A Ponzone

1.1k total citations
56 papers, 729 citations indexed

About

A Ponzone is a scholar working on Clinical Biochemistry, Molecular Biology and Genetics. According to data from OpenAlex, A Ponzone has authored 56 papers receiving a total of 729 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Clinical Biochemistry, 25 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in A Ponzone's work include Metabolism and Genetic Disorders (33 papers), Biochemical and Molecular Research (16 papers) and Neonatal Health and Biochemistry (10 papers). A Ponzone is often cited by papers focused on Metabolism and Genetic Disorders (33 papers), Biochemical and Molecular Research (16 papers) and Neonatal Health and Biochemistry (10 papers). A Ponzone collaborates with scholars based in Italy, Switzerland and Australia. A Ponzone's co-authors include Richard G.H. Cotton, Irma Dianzani, Ornella Guardamagna, Marco Spada, A. Niederwieser, H.‐Ch. Curtius, Nenad Blau, Clara Camaschella, Riccardo Ponzone and L. Kierat and has published in prestigious journals such as Neurology, Trends in Genetics and The Journal of Pediatrics.

In The Last Decade

A Ponzone

55 papers receiving 710 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A Ponzone Italy 16 468 366 160 132 127 56 729
Niels Gregersen Denmark 14 535 1.1× 630 1.7× 86 0.5× 70 0.5× 121 1.0× 28 935
L. Kierat Switzerland 13 266 0.6× 271 0.7× 90 0.6× 63 0.5× 139 1.1× 26 496
Patrik Feyh Germany 11 349 0.7× 277 0.8× 86 0.5× 75 0.6× 133 1.0× 18 477
Alan S. Lidsky United States 9 577 1.2× 582 1.6× 39 0.2× 94 0.7× 295 2.3× 10 855
Alice Masurel‐Paulet France 15 164 0.4× 344 0.9× 105 0.7× 79 0.6× 63 0.5× 26 800
Elena Martín‐Hernández Spain 16 331 0.7× 408 1.1× 69 0.4× 52 0.4× 88 0.7× 41 596
Andrew A.M. Morris United Kingdom 11 606 1.3× 701 1.9× 40 0.3× 39 0.3× 70 0.6× 16 851
Annette S. Feigenbaum Canada 11 387 0.8× 374 1.0× 73 0.5× 54 0.4× 87 0.7× 13 620
Christine Makowski Germany 10 143 0.3× 229 0.6× 94 0.6× 33 0.3× 37 0.3× 18 480
B. Bertagnolio Italy 13 184 0.4× 249 0.7× 27 0.2× 25 0.2× 61 0.5× 21 470

Countries citing papers authored by A Ponzone

Since Specialization
Citations

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

Fields of papers citing papers by A Ponzone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A Ponzone

This figure shows the co-authorship network connecting the top 25 collaborators of A Ponzone. A scholar is included among the top collaborators of A 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 A Ponzone. A 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.
Leuzzi, Vincenzo, Alberto Burlina, R. Cerone, et al.. (2010). Phenotypic variability, neurological outcome and genetics background of 6‐pyruvoyl‐tetrahydropterin synthase deficiency. Clinical Genetics. 77(3). 249–257. 48 indexed citations
2.
Dianzani, Irma, Luisa De Sanctis, Marco Spada, & A Ponzone. (2000). Genetic testing of hyperphenylalaninemias. 12(2). 71–82. 1 indexed citations
3.
Spada, Marco, et al.. (1998). Phenylalanine and tyrosine metabolism in phenylketonuria heterozygotes: Influence of different phenylalanine hydroxylase mutations. Journal of Inherited Metabolic Disease. 21(3). 236–239. 7 indexed citations
4.
Spada, Marco, Nenad Blau, Concetta Meli, et al.. (1996). Different Strategies In the Treatment of Dihydropteridine Reductase Deficiency. Pteridines. 7(3). 107–109. 5 indexed citations
5.
Spada, Marco, et al.. (1995). Deprenyl in 6-Pyruvoyl Tetrahydropterin Synthase Deficiency. Pteridines. 6(3). 144–146. 3 indexed citations
6.
Dianzani, Irma, Per M. Knappskog, Luisa De Sanctis, et al.. (1995). Novel missense mutation in the phenylalanine hydroxylase gene leading to complete loss of enzymatic activity. Human Mutation. 6(3). 247–249. 4 indexed citations
7.
Spada, Marco, Ornella Guardamagna, Daniel Rabier, et al.. (1994). Recurrent episodes of bizarre behavior in a boy with ornithine transcarbamylase deficiency: Diagnostic failure of protein loading and allopurinol challenge tests. The Journal of Pediatrics. 125(2). 249–251. 19 indexed citations
8.
Blau, Nenad, L. Kierat, A. Matasović, et al.. (1994). Antenatal diagnosis of tetrahydrobiopterin deficiency by quantification of pterins in amniotic fluid and enzyme activity in fetal and extrafetal tissue. Clinica Chimica Acta. 226(2). 159–169. 11 indexed citations
9.
Ponzone, A, Ornella Guardamagna, Marco Spada, et al.. (1993). Hyperphenylalaninemia and pterin metabolism in serum and erythrocytes. Clinica Chimica Acta. 216(1-2). 63–71. 23 indexed citations
10.
Ponzone, A, Ornella Guardamagna, Marco Spada, et al.. (1993). Differential diagnosis of hyperphenylalaninaemia by a combined phenylalanine-tetrahydrobiopterin loading test. European Journal of Pediatrics. 152(8). 655–661. 31 indexed citations
11.
Gregersen, Niels, Vibeke Winter, Diana Curtis, et al.. (1993). Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency: The Prevalent Mutation G985 (K304E) Is Subject to a Strong Founder Effect from Northwestern Europe. Human Heredity. 43(6). 342–350. 55 indexed citations
12.
Dianzani, Irma, Clara Camaschella, A Ponzone, & Richard G.H. Cotton. (1993). Dilemmas and progress in mutation detection. Trends in Genetics. 9(12). 403–405. 33 indexed citations
13.
Ponzone, A, Ornella Guardamagna, Irma Dianzani, et al.. (1993). Catalytic Activity of Tetrahydrobiopterin in Dihydropteridine Reductase Deficiency and Indications for Treatment. Pediatric Research. 33(2). 125–128. 12 indexed citations
14.
Blau, Nenad, A. Niederwieser, H.‐Ch. Curtius, et al.. (1989). Prenatal Diagnosis of Atypical Phenylketonuria. Journal of Inherited Metabolic Disease. 12(S2). 295–298. 6 indexed citations
15.
Cotton, Richard G.H., et al.. (1986). Tetrahydrobiopterin non‐responsiveness in dihydropteridine reductase deficiency is associated with the presence of mutant protein. Journal of Inherited Metabolic Disease. 9(3). 239–243. 18 indexed citations
16.
Arosio, Paolo, et al.. (1984). Ferritin in Human Milk. Acta Paediatrica. 73(2). 271–272. 8 indexed citations
17.
Stella, L., et al.. (1974). [Therapy of diabetes insipidus with chlorpropamide].. PubMed. 26(38). 1924–9. 1 indexed citations
18.
Ansaldi, N, C. De Sanctis, Carlo Fabris, & A Ponzone. (1970). [Lymphocyte blast formation induced in vitro by phytohemagglutinin and by gluten in children with celiac disease].. PubMed. 22(39). 1907–12. 2 indexed citations
19.
Gavosto, F, et al.. (1969). Different Blast Kinetics in Acute Myeloblastic and Lymphoblastic Leukaemia. Acta Haematologica. 41(4). 215–224. 7 indexed citations
20.
Gavosto, F, et al.. (1969). Unusual blast proliferation and kinetics in acute lymphoblastic leukaemia. European Journal of Cancer (1965). 5(4). 343–348. 4 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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