Eduardo S. Cantú

648 citations
18 papers · 499 indexed · h-index 10
Topics
Genomic variations and chromosomal abnormalities (11 papers)Prenatal Screening and Diagnostics (7 papers)Genetic Syndromes and Imprinting (5 papers)
Journals
SHILAP Revista de lepidopterologíaBloodAnnals of Neurology

In The Last Decade

Eduardo S. Cantú

18 papers receiving 487 citations

Peers

Eduardo S. Cantú
Comparison fields: 5 of 38
  • Genetics 304
  • Molecular Biology 288
  • Pediatrics, Perinatology and Child Health 133
  • Hematology 107
  • Public Health, Environmental and Occupational Health 47
Replace F. Prieto with:
F. Prieto Spain
Michael J. Macera United States
J L Watt United Kingdom
Rachel D. Burnside United States
Judith Dagan Israel
V. D. Marković Canada
M. Chery France
Iskra Petković Croatia
Donatella Fantasia Italy
Carmelo Laganà Italy
Eduardo S. Cantú relative to F. Prieto Spain F. Prieto's profile →
Citations per field
00.5×1.5×2.0×
F. Prieto · 1×
Citations per year

Countries citing papers authored by Eduardo S. Cantú

Since Specialization
Citations

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

Fields of papers citing papers by Eduardo S. Cantú

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eduardo S. Cantú

This figure shows the co-authorship network connecting the top 25 collaborators of Eduardo S. Cantú. A scholar is included among the top collaborators of Eduardo S. Cantú 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 Eduardo S. Cantú. Eduardo S. Cantú is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
#WorkIndexed citations
1 1
2
Discrepant Cytogenetic and Interphase Fluorescence In Situ Hybridization (I-FISH) Results from Bone Marrow Specimens of Patients with Hematologic Neoplasms.
2
3 9
4 11
5 5
6 168
7 23
8 4
9 60
10 13
11 77
12 61
13 15
14 23
15 15
16 1
17 7
18 4

About Eduardo S. Cantú

Eduardo S. Cantú is a scholar working on Genetics, Hematology and Pediatrics, Perinatology and Child Health, having authored 18 papers that have together received 499 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Prenatal Screening and Diagnostics (7 papers) and Genetic Syndromes and Imprinting (5 papers). The work is most often cited by research in Genetics (304 citations), Hematology (107 citations) and Pediatrics, Perinatology and Child Health (133 citations). Eduardo S. Cantú has collaborated with scholars based in United States and United Kingdom. Frequent co-authors include Charles A. Williams, G. Shashidhar Pai, Jill E. Hendrickson, Robert D. Nicholls, Brian A. Gray, John W. Stone, Wayne Gottlieb, Frederick G. Behm, Jaime L. Frías and Norman A. Doggett. Their work appears in journals such as SHILAP Revista de lepidopterología, Blood and Annals of Neurology.

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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