E S Cantú

425 total citations
7 papers, 269 citations indexed

About

E S Cantú is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, E S Cantú has authored 7 papers receiving a total of 269 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Plant Science. Recurrent topics in E S Cantú's 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). E S Cantú is often cited by papers focused on 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). E S Cantú collaborates with scholars based in United States. E S Cantú's 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 and has published in prestigious journals such as Journal of Medical Genetics, American Journal of Medical Genetics and PubMed.

In The Last Decade

E S Cantú

7 papers receiving 247 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
E S Cantú United States	6	248	131	69	36	31	7	269
Л. П. Назаренко Russia	10	155 0.6×	141 1.1×	38 0.6×	55 1.5×	18 0.6×	45	244
W. Ted Brown United States	9	244 1.0×	202 1.5×	18 0.3×	22 0.6×	17 0.5×	11	326
Isidora López‐Pajares Spain	10	187 0.8×	113 0.9×	60 0.9×	55 1.5×	32 1.0×	11	242
Arthur W. Grix United States	5	95 0.4×	105 0.8×	46 0.7×	4 0.1×	23 0.7×	6	197
Catherine Ozilou France	10	273 1.1×	118 0.9×	72 1.0×	67 1.9×	5 0.2×	11	319
Yannis Duffourd France	6	140 0.6×	121 0.9×	17 0.2×	9 0.3×	34 1.1×	14	218
Bénédicte Duban‐Bedu France	10	154 0.6×	93 0.7×	39 0.6×	33 0.9×	16 0.5×	12	214
Chloe X. Yap Australia	5	218 0.9×	82 0.6×	9 0.1×	25 0.7×	27 0.9×	9	313
Catherine Mercer United Kingdom	7	151 0.6×	114 0.9×	55 0.8×	53 1.5×	25 0.8×	8	231
Natalie Blagowidow United States	6	157 0.6×	190 1.5×	22 0.3×	25 0.7×	5 0.2×	10	253

Countries citing papers authored by E S Cantú

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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7 of 7 papers shown

1.

Joseph, Maries, et al.. (1996). Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation.. Journal of Medical Genetics. 33(11). 906–911. 26 indexed citations

2.

Cantú, E S, et al.. (1995). An atypical Turner syndrome patient with ring X chromosome mosaicism.. PubMed. 25(1). 60–5. 10 indexed citations

3.

Williams, Charles A., Roberto T. Zori, John W. Stone, et al.. (1990). Maternal origin of 15q11–13 deletions in Angelman syndrome suggests a role for genomic imprinting. American Journal of Medical Genetics. 35(3). 350–353. 95 indexed citations

4.

Cantú, E S, et al.. (1990). Cytogenetic survey for autistic fragile X carriers in a mental retardation center.. PubMed. 94(4). 442–7. 10 indexed citations

5.

Thomas, I. T., et al.. (1989). Association of pigmentary anomalies with chromosomal and genetic mosaicism and chimerism.. PubMed. 45(2). 193–205. 115 indexed citations

6.

Cantú, E S, et al.. (1988). Selective protection of specific DNA sequences in the heterochromatin of C-banded human Y chromosomes.. PubMed. 43(6). 948–53. 2 indexed citations

7.

Cantú, E S, Robert L. Nussbaum, Susan Airhart, & David H. Ledbetter. (1985). Fragile (X) expression induced by FUdR is transient and inversely related to levels of thymidylate synthase activity.. PubMed. 37(5). 947–55. 11 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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