Giulia Polo

1.3k total citations
29 papers, 871 citations indexed

About

Giulia Polo is a scholar working on Physiology, Epidemiology and Clinical Biochemistry. According to data from OpenAlex, Giulia Polo has authored 29 papers receiving a total of 871 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Physiology, 8 papers in Epidemiology and 8 papers in Clinical Biochemistry. Recurrent topics in Giulia Polo's work include Lysosomal Storage Disorders Research (18 papers), Metabolism and Genetic Disorders (8 papers) and Cellular transport and secretion (6 papers). Giulia Polo is often cited by papers focused on Lysosomal Storage Disorders Research (18 papers), Metabolism and Genetic Disorders (8 papers) and Cellular transport and secretion (6 papers). Giulia Polo collaborates with scholars based in Italy, United States and Australia. Giulia Polo's co-authors include Alberto Burlina, Alessandro P. Burlina, Chiara Cazzorla, Laura Rubert, Giovanni Duro, Leonardo Salviati, Mario Plebani, Martina Zaninotto, Albina Tummolo and Andrea Dardis and has published in prestigious journals such as Blood, Scientific Reports and Nutrients.

In The Last Decade

Giulia Polo

29 papers receiving 856 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Giulia Polo Italy	17	589	248	228	200	165	29	871
Ana Marcão Portugal	12	402 0.7×	188 0.8×	159 0.7×	169 0.8×	128 0.8×	22	616
María Josep Coll Spain	19	703 1.2×	370 1.5×	158 0.7×	228 1.1×	218 1.3×	37	1.1k
Clare Beesley United Kingdom	17	607 1.0×	288 1.2×	189 0.8×	262 1.3×	240 1.5×	29	980
Raquel Dodelson de Kremer Argentina	17	266 0.5×	395 1.6×	120 0.5×	145 0.7×	93 0.6×	52	735
Severo Pagliardini Italy	11	795 1.3×	193 0.8×	76 0.3×	373 1.9×	267 1.6×	14	988
Simona Fecarotta Italy	17	299 0.5×	207 0.8×	75 0.3×	165 0.8×	82 0.5×	41	775
Ricardo Flores Pires Brazil	15	338 0.6×	286 1.2×	251 1.1×	121 0.6×	81 0.5×	36	624
Alain Fouilhoux France	12	314 0.5×	149 0.6×	134 0.6×	178 0.9×	50 0.3×	22	533
Dimitar Gavrilov United States	15	345 0.6×	403 1.6×	437 1.9×	102 0.5×	83 0.5×	35	901
Janet A. Thomas United States	18	454 0.8×	505 2.0×	481 2.1×	149 0.7×	58 0.4×	40	1.1k

Countries citing papers authored by Giulia Polo

Since Specialization

Citations

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

Fields of papers citing papers by Giulia Polo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giulia Polo

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

Kubaski, Francyne, Inês Sousa, Camilo Silva, et al.. (2023). Pilot Study of Newborn Screening for Six Lysosomal Diseases in Brazil. SSRN Electronic Journal. 1 indexed citations

Kubaski, Francyne, Inês Sousa, Camilo Silva, et al.. (2023). Pilot study of newborn screening for six lysosomal diseases in Brazil. Molecular Genetics and Metabolism. 140(1-2). 107654–107654. 9 indexed citations

Kubaski, Francyne, Alberto Burlina, Giulia Polo, et al.. (2022). Experience of the NPC Brazil Network with a Comprehensive Program for the Screening and Diagnosis of Niemann-Pick Disease Type C. International Journal of Neonatal Screening. 8(3). 39–39. 2 indexed citations

Gragnaniello, Vincenza, Alessandro P. Burlina, Stijn L.M. in ‘t Groen, et al.. (2022). Newborn screening for Pompe disease in Italy: Long-term results and future challenges. Molecular Genetics and Metabolism Reports. 33. 100929–100929. 22 indexed citations

Gragnaniello, Vincenza, Alessandro P. Burlina, Giulia Polo, et al.. (2021). Newborn Screening for Fabry Disease in Northeastern Italy: Results of Five Years of Experience. Biomolecules. 11(7). 951–951. 33 indexed citations

Burlina, Alberto, Giulia Polo, Vincenza Gragnaniello, et al.. (2021). Detection of 3-O-methyldopa in dried blood spots for neonatal diagnosis of aromatic L-amino-acid decarboxylase deficiency: The northeastern Italian experience. Molecular Genetics and Metabolism. 133(1). 56–62. 17 indexed citations

Kubaski, Francyne, Inês Sousa, Alexandre Wagner Silva de Souza, et al.. (2020). Neonatal Screening for MPS Disorders in Latin America: A Survey of Pilot Initiatives. International Journal of Neonatal Screening. 6(4). 90–90. 9 indexed citations

Gragnaniello, Vincenza, Laura Rubert, Francesca Manzoni, et al.. (2020). Report of Five Years of Experience in Neonatal Screening for Mucopolysaccharidosis Type I and Review of the Literature. International Journal of Neonatal Screening. 6(4). 85–85. 12 indexed citations

Polo, Giulia, Laura Rubert, Chiara Cazzorla, et al.. (2020). The combined use of enzyme activity and metabolite assays as a strategy for newborn screening of mucopolysaccharidosis type I. Clinical Chemistry and Laboratory Medicine (CCLM). 58(12). 2063–2072. 16 indexed citations

10.

Burlina, Alberto, Giulia Polo, Laura Rubert, et al.. (2019). Implementation of Second-Tier Tests in Newborn Screening for Lysosomal Disorders in North Eastern Italy. International Journal of Neonatal Screening. 5(2). 24–24. 53 indexed citations

11.

Polo, Giulia, Alessandro P. Burlina, Enzo Ranieri, et al.. (2019). Plasma and dried blood spot lysosphingolipids for the diagnosis of different sphingolipidoses: a comparative study. Clinical Chemistry and Laboratory Medicine (CCLM). 57(12). 1863–1874. 67 indexed citations

12.

Burlina, Alessandro P., et al.. (2019). Large Neutral Amino Acid Therapy Increases Tyrosine Levels in Adult Patients with Phenylketonuria: A Long-Term Study. Nutrients. 11(10). 2541–2541. 16 indexed citations

13.

Williams, Monique, Alberto Burlina, Laura Rubert, et al.. (2018). N-Acetylglutamate Synthase Deficiency Due to a Recurrent Sequence Variant in the N-acetylglutamate Synthase Enhancer Region. Scientific Reports. 8(1). 15436–15436. 8 indexed citations

14.

Cazzorla, Chiara, Giacomo Biasucci, Vincenzo Leuzzi, et al.. (2018). Living with phenylketonuria in adulthood: The PKU ATTITUDE study. Molecular Genetics and Metabolism Reports. 16. 39–45. 79 indexed citations

15.

Donati, Maria Alice, Elisabetta Pasquini, Marco Spada, Giulia Polo, & Alberto Burlina. (2018). Newborn screening in mucopolysaccharidoses. The Italian Journal of Pediatrics/Italian journal of pediatrics. 44(S2). 126–126. 51 indexed citations

16.

Burlina, Alberto, et al.. (2016). Clinical experience with N-carbamylglutamate in a single-centre cohort of patients with propionic and methylmalonic aciduria. Molecular Genetics and Metabolism Reports. 8. 34–40. 16 indexed citations

17.

Reunert, Janine, Amelie S. Lotz‐Havla, Giulia Polo, et al.. (2015). Niemann-Pick Type C-2 Disease: Identification by Analysis of Plasma Cholestane-3β,5α,6β-Triol and Further Insight into the Clinical Phenotype. JIMD Reports. 23. 17–26. 36 indexed citations

18.

Polo, Giulia, Alessandro P. Burlina, Francesca Furlan, et al.. (2015). High level of oxysterols in neonatal cholestasis: a pitfall in analysis of biochemical markers for Niemann-Pick type C disease. Clinical Chemistry and Laboratory Medicine (CCLM). 54(7). 1221–1229. 36 indexed citations

19.

Cazzorla, Chiara, Luca Cegolon, Alessandro P. Burlina, et al.. (2014). Quality of Life (QoL) assessment in a cohort of patients with Phenylketonuria. BMC Public Health. 14(1). 1243–1243. 40 indexed citations

20.

Vettori, Andrea, Enrico Moro, Giovanni Vazza, et al.. (2010). Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy. Neuromuscular Disorders. 21(1). 58–67. 35 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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