E S Cantú
- Genetics top 10%
- Molecular Biology
- Pediatrics, Perinatology and Child Health
- Plant Science
- Cell Biology
- Co-authors
- David B. FlanneryJaime L. FríasI. T. ThomasJanet G. GrahamBrian A. GrayJohn W. StoneCharles A. WilliamsRoberto T. Zori
- Topics
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers)Genetics and Neurodevelopmental Disorders (2 papers)Chromosomal and Genetic Variations (2 papers)
- Partner nations
- United States
In The Last Decade
E S Cantú
7 papers receiving 247 citations
Peers
Comparison fields: 5 of 42
- Genetics 248
- Molecular Biology 131
- Pediatrics, Perinatology and Child Health 69
- Plant Science 36
- Cell Biology 31
Countries citing papers authored by E S Cantú
This map shows the geographic impact of E 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 E 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 E S Cantú more than expected).
Fields of papers citing papers by E S Cantú
This network shows the impact of papers produced by E 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 E S Cantú. The network helps show where E S Cantú may publish in the future.
Co-authorship network of co-authors of E S Cantú
This figure shows the co-authorship network connecting the top 25 collaborators of E S Cantú. A scholar is included among the top collaborators of E 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 E S Cantú. E S Cantú is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 26 | |
| 2 | An atypical Turner syndrome patient with ring X chromosome mosaicism. | 10 |
| 3 | 95 | |
| 4 | Cytogenetic survey for autistic fragile X carriers in a mental retardation center. | 10 |
| 5 | Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism. | 115 |
| 6 | Selective protection of specific DNA sequences in the heterochromatin of C-banded human Y chromosomes. | 2 |
| 7 | Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activity. | 11 |
About E S Cantú
E S Cantú is a scholar working on Genetics, Gender Studies and Cancer Research, having authored 7 papers that have together received 269 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Genetics (248 citations), Pediatrics, Perinatology and Child Health (69 citations) and Dermatology (22 citations). E S Cantú has collaborated with scholars based in United States. Frequent co-authors include David B. Flannery, Jaime L. Frías, I. T. Thomas, Janet G. Graham, Brian A. Gray, John W. Stone, Charles A. Williams, Roberto T. Zori, Harry Ostrer and Maries Joseph. Their work appears in journals such as Journal of Medical Genetics, American Journal of Medical Genetics and PubMed.
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.