Barbara Castellotti

7.0k total citations
65 papers, 1.8k citations indexed

About

Barbara Castellotti is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Barbara Castellotti has authored 65 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 20 papers in Cellular and Molecular Neuroscience and 18 papers in Genetics. Recurrent topics in Barbara Castellotti's work include Genetics and Neurodevelopmental Disorders (15 papers), Mitochondrial Function and Pathology (14 papers) and Genetic Neurodegenerative Diseases (14 papers). Barbara Castellotti is often cited by papers focused on Genetics and Neurodevelopmental Disorders (15 papers), Mitochondrial Function and Pathology (14 papers) and Genetic Neurodegenerative Diseases (14 papers). Barbara Castellotti collaborates with scholars based in Italy, United States and France. Barbara Castellotti's co-authors include Cinzia Gellera, Caterina Mariotti, Franco Taroni, Vincenzo Silani, Nicola Ticozzi, Davide Pareyson, Antonia Ratti, Stefano Di Donato, Giovanna Zorzi and Letizia Mazzini and has published in prestigious journals such as Brain, Neurology and Brain Research.

In The Last Decade

Barbara Castellotti

65 papers receiving 1.8k citations

Peers

Countries citing papers authored by Barbara Castellotti

Since Specialization

Citations

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

Fields of papers citing papers by Barbara Castellotti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Castellotti

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

#	Work	Indexed citations
1	Severe epilepsy phenotypes in adults with succinic semialdehyde dehydrogenase deficiency: Novel clinical and therapeutic insights from an Italian multicenter retrospective cohort study 2025 ·Seizure ·Laura Canafoglia, Mario Mastrangelo, Marco Russo, Jacopo C. DiFrancesco, Andrea Stabile, Fabio Martino Doniselli, Roberta Di Giacomo, Giuseppe Didato, Silvia Esposito, Claudio Caccia, Francesco Pisani, Emilio Russo, Romana Rizzi, Cinzia Gellera, Barbara Castellotti	2
2	Next‐generation sequencing in pediatric‐onset epilepsies: Analysis with target panels and personalized therapeutic approach 2024 ·Epilepsia Open ·Barbara Castellotti, Francesca Ragona, Elena Freri, (unknown), (unknown), (unknown), Roberta Solazzi, Silvana Franceschetti, Franco Taroni, Laura Canafoglia, Cinzia Gellera, Tiziana Granata, Jacopo C. DiFrancesco	2
3	Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with KCNT1-related drug-resistant focal epilepsy 2024 ·Frontiers in Cellular Neuroscience ·Ilaria Mosca, Elena Freri, Paolo Ambrosino, (unknown), Tiziana Granata, Laura Canafoglia, Francesca Ragona, Roberta Solazzi, (unknown), Barbara Castellotti, (unknown), Cinzia Gellera, Jacopo C. DiFrancesco, Maria Virginia Soldovieri, Maurizio Taglialatela	4
4	A novel KCNC1 gain‐of‐function variant causing developmental and epileptic encephalopathy: “Precision medicine” approach with fluoxetine 2023 ·Epilepsia ·Paolo Ambrosino, Francesca Ragona, Ilaria Mosca, (unknown), Laura Canafoglia, Roberta Solazzi, Ilaria Rivolta, Elena Freri, Tiziana Granata, (unknown), Barbara Castellotti, Cinzia Gellera, Maria Virginia Soldovieri, Jacopo C. DiFrancesco, Maurizio Taglialatela	10
5	Progressive myoclonus epilepsies due to SEMA6B mutations. New variants and appraisal of published phenotypes 2023 ·Epilepsia Open ·Barbara Castellotti, Laura Canafoglia, Elena Freri, (unknown), (unknown), Stefania Magri, Jacopo C. DiFrancesco, Martina Fanella, Carlo Di Bonaventura, Alessandra Morano, Tiziana Granata, Cinzia Gellera, Silvana Franceschetti, Roberto Michelucci	6
6	Case report: A novel pathogenic FRMD7 variant in a Turner syndrome patient with familial idiopathic infantile nystagmus 2023 ·Frontiers in Neurology ·(unknown), Claudia Ciaccio, Barbara Castellotti, Francesca L. Sciacca, Chiara Pantaleoni, Stefano D’Arrigo	2
7	Do the functional properties of HCN1 mutants correlate with the clinical features in epileptic patients? 2021 ·Progress in Biophysics and Molecular Biology ·Alessandro Porro, Gerardo Abbandonato, Valentina Veronesi, (unknown), Anna Binda, Laura Antolini, Tiziana Granata, Barbara Castellotti, Carla Marini, Anna Moroni, Jacopo C. DiFrancesco, Ilaria Rivolta	14
8	Severe epilepsy in CNTNAP2-related Pitt-Hopkins-like syndrome successfully treated with stiripentol 2021 ·Seizure ·Elena Freri, Barbara Castellotti, Laura Canafoglia, Francesca Ragona, Roberta Solazzi, (unknown), Stefania Magri, (unknown), Stefano D’Arrigo, Cinzia Gellera, Jacopo C. DiFrancesco, Tiziana Granata	7
9	Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy 2020 ·Pharmacological Research ·Maria Virginia Soldovieri, Elena Freri, Paolo Ambrosino, Ilaria Rivolta, Ilaria Mosca, Anna Binda, (unknown), Francesca Ragona, Laura Canafoglia, (unknown), Roberta Solazzi, Tiziana Granata, Barbara Castellotti, (unknown), Cinzia Gellera, Audrey Labalme, Gaëtan Lesca, Jacopo C. DiFrancesco, Maurizio Taglialatela	13
10	A novel de novo HCN1 loss-of-function mutation in genetic generalized epilepsy causing increased neuronal excitability 2018 ·Neurobiology of Disease ·(unknown), Jacopo C. DiFrancesco, Raffaella Milanesi, Giulia Campostrini, Barbara Castellotti, Annalisa Bucchi, Mirko Baruscotti, Carlo Ferrarese, Silvana Franceschetti, Laura Canafoglia, Francesca Ragona, Elena Freri, Angelo Labate, Antonio Gambardella, Cinzia Costa, Ilaria Rivolta, Cinzia Gellera, Tiziana Granata, Andrea Barbuti, Dario DiFrancesco	34
11	ASAH1 variant causing a mild SMA phenotype with no myoclonic epilepsy: a clinical, biochemical and molecular study 2016 ·European Journal of Human Genetics ·Massimiliano Filosto, Massimo Aureli, Barbara Castellotti, Fabrizio Rinaldi, (unknown), Manuela Valsecchi, Susanna Lualdi, (unknown), Viviana Pensato, Silvia Rota, Cinzia Gellera, Mirella Filocamo, Alessandro Padovani	18
12	Hyperargininemia: 7-Month Follow-Up Under Sodium Benzoate Therapy in an Italian Child Presenting Progressive Spastic Paraparesis, Cognitive Decline, and Novel Mutation in ARG1 Gene 2014 ·Pediatric Neurology ·Giovanni Baranello, Enrico Alfei, Diego Martinelli, (unknown), (unknown), Carlo Dionisi‐Vici, Cinzia Gellera, Barbara Castellotti	9
13	Granny trips down: is she carrying the big bad wolf? 2012 ·Neurological Sciences ·Lucio Tremolizzo, (unknown), Graziella Uziel, Barbara Castellotti, Cinzia Gellera, Carlo Ferrarese, Ildebrando Appollonio	2
14	Paroxysmal exercise-induced dyskinesia with self-limiting partial epilepsy: A novel GLUT-1 mutation with benign phenotype 2011 ·Parkinsonism & Related Disorders ·Tommaso Bovi, Alfonso Fasano, (unknown), Cinzia Gellera, Barbara Castellotti, Elena Fontana, Michèle Tinazzi	12
15	Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 2011 ·Journal of Neurology Neurosurgery & Psychiatry ·Roberto Del Bo, Cinzia Tiloca, Viviana Pensato, Lucia Corrado, Antonia Ratti, Nicola Ticozzi, Stefania Corti, Barbara Castellotti, Letizia Mazzini, Gianni Sorarú, Cristina Cereda, Sandra D’Alfonso, Cinzia Gellera, Giacomo P. Comi, Vincenzo Silani	77
16	Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis 2007 ·Neurogenetics ·Cinzia Gellera, Claudia Colombrita, Nicola Ticozzi, Barbara Castellotti, Cinzia Bragato, Antonia Ratti, Franco Taroni, Vincenzo Silani	90
17	Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPAgene in Italian families 2004 ·Neurological Sciences ·Caterina Mariotti, Cinzia Gellera, M. Rimoldi, Rossana Mineri, Graziella Uziel, Giovanna Zorzi, Davide Pareyson, G. Piccolo, D. Gambi, Silvia Piacentini, Ferdinando Squitieri, Ruggero Capra, Barbara Castellotti, S. Di Donato	101
18	Autosomal dominant cerebellar ataxias: Genotype frequency and clinical/molecular correlations 1997 ·The Italian Journal of Neurological Sciences ·Davide Pareyson, Cinzia Gellera, Barbara Castellotti, (unknown), (unknown), (unknown), F. Girotti, Caterina Mariotti, Stefano DiDonato	1
19	Mapping of genes predisposing to idiopathic generalized epilepsy 1995 ·Human Molecular Genetics ·Federico Zara, (unknown), G. Avanzini, Stefano Di Donato, Barbara Castellotti, Pragna I. Patel, Massimo Pandolfo	93
20	Kennedy's disease: clinical and molecular study of two Italian families 1995 ·Neurological Sciences ·Davide Pareyson, Barbara Castellotti, Sara Botti, (unknown), Cinzia Gellera, Franco Taroni, Angelo Sghirlanzoni	1

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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