Pietro Strisciuglio

4.2k total citations
131 papers, 2.9k citations indexed

About

Pietro Strisciuglio is a scholar working on Molecular Biology, Physiology and Rheumatology. According to data from OpenAlex, Pietro Strisciuglio has authored 131 papers receiving a total of 2.9k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Molecular Biology, 36 papers in Physiology and 26 papers in Rheumatology. Recurrent topics in Pietro Strisciuglio's work include Lysosomal Storage Disorders Research (24 papers), Metabolism and Genetic Disorders (22 papers) and Folate and B Vitamins Research (12 papers). Pietro Strisciuglio is often cited by papers focused on Lysosomal Storage Disorders Research (24 papers), Metabolism and Genetic Disorders (22 papers) and Folate and B Vitamins Research (12 papers). Pietro Strisciuglio collaborates with scholars based in Italy, United States and Netherlands. Pietro Strisciuglio's co-authors include Daniela Concolino, Generoso Andria, Giancarlo Parenti, William S. Sly, Licia Pensabene, Rossella Parini, Peiyi Hu, Giuseppe Bonapace, Gianfranco Sebastio and Francesco Pallone and has published in prestigious journals such as Journal of Clinical Investigation, Nature Genetics and Gastroenterology.

In The Last Decade

Pietro Strisciuglio

126 papers receiving 2.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pietro Strisciuglio Italy 30 1.1k 656 597 532 442 131 2.9k
B. Kristiansson Sweden 30 1.3k 1.2× 484 0.7× 599 1.0× 335 0.6× 172 0.4× 81 2.7k
Daniela Concolino Italy 24 630 0.6× 147 0.2× 217 0.4× 661 1.2× 260 0.6× 130 1.9k
Mariacarolina Salerno Italy 36 945 0.9× 371 0.6× 119 0.2× 282 0.5× 187 0.4× 160 3.7k
S Tarui Japan 31 756 0.7× 929 1.4× 112 0.2× 419 0.8× 177 0.4× 126 3.4k
Yeong‐Hau H. Lien United States 32 953 0.9× 345 0.5× 85 0.1× 620 1.2× 223 0.5× 85 3.1k
Tohru Yorifuji Japan 35 1.5k 1.4× 982 1.5× 670 1.1× 381 0.7× 192 0.4× 168 3.6k
Michael Sørensen Denmark 32 274 0.3× 1.3k 1.9× 228 0.4× 208 0.4× 810 1.8× 122 2.8k
Michael T. Geraghty United States 36 1.9k 1.7× 337 0.5× 913 1.5× 422 0.8× 351 0.8× 121 3.6k
D. J. Carson United Kingdom 23 260 0.2× 509 0.8× 117 0.2× 263 0.5× 135 0.3× 69 1.7k
Ina Knerr Germany 29 808 0.8× 278 0.4× 626 1.0× 486 0.9× 193 0.4× 110 2.5k

Countries citing papers authored by Pietro Strisciuglio

Since Specialization
Citations

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

Fields of papers citing papers by Pietro Strisciuglio

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pietro Strisciuglio

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

All Works

20 of 20 papers shown
1.
Fecarotta, Simona, Valeria De Pasquale, Pietro Strisciuglio, et al.. (2025). Digital microfluidic platform for dried blood spot newborn screening of lysosomal storage diseases in Campania region (Italy): Findings from the first year pilot project. Molecular Genetics and Metabolism. 144(2). 109008–109008. 1 indexed citations
2.
Rossi, Alessandro, Chiara Simeoli, Rosario Pivonello, et al.. (2024). Endocrine involvement in hepatic glycogen storage diseases: pathophysiology and implications for care. Reviews in Endocrine and Metabolic Disorders. 25(4). 707–725. 4 indexed citations
3.
Borrelli, Melissa, Roberto Rongo, Elena Cantone, et al.. (2022). Obstructive Sleep Apnoea in Children with Down Syndrome: A Multidisciplinary Approach. Journal of Personalized Medicine. 13(1). 71–71. 5 indexed citations
4.
Scala, Iris, Daniela Concolino, Giulia Esposito, et al.. (2021). Beneficial Effects of Slow-Release Large Neutral Amino Acids after a Phenylalanine Oral Load in Patients with Phenylketonuria. Nutrients. 13(11). 4012–4012. 4 indexed citations
5.
6.
D’Amico, Alessandra, Carmen L. Rosano, Luca Pannone, et al.. (2021). Clinical variability of neurofibromatosis 1: A modifying role of cooccurring PTPN11 variants and atypical brain MRI findings. Clinical Genetics. 100(5). 563–572. 5 indexed citations
7.
Riccio, Maria Pia, et al.. (2021). Expanding the neurological and behavioral phenotype of White-Sutton syndrome: a case report. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 47(1). 148–148. 4 indexed citations
8.
9.
Fischetto, Rita, Maria Margherita Mancardi, Thea Giacomini, et al.. (2020). Substrate reduction therapy with Miglustat in pediatric patients with GM1 type 2 gangliosidosis delays neurological involvement: A multicenter experience. Molecular Genetics & Genomic Medicine. 8(10). e1371–e1371. 20 indexed citations
10.
Rocco, Maja Di, Alessio Di Fonzo, Antonio Barbato, et al.. (2020). Parkinson’s disease in Gaucher disease patients: what’s changing in the counseling and management of patients and their relatives?. Orphanet Journal of Rare Diseases. 15(1). 262–262. 5 indexed citations
11.
Fecarotta, Simona, Vincenza Gragnaniello, Roberto Della Casa, et al.. (2018). Steroid therapy in an alpha-dystroglycanopathy due to GMPPB gene mutations: A case report. Neuromuscular Disorders. 28(11). 956–960. 4 indexed citations
12.
Oderda, Giuseppina, P. Lerro, Gian Luigi de’Angelis, et al.. (2004). Dual vs. Triple Therapy for Childhood Helicobacter pylori Gastritis: a Double‐Blind Randomized Multicentre Trial. Helicobacter. 9(4). 293–301. 28 indexed citations
13.
Andria, Generoso, Daniela Concolino, Maria Piccione, et al.. (2003). Down syndrome and breastfeeding. Acta Paediatrica. 92(12). 1479–1481. 31 indexed citations
14.
Luzza, Francesco, Maria Imeneo, Licia Pensabene, et al.. (2000). Evidence favouring the gastro-oral route in the transmission of Helicobacter pylori infection in children. European Journal of Gastroenterology & Hepatology. 12(6). 623–627. 17 indexed citations
15.
Santamaria, Francesca, Giancarlo Parenti, Guido De Guidi, et al.. (1998). Pulmonary Manifestations of Gaucher Disease: An Increased Risk for L444P Homozygotes?. American Journal of Respiratory and Critical Care Medicine. 157(3). 985–989. 42 indexed citations
16.
Santamaria, Francesca, Giancarlo Parenti, Guido De Guidi, et al.. (1996). Early Detection of Lung Involvement in Lysinuric Protein Intolerance: Role of High-Resolution Computed Tomography and Radioisotopic Methods. American Journal of Respiratory and Critical Care Medicine. 153(2). 731–735. 34 indexed citations
17.
Concolino, Daniela, et al.. (1993). Long survival of a patient with Marshall-Smith syndrome without respiratory complications.. Journal of Medical Genetics. 30(10). 877–879. 20 indexed citations
18.
Parenti, Giancarlo, R. de Franchis, Vincenzo Farina, et al.. (1992). Clinical variability of cardio‐facio‐cutaneous syndrome: report of two additional cases. Clinical Genetics. 42(4). 206–209. 13 indexed citations
19.
Ballabio, Andrea, Massimo Zollo, Rosalba Carrozzo, et al.. (1991). Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X‐linked ichthyosis due to steroid sulfatase deficiency. American Journal of Medical Genetics. 41(2). 184–187. 16 indexed citations
20.
Andria, Generoso, Paola Di Natale, Ennio Del Giudice, Pietro Strisciuglio, & Patrizia Murino. (1979). Sanfilippo B syndrome (MPS III B): mild and severe forms within the same sibship. Clinical Genetics. 15(6). 500–504. 29 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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