R. Cerone

3.8k total citations · 1 hit paper
62 papers, 2.3k citations indexed

About

R. Cerone is a scholar working on Clinical Biochemistry, Molecular Biology and Rheumatology. According to data from OpenAlex, R. Cerone has authored 62 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Clinical Biochemistry, 27 papers in Molecular Biology and 24 papers in Rheumatology. Recurrent topics in R. Cerone's work include Metabolism and Genetic Disorders (42 papers), Folate and B Vitamins Research (23 papers) and Amino Acid Enzymes and Metabolism (12 papers). R. Cerone is often cited by papers focused on Metabolism and Genetic Disorders (42 papers), Folate and B Vitamins Research (23 papers) and Amino Acid Enzymes and Metabolism (12 papers). R. Cerone collaborates with scholars based in Italy, United States and Switzerland. R. Cerone's co-authors include Generoso Andria, Harvey L. Levy, K. D. Pettigrew, G. H. J. Boers, Irvin L. Bromberg, Flemming Skovby, S. Harvey Mudd, Reed E. Pyeritz, Bridget Wilcken and Giuseppe Minniti and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and Journal of Chromatography A.

In The Last Decade

R. Cerone

61 papers receiving 2.2k citations

Hit Papers

align trajectories

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.

The natural history of homocystinuria due to cystathionine beta-synthase deficiency.

1985 960 citations Generoso Andria, R. Cerone et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R. Cerone Italy	22	1.3k	1.0k	777	328	309	62	2.3k
D. P. Brenton United Kingdom	24	691 0.5×	849 0.8×	656 0.8×	182 0.6×	377 1.2×	63	1.9k
John H. Walter United Kingdom	20	589 0.5×	1.2k 1.2×	874 1.1×	163 0.5×	474 1.5×	39	1.9k
Guy Touati France	33	434 0.3×	1.9k 1.8×	1.4k 1.9×	571 1.7×	540 1.7×	94	3.7k
F. Maillot France	22	523 0.4×	1.2k 1.1×	837 1.1×	169 0.5×	962 3.1×	150	2.3k
Isabel Rivera Portugal	19	622 0.5×	421 0.4×	768 1.0×	184 0.6×	168 0.5×	56	1.5k
Godfried H.J. Boers Netherlands	34	3.6k 2.8×	721 0.7×	598 0.8×	1.5k 4.7×	328 1.1×	47	4.7k
Chanika Phornphutkul United States	22	291 0.2×	495 0.5×	728 0.9×	365 1.1×	372 1.2×	56	2.0k
Marco Spada Italy	28	716 0.6×	1.0k 1.0×	1.1k 1.4×	135 0.4×	1.6k 5.3×	132	3.1k
Terry G. J. Derks Netherlands	26	834 0.6×	729 0.7×	677 0.9×	226 0.7×	598 1.9×	106	2.0k
Sarah C. Grünert Germany	22	564 0.4×	726 0.7×	716 0.9×	102 0.3×	333 1.1×	86	1.6k

Countries citing papers authored by R. Cerone

Since Specialization

Citations

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

Fields of papers citing papers by R. Cerone

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Cerone

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

Muntau, Ania C., Darius J. Adams, Amaya Bélanger-Quintana, et al.. (2019). International best practice for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria. Molecular Genetics and Metabolism. 127(1). 1–11. 43 indexed citations

Panfoli, Isabella, Michela Cassanello, Matteo Bruschettini, et al.. (2016). Why do premature newborn infants display elevated blood adenosine levels?. Medical Hypotheses. 90. 53–56. 15 indexed citations

Cerone, R., Generoso Andria, Marcello Giovannini, et al.. (2013). Testing for Tetrahydrobiopterin Responsiveness in Patients with Hyperphenylalaninemia due to Phenylalanine Hydroxylase Deficiency. Advances in Therapy. 30(3). 212–228. 12 indexed citations

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

Nogueira, Célia, Chiara Aiello, R. Cerone, et al.. (2008). Spectrum of MMACHC mutations in Italian and Portuguese patients with combined methylmalonic aciduria and homocystinuria, cblC type. Molecular Genetics and Metabolism. 93(4). 475–480. 72 indexed citations

Signorello, Maria Grazia, Giorgio Luciano Viviani, U Armani, et al.. (2007). Homocysteine, reactive oxygen species and nitric oxide in type 2 diabetes mellitus. Thrombosis Research. 120(4). 607–613. 38 indexed citations

Amato, Stefano, et al.. (2005). von Willebrand factor multimer composition is modified following oral methionine load in women with thrombosis, but not in healthy women. Blood Coagulation & Fibrinolysis. 16(4). 267–273. 5 indexed citations

Minniti, Giuseppe, et al.. (2004). Isolated sulphite oxidase deficiency: clinical and biochemical features in an Italian patient. Journal of Inherited Metabolic Disease. 27(1). 101–102. 5 indexed citations

Cerone, R., et al.. (2003). Long-term follow-up of a patient with mild tetrahydrobiopterin-responsive phenylketonuria. Molecular Genetics and Metabolism. 81(2). 137–139. 33 indexed citations

10.

Cánepa, Alberto, Alba Carrea, Gianluca Caridi, et al.. (2003). Homocysteine, folate, vitamin B12 levels, and C677T MTHFR mutation in children with renal failure. Pediatric Nephrology. 18(3). 225–229. 14 indexed citations

11.

Biancheri, Roberta, R. Cerone, Andrea Rossi, et al.. (2002). Early‐onset Cobalamin C/D Deficiency: Epilepsy and Electroencephalographic Features. Epilepsia. 43(6). 616–622. 24 indexed citations

12.

Minniti, Giuseppe, et al.. (1998). Purines and Pyrimidines Determination in Urine Using High-Performance Liquid Chromatography. Advances in experimental medicine and biology. 431. 843–848. 7 indexed citations

13.

Bonioli, E, Antonio Di Stefano, U. Caruso, et al.. (1998). Fumarate hydratase deficiency. Journal of Inherited Metabolic Disease. 21(4). 435–436. 13 indexed citations

14.

Cerone, R., et al.. (1997). Tyrosinemia type III: diagnosis and ten‐year follow‐up. Acta Paediatrica. 86(9). 1013–1015. 30 indexed citations

15.

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

16.

Cerone, R., et al.. (1994). SYNDROME HEMOLYTIQUE ET UREMIQUE NEONATAL, ACIDURIE METHYLMALONIQUE ET HOMOCYSTINURIE PAR DEFICIT INTRACELLULAIRE DE LA VITAMINE B12 [1]. Archives de Pédiatrie. 1(8). 762–763. 5 indexed citations

17.

Marescau, Bart, Peter P. De Deyn, Ijaz A. Qureshi, et al.. (1992). The pathobiochemistry of uremia and hyperargininemia further demonstrates a metabolic relationship between urea and guanidinosuccinic acid. Metabolism. 41(9). 1021–1024. 20 indexed citations

18.

Okano, Yoshiyuki, Tao Wang, Randy C. Eisensmith, et al.. (1991). Phenylketonuria missense mutations in the Mediterranean. Genomics. 9(1). 96–103. 51 indexed citations

19.

Cerone, R., et al.. (1991). Acute neonatal isovaleric acidaemia presented without acidosis or ketonuria. Journal of Inherited Metabolic Disease. 14(1). 111–111. 1 indexed citations

20.

Perfumo, Francesco, Enrico Verrina, Corrado Romano, et al.. (1986). Studio degli aminoacidi plasmatici nel bambino dializzato: confronto tra emodialisi e dialisi peritoneale ambulatoriale continua.. 8(3). 341–345. 2 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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