Elisa Bettella

678 total citations
14 papers, 324 citations indexed

About

Elisa Bettella is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Elisa Bettella has authored 14 papers receiving a total of 324 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Psychiatry and Mental health. Recurrent topics in Elisa Bettella's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (3 papers) and Epilepsy research and treatment (3 papers). Elisa Bettella is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (3 papers) and Epilepsy research and treatment (3 papers). Elisa Bettella collaborates with scholars based in Italy, United States and Serbia. Elisa Bettella's co-authors include Rita Fabbri, A. Viarengo, M. Lafaurie, Bruno Burlando, Alessandra Murgia, Stefano Sartori, Roberta Polli, Gabriella Di Rosa, Clementina Boniver and Emanuela Leonardi and has published in prestigious journals such as International Journal of Molecular Sciences, European Journal of Human Genetics and Marine Environmental Research.

In The Last Decade

Elisa Bettella

13 papers receiving 307 citations

Peers

Countries citing papers authored by Elisa Bettella

Since Specialization

Citations

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

Fields of papers citing papers by Elisa Bettella

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Bettella

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

All Works

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14 of 14 papers shown

#	Work	Indexed citations
1	Somatic Instability Leading to Mosaicism in Fragile X Syndrome and Associated Disorders: Complex Mechanisms, Diagnostics, and Clinical Relevance 2024 ·International Journal of Molecular Sciences ·Dragana Protić, Roberta Polli, Elisa Bettella, Karen Usdin, Alessandra Murgia, Flora Tassone	0
2	Identification of SETBP1 Mutations by Gene Panel Sequencing in Individuals With Intellectual Disability or With “Developmental and Epileptic Encephalopathy” 2020 ·Frontiers in Neurology ·Emanuela Leonardi, Elisa Bettella, Maria Federica Pelizza, Maria Cristina Aspromonte, Roberta Polli, Clementina Boniver, Stefano Sartori, Donatella Milani, Alessandra Murgia	15
3	Frequency of Usher gene mutations in non-syndromic hearing loss: higher variability of the Usher phenotype 2020 ·Journal of Human Genetics ·(unknown), Elisa Bettella, Roberta Polli, Emanuela Leonardi, Maria Cristina Aspromonte, (unknown), Franco Stanzial, Francesco Benedicenti, Alberto Sensi, Andrea Ciorba, Stefania Bigoni, Elona Cama, Pietro Scimemi, Rosamaria Santarelli, Alessandra Murgia	9
4	A Novel WAC Loss of Function Mutation in an Individual Presenting with Encephalopathy Related to Status Epilepticus during Sleep (ESES) 2020 ·Genes ·Emanuela Leonardi, (unknown), Maria Cristina Aspromonte, Roberta Polli, (unknown), Claudia Ciaccio, (unknown), Elisa Bettella, (unknown), Elisa Cainelli, Stefania Boni, Stefano Sartori, Chiara Pantaleoni, Clementina Boniver, Alessandra Murgia	14
5	Brain malformations associated to Aldh7a1 gene mutations: Report of a novel homozygous mutation and literature review 2018 ·European Journal of Paediatric Neurology ·Irene Toldo, Claudia Bonardi, Elisa Bettella, Roberta Polli, Giacomo Talenti, Alberto Burlina, Stefano Sartori, Alessandra Murgia	17
6	A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members 2017 ·International Journal of Pediatric Otorhinolaryngology ·(unknown), Elisa Bettella, Roberta Polli, Elona Cama, Pietro Scimemi, Rosamaria Santarelli, Alessandra Murgia	13
7	Identification of Four NovelPCDH19Mutations and Prediction of Their Functional Impact 2014 ·Annals of Human Genetics ·Emanuela Leonardi, Stefano Sartori, Marilena Vecchi, Elisa Bettella, Roberta Polli, Luca De Palma, Clementina Boniver, Alessandra Murgia	14
8	14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype 2012 ·European Journal of Human Genetics ·Carolyn Ellaway, Gladys Ho, Elisa Bettella, (unknown), Felicity Collins, Anna Hackett, F. Ellis McKenzie, Artur Darmanian, Gregory B. Peters, Kerry Fagan, John Christodoulou	44
9	Early‐onset epileptic encephalopathy in a girl carrying a truncating mutation of the ARX gene: rethinking the ARX phenotype in females 2012 ·Clinical Genetics ·Elisa Bettella, Gabriella Di Rosa, Roberta Polli, Emanuela Leonardi, Giovanni Tortorella, Stefano Sartori, Alessandra Murgia	8
10	Pathogenic Role of the X-Linked Cyclin-Dependent Kinase-Like 5 and Aristaless-Related Homeobox Genes in Epileptic Encephalopathy of Unknown Etiology With Onset in the First Year of Life 2011 ·Journal of Child Neurology ·Stefano Sartori, Roberta Polli, Elisa Bettella, (unknown), (unknown), Marilena Vecchi, Lucio Giordano, Patrizia Accorsi, Gabriella Di Rosa, Irene Toldo, Nelia Zamponi, Francesca Darra, Bernardo Dalla Bernardina, Giorgio Perilongo, Clementina Boniver, Alessandra Murgia	23
11	Familial Ohtahara syndrome due to a novel ARX gene mutation 2010 ·American Journal of Medical Genetics Part A ·Lucio Giordano, Stefano Sartori, Silvia Russo, Patrizia Accorsi, Jessica Galli, Alessandra Tiberti, Elisa Bettella, Margherita Marchi, Aglaia Vignoli, Francesca Darra, Alessandra Murgia, Bernardo Dalla Bernardina	22
12	A novel CDKL5 mutation in a 47,XXY boy with the early‐onset seizure variant of Rett syndrome 2009 ·American Journal of Medical Genetics Part A ·Stefano Sartori, Gabriella Di Rosa, Roberta Polli, Elisa Bettella, (unknown), Gaetano Tortorella, Alessandra Murgia	33
13	Heavy metal inhibition of EROD activity in liver microsomes from the bass Dicentrarchus labrax exposed to organic xenobiotics: Role of GSH in the reduction of heavy metal effects 1997 ·Marine Environmental Research ·A. Viarengo, Elisa Bettella, Rita Fabbri, Bruno Burlando, M. Lafaurie	107
14	Dependence of chick killing on nest density in a colony of yellow‐legged gull(Larus cachinnans michaellis) 1995 ·Bolletino di zoologia ·G. Marin, Elisa Bettella, Andrea Pilastro, Stefano Amato, (unknown)	5

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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