Sonia Amabile

497 total citations
12 papers, 242 citations indexed

About

Sonia Amabile is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Sonia Amabile has authored 12 papers receiving a total of 242 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 2 papers in Cognitive Neuroscience. Recurrent topics in Sonia Amabile's work include Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). Sonia Amabile is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). Sonia Amabile collaborates with scholars based in Italy, United States and France. Sonia Amabile's co-authors include Fabio Acquaviva, Mariateresa Falco, Francesca Ariani, Alessandra Renieri, Ilaria Meloni, Johannes Hell, Caterina Lo Rizzo, Tommaso Patriarchi, Francesca Mari and Elisa Landucci and has published in prestigious journals such as SHILAP Revista de lepidopterología, Oxidative Medicine and Cellular Longevity and European Journal of Human Genetics.

In The Last Decade

Sonia Amabile

12 papers receiving 239 citations

Peers

Sonia Amabile

GENET

CMN

Emilie Landais France

Roberta De Filippis Italy

Caterina Lo Rizzo Italy

Aline Dubos France

Sébastien Moutton France

Daji Guo China

Daniëlle G.M. Bosch Netherlands

Joseph Goodliffe United States

Christina N. Vallianatos United States

Midori Sugawara Japan

Emilie Landais France

Sonia Amabile

177 ×1.1

GENET

117 ×0.8

40 ×1.2

24 ×0.8

CMN

17 ×0.8

Citations per year, relative to Sonia Amabile Sonia Amabile (= 1×) peers Emilie Landais

Countries citing papers authored by Sonia Amabile

Since Specialization

Citations

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

Fields of papers citing papers by Sonia Amabile

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sonia Amabile

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

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

Stefano, Vincenzo Di, Antonino Lupica, Simona Maccora, et al.. (2024). AChR-seropositive myasthenia gravis in muscular dystrophy: diagnostic pitfalls and clinical management challenges. Neurological Sciences. 46(1). 125–132. 4 indexed citations

D’Agostino, Ylenia, Domenico Palumbo, Maria Rosaria Rusciano, et al.. (2022). Whole-Exome Sequencing Revealed New Candidate Genes for Human Dilated Cardiomyopathy. Diagnostics. 12(10). 2411–2411. 4 indexed citations

Salvati, Annamaria, Ileana Carnevali, Elena Alexandrova, et al.. (2022). Targeted molecular profiling of epithelial ovarian cancer from Italian BRCA wild-type patients with a BRCA and PARP pathways gene panel. Experimental and Molecular Pathology. 128. 104833–104833. 3 indexed citations

Rosanio, Francesco Maria, et al.. (2021). Perinatal‐lethal Gaucher disease presenting with blueberry muffin lesions. Pediatric Dermatology. 38(5). 1357–1358. 2 indexed citations

Amabile, Sonia, et al.. (2020). DYNC1H1‐related disorders: A description of four new unrelated patients and a comprehensive review of previously reported variants. American Journal of Medical Genetics Part A. 182(9). 2049–2057. 28 indexed citations

Falco, Luigia De, et al.. (2019). Detection of SRY‐positive46,XX male syndrome by the analysis of cell‐free fetal DNA via non‐invasive prenatal testing. SHILAP Revista de lepidopterología. 7(10). 1977–1981. 5 indexed citations

Falco, Mariateresa, Sonia Amabile, & Fabio Acquaviva. (2017). <em>RAI1</em> gene mutations: mechanisms of Smith–Magenis Syndrome. The Application of Clinical Genetics. Volume 10. 85–94. 36 indexed citations

Mucciolo, Mafalda, Chiara Di Marco, Roberto Canitano, et al.. (2016). A Genome Wide Copy Number Variations Analysis in Autism Spectrum Disorder (Asd) and Intellectual Disability (Id) in Italian Families. Journal of Genetic Syndromes & Gene Therapy. 7(5). 2 indexed citations

Frullanti, Elisa, Sonia Amabile, Elisa Landucci, et al.. (2015). Altered expression of neuropeptides in FoxG1-null heterozygous mutant mice. European Journal of Human Genetics. 24(2). 252–257. 8 indexed citations

10.

Patriarchi, Tommaso, Sonia Amabile, Elisa Frullanti, et al.. (2015). Imbalance of excitatory/inhibitory synaptic protein expression in iPSC-derived neurons from FOXG1+/− patients and in foxg1+/− mice. European Journal of Human Genetics. 24(6). 871–880. 47 indexed citations

11.

Signorini, Cinzia, Silvia Leoncini, Claudio De Felice, et al.. (2014). Redox Imbalance and Morphological Changes in Skin Fibroblasts in Typical Rett Syndrome. Oxidative Medicine and Cellular Longevity. 2014. 1–10. 46 indexed citations

12.

Patriarchi, Tommaso, Mariangela Amenduni, Sonia Amabile, et al.. (2014). GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells. European Journal of Human Genetics. 23(2). 195–201. 57 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.

Explore authors with similar magnitude of impact