A. Matasović

483 total citations
21 papers, 330 citations indexed

About

A. Matasović is a scholar working on Clinical Biochemistry, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, A. Matasović has authored 21 papers receiving a total of 330 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Clinical Biochemistry, 12 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in A. Matasović's work include Metabolism and Genetic Disorders (14 papers), Biochemical and Molecular Research (7 papers) and Amino Acid Enzymes and Metabolism (5 papers). A. Matasović is often cited by papers focused on Metabolism and Genetic Disorders (14 papers), Biochemical and Molecular Research (7 papers) and Amino Acid Enzymes and Metabolism (5 papers). A. Matasović collaborates with scholars based in Switzerland, Italy and United States. A. Matasović's co-authors include A. Niederwieser, Ernst Leumann, Nenad Blau, Andreas Dietl, H.‐Ch. Curtius, Jean‐Louis Dhondt, Claus W. Heizmann, B Steinmann, Thomas Küster and D. M. Danks and has published in prestigious journals such as Journal of Biological Chemistry, Biochemical and Biophysical Research Communications and FEBS Letters.

In The Last Decade

A. Matasović

20 papers receiving 307 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. Matasović Switzerland 12 187 145 93 76 68 21 330
J Bardet France 11 187 1.0× 134 0.9× 63 0.7× 72 0.9× 28 0.4× 28 335
Theresa M. Wunz United States 12 60 0.3× 144 1.0× 115 1.2× 57 0.8× 11 0.2× 17 336
Mitsuharu Kajita Japan 12 132 0.7× 166 1.1× 45 0.5× 65 0.9× 7 0.1× 26 363
S. Rovidati Italy 8 81 0.4× 172 1.2× 48 0.5× 22 0.3× 43 0.6× 10 514
George E. Nichoalds United States 8 58 0.3× 150 1.0× 38 0.4× 71 0.9× 22 0.3× 13 413
Thomas Mehrens Germany 7 77 0.4× 109 0.8× 73 0.8× 73 1.0× 13 0.2× 10 379
Ronald L. George United States 6 109 0.6× 128 0.9× 71 0.8× 112 1.5× 5 0.1× 6 343
Runa NJÅLSSON Sweden 10 34 0.2× 239 1.6× 29 0.3× 207 2.7× 33 0.5× 11 438
Yan-Wo Chan Hong Kong 13 47 0.3× 115 0.8× 24 0.3× 31 0.4× 45 0.7× 21 264
B Egestad Sweden 14 162 0.9× 164 1.1× 102 1.1× 8 0.1× 13 0.2× 19 686

Countries citing papers authored by A. Matasović

Since Specialization
Citations

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

Fields of papers citing papers by A. Matasović

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Matasović

This figure shows the co-authorship network connecting the top 25 collaborators of A. Matasović. A scholar is included among the top collaborators of A. Matasović 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. Matasović. A. Matasović 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.
Blau, Nenad, Alessandra Baumer, Mariluce Riegel, et al.. (2000). Isolated central form of tetrahydrobiopterin deficiency associated with hemizygosity on chromosome 11q and a mutant allele of PTPS. Human Mutation. 16(1). 54–60. 8 indexed citations
2.
3.
Blau, Nenad, et al.. (1998). Simultaneous Determination of Oxalate, Glycolate, Citrate, and Sulfate from Dried Urine Filter Paper Spots in a Pediatric Population. Clinical Chemistry. 44(7). 1554–1556. 24 indexed citations
4.
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
5.
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
6.
Ponzone, A, Irma Dianzani, Marco Spada, et al.. (1993). Prenatal diagnosis in primary hyperphenylalaninemias. 6. 158–167. 2 indexed citations
7.
Guardamagna, Ornella, Marco Spada, A Ponzone, et al.. (1991). Prenatal Diagnosis of Dihydropteridine Reductase Deficiency in a Twin Pregnancy. Pteridines. 3(1-2). 19–21. 1 indexed citations
8.
Leumann, Ernst, Andreas Dietl, & A. Matasović. (1990). Urinary oxalate and glycolate excretion in healthy infants and children. Pediatric Nephrology. 4(5). 493–497. 50 indexed citations
9.
Curtius, H.‐Ch., A. Matasović, Gabriele Schoedon, et al.. (1990). 7-Substituted pterins. A new class of mammalian pteridines.. Journal of Biological Chemistry. 265(7). 3923–3930. 27 indexed citations
10.
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
11.
Blau, Nenad, H.‐Ch. Curtius, A. Matasović, et al.. (1989). Primapterinuria: A New Variant of Atypical Phenylketonuria. Journal of Inherited Metabolic Disease. 12(S2). 335–338. 19 indexed citations
12.
Curtius, H.‐Ch., et al.. (1988). Primapterin, anapterin, and 6-oxo-primapterin, three new 7-substituted pterins identified in a patient with hyperphenylalaninemia. Biochemical and Biophysical Research Communications. 153(2). 715–721. 40 indexed citations
13.
Küster, Thomas, A. Matasović, & A. Niederwieser. (1984). Application of gas chromatography—mass spectrometry to the study of biopterin metabolism in man. Journal of Chromatography A. 290. 303–310. 8 indexed citations
14.
Niederwieser, A., et al.. (1980). 3′‐hydroxysepiapterin in patients with dihydrobiopterin deficiency. FEBS Letters. 118(2). 299–302. 14 indexed citations
15.
Niederwieser, A., A. Matasović, & Ernst Leumann. (1978). Glycolic acid in urine. A colorimetric method with values in normal adult controls and in patients with primary hyperoxaluria. Clinica Chimica Acta. 89(1). 13–23. 24 indexed citations
16.
Niederwieser, A., B Steinmann, & A. Matasović. (1978). New bromisoval (bromural) metabolites in human urine: a-(cystein-S-yl)isovalerylurea, a-(N-acetylcystein-S-yl)isovalerylurea and a-(cysteamin-S-yl)isovaleric acid. Journal of Chromatography A. 147. 163–176. 14 indexed citations
17.
Niederwieser, A., et al.. (1978). New tyrosine metabolites in humans: Hawkinsin and cis- and trans-4-hydroxycyclohexylacetic acids. Journal of Chromatography B Biomedical Sciences and Applications. 146(2). 207–212. 11 indexed citations
18.
Niederwieser, A., A. Matasović, P. Tippett, & D. M. Danks. (1977). A new sulfur amino acid, named hawkinsin, identified in a baby with transient tyrosinemia and her mother. Clinica Chimica Acta. 76(3). 345–356. 23 indexed citations
19.
Niederwieser, A., Paola Giliberti, & A. Matasović. (1975). Nε-/l-DEOXYFRUCTOSYL/-LYSINE IN URINE AFTER INGESTION OF A LACTOSE FREE, GLUCOSE CONTAINING MILK FORMULA. Pediatric Research. 9(11). 867–867. 6 indexed citations
20.
Niederwieser, A., Paola Giliberti, & A. Matasović. (1975). N∊-/l-DEOXYFRUCTOSYL/-LYSINE IN URINE AFTER INGESTION OF A LACTOSE FREE, GLUCOSE CONTAINING MILK FORMULA. Pediatric Research. 9(11). 867–867. 1 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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