Claudia Strafella

1.3k total citations
57 papers, 834 citations indexed

About

Claudia Strafella is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Claudia Strafella has authored 57 papers receiving a total of 834 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 10 papers in Ophthalmology and 10 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Claudia Strafella's work include Muscle Physiology and Disorders (9 papers), Retinal Diseases and Treatments (9 papers) and SARS-CoV-2 and COVID-19 Research (6 papers). Claudia Strafella is often cited by papers focused on Muscle Physiology and Disorders (9 papers), Retinal Diseases and Treatments (9 papers) and SARS-CoV-2 and COVID-19 Research (6 papers). Claudia Strafella collaborates with scholars based in Italy, Albania and United Kingdom. Claudia Strafella's co-authors include Emiliano Giardina, Raffaella Cascella, Valerio Caputo, Giuseppe Novelli, Andrea Termine, Stefania Zampatti, Carlo Caltagirone, Federico Ricci, Paola Borgiani and Andrea Cusumano and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Human Molecular Genetics.

In The Last Decade

Claudia Strafella

54 papers receiving 822 citations

Peers

Claudia Strafella

OPHTH

IMMUN

RNMI

Raffaella Cascella Italy

Valerio Caputo Italy

Richard K. Lee United States

Vedam L. Ramprasad India

Alka Chaubey United States

Shinobu Kura Japan

Laura Collins United States

Heidi Roehrich United States

Dina J. Zand United States

Shen Wu China

Raffaella Cascella Italy

Claudia Strafella

417 ×1.2

210 ×1.3

OPHTH

162 ×1.2

IMMUN

103 ×1.1

114 ×1.2

RNMI

Citations per year, relative to Claudia Strafella Claudia Strafella (= 1×) peers Raffaella Cascella

Countries citing papers authored by Claudia Strafella

Since Specialization

Citations

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

Fields of papers citing papers by Claudia Strafella

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudia Strafella

This figure shows the co-authorship network connecting the top 25 collaborators of Claudia Strafella. A scholar is included among the top collaborators of Claudia Strafella 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 Claudia Strafella. Claudia Strafella 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

Zampatti, Stefania, et al.. (2025). Sample Tracking Tool: A Comprehensive Approach Based on OpenArray Technology and R Scripting for Genomic Sample Monitoring. Diagnostics. 15(2). 149–149.

Zampatti, Stefania, et al.. (2024). RHO Variants and Autosomal Dominant Retinitis Pigmentosa: Insights from the Italian Genetic Landscape. Genes. 15(9). 1158–1158. 1 indexed citations

Strafella, Claudia, et al.. (2024). Federated Learning: Breaking Down Barriers in Global Genomic Research. Genes. 15(12). 1650–1650. 8 indexed citations

Zampatti, Stefania, et al.. (2024). AI-Powered Neurogenetics: Supporting Patient’s Evaluation with Chatbot. Genes. 16(1). 29–29. 1 indexed citations

Zampatti, Stefania, et al.. (2024). Innovations in Medicine: Exploring ChatGPT’s Impact on Rare Disorder Management. Genes. 15(4). 421–421. 8 indexed citations

Strafella, Claudia, Luca Colantoni, Guido Primiano, et al.. (2023). Characterization of D4Z4 alleles and assessment of de novo cases in Facioscapulohumeral dystrophy (FSHD) in a cohort of Italian families. Clinical Genetics. 105(3). 335–339. 3 indexed citations

Caputo, Valerio, et al.. (2023). Epigenetic profiling of the D4Z4 locus: Optimization of the protocol for studying DNA methylation at single CpG site level. Electrophoresis. 44(19-20). 1588–1594. 1 indexed citations

Manzo, L., et al.. (2021). Evaluation of OpenArray™ as a Genotyping Method for Forensic DNA Phenotyping and Human Identification. Genes. 12(2). 221–221. 15 indexed citations

Caputo, Valerio, Claudia Strafella, Terenzio Cosio, et al.. (2021). Pharmacogenomics: An Update on Biologics and Small-Molecule Drugs in the Treatment of Psoriasis. Genes. 12(9). 1398–1398. 32 indexed citations

10.

Strafella, Claudia, Raffaella Cascella, Valerio Caputo, et al.. (2021). Deregulation of ncRNA in Neurodegenerative Disease: Focus on circRNA, lncRNA and miRNA in Amyotrophic Lateral Sclerosis. Frontiers in Genetics. 12. 784996–784996. 27 indexed citations

11.

Strafella, Claudia, Valerio Caputo, Andrea Termine, et al.. (2021). Genetic Determinants Highlight the Existence of Shared Etiopathogenetic Mechanisms Characterizing Age-Related Macular Degeneration and Neurodegenerative Disorders. Frontiers in Neurology. 12. 626066–626066. 11 indexed citations

12.

Strafella, Claudia, Valerio Caputo, Andrea Termine, et al.. (2020). Analysis of ACE2 Genetic Variability among Populations Highlights a Possible Link with COVID-19-Related Neurological Complications. Genes. 11(7). 741–741. 60 indexed citations

13.

Caputo, Valerio, Claudia Strafella, Andrea Termine, et al.. (2020). RNAseq-Based Prioritization Revealed COL6A5, COL8A1, COL10A1 and MIR146A as Common and Differential Susceptibility Biomarkers for Psoriasis and Psoriatic Arthritis: Confirmation from Genotyping Analysis of 1417 Italian Subjects. International Journal of Molecular Sciences. 21(8). 2740–2740. 16 indexed citations

14.

Caputo, Valerio, Andrea Termine, Claudia Strafella, Emiliano Giardina, & Raffaella Cascella. (2020). Shared (epi)genomic background connecting neurodegenerative diseases and type 2 diabetes. World Journal of Diabetes. 11(5). 155–164. 8 indexed citations

15.

Strafella, Claudia, Valerio Caputo, G. Pagliaroli, et al.. (2019). Limb-Girdle Muscular Dystrophies (LGMDs): The Clinical Application of NGS Analysis, a Family Case Report. Frontiers in Neurology. 10. 619–619. 10 indexed citations

16.

Zampatti, Stefania, Luca Colantoni, Claudia Strafella, et al.. (2019). Facioscapulohumeral muscular dystrophy (FSHD) molecular diagnosis: from traditional technology to the NGS era. Neurogenetics. 20(2). 57–64. 18 indexed citations

17.

Cascella, Raffaella, Claudia Strafella, Valerio Caputo, et al.. (2018). Digenic Inheritance of Shortened Repeat Units of the D4Z4 Region and a Loss-of-Function Variant in SMCHD1 in a Family With FSHD. Frontiers in Neurology. 9. 1027–1027. 10 indexed citations

18.

Cascella, Raffaella, Claudia Strafella, L. Manzo, et al.. (2017). Assessing individual risk for AMD with genetic counseling, family history, and genetic testing. Eye. 32(2). 446–450. 20 indexed citations

19.

Cascella, Raffaella, Claudia Strafella, Valerio Caputo, et al.. (2017). Towards the application of precision medicine in Age-Related Macular Degeneration. Progress in Retinal and Eye Research. 63. 132–146. 55 indexed citations

20.

Cascella, Raffaella, Claudia Strafella, Stefania Zampatti, et al.. (2014). Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01. The Pharmacogenomics Journal. 15(2). 196–200. 27 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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