Andrea Dardis

4.2k total citations
98 papers, 2.6k citations indexed

About

Andrea Dardis is a scholar working on Physiology, Molecular Biology and Organic Chemistry. According to data from OpenAlex, Andrea Dardis has authored 98 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Physiology, 30 papers in Molecular Biology and 27 papers in Organic Chemistry. Recurrent topics in Andrea Dardis's work include Lysosomal Storage Disorders Research (76 papers), Carbohydrate Chemistry and Synthesis (27 papers) and Glycogen Storage Diseases and Myoclonus (20 papers). Andrea Dardis is often cited by papers focused on Lysosomal Storage Disorders Research (76 papers), Carbohydrate Chemistry and Synthesis (27 papers) and Glycogen Storage Diseases and Myoclonus (20 papers). Andrea Dardis collaborates with scholars based in Italy, United States and Argentina. Andrea Dardis's co-authors include Bruno Bembi, Stefania Zampieri, Mirella Filocamo, Giovanni Ciana, Emanuele Buratti, Paolo Peruzzo, Tommaso Beccari, Annalisa Sechi, Silvia Paciotti and María Gabriela Pittis and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Andrea Dardis

94 papers receiving 2.6k citations

Peers

Andrea Dardis

PHYSI

RHEUM

Joan Keutzer United States

Frédéric Sedel France

Helen Michelakakis Greece

Bruno Bembi Italy

Kim M. Hemsley Australia

Olimpia Musumeci Italy

Mercè Pineda Spain

Ruth Navon Israel

Alessandro Simonati Italy

Marcus Deschauer Germany

Joan Keutzer United States

Andrea Dardis

2.3k ×1.2

PHYSI

498 ×0.7

561 ×1.1

662 ×1.4

RHEUM

598 ×1.2

Citations per year, relative to Andrea Dardis Andrea Dardis (= 1×) peers Joan Keutzer

Countries citing papers authored by Andrea Dardis

Since Specialization

Citations

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

Fields of papers citing papers by Andrea Dardis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrea Dardis

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

Peruzzo, Paolo, Natascha Bergamin, Alessandra Longo, et al.. (2025). Rescue of common and rare exon 2 skipping variants of the GAA gene using modified U1 snRNA. Molecular Medicine. 31(1). 45–45.

D’Avanzo, Francesca, Alessandra Zanetti, Andrea Dardis, et al.. (2023). Mucopolysaccharidoses Differential Diagnosis by Mass Spectrometry-Based Analysis of Urine Free Glycosaminoglycans—A Diagnostic Prediction Model. Biomolecules. 13(3). 532–532. 2 indexed citations

Zampieri, Stefania, Antonio Barbato, Agata Fiumara, et al.. (2021). Accurate Molecular Diagnosis of Gaucher Disease Using Clinical Exome Sequencing as a First-Tier Test. International Journal of Molecular Sciences. 22(11). 5538–5538. 7 indexed citations

Ladelfa, María Fátima, Leticia Y. Peche, Stefania Zampieri, et al.. (2021). Expression of the tumor-expressed protein MageB2 enhances rRNA transcription. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1868(7). 119015–119015. 4 indexed citations

Dardis, Andrea, et al.. (2020). Pre-mRNA splicing defects and RNA binding protein involvement in Niemann Pick type C disease. Journal of Biotechnology. 318. 20–30. 4 indexed citations

Colaço, Alexandria, Elias Adriaenssens, Lianne C. Davis, et al.. (2019). Mechanistic convergence and shared therapeutic targets in Niemann‐Pick disease. Journal of Inherited Metabolic Disease. 43(3). 574–585. 15 indexed citations

Bergsma, Atze J., Stijn L.M. in ‘t Groen, Nadine A. M. E. van der Beek, et al.. (2019). A genetic modifier of symptom onset in Pompe disease. EBioMedicine. 43. 553–561. 33 indexed citations

Peruzzo, Paolo, et al.. (2017). Glycogen Reduction in Myotubes of Late-Onset Pompe Disease Patients Using Antisense Technology. Molecular Therapy. 25(9). 2117–2128. 25 indexed citations

Canterini, Sonia, Jessica Dragotto, Andrea Dardis, et al.. (2017). Shortened primary cilium length and dysregulated Sonic hedgehog signaling in Niemann-Pick C1 disease. Human Molecular Genetics. 26(12). 2277–2289. 53 indexed citations

10.

Devigili, Grazia, Giovanni Ciana, Andrea Dardis, et al.. (2017). Chronic pain in Gaucher disease: skeletal or neuropathic origin?. Orphanet Journal of Rare Diseases. 12(1). 148–148. 20 indexed citations

11.

Dardis, Andrea, Stefania Zampieri, Sonia Canterini, et al.. (2016). Altered localization and functionality of TAR DNA Binding Protein 43 (TDP-43) in niemann- pick disease type C. Acta Neuropathologica Communications. 4(1). 52–52. 29 indexed citations

12.

D’Amico, Adele, Enrico Bertini, Andrea Dardis, et al.. (2013). Efficacy of Miglustat in Niemann–Pick C disease: A single centre experience. Molecular Genetics and Metabolism. 110(3). 329–335. 16 indexed citations

13.

Dardis, Andrea, Stefania Zampieri, Cristiana Stuani, et al.. (2013). Functional characterization of the common c.-32-13T>G mutation of GAA gene: identification of potential therapeutic agents. Nucleic Acids Research. 42(2). 1291–1302. 38 indexed citations

14.

Grossi, Serena, Marta Deganuto, Camillo Rosano, et al.. (2013). Functional analysis of 11 novel GBA alleles. European Journal of Human Genetics. 22(4). 511–516. 41 indexed citations

15.

Rocco, Maja Di, Andrea Dardis, Annalisa Madeo, Rita Barone, & Agata Fiumara. (2012). Early Miglustat Therapy in Infantile Niemann-Pick Disease Type C. Pediatric Neurology. 47(1). 40–43. 24 indexed citations

16.

Filippi, Paola De, Sabrina Ravaglia, Bruno Bembi, et al.. (2010). The angiotensin-converting enzyme insertion/deletion polymorphism modifies the clinical outcome in patients with Pompe disease. Genetics in Medicine. 12(4). 206–211. 24 indexed citations

17.

Zampieri, Stefania, Synthia H. Mellon, Terry D. Butters, et al.. (2008). Oxidative stress in NPC1 deficient cells: protective effect of allopregnanolone. Journal of Cellular and Molecular Medicine. 13(9b). 3786–3796. 99 indexed citations

18.

Bembi, Bruno, Mirella Filocamo, Giancarlo Parenti, et al.. (2006). Mutation profile of theGAA gene in 40 Italian patients with late onset glycogen storage disease type II. Human Mutation. 27(10). 999–1006. 103 indexed citations

19.

Dardis, Andrea & W L Miller. (2003). Dexamethasone does not exert direct intracellular feedback on steroidogenesis in human adrenal NCI-H295A cells. Journal of Endocrinology. 179(1). 131–142. 21 indexed citations

20.

Dardis, Andrea, Nora Saraco, Marco A. Rivarola, & Alicia Belgorosky. (1999). Decrease in the Expression of the 3β-Hydroxysteroid Dehydrogenase Gene in Human Adrenal Tissue during Prepuberty and Early Puberty: Implications for the Mechanism of Adrenarche. Pediatric Research. 45(3). 384–388. 41 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