E. Orye

721 total citations
35 papers, 590 citations indexed

About

E. Orye is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, E. Orye has authored 35 papers receiving a total of 590 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 11 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in E. Orye's work include Genomic variations and chromosomal abnormalities (22 papers), Prenatal Screening and Diagnostics (9 papers) and Chromosomal and Genetic Variations (9 papers). E. Orye is often cited by papers focused on Genomic variations and chromosomal abnormalities (22 papers), Prenatal Screening and Diagnostics (9 papers) and Chromosomal and Genetic Variations (9 papers). E. Orye collaborates with scholars based in Belgium and Netherlands. E. Orye's co-authors include Margarita Craen, C Hooft, G. Dacremont, Henri Verhaaren, D. Carton, J. Kint, Hendrik van Egmond, Yves Benoît, Marc Coppens and Marleen Praet and has published in prestigious journals such as Science, The Lancet and Heart.

In The Last Decade

E. Orye

32 papers receiving 531 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Orye Belgium 14 311 233 137 122 85 35 590
Atsuko Fujimoto United States 19 489 1.6× 310 1.3× 267 1.9× 153 1.3× 126 1.5× 45 868
M.M. Aronson United States 13 213 0.7× 264 1.1× 90 0.7× 83 0.7× 50 0.6× 48 498
T. M. Schroeder Germany 13 231 0.7× 716 3.1× 62 0.5× 173 1.4× 61 0.7× 33 967
Mildred L. Kistenmacher United States 12 326 1.0× 315 1.4× 138 1.0× 119 1.0× 31 0.4× 17 595
F Chavin-Colin France 14 413 1.3× 352 1.5× 202 1.5× 133 1.1× 7 0.1× 24 640
K. L. Ying United States 12 252 0.8× 267 1.1× 75 0.5× 81 0.7× 5 0.1× 18 497
WB Bias United States 9 132 0.4× 134 0.6× 57 0.4× 37 0.3× 39 0.5× 14 537
Sparkes Rs United States 11 132 0.4× 143 0.6× 72 0.5× 42 0.3× 27 0.3× 30 382
M. L. Kwee Netherlands 13 320 1.0× 426 1.8× 91 0.7× 57 0.5× 20 0.2× 24 640
Chris Fisher United Kingdom 14 227 0.7× 708 3.0× 235 1.7× 54 0.4× 158 1.9× 28 1.3k

Countries citing papers authored by E. Orye

Since Specialization
Citations

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

Fields of papers citing papers by E. Orye

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. Orye. 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. Orye. The network helps show where E. Orye may publish in the future.

Co-authorship network of co-authors of E. Orye

This figure shows the co-authorship network connecting the top 25 collaborators of E. Orye. A scholar is included among the top collaborators of E. Orye 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. Orye. E. Orye 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.
Speleman, Frank, Jules G. Leroy, Nadine Van Roy, et al.. (1991). Pallister‐killian syndrome: Characterization of the isochromosome 12p by fluorescent In Situ hybridization. American Journal of Medical Genetics. 41(3). 381–387. 50 indexed citations
2.
Orye, E., et al.. (1985). Trisomy 10p, due to an unusual translocation.. PubMed. 33(1). 63–6. 4 indexed citations
3.
Orye, E., Geneviève Laureys, & Henri Verhaaren. (1985). Mosaic and non-mosaic trisomy 15q2.. PubMed. 28(1). 58–60. 2 indexed citations
4.
Orye, E., et al.. (1985). Extra Yq and partial monosomy 12p due to a Y;12 translocation in a boy with features of the 12p deletion syndrome.. Journal of Medical Genetics. 22(3). 222–224. 4 indexed citations
5.
Orye, E., Jean Plum, & Magda De Smedt. (1984). β-Glucuronidase activity in human T and B lymphocytes and the Tμ and Tγ subpopulations. Histochemistry and Cell Biology. 81(3). 287–290. 5 indexed citations
6.
Orye, E., et al.. (1983). Distal trisomy 14q due to tandem duplication (q24 leads to q32).. PubMed. 26(4). 238–9. 12 indexed citations
7.
8.
Orye, E., et al.. (1983). A new, simple and rapid method for enumerating human T lymphocytes in full blood: the E. coli (ATCC 11303) rosette test. Journal of Immunological Methods. 60(3). 369–377. 1 indexed citations
9.
Berghe, Herman Van den, Kristina Vermaelen, Yves Benoît, et al.. (1983). Pentasomy 21 characterizing spontaneously regressing congenital acute leukemia. Cancer Genetics and Cytogenetics. 9(1). 19–23. 25 indexed citations
10.
11.
12.
Orye, E. & Margarita Craen. (1974). A t(21q21q) Ring Chromosome. Human Heredity. 24(3). 253–258. 11 indexed citations
13.
14.
15.
Orye, E., et al.. (1972). [Familial partial trisomy 18].. PubMed. 26(1). 41–52. 1 indexed citations
16.
Orye, E., et al.. (1969). A Probable Pericentric Inversion of a G/G Translocation Chromosome in a Mentally Retarded Child with Mongoloid Traits. Human Heredity. 19(3). 288–298. 4 indexed citations
17.
Hooft, C, et al.. (1968). [Turner's syndrome and a probable pericentric inversion of chromosome 2(45, X, 2(p+q-))].. PubMed. 11(3). 181–3. 4 indexed citations
18.
Hooft, C, et al.. (1968). [Ring chromosome 18].. PubMed. 22(2). 69–88. 8 indexed citations
19.
Orye, E., et al.. (1967). Familial D/D and D/G, translocation.. PubMed. 22(1). 36–40. 9 indexed citations
20.
Orye, E., et al.. (1967). [Deletion of the short arms of chromosome 18].. PubMed. 35(9). 277–84. 5 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Atsuko Fujimoto Breakdown of academic impact, for papers by M.M. Aronson Breakdown of academic impact, for papers by T. M. Schroeder Breakdown of academic impact, for papers by Mildred L. Kistenmacher Breakdown of academic impact, for papers by F Chavin-Colin Breakdown of academic impact, for papers by K. L. Ying Breakdown of academic impact, for papers by WB Bias Breakdown of academic impact, for papers by Sparkes Rs Breakdown of academic impact, for papers by M. L. Kwee Breakdown of academic impact, for papers by Chris Fisher
Rankless by CCL
2026