Thea Giacomini

1.0k total citations
32 papers, 222 citations indexed

About

Thea Giacomini is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Thea Giacomini has authored 32 papers receiving a total of 222 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 13 papers in Molecular Biology and 7 papers in Psychiatry and Mental health. Recurrent topics in Thea Giacomini's work include Genetics and Neurodevelopmental Disorders (11 papers), Epilepsy research and treatment (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Thea Giacomini is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), Epilepsy research and treatment (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). Thea Giacomini collaborates with scholars based in Italy, United States and Russia. Thea Giacomini's co-authors include Maria Margherita Mancardi, Mariasavina Severino, Giovanni Morana, Lino Nobili, Sarà Uccella, Patrizia Ronchetto, Elisa Tassano, Giorgio Gimelli, Maria Stella Vari and Livia Pisciotta and has published in prestigious journals such as Clinical Neurophysiology, American Journal of Clinical Pathology and Journal of Neuroimmunology.

In The Last Decade

Thea Giacomini

31 papers receiving 221 citations

Peers

Thea Giacomini

GENET

PMH

NEURO

Pia Bernardo Italy

Hirofumi Kashii Japan

Marisela Dy-Hollins United States

Michael Alber Germany

Anaita Hegde India

Shakti Agrawal United Kingdom

Pınar Tektürk Türkiye

Barbara Hallinan United States

Esther Ganelin‐Cohen Israel

Chloe Stutterd Australia

Pia Bernardo Italy

Thea Giacomini

77 ×1.0

91 ×1.2

GENET

36 ×0.8

PMH

81 ×2.0

NEURO

39 ×1.3

Citations per year, relative to Thea Giacomini Thea Giacomini (= 1×) peers Pia Bernardo

Countries citing papers authored by Thea Giacomini

Since Specialization

Citations

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

Fields of papers citing papers by Thea Giacomini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thea Giacomini

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

Bodria, Monica, Thea Giacomini, Domenico Tortora, et al.. (2024). Brain and spine malformations and neurodevelopmental disorders in a cohort of children with CAKUT. Pediatric Nephrology. 39(7). 2115–2129. 1 indexed citations

Gastaldi, Matteo, Matilde Inglese, Andrea Rossi, et al.. (2023). Asynchronous combined central and peripheral demyelination (CCPD) in a girl with anti-MOG positivity: A case report and review of the literature. Journal of Neuroimmunology. 384. 578213–578213. 4 indexed citations

Mancardi, Maria Margherita, Antonella Riva, Thea Giacomini, et al.. (2023). The phenotypic spectrum of epilepsy associated with periventricular nodular heterotopia. Journal of Neurology. 270(8). 3934–3945. 5 indexed citations

Tortora, Domenico, Mariasavina Severino, Alessandro Consales, et al.. (2022). Comparison of Qualitative and Quantitative Analyses of MR-Arterial Spin Labeling Perfusion Data for the Assessment of Pediatric Patients with Focal Epilepsies. Diagnostics. 12(4). 811–811. 8 indexed citations

Riva, Antonella, Gianluca Piccolo, Noemi Brolatti, et al.. (2022). Acute Neurological Presentation in Children With SARS-CoV-2 Infection. Frontiers in Pediatrics. 10. 909849–909849. 6 indexed citations

Giacomini, Thea, Giulia Nobile, Oliviero Bruni, et al.. (2022). On the role of REM sleep microstructure in suppressing interictal spikes in Electrical Status Epilepticus during Sleep. Clinical Neurophysiology. 136. 62–68. 13 indexed citations

Giacomini, Thea, Marcello Scala, Giulia Nobile, et al.. (2022). De novo POLR2A p.(Ile457Thr) variant associated with early-onset encephalopathy and cerebellar atrophy: expanding the phenotypic spectrum. Brain and Development. 44(7). 480–485. 4 indexed citations

Pisciotta, Livia, Maria Margherita Mancardi, Michela Stagnaro, et al.. (2021). Alternating Hemiplegia of Childhood in a Child Harboring a Novel TBC1D24 Mutation: Case Report and Literature Review. Neuropediatrics. 53(1). 69–74. 1 indexed citations

Mancardi, Maria Margherita, Claudia Nesti, Laura Siri, et al.. (2021). Focal status and acute encephalopathy in a 13-year-old boy with de novo DNM1L mutation: Video-polygraphic pattern and clues for differential diagnosis. Brain and Development. 43(5). 644–651. 6 indexed citations

10.

Giacomini, Thea, Livia Pisciotta, Claudia Nesti, et al.. (2020). Optic Atrophy and Generalized Chorea in a Patient Harboring an OPA10/RTN4IP1 Pathogenic Variant. Neuropediatrics. 51(6). 425–429. 4 indexed citations

11.

Fischetto, Rita, Maria Margherita Mancardi, Thea Giacomini, et al.. (2020). Substrate reduction therapy with Miglustat in pediatric patients with GM1 type 2 gangliosidosis delays neurological involvement: A multicenter experience. Molecular Genetics & Genomic Medicine. 8(10). e1371–e1371. 20 indexed citations

12.

Tortora, Domenico, Marta Bertamino, Marcello Scala, et al.. (2020). Spatial coefficient of variation applied to arterial spin labeling MRI may contribute to predict surgical revascularization outcomes in pediatric moyamoya vasculopathy. Neuroradiology. 62(8). 1003–1015. 15 indexed citations

13.

Amadori, Elisabetta, Marcello Scala, Maria Stella Vari, et al.. (2020). Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the ‘beyond epilepsy’ project. The Italian Journal of Pediatrics/Italian journal of pediatrics. 46(1). 92–92. 22 indexed citations

14.

Giacomini, Thea, Maria Stella Vari, Giulia Prato, et al.. (2019). Epileptic Encephalopathy, Myoclonus–Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene. Neuropediatrics. 50(5). 327–331. 6 indexed citations

15.

Micalizzi, Concetta, Thea Giacomini, Matteo Gastaldi, et al.. (2019). Bortezomib-Responsive Refractory Anti-N-Methyl-d-Aspartate Receptor Encephalitis. Pediatric Neurology. 103. 61–64. 24 indexed citations

16.

Giacomini, Thea, Livia Pisciotta, Giulia Prato, et al.. (2019). Severe early-onset developmental and epileptic encephalopathy (DEE) associated with novel compound heterozygous pathogenic variants in SLC25A22: Case report and literature review. Seizure. 70. 56–58. 5 indexed citations

17.

Tassano, Elisa, Sarà Uccella, Thea Giacomini, et al.. (2018). Intragenic Microdeletion of ULK4 and Partial Microduplication of BRWD3 in Siblings with Neuropsychiatric Features and Obesity. Cytogenetic and Genome Research. 156(1). 14–21. 10 indexed citations

18.

Tassano, Elisa, Sarà Uccella, Thea Giacomini, et al.. (2018). Clinical and Molecular Characterization of Two Patients with CNTN6 Copy Number Variations. Cytogenetic and Genome Research. 156(3). 144–149. 6 indexed citations

19.

Tassano, Elisa, et al.. (2017). Characterization of the Phenotype Associated with Microduplication Reciprocal to NF1 Microdeletion Syndrome. Cytogenetic and Genome Research. 152(1). 22–28.

20.

Pintaudi, Maria, Maria Grazia Calevo, Aglaia Vignoli, et al.. (2015). Antiepileptic drugs in Rett Syndrome. European Journal of Paediatric Neurology. 19(4). 446–452. 15 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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