Daniele Frattini

1.1k total citations
59 papers, 464 citations indexed

About

Daniele Frattini is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Daniele Frattini has authored 59 papers receiving a total of 464 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 25 papers in Cellular and Molecular Neuroscience and 19 papers in Genetics. Recurrent topics in Daniele Frattini's work include Hereditary Neurological Disorders (17 papers), Neurological diseases and metabolism (13 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Daniele Frattini is often cited by papers focused on Hereditary Neurological Disorders (17 papers), Neurological diseases and metabolism (13 papers) and Genetics and Neurodevelopmental Disorders (13 papers). Daniele Frattini collaborates with scholars based in Italy, United States and Switzerland. Daniele Frattini's co-authors include Carlo Fusco, Elvio Della Giustina, Carlotta Spagnoli, Francesco Pisani, Grazia Salerno, Alessandro Iodice, S. Giovannini, Marcella Zollino, Giovanni Neri and Giuseppe Gobbi and has published in prestigious journals such as International Journal of Molecular Sciences, Epilepsia and Developmental Medicine & Child Neurology.

In The Last Decade

Daniele Frattini

53 papers receiving 456 citations

Peers

Countries citing papers authored by Daniele Frattini

Since Specialization

Citations

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

Fields of papers citing papers by Daniele Frattini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniele Frattini

This figure shows the co-authorship network connecting the top 25 collaborators of Daniele Frattini. A scholar is included among the top collaborators of Daniele Frattini 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 Daniele Frattini. Daniele Frattini 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	Myoclonic reflex and non‐reflex seizures in a female child with Coffin–Lowry syndrome: Clinical vignette 2025 ·Epileptic Disorders ·(unknown), (unknown), Carlotta Spagnoli, (unknown), A Cavalli, Stefano Giuseppe Caraffi, (unknown), (unknown), Roberta Russo, Iris Scala, Roberta Zuntini, Livia Garavelli, Daniele Frattini, Carlo Fusco	1
2	Axonal motor polyneuropathy in a 13 years old Girl with a de Novo variant in ADNP 2025 ·Neurogenetics ·(unknown), (unknown), Stefano Giuseppe Caraffi, (unknown), Simonetta Rosato, (unknown), Carlotta Spagnoli, A Cavalli, (unknown), (unknown), (unknown), Ivan Ivanovski, Livia Garavelli, Daniele Frattini, Carlo Fusco	0
3	Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study 2024 ·International Journal of Molecular Sciences ·(unknown), Carlotta Spagnoli, Stefano Giuseppe Caraffi, A Cavalli, (unknown), (unknown), Valentina De Giorgis, Daniele Frattini, (unknown), Silvia Masnada, Angela Peron, (unknown), Costanza Varesio, Luigina Spaccini, Aglaia Vignoli, Maria Paola Canevini, Pierangelo Veggiotti, Livia Garavelli, Carlo Fusco	9
4	Guillain-Barrè Syndrome—Retrospective Analysis of Data from a Cohort of Patients Referred to a Tertiary Care Pediatric Neuromuscular Center from 2000 to 2017: Electrophysiological Findings, Outcomes, and a Brief Literature Review 2024 ·Medicina ·(unknown), (unknown), (unknown), (unknown), Carlotta Spagnoli, Daniele Frattini, Elvio Della Giustina, (unknown), Carlo Fusco	1
5	Early-onset dysphagia and severe neurodevelopmental disorder as early signs in a patient with two novel variants in NARS1: a case report and brief review of the literature 2024 ·Neurogenetics ·(unknown), (unknown), Carlotta Spagnoli, (unknown), Stefano Giuseppe Caraffi, (unknown), (unknown), Daniele Frattini, (unknown), A Cavalli, Livia Garavelli, Carlo Fusco	2
6	Heterozygous truncating variant of TAOK1 in a boy with periventricular nodular heterotopia: a case report and literature review of TAOK1-related neurodevelopmental disorders 2024 ·BMC Medical Genomics ·A Cavalli, Stefano Giuseppe Caraffi, (unknown), (unknown), Manuela Napoli, Daniele Frattini, Carlotta Spagnoli, Livia Garavelli, Carlo Fusco	1
7	A Novel Family with Demyelinating Charcot–Marie–Tooth Disease Caused by a Mutation in the PMP2 Gene: A Case Series of Nine Patients and a Brief Review of the Literature 2023 ·Children ·(unknown), (unknown), Carlotta Spagnoli, Daniele Frattini, (unknown), Carlo Fusco	0
8	Severe Neurodevelopmental Disorder in Autosomal Recessive Spinocerebellar Ataxia 13 (SCAR13) Caused by Two Novel Frameshift Variants in GRM1 2023 ·The Cerebellum ·(unknown), (unknown), (unknown), Stefano Giuseppe Caraffi, (unknown), (unknown), Daniele Frattini, Carlotta Spagnoli, (unknown), (unknown), (unknown), Livia Garavelli, Carlo Fusco	2
9	Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures 2023 ·Frontiers in Neurology ·(unknown), Marzia Pollazzon, Cecilia Mancini, (unknown), (unknown), Simone Pizzi, Daniele Frattini, Carlotta Spagnoli, Stefano Giuseppe Caraffi, Roberta Zuntini, (unknown), Marcello Niceta, Francesca Clementina Radio, Marco Tartaglia, Livia Garavelli, Carlo Fusco	3
10	Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes 2023 ·Genes ·(unknown), Laura Bernardini, Marzia Pollazzon, Maria Grazia Giuffrida, Valentina Guida, (unknown), (unknown), (unknown), Manuela Napoli, Simonetta Rosato, (unknown), (unknown), Stefano Giuseppe Caraffi, Anita Wischmeijer, Daniele Frattini, Antonio Novelli, Livia Garavelli	2
11	Aromatic L-Amino-Acid Decarboxylase Deficiency Screening by Analysis of 3-O-Methyldopa in Dried Blood Spots: Results of a Multicentric Study in Neurodevelopmental Disorders 2023 ·Genes ·(unknown), Carlotta Spagnoli, Melissa Bellini, (unknown), (unknown), (unknown), (unknown), (unknown), Emanuela Claudia Turco, (unknown), (unknown), Duccio Maria Cordelli, Giacomo Biasucci, Daniele Frattini, Carlo Fusco	0
12	Tolosa-Hunt syndrome and recurrent painful ophthalmoplegic neuropathy, case reports: what to do and when? 2023 ·The Italian Journal of Pediatrics/Italian journal of pediatrics ·Daniele Frattini, Alessandro Iodice, Carlotta Spagnoli, (unknown), (unknown), (unknown), Carlo Fusco	1
13	Further delineation of PIGB-related early infantile epileptic encephalopathy 2021 ·European Journal of Medical Genetics ·(unknown), Carlotta Spagnoli, (unknown), Grazia Salerno, Daniele Frattini, (unknown), Francesco Pisani, Carlo Fusco	2
14	Pharmacological Treatment of Severe Breathing Abnormalities in a Case of HNRNPU Epileptic Encephalopathy 2021 ·Molecular Syndromology ·Carlotta Spagnoli, (unknown), Grazia Salerno, Daniele Frattini, Juha Koskenvuo, Carlo Fusco	3
15	Early-onset Dopamine Transporter Deficiency Syndrome: Long-term Follow-up 2020 ·Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques ·(unknown), Carlotta Spagnoli, (unknown), Grazia Salerno, (unknown), Daniele Frattini, Francesco Pisani, Carlo Fusco	3
16	Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrum 2018 ·Brain and Development ·Alessandro Iodice, Miryam Carecchio, Giovanna Zorzi, Barbara Garavaglia, Carlotta Spagnoli, Grazia Salerno, Daniele Frattini, Niccolò E. Mencacci, Federica Invernizzi, Liana Veneziano, Elide Mantuano, Marco Angriman, Carlo Fusco	6
17	Expanding phenotype of PRRT2 gene mutations: A new case with epilepsy and benign myoclonus of early infancy 2016 ·European Journal of Paediatric Neurology ·(unknown), Alessandro Iodice, Carlotta Spagnoli, Grazia Salerno, (unknown), Daniele Frattini, Carlo Fusco	15
18	Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis 2016 ·Brain and Development ·Alessandro Iodice, Carlotta Spagnoli, Grazia Salerno, Daniele Frattini, (unknown), (unknown), Francesco Pisani, Carlo Fusco	25
19	Downbeat nystagmus as the presenting symptom of infantile neuroaxonal dystrophy: A case report 2014 ·Brain and Development ·Daniele Frattini, Nardo Nardocci, Rosario Pascarella, Celeste Panteghini, Barbara Garavaglia, Carlo Fusco	7
20	Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation 2009 ·Brain and Development ·Carlo Fusco, Daniele Frattini, Enrico Farnetti, Davide Nicoli, Bruno Casali, (unknown), Andrea Nuccitelli, Elvio Della Giustina	23

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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