Aron J. Diament

827 total citations
59 papers, 561 citations indexed

About

Aron J. Diament is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Aron J. Diament has authored 59 papers receiving a total of 561 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 14 papers in Pediatrics, Perinatology and Child Health and 14 papers in Genetics. Recurrent topics in Aron J. Diament's work include Genetic Neurodegenerative Diseases (7 papers), Epilepsy research and treatment (7 papers) and Metabolism and Genetic Disorders (5 papers). Aron J. Diament is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Epilepsy research and treatment (7 papers) and Metabolism and Genetic Disorders (5 papers). Aron J. Diament collaborates with scholars based in Brazil, United States and Chile. Aron J. Diament's co-authors include Fernando Kok, José Luiz Dias Gherpelli, Mayana Zatz, Angela Maria Vianna‐Morgante, Anita Wajntal, Célia Priszkulnik Koiffmann, Maria Luíza Giraldes de Manreza, Beatriz Helena Lefèvre, Milberto Scaff and Suely Kazue Nagahashi Marie and has published in prestigious journals such as Clinical Chemistry, Epilepsia and Journal of Medical Genetics.

In The Last Decade

Aron J. Diament

48 papers receiving 529 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Aron J. Diament Brazil 14 214 152 143 127 85 59 561
D Fontan France 14 271 1.3× 152 1.0× 185 1.3× 181 1.4× 31 0.4× 43 719
Ignacio Pascual Castroviejo Spain 11 170 0.8× 216 1.4× 236 1.7× 182 1.4× 30 0.4× 67 600
A. Hori Germany 15 158 0.7× 99 0.7× 58 0.4× 151 1.2× 70 0.8× 50 766
V. Colamaria Italy 14 105 0.5× 142 0.9× 233 1.6× 165 1.3× 31 0.4× 29 552
A. Mrabet Tunisia 12 184 0.9× 128 0.8× 201 1.4× 143 1.1× 26 0.3× 59 716
Akira Sudo Japan 14 307 1.4× 79 0.5× 122 0.9× 83 0.7× 21 0.2× 35 685
Nobutsune Ishikawa Japan 15 143 0.7× 148 1.0× 144 1.0× 129 1.0× 23 0.3× 52 638
D. L. Keene Canada 11 131 0.6× 86 0.6× 478 3.3× 333 2.6× 46 0.5× 18 679
Yoshihisa Higuchi Japan 14 221 1.0× 42 0.3× 66 0.5× 163 1.3× 46 0.5× 31 518
Pen‐Jung Wang Taiwan 12 98 0.5× 75 0.5× 96 0.7× 108 0.9× 17 0.2× 51 399

Countries citing papers authored by Aron J. Diament

Since Specialization
Citations

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

Fields of papers citing papers by Aron J. Diament

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aron J. Diament. 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 Aron J. Diament. The network helps show where Aron J. Diament may publish in the future.

Co-authorship network of co-authors of Aron J. Diament

This figure shows the co-authorship network connecting the top 25 collaborators of Aron J. Diament. A scholar is included among the top collaborators of Aron J. Diament 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 Aron J. Diament. Aron J. Diament 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.
Casella, Erasmo Barbante, et al.. (2005). Episodic somnolence in an infant with Riley-Day syndrome. Pediatric Neurology. 32(4). 273–274. 1 indexed citations
2.
Reed, Umbertina Conti, Rubens Reimão, Fernando Kok, et al.. (2002). Schwartz-jampel syndrome: report of five cases. Arquivos de Neuro-Psiquiatria. 60(3B). 734–738. 8 indexed citations
3.
Fridman, Cíntia, et al.. (2000). Paternal UPD15: Further genetic and clinical studies in four Angelman syndrome patients. American Journal of Medical Genetics. 92(5). 322–327. 31 indexed citations
4.
Reed, Umbertina Conti, Ana Maria Crous Tsanaclis, Mariz Vainzof, et al.. (1999). Merosin-positive congenital muscular dystrophy in two siblings with cataract and slight mental retardation. Brain and Development. 21(4). 274–278. 6 indexed citations
5.
Diament, Aron J., et al.. (1998). Migraine in Childhood and Adolescence. A Critical Study of the Diagnostic Criteria and of the Influence of Age on Clinical Findings. Cephalalgia. 18(6). 333–341. 42 indexed citations
6.
Manreza, Maria Luíza Giraldes de, et al.. (1997). Treatment of febrile seizures with intermittent clobazam. Arquivos de Neuro-Psiquiatria. 55(4). 757–761. 13 indexed citations
7.
Marie, Suely Kazue Nagahashi, et al.. (1996). Congenital muscular dystrophy with cerebral white matter hypodensity. Correlation of clinical features and merosin deficiency. Brain and Development. 18(1). 53–58. 18 indexed citations
8.
Gherpelli, José Luiz Dias, Lídia Nagae, & Aron J. Diament. (1995). Dopa-sensitive progressive dystonia of childhood with diurnal fluctuations of symptoms: a case report. Arquivos de Neuro-Psiquiatria. 53(2). 298–301. 7 indexed citations
9.
Rosemberg, Sérgio, et al.. (1993). Brain Tumors in the First Two Years of Life: A Review of Forty Cases. Pediatric Neurosurgery. 19(4). 180–185. 17 indexed citations
10.
Koiffmann, Célia Priszkulnik, et al.. (1993). Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): Further evidence of localization at Xp11. American Journal of Medical Genetics. 46(5). 529–533. 25 indexed citations
11.
Kok, Fernando, et al.. (1992). Sindrome de rett: achados clinicos e polissonograficos em 2 irmas. Arquivos de Neuro-Psiquiatria. 50. 116. 1 indexed citations
12.
Tsanaclis, Ana Maria Crous, et al.. (1992). Miopatia centronuclear (miotubular): relato de caso. 47(5). 1 indexed citations
13.
Gherpelli, José Luiz Dias, et al.. (1992). Discontinuing Medication in Epileptic Children: A Study of Risk Factors Related to Recurrence. Epilepsia. 33(4). 681–686. 50 indexed citations
14.
Gherpelli, José Luiz Dias, et al.. (1992). Seizure recurrence in infants with neonatal convulsions a follow-up study: estudo evolutivo. Arquivos de Neuro-Psiquiatria. 50(1). 31–36. 7 indexed citations
15.
Kok, Fernando, et al.. (1990). In search of a genetic basis for the Rett syndrome. Human Genetics. 86(2). 131–4. 19 indexed citations
16.
Moretti‐Ferreira, Danilo, et al.. (1989). Macrocephaly, multiple lipomas, and hemangiomata (Bannayan‐Zonana syndrome): Genetic heterogeneity or autosomal dominant locus with at least two different allelic forms?. American Journal of Medical Genetics. 34(4). 548–551. 22 indexed citations
17.
Barbosa, Egberto Reis, et al.. (1985). Coréia familiar benigna: relato de dois casos. Arquivos de Neuro-Psiquiatria. 43(2). 181–186.
18.
Diament, Aron J., et al.. (1982). Epidemiologia em neurologia infantil : estudo dos diagnosticos mais comuns. 37(5). 199–205. 6 indexed citations
19.
Lacassie, Yves, et al.. (1980). Abstracts: 16th Annual Meeting Sociedad Latinoamericana de Investigacion Pediatrica. Pediatric Research. 14(1). 70–80. 1 indexed citations
20.
Diament, Aron J., et al.. (1960). Infecção piógena do espaço epidural raquidiano em criança. Arquivos de Neuro-Psiquiatria. 18(1). 53–57. 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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