N. Chamoles

1.0k total citations
20 papers, 498 citations indexed

About

N. Chamoles is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, N. Chamoles has authored 20 papers receiving a total of 498 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in N. Chamoles's work include Metabolism and Genetic Disorders (6 papers), Biochemical and Molecular Research (4 papers) and Neonatal Health and Biochemistry (3 papers). N. Chamoles is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Biochemical and Molecular Research (4 papers) and Neonatal Health and Biochemistry (3 papers). N. Chamoles collaborates with scholars based in Argentina, United States and France. N. Chamoles's co-authors include R Humbel, D. Karcher, Andrea Schenone, José E. Abdenur, Wolfgang Zeman, Laura De Gregorio, William L. Nyhan, A. Löwenthal, Jean Marie Saudubray and Szabolcs Udvari and has published in prestigious journals such as Brain Research, Human Molecular Genetics and Clinica Chimica Acta.

In The Last Decade

N. Chamoles

19 papers receiving 458 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
N. Chamoles Argentina	11	302	230	120	76	66	20	498
M. DiRocco Italy	8	353 1.2×	244 1.1×	78 0.7×	48 0.6×	64 1.0×	11	497
Rebecca Mardach United States	11	193 0.6×	164 0.7×	100 0.8×	82 1.1×	53 0.8×	17	351
L. J. M. Spaapen Netherlands	15	492 1.6×	210 0.9×	216 1.8×	177 2.3×	83 1.3×	37	780
S Scheibenreiter Austria	10	176 0.6×	267 1.2×	58 0.5×	71 0.9×	30 0.5×	35	416
Ricardo Flores Pires Brazil	15	286 0.9×	251 1.1×	338 2.8×	94 1.2×	92 1.4×	36	624
J. M. van der Klei‐van Moorsel Netherlands	9	586 1.9×	254 1.1×	110 0.9×	31 0.4×	46 0.7×	10	786
H. W. Moser United States	11	233 0.8×	91 0.4×	144 1.2×	29 0.4×	33 0.5×	29	372
Bing-Zhi Yang United States	13	232 0.8×	159 0.7×	160 1.3×	39 0.5×	170 2.6×	18	445
L. Sweetman United States	13	272 0.9×	175 0.8×	35 0.3×	51 0.7×	36 0.5×	23	411
María Teresa García‐Silva Spain	12	392 1.3×	234 1.0×	83 0.7×	82 1.1×	88 1.3×	24	595

Countries citing papers authored by N. Chamoles

Since Specialization

Citations

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

Fields of papers citing papers by N. Chamoles

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of N. Chamoles

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

Gregorio, Laura De, et al.. (2000). An Unexpected Affected Female Patient in a Classical Lesch–Nyhan Family. Molecular Genetics and Metabolism. 69(3). 263–268. 30 indexed citations

Nuoffer, Jean‐Marc, Pascale de Lonlay, Carlos A. Bana e Costa, et al.. (2000). Familial neonatal SIDS revealing carnitine-acylcarnitine translocase deficiency. European Journal of Pediatrics. 159(1-2). 82–85. 12 indexed citations

Chamoles, N., et al.. (2000). An unexpected female patient within a classical Lesch-Nyhan family. Genetics in Medicine. 2(1). 104–104.

Abdenur, José E., et al.. (1998). Diagnosis of isovaleric acidaemia by tandem mass spectrometry: False positive result due to pivaloylcarnitine in a newborn screening programme. Journal of Inherited Metabolic Disease. 21(6). 624–630. 68 indexed citations

Cormand, Bru, Laura Gort, Cristina Campoy, et al.. (1998). Mutation analysis of Gaucher disease patients from Argentina: High prevalence of the RecNciI mutation. American Journal of Medical Genetics. 80(4). 343–351. 35 indexed citations

Consalvo, D., et al.. (1997). [Severe cardiac failure in Kearns-Sayre syndrome].. PubMed. 57(1). 67–71. 4 indexed citations

Tenembaum, Silvia, et al.. (1997). 4-13-12 Multiphasic disseminated encephalomyelitis and multiple sclerosis in children: Diagnostic clues. Journal of the Neurological Sciences. 150. S230–S230. 1 indexed citations

Andresen, Brage Storstein, Peter Bross, Szabolcs Udvari, et al.. (1997). The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype?. Human Molecular Genetics. 6(5). 695–707. 105 indexed citations

Chamoles, N., et al.. (1996). [Autoimmune hypoglycemia syndrome with specific anti-human insulin antibodies].. PubMed. 56(3). 279–83. 7 indexed citations

10.

Barth, P. G., Georg F. Hoffmann, J. Jaeken, et al.. (1993). l‐2‐Hydroxyglutaric acidaemia: Clinical and biochemical findings in 12 patients and preliminary report onl‐2‐hydroxyacid dehydrogenase. Journal of Inherited Metabolic Disease. 16(4). 753–761. 70 indexed citations

11.

Pavlovsky, S, et al.. (1983). Neuropsychological study in patients with ALL. Two different CNS prevention therapies--cranial irradiation plus IT methotrexate vs. IT methotrexate alone.. PubMed. 5(1). 79–86. 29 indexed citations

12.

Humbel, R & N. Chamoles. (1972). Sequential thin layer chromatography of urinary acidic glycosaminglycans. Clinica Chimica Acta. 40(1). 290–293. 75 indexed citations

13.

Karcher, D., Wolfgang Zeman, A. Löwenthal, & N. Chamoles. (1970). Studies on alpha albumin in nervous tissue. I. Biochemical investigations. Brain Research. 17(2). 307–314. 9 indexed citations

14.

Chamoles, N., D. Karcher, Wolfgang Zeman, & A. Löwenthal. (1970). Studies on alpha albumin in nervous tissue. II. Topographical distribution in normal tissue. Brain Research. 17(2). 315–324. 10 indexed citations

15.

Chamoles, N. & D. Karcher. (1970). Isoelectro-focusing en acrylamide de la lacticodés-hydrogénase hydrosoluble de tissus humains. Clinica Chimica Acta. 30(2). 359–364. 14 indexed citations

16.

Chamoles, N. & D. Karcher. (1970). Corrélation entre l'enzymogramme classique de la lacticodéshydrogénase et son fractionnement par isoelectrofocusing en gel d'acrylamide. Clinica Chimica Acta. 30(2). 337–341. 14 indexed citations

17.

Zeman, Wolfgang, D. Karcher, N. Chamoles, & A. Löwenthal. (1970). Studies on alpha albumin in nervous tissue. III. Observations on pathological specimens. Brain Research. 17(2). 325–334. 8 indexed citations

18.

Karcher, D., N. Chamoles, Wolfgang Zeman, & A. Löwenthal. (1969). [Hydrosoluble proteins of the nervous system of man and the animal].. PubMed. 48. 73–6. 4 indexed citations

19.

Chamoles, N., et al.. (1968). [Recent study on the significance of diffuse sclerosis of the Schilder type (1912) in children. 1. Anatomoclinical aspect of a sporadic case].. PubMed. 68(11). 837–50. 1 indexed citations

20.

Chamoles, N., et al.. (1965). [Painful shoulder-hand syndrome. Drug-induced iatrogenic disease].. PubMed. 79(4). 165–9. 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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