Alessia Azzarà

419 total citations
36 papers, 292 citations indexed

About

Alessia Azzarà is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Alessia Azzarà has authored 36 papers receiving a total of 292 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 13 papers in Genetics and 6 papers in Cancer Research. Recurrent topics in Alessia Azzarà's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Alessia Azzarà is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (4 papers). Alessia Azzarà collaborates with scholars based in Italy, Czechia and Switzerland. Alessia Azzarà's co-authors include Roberto Scarpato, Fiorella Gurrieri, Angelo Valetto, Veronica Bertini, C Giovannini, Chiara Pirillo, Eugenio Sangiorgi, Carlos García‐Crespo, Carla Lintas and Simona Piaggi and has published in prestigious journals such as PLoS ONE, Food and Chemical Toxicology and Mutation research. Fundamental and molecular mechanisms of mutagenesis.

In The Last Decade

Alessia Azzarà

33 papers receiving 275 citations

Peers

Alessia Azzarà

GENET

PPCH

IMMUN

Yubin Li China

Ali Khodadadian Iran

Bowen Niu China

Maria Cândida Pinheiro Baracat Brazil

Asmarinah Asmarinah Indonesia

Jianjun Hu China

Wei-Jie Zhu China

Jason Yongha Kim South Korea

Wen Lin China

Paweł Kordowitzki Poland

Yubin Li China

Alessia Azzarà

125 ×1.0

26 ×0.4

GENET

77 ×1.8

PPCH

29 ×0.8

46 ×1.3

IMMUN

Citations per year, relative to Alessia Azzarà Alessia Azzarà (= 1×) peers Yubin Li

Countries citing papers authored by Alessia Azzarà

Since Specialization

Citations

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

Fields of papers citing papers by Alessia Azzarà

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alessia Azzarà

This figure shows the co-authorship network connecting the top 25 collaborators of Alessia Azzarà. A scholar is included among the top collaborators of Alessia Azzarà 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 Alessia Azzarà. Alessia Azzarà 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:

20 of 20 papers shown

Bottillo, Irene, Luigi Laino, Alessia Azzarà, et al.. (2024). A pathogenic variant in the FLCN gene presenting with pure dementia: is autophagy at the intersection between neurodegeneration and cancer?. Frontiers in Neuroscience. 17. 1304080–1304080.

Azzarà, Alessia, et al.. (2024). Exome Profiling Suggests Combined Effect of Myeloperoxidase, Toll-Like Receptors, and Metallopeptidase in Hidradenitis Suppurativa. Biomedicines. 12(11). 2498–2498.

Lintas, Carla, et al.. (2024). Exploring the Role of the MUTYH Gene in Breast, Ovarian and Endometrial Cancer. Genes. 15(5). 554–554. 3 indexed citations

Azzarà, Alessia, Carla Lintas, Fabio Pilato, et al.. (2023). Melkersson–Rosenthal Syndrome and Migraine: A New Phenotype Associated with SCN1A Variants?. Genes. 14(7). 1482–1482. 1 indexed citations

Lintas, Carla, Angelo Facchiano, Alessia Azzarà, et al.. (2023). Deletion of a Single Lysine Residue at Position 292 of CAMK2A Disrupts Protein Function, Causing Severe Epileptic Encephalopathy and Intellectual Disability. Genes. 14(7). 1353–1353. 3 indexed citations

Sangiorgi, Eugenio, Alessia Azzarà, Elena Verrecchia, et al.. (2023). Identification by Exome Sequencing of Predisposing Variants in Familial Cases of Autoinflammatory Recurrent Fevers. Genes. 14(7). 1310–1310.

Lintas, Carla, Alessia Azzarà, Chiara Gregorj, et al.. (2023). Maternal Epigenetic Dysregulation as a Possible Risk Factor for Neurodevelopmental Disorders. Genes. 14(3). 585–585. 4 indexed citations

Azzarà, Alessia, Carla Lintas, Laura Bernardini, et al.. (2023). A new gene for autosomal dominant facial palsy/migraine identified in a family by whole exome sequencing. European Journal of Neurology. 31(1). e16088–e16088. 1 indexed citations

Azzarà, Alessia, et al.. (2022). Genetic variants determine intrafamilial variability of SARS-CoV-2 clinical outcomes in 19 Italian families. PLoS ONE. 17(10). e0275988–e0275988. 5 indexed citations

10.

Azzarà, Alessia, Eugenio Sangiorgi, Fiorella Gurrieri, et al.. (2021). Results of a Gene Panel Approach in a Cohort of Patients with Incomplete Distal Renal Tubular Acidosis and Nephrolithiasis. Kidney & Blood Pressure Research. 46(4). 469–474. 10 indexed citations

11.

Azzarà, Alessia, et al.. (2021). Identification of new candidate genes for spina bifida through exome sequencing. Child s Nervous System. 37(8). 2589–2596. 10 indexed citations

12.

Azzarà, Alessia, Silvia Giovanelli, Simona Piaggi, et al.. (2020). Assessing the cytotoxic/genotoxic activity and estrogenic/antiestrogenic potential of essential oils from seven aromatic plants. Food and Chemical Toxicology. 138. 111205–111205. 19 indexed citations

13.

Bertini, Veronica, Alessia Azzarà, Annalisa Legitimo, et al.. (2017). Deletion Extents Are Not the Cause of Clinical Variability in 22q11.2 Deletion Syndrome: Does the Interaction between DGCR8 and miRNA-CNVs Play a Major Role?. Frontiers in Genetics. 8. 47–47. 17 indexed citations

14.

Bertini, Veronica, Rossella Bruno, Alessia Azzarà, et al.. (2017). Maternal Uniparental Disomy 14 (Temple Syndrome) as a Result of a Robertsonian Translocation. Molecular Syndromology. 8(3). 131–138. 13 indexed citations

15.

Bertini, Veronica, Angelo Valetto, Alessia Azzarà, et al.. (2017). A Case of 22q11 Deletion Syndrome (22q11DS) with a Panayiotopoulos Epileptic Pattern: Are Additional Copy-Number Variations a Possible Second Hit in Modulating the 22q11DS Phenotype?. Frontiers in Pediatrics. 5. 48–48. 4 indexed citations

16.

Azzarà, Alessia, Chiara Pirillo, C Giovannini, Giovanni Federico, & Roberto Scarpato. (2016). Different repair kinetic of DSBs induced by mitomycin C in peripheral lymphocytes of obese and normal weight adolescents. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 789. 9–14. 22 indexed citations

17.

Ry, Silvia Del, Manuela Cabiati, Letizia Guiducci, et al.. (2014). Transcriptional Alterations of ET-1 Axis and DNA Damage in Lung Tissue of a Rat Obesity Model. DNA and Cell Biology. 34(3). 170–177. 4 indexed citations

18.

Scarpato, Roberto, Alessia Azzarà, Francesco Ghetti, et al.. (2013). Kinetics of nuclear phosphorylation ( -H2AX) in human lymphocytes treated in vitro with UVB, bleomycin and mitomycin C. Mutagenesis. 28(4). 465–473. 25 indexed citations

19.

Sbrana, Silverio, L. Ruocco, Renato Vanacore, Alessia Azzarà, & Federico Ambrogi. (1993). In vitro effects of an immunoglobulin preparation for intravenous use (IVIG) on T-cells activation.. PubMed. 25(1). 35–7. 9 indexed citations

20.

Petrini, Massimiliano, et al.. (1981). Increased PHA response to thymostimulin in the elderly. Current Therapeutic Research. 30(3). 367–371. 4 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