and Reports. 21(3). 816–833. 1 indexed citations

Conteduca, Giuseppina, Chiara Baldo, Sımona Baldassari, et al.. (2024). Generation of IGGi003-A induced pluripotent stem cell line from a patient with Sotos Syndrome carrying c.1633delA NSD1 variant in exon 5. Stem Cell Research. 76. 103324–103324. 1 indexed citations

Iacomino, Michele, Sara Fortuna, Jennifer Howe, et al.. (2024). Allelic heterogeneity and abnormal vesicle recycling in PLAA-related neurodevelopmental disorders. Frontiers in Molecular Neuroscience. 17. 1268013–1268013. 1 indexed citations

D’Onofrio, Gianluca, Marcello Scala, Mariasavina Severino, et al.. (2023). Expanding the phenotype associated with biallelic SLC20A2 variants. European Journal of Human Genetics. 31(7). 725–729.

Baldassari, Sımona, Chiara Cervetto, Floriana Fruscione, et al.. (2022). Vesicular Glutamate Release from Feeder-FreehiPSC-Derived Neurons. International Journal of Molecular Sciences. 23(18). 10545–10545. 8 indexed citations

Conteduca, Giuseppina, Chiara Baldo, Monica Traverso, et al.. (2022). Generation of induced pluripotent stem cell lines from a patient with Sotos syndrome carrying 5q35 microdeletion. Stem Cell Research. 66. 103007–103007. 1 indexed citations

Madia, Francesca, Patrizia De Marco, Marzia Ognibene, et al.. (2022). Clinical and genetic analysis of patients with segmental overgrowth features and somatic mammalian target of rapamycin (mTOR) pathway disruption: Possible novel clinical issues. Birth Defects Research. 114(20). 1440–1448. 1 indexed citations

Braccia, Clarissa, Oliver M. Crook, Lisa M. Breckels, et al.. (2022). CFTR Rescue by Lumacaftor (VX-809) Induces an Extensive Reorganization of Mitochondria in the Cystic Fibrosis Bronchial Epithelium. Cells. 11(12). 1938–1938. 8 indexed citations

10.

Piccolo, Gianluca, Giuseppe d’Annunzio, Elisabetta Amadori, et al.. (2021). Neuromuscular and Neuroendocrinological Features Associated With ZC4H2-Related Arthrogryposis Multiplex Congenita in a Sicilian Family: A Case Report. Frontiers in Neurology. 12. 704747–704747. 6 indexed citations

11.

Baldassari, Sımona, Ilaria Musante, Michele Iacomino, et al.. (2020). Brain Organoids as Model Systems for Genetic Neurodevelopmental Disorders. Frontiers in Cell and Developmental Biology. 8. 590119–590119. 39 indexed citations

12.

Aprile, Davide, Floriana Fruscione, Sımona Baldassari, et al.. (2019). TBC1D24 regulates axonal outgrowth and membrane trafficking at the growth cone in rodent and human neurons. Cell Death and Differentiation. 26(11). 2464–2478. 27 indexed citations

13.

Gazzerro, Elisabetta, Stefania Assereto, Sımona Baldassari, et al.. (2018). The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan–Deficient Muscular Dystrophy. American Journal Of Pathology. 189(2). 354–369. 10 indexed citations

14.

Fruscione, Floriana, Pierluigi Valente, Bruno Sterlini, et al.. (2018). PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity. Brain. 141(4). 1000–1016. 91 indexed citations

15.

Baskin, Jeremy M., Xudong Wu, Romain Christiano, et al.. (2015). The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane. Nature Cell Biology. 18(1). 132–138. 85 indexed citations

16.

Gazzerro, Elisabetta, Sımona Baldassari, Stefania Assereto, et al.. (2015). Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X Axis. American Journal Of Pathology. 185(12). 3349–3360. 44 indexed citations

17.

Kondo, Yoichi, Abigail B. Radcliff, Sımona Baldassari, et al.. (2013). Spontaneous Optic Nerve Compression in the Osteopetrotic (op/op) Mouse: A Novel Model of Myelination Failure. Journal of Neuroscience. 33(8). 3514–3525. 8 indexed citations

18.

Traverso, Monica, Stefania Assereto, Elisabetta Gazzerro, et al.. (2013). Novel FAM126A mutations in hypomyelination and congenital cataract disease. Biochemical and Biophysical Research Communications. 439(3). 369–372. 13 indexed citations

19.

Gazzerro, Elisabetta, Sımona Baldassari, Caterina Giacomini, et al.. (2012). Hyccin, the Molecule Mutated in the Leukodystrophy Hypomyelination and Congenital Cataract (HCC), Is a Neuronal Protein. PLoS ONE. 7(3). e32180–e32180. 20 indexed citations

20.

Traverso, Monica, Özge Özalp Yüreğir, Aviva Mimouni-Bloch, et al.. (2012). Hypomyelination and congenital cataract: Identification of novel mutations in two unrelated families. European Journal of Paediatric Neurology. 17(1). 108–111. 4 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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