Severo Pagliardini

1.6k total citations · 1 hit paper
14 papers, 988 citations indexed

About

Severo Pagliardini is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, Severo Pagliardini has authored 14 papers receiving a total of 988 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Physiology and 4 papers in Clinical Biochemistry. Recurrent topics in Severo Pagliardini's work include Lysosomal Storage Disorders Research (5 papers), Metabolism and Genetic Disorders (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). Severo Pagliardini is often cited by papers focused on Lysosomal Storage Disorders Research (5 papers), Metabolism and Genetic Disorders (4 papers) and Glycogen Storage Diseases and Myoclonus (3 papers). Severo Pagliardini collaborates with scholars based in Italy, United States and Belgium. Severo Pagliardini's co-authors include Marco Spada, Alberto Ponzone, Robert J. Desnick, Geetha Thiagarajan, Turgut Tükel, Hitoshi Sakuraba, Makiko Yasuda, Veronica Pagliardini, Francesco Porta and Giancarlo Parenti and has published in prestigious journals such as The American Journal of Human Genetics, Nutrients and Clinica Chimica Acta.

In The Last Decade

Severo Pagliardini

14 papers receiving 956 citations

Hit Papers

High Incidence of Later-O... 2006 2026 2012 2019 2006 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. High Incidence of Later-Onset Fabry Disease Revealed by Newborn Screening*
    2006 713 citations Marco Spada, Severo Pagliardini et al. The American Journal of Human Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Severo Pagliardini Italy 11 795 373 267 263 216 14 988
Bouwien E. Smid Netherlands 12 797 1.0× 362 1.0× 256 1.0× 210 0.8× 245 1.1× 13 860
Margaret Timmons United States 8 603 0.8× 267 0.7× 196 0.7× 180 0.7× 220 1.0× 10 761
Giulia Polo Italy 17 589 0.7× 200 0.5× 165 0.6× 132 0.5× 151 0.7× 29 871
Roberta Ricci Italy 10 458 0.6× 267 0.7× 103 0.4× 201 0.8× 171 0.8× 15 752
Ana Marcão Portugal 12 402 0.5× 169 0.5× 128 0.5× 160 0.6× 95 0.4× 22 616
Carmela Zizzo Italy 14 384 0.5× 140 0.4× 122 0.5× 118 0.4× 117 0.5× 34 490
Celeste Decker United States 17 550 0.7× 258 0.7× 52 0.2× 236 0.9× 46 0.2× 21 685
Simona Fecarotta Italy 17 299 0.4× 165 0.4× 82 0.3× 144 0.5× 121 0.6× 41 775
Alexander Broomfield United Kingdom 14 358 0.5× 124 0.3× 81 0.3× 137 0.5× 54 0.3× 54 613
Miriam Rigoldi Italy 16 286 0.4× 114 0.3× 88 0.3× 228 0.9× 42 0.2× 29 544

Countries citing papers authored by Severo Pagliardini

Since Specialization
Citations

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

Fields of papers citing papers by Severo Pagliardini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Severo Pagliardini

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

All Works

14 of 14 papers shown
1.
Mussa, Alessandro, Veronica Pagliardini, Severo Pagliardini, et al.. (2019). Longitudinal Monitoring of Alpha-Fetoprotein by Dried Blood Spot for Hepatoblastoma Screening in Beckwith–Wiedemann Syndrome. Cancers. 11(1). 86–86. 9 indexed citations
2.
Dato, Fabiola Di, Maria Grazia Caprio, Severo Pagliardini, et al.. (2019). Daily Fructose Traces Intake and Liver Injury in Children with Hereditary Fructose Intolerance. Nutrients. 11(10). 2397–2397. 14 indexed citations
3.
Porta, Francesco, Veronica Pagliardini, Severo Pagliardini, et al.. (2017). Neonatal screening for biotinidase deficiency: A 30-year single center experience. Molecular Genetics and Metabolism Reports. 13. 80–82. 11 indexed citations
4.
Porta, Francesco, Severo Pagliardini, Veronica Pagliardini, Alberto Ponzone, & Marco Spada. (2015). Newborn screening for galactosemia: a 30-year single center experience. World Journal of Pediatrics. 11(2). 160–164. 18 indexed citations
5.
Mussa, Alessandro, Severo Pagliardini, Veronica Pagliardini, et al.. (2014). α-Fetoprotein assay on dried blood spot for hepatoblastoma screening in children with overgrowth-cancer predisposition syndromes. Pediatric Research. 76(6). 544–548. 10 indexed citations
6.
Pagliardini, Veronica, Severo Pagliardini, Lucia Corrado, et al.. (2014). Chitotriosidase and lysosomal enzymes as potential biomarkers of disease progression in amyotrophic lateral sclerosis: A survey clinic-based study. Journal of the Neurological Sciences. 348(1-2). 245–250. 31 indexed citations
7.
Spada, Marco, Francesco Porta, Liliana Vercelli, et al.. (2013). Screening for later-onset Pompe's disease in patients with paucisymptomatic hyperCKemia. Molecular Genetics and Metabolism. 109(2). 171–173. 35 indexed citations
8.
Paciotti, Silvia, Emanuele Persichetti, Severo Pagliardini, et al.. (2012). First pilot newborn screening for four lysosomal storage diseases in an Italian region: Identification and analysis of a putative causative mutation in the GBA gene. Clinica Chimica Acta. 413(23-24). 1827–1831. 46 indexed citations
9.
Kotanko, Peter, Marco Spada, Severo Pagliardini, et al.. (2009). Anderson-Fabry disease: a case-finding study among male kidney transplant recipients in Austria. Transplant International. 22(3). 287–292. 29 indexed citations
10.
Calvo, Pier Luigi, Severo Pagliardini, M. Baldi, et al.. (2008). Long‐standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx. Journal of Inherited Metabolic Disease. 31(S2). 437–440. 9 indexed citations
11.
Spada, Marco, Severo Pagliardini, Makiko Yasuda, et al.. (2006). High Incidence of Later-Onset Fabry Disease Revealed by Newborn Screening*. The American Journal of Human Genetics. 79(1). 31–40. 713 indexed citations breakdown →
12.
Mandato, Claudia, Lena Brive, Yoshiaki Miura, et al.. (2006). Cryptogenic Liver Disease in Four Children: A Novel Congenital Disorder of Glycosylation. Pediatric Research. 59(2). 293–298. 38 indexed citations
13.
Rocco, Mattia, Thierry Hennet, Claudia E. Grubenmann, et al.. (2005). Congenital disorder of glycosylation (CDG) Ig: Report on a patient and review of the literature. Journal of Inherited Metabolic Disease. 28(6). 1162–1164. 18 indexed citations
14.
Silengo, Margherita, Mariella Valenzise, Severo Pagliardini, & Marco Spada. (2003). Hair changes in congenital disorders of glycosylation (CDG type 1). European Journal of Pediatrics. 162(2). 114–115. 7 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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