Maria Bottitta

656 total citations
12 papers, 406 citations indexed

About

Maria Bottitta is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Maria Bottitta has authored 12 papers receiving a total of 406 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Cognitive Neuroscience. Recurrent topics in Maria Bottitta's work include Genetics and Neurodevelopmental Disorders (9 papers), Congenital heart defects research (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Maria Bottitta is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Congenital heart defects research (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Maria Bottitta collaborates with scholars based in Italy. Maria Bottitta's co-authors include Maurizio Elia, Raffaele Ferri, S Musumeci, Carmela Scuderi, Simonetta Panerai, Stefano Del Gracco, Giuseppe Calabrese, Lucia Grillo, Marco Carotenuto and Marco Fichera and has published in prestigious journals such as Neurology, International Journal of Psychophysiology and Journal of Child Neurology.

In The Last Decade

Maria Bottitta

11 papers receiving 374 citations

Peers

Maria Bottitta

GENET

CN

PMH

MB

ECP

Carmela Scuderi Italy

Markéta Havlovičová Czechia

Hélène De Leersnyder France

Aleksandra Djukic United States

Diane C. Lanham United States

Athina Ververi Greece

Marie-Christine Ottet Switzerland

Juthamas Wirojanan Thailand

Deana D. Li United States

Derek Sayre Andrews United States

Carmela Scuderi Italy

Maria Bottitta

187 ×0.8

GENET

186 ×1.0

CN

120 ×1.1

PMH

146 ×1.6

MB

53 ×1.1

ECP

Citations per year, relative to Maria Bottitta Maria Bottitta (= 1×) peers Carmela Scuderi

Countries citing papers authored by Maria Bottitta

Since Specialization

Citations

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

Fields of papers citing papers by Maria Bottitta

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Bottitta

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Bottitta. A scholar is included among the top collaborators of Maria Bottitta 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 Maria Bottitta. Maria Bottitta is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

1.

Greco, Donatella, Simone Treccarichi, Maria Bottitta, et al.. (2025). Clinical Application of a Customized Gene Panel for Identifying Autism Spectrum Disorder-Associated Variants. Medicina. 61(7). 1273–1273.

2.

Treccarichi, Simone, Francesco Calı̀, Mirella Vinci, et al.. (2024). Implications of a De Novo Variant in the SOX12 Gene in a Patient with Generalized Epilepsy, Intellectual Disability, and Childhood Emotional Behavioral Disorders. Current Issues in Molecular Biology. 46(7). 6407–6422. 2 indexed citations

3.

Coppola, Antonietta, Maria Bottitta, Giuseppe Calabrese, et al.. (2014). Seizures and EEG pattern in the 22q13.3 deletion syndrome: Clinical report of six Italian cases. Seizure. 23(9). 774–779. 43 indexed citations

4.

Elia, Maurizio, Maria Bottitta, Lucia Grillo, et al.. (2012). An atypical patient with Cowden syndrome and PTEN gene mutation presenting with cortical malformation and focal epilepsy. Brain and Development. 34(10). 873–876. 38 indexed citations

5.

Grillo, Lucia, S Reitano, Maria Bottitta, et al.. (2010). Familial 1.1 Mb deletion in chromosome Xq22.1 associated with mental retardation and behavioural disorders in female patients. European Journal of Medical Genetics. 53(2). 113–116. 33 indexed citations

6.

Elia, Maurizio, Raffaele Ferri, Maria Bottitta, et al.. (2008). CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy. Neurology. 71(13). 997–999. 71 indexed citations

7.

Elia, Maurizio, Raffaele Ferri, S Musumeci, et al.. (2000). Sleep in subjects with autistic disorder: a neurophysiological and psychological study. Brain and Development. 22(2). 88–92. 141 indexed citations

8.

Elia, Maurizio, Raffaele Ferri, S Musumeci, et al.. (2000). Clinical Correlates of Brain Morphometric Features of Subjects With Low-Functioning Autistic Disorder. Journal of Child Neurology. 15(8). 504–508. 41 indexed citations

9.

Elia, Maurizio, et al.. (1998). Sindrome del cromosoma 20 ad anello ed epilessia: Descrizione di un caso. 265–266. 1 indexed citations

10.

Elia, Maurizio, S Musumeci, Raffaele Ferri, et al.. (1998). Familial Cortical Tremor, Epilepsy, and Mental Retardation. Archives of Neurology. 55(12). 1569–1569. 33 indexed citations

11.

Elia, Maurizio, et al.. (1998). 518 Sleep in autism. International Journal of Psychophysiology. 30(1-2). 200–200. 1 indexed citations

12.

Elia, Maurizio, L. Manfrè, Raffaele Ferri, et al.. (1997). Brain Morphometry and Psychobehavioural Measures in Autistic Low-Functioning Subjects. Rivista di Neuroradiologia. 10(4). 431–436. 2 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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