Carlos Eduardo Steiner

1.7k total citations
58 papers, 586 citations indexed

About

Carlos Eduardo Steiner is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Carlos Eduardo Steiner has authored 58 papers receiving a total of 586 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 23 papers in Molecular Biology and 15 papers in Rheumatology. Recurrent topics in Carlos Eduardo Steiner's work include Lysosomal Storage Disorders Research (14 papers), Genomic variations and chromosomal abnormalities (10 papers) and Glycogen Storage Diseases and Myoclonus (9 papers). Carlos Eduardo Steiner is often cited by papers focused on Lysosomal Storage Disorders Research (14 papers), Genomic variations and chromosomal abnormalities (10 papers) and Glycogen Storage Diseases and Myoclonus (9 papers). Carlos Eduardo Steiner collaborates with scholars based in Brazil, United States and Germany. Carlos Eduardo Steiner's co-authors include Antonia Paula Marques‐de‐Faria, Marilisa M. Guerreiro, Paulo Dalgalarrondo, Fernando Cendes, Li M. Li, Leonardo Bonilha, Chris Rorden, Mark A. Eckert, Angelina Xavier Acosta and Ida Vanessa Döederlein Schwartz and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Gene.

In The Last Decade

Carlos Eduardo Steiner

54 papers receiving 567 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Carlos Eduardo Steiner Brazil 15 203 157 145 143 79 58 586
Erika F. Augustine United States 16 139 0.7× 209 1.3× 363 2.5× 109 0.8× 133 1.7× 69 879
Elisabetta Bolognesi Italy 21 207 1.0× 257 1.6× 94 0.6× 202 1.4× 36 0.5× 50 973
Stacey Clardy United States 18 120 0.6× 173 1.1× 61 0.4× 94 0.7× 125 1.6× 75 1.2k
Yi Guo China 18 145 0.7× 372 2.4× 91 0.6× 137 1.0× 31 0.4× 77 1.1k
Edvige Veneselli Italy 17 210 1.0× 190 1.2× 105 0.7× 236 1.7× 159 2.0× 41 1.1k
J.L. Haines United States 15 319 1.6× 247 1.6× 54 0.4× 300 2.1× 32 0.4× 20 853
Soo Yeon Kim South Korea 17 197 1.0× 327 2.1× 74 0.5× 61 0.4× 36 0.5× 109 899
Euthymia Vargìami Greece 13 158 0.8× 155 1.0× 57 0.4× 162 1.1× 33 0.4× 35 543
José Pedro Vieira Portugal 15 250 1.2× 228 1.5× 36 0.2× 179 1.3× 51 0.6× 48 702
Christopher Severson United States 10 122 0.6× 121 0.8× 41 0.3× 130 0.9× 59 0.7× 13 778

Countries citing papers authored by Carlos Eduardo Steiner

Since Specialization
Citations

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

Fields of papers citing papers by Carlos Eduardo Steiner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Carlos Eduardo Steiner. 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 Carlos Eduardo Steiner. The network helps show where Carlos Eduardo Steiner may publish in the future.

Co-authorship network of co-authors of Carlos Eduardo Steiner

This figure shows the co-authorship network connecting the top 25 collaborators of Carlos Eduardo Steiner. A scholar is included among the top collaborators of Carlos Eduardo Steiner 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 Carlos Eduardo Steiner. Carlos Eduardo Steiner 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.
2.
Steiner, Carlos Eduardo, et al.. (2024). Clinical Findings in a Series of Thirty Eight Patients with Williams-Beuren Syndrome. Cytogenetic and Genome Research. 164(3-4). 1–9.
3.
4.
Steiner, Carlos Eduardo, et al.. (2023). Sjogren-Larsson syndrome brain volumetric reductions demonstrated with an automated software. Arquivos de Neuro-Psiquiatria. 81(9). 809–815. 1 indexed citations
5.
Stöckler‐Ipsiroglu, Sylvia, Nahid Yazdanpanah, Mojgan Yazdanpanah, et al.. (2021). Morquio‐like dysostosis multiplex presenting with neuronopathic features is a distinct GLB1‐related phenotype. JIMD Reports. 60(1). 23–31. 3 indexed citations
6.
Steiner, Carlos Eduardo, Chong Ae Kim, Charles Marques Lourenço, et al.. (2019). Clinical findings in Brazilian patients with adult GM1 gangliosidosis. JIMD Reports. 49(1). 96–106. 7 indexed citations
7.
Simioni, Milena, François Artiguenave, Vincent Meyer, et al.. (2017). Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes. Molecular Syndromology. 8(4). 187–194. 6 indexed citations
8.
Camelo, José Simon, Greice Andreotti de Molfetta, Carolina Fischinger Moura de Souza, et al.. (2016). Clinical profile and molecular characterization of Galactosemia in Brazil: identification of seven novel mutations. BMC Medical Genetics. 17(1). 39–39. 12 indexed citations
9.
Bender, Fernanda, et al.. (2015). Medical Costs Related to Enzyme Replacement Therapy for Mucopolysaccharidosis Types I, II, and VI in Brazil: A Multicenter Study. Value in Health Regional Issues. 8. 99–106. 8 indexed citations
10.
Simioni, Milena, Carlos Eduardo Steiner, & Vera Lúcia Gil‐da‐Silva‐Lopes. (2015). De novo double reciprocal translocations in addition to partial monosomy at another chromosome: A very rare case. Gene. 573(1). 166–170. 5 indexed citations
11.
Adur, Javier, Lilia Freire Rodrigues D’Souza-Li, Carlos Eduardo Steiner, et al.. (2013). The Severity of Osteogenesis Imperfecta and Type I Collagen Pattern in Human Skin as Determined by Nonlinear Microscopy: Proof of Principle of a Diagnostic Method. PLoS ONE. 8(7). e69186–e69186. 15 indexed citations
12.
Steiner, Carlos Eduardo, et al.. (2013). Cognitive and behavioral heterogeneity in genetic syndromes. Jornal de Pediatria. 90(2). 155–160. 12 indexed citations
13.
Nogueira, Roberto José Negrão, et al.. (2011). Anthropometric and body-mass composition suggests an intrinsic feature in Williams-Beuren syndrome. Revista da Associação Médica Brasileira. 57(6). 681–685. 10 indexed citations
14.
Steiner, Carlos Eduardo, et al.. (2010). Mucopolysaccharidosis type II: skeletal–muscle system involvement. Journal of Pediatric Orthopaedics B. 19(4). 313–317. 4 indexed citations
15.
Alexandrino, Fabiana, et al.. (2008). Type II autosomal recessive cutis laxa: Report of another patient and molecular studies concerning three candidate genes. American Journal of Medical Genetics Part A. 146A(21). 2740–2745. 1 indexed citations
16.
Steiner, Carlos Eduardo, Angelina Xavier Acosta, Marilisa M. Guerreiro, & Antonia Paula Marques‐de‐Faria. (2007). Genotype And Natural History In Unrelated Individuals With Phenylketonuria And Autistic Behavior.. Americanae (AECID Library). 3 indexed citations
17.
Steiner, Carlos Eduardo, et al.. (2007). What Syndrome Is This?. Pediatric Dermatology. 24(3). 313–315. 3 indexed citations
18.
Steiner, Carlos Eduardo, Marilisa M. Guerreiro, & Antonia Paula Marques‐de‐Faria. (2004). Brief Report: Acrocallosal Syndrome and Autism. Journal of Autism and Developmental Disorders. 34(6). 723–726. 10 indexed citations
19.
Behrens, Otto K., et al.. (1999). [Efficacy of ultrasound screening in pregnancy].. PubMed. 121(5). 228–32. 1 indexed citations
20.
Lopes‐Cendes, Íscia, et al.. (1996). Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1. Arquivos de Neuro-Psiquiatria. 54(3). 412–418. 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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