Alberto Ponzone

2.8k total citations · 1 hit paper
34 papers, 1.8k citations indexed

About

Alberto Ponzone is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Alberto Ponzone has authored 34 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Clinical Biochemistry, 11 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Alberto Ponzone's work include Metabolism and Genetic Disorders (22 papers), Folate and B Vitamins Research (9 papers) and Neonatal Health and Biochemistry (8 papers). Alberto Ponzone is often cited by papers focused on Metabolism and Genetic Disorders (22 papers), Folate and B Vitamins Research (9 papers) and Neonatal Health and Biochemistry (8 papers). Alberto Ponzone collaborates with scholars based in Italy, Switzerland and Australia. Alberto Ponzone's co-authors include Marco Spada, Severo Pagliardini, Hitoshi Sakuraba, Geetha Thiagarajan, Turgut Tükel, Robert J. Desnick, Makiko Yasuda, Irma Dianzani, Francesco Porta and Manuela Ceccarelli and has published in prestigious journals such as PEDIATRICS, Annals of the New York Academy of Sciences and Journal of the American Society of Nephrology.

In The Last Decade

Alberto Ponzone

33 papers receiving 1.7k citations

Hit Papers

High Incidence of Later-Onset Fabry Disease Revealed by N... 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
Alberto Ponzone Italy 15 850 631 546 455 353 34 1.8k
Guillem Pintos‐Morell Spain 25 1.3k 1.6× 449 0.7× 490 0.9× 526 1.2× 558 1.6× 94 2.2k
Klary E. Niezen‐Koning Netherlands 22 930 1.1× 522 0.8× 709 1.3× 395 0.9× 367 1.0× 59 1.8k
Marco Spada Italy 28 1.6k 1.9× 1.0k 1.6× 1.1k 2.0× 716 1.6× 700 2.0× 132 3.1k
Anaïs Brassier France 19 714 0.8× 389 0.6× 608 1.1× 168 0.4× 230 0.7× 84 1.7k
Federica Deodato Italy 23 640 0.8× 608 1.0× 801 1.5× 404 0.9× 217 0.6× 55 1.7k
Julian Raiman Canada 24 738 0.9× 334 0.5× 559 1.0× 439 1.0× 331 0.9× 58 1.5k
José E. Abdenur United States 24 446 0.5× 818 1.3× 978 1.8× 454 1.0× 102 0.3× 63 1.8k
Wenjuan Qiu China 22 378 0.4× 606 1.0× 730 1.3× 373 0.8× 142 0.4× 146 1.5k
Carolina Fischinger Moura de Souza Brazil 19 427 0.5× 362 0.6× 507 0.9× 279 0.6× 170 0.5× 110 1.2k
Deborah Marsden United States 24 532 0.6× 1.2k 1.9× 854 1.6× 283 0.6× 91 0.3× 65 1.8k

Countries citing papers authored by Alberto Ponzone

Since Specialization
Citations

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

Fields of papers citing papers by Alberto Ponzone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alberto Ponzone

This figure shows the co-authorship network connecting the top 25 collaborators of Alberto Ponzone. A scholar is included among the top collaborators of Alberto Ponzone 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 Alberto Ponzone. Alberto Ponzone 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.
Porta, Francesco, Alberto Ponzone, & Marco Spada. (2020). Neonatal phenylalanine wash-out in phenylketonuria. Metabolic Brain Disease. 35(7). 1225–1229. 4 indexed citations
2.
Porta, Francesco, Alberto Ponzone, & Marco Spada. (2020). Phenylalanine and tyrosine metabolism in DNAJC12 deficiency: A comparison between inherited hyperphenylalaninemias and healthy subjects. European Journal of Paediatric Neurology. 28. 77–80. 9 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, Alberto Ponzone, & Marco Spada. (2016). Long-term safety and effectiveness of pramipexole in tetrahydrobiopterin deficiency. European Journal of Paediatric Neurology. 20(6). 839–842. 9 indexed citations
5.
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
6.
Porta, Francesco, Alberto Ponzone, & Marco Spada. (2015). Short prolactin profile for monitoring treatment in BH4 deficiency. European Journal of Paediatric Neurology. 19(3). 360–363. 9 indexed citations
7.
Porta, Francesco, Alberto Ponzone, & Marco Spada. (2015). Target Prolactin Range in Treatment of Tetrahydrobiopterin Deficiency. The Journal of Pediatrics. 168. 236–239.e1. 2 indexed citations
8.
Porta, Francesco, Alessandro Mussa, Giuseppina Baldassarre, et al.. (2015). Genealogy of breastfeeding. European Journal of Pediatrics. 175(1). 105–112. 6 indexed citations
9.
Porta, Francesco, Alessandro Mussa, Daniela Concolino, Marco Spada, & Alberto Ponzone. (2012). Dopamine agonists in dihydropteridine reductase deficiency. Molecular Genetics and Metabolism. 105(4). 582–584. 11 indexed citations
10.
Ferraris, Silvio, Emanuela Garelli, Adriana Carando, et al.. (2009). HDR syndrome: A novel “de novo” mutation in GATA3 gene. American Journal of Medical Genetics Part A. 149A(4). 770–775. 36 indexed citations
11.
Ponzone, Alberto, et al.. (2009). Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiency. Metabolism. 59(5). 645–652. 12 indexed citations
12.
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 →
13.
Ponzone, Alberto, Marco Spada, Silvio Ferraris, Irma Dianzani, & Luisa De Sanctis. (2003). Dihydropteridine reductase deficiency in man: From biology to treatment. Medicinal Research Reviews. 24(2). 127–150. 59 indexed citations
14.
Dianzani, Irma, Ulf Landegren, Clara Camaschella, et al.. (1999). Fifth International Mutation Detection Workshop, May 13-16, 1999, Vicoforte, Italy. Human Mutation. 14(6). 451–453. 4 indexed citations
15.
Guldberg, Per, Françoise Rey, Johannes Zschocke, et al.. (1998). A European Multicenter Study of Phenylalanine Hydroxylase Deficiency: Classification of 105 Mutations and a General System for Genotype-Based Prediction of Metabolic Phenotype. The American Journal of Human Genetics. 63(1). 71–79. 278 indexed citations
16.
Dianzani, Irma, Luisa De Sanctis, Peter M. Smooker, et al.. (1998). Dihydropteridine reductase deficiency: Physical structure of the QDPR gene, identification of two new mutations and genotype–phenotype correlations. Human Mutation. 12(4). 267–273. 34 indexed citations
17.
Thöny, Beat, A. Matasović, Claus W. Heizmann, et al.. (1997). Identification of mutations causing 6-pyruvoyl-tetrahydropterin synthase deficiency in four Italian families. Human Mutation. 10(1). 25–35. 21 indexed citations
18.
Sanctis, Luisa De, Carla Alliaudi, Marco Spada, et al.. (1996). Mutations and Phenotypes In Dihydropteridine Reductase Deficiency in Italy. Pteridines. 7(3). 103–106. 2 indexed citations
19.
Gasparini, Paolo, Marı́a Julia Calonge, Luigi Bisceglia, et al.. (1995). Molecular genetics of cystinuria: identification of four new mutations and seven polymorphisms, and evidence for genetic heterogeneity.. PubMed. 57(4). 781–8. 72 indexed citations
20.
Romano, Valentino, Irma Dianzani, Alberto Ponzone, et al.. (1994). Prenatal diagnosis by minisatellite analysis in italian families with phenylketonuria. Prenatal Diagnosis. 14(10). 959–962. 8 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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