Ellen Magenis

2.0k total citations
31 papers, 1.4k citations indexed

About

Ellen Magenis is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ellen Magenis has authored 31 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 15 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ellen Magenis's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Ellen Magenis is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers). Ellen Magenis collaborates with scholars based in United States, Ireland and Canada. Ellen Magenis's co-authors include Leland Allen, John M. Opitz, Jacob A. Reiss, Gail Waldstein, Ann C. M. Smith, Martin B. Lahr, Loris McGavran, James F. Reynolds, Hiroko Kawashima and Julie R. Korenberg and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Ellen Magenis

30 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ellen Magenis United States 18 815 694 245 215 191 31 1.4k
Bruno Leheup France 29 758 0.9× 1.1k 1.6× 215 0.9× 125 0.6× 149 0.8× 97 2.2k
Emilio Donti Italy 21 404 0.5× 836 1.2× 267 1.1× 608 2.8× 108 0.6× 96 1.6k
A. Moseley United States 5 890 1.1× 834 1.2× 94 0.4× 149 0.7× 92 0.5× 10 1.6k
Luitgard M. Neumann Germany 20 1.0k 1.2× 708 1.0× 110 0.4× 73 0.3× 110 0.6× 46 1.7k
S Malcolm United Kingdom 31 1.1k 1.4× 1.2k 1.7× 210 0.9× 78 0.4× 248 1.3× 71 2.3k
Dvorah Abeliovich Israel 31 1.4k 1.7× 1.5k 2.1× 158 0.6× 105 0.5× 450 2.4× 98 3.0k
David Geneviève France 24 1.1k 1.4× 1.3k 1.9× 168 0.7× 55 0.3× 202 1.1× 80 2.3k
Mitsuo Masuno Japan 21 1.1k 1.3× 1.4k 2.0× 100 0.4× 67 0.3× 180 0.9× 86 2.3k
Adele Schneider United States 23 1.2k 1.5× 908 1.3× 502 2.0× 51 0.2× 366 1.9× 67 2.2k
Anna Rajab Oman 23 628 0.8× 1.2k 1.7× 170 0.7× 83 0.4× 180 0.9× 58 1.9k

Countries citing papers authored by Ellen Magenis

Since Specialization
Citations

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

Fields of papers citing papers by Ellen Magenis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ellen Magenis

This figure shows the co-authorship network connecting the top 25 collaborators of Ellen Magenis. A scholar is included among the top collaborators of Ellen Magenis 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 Ellen Magenis. Ellen Magenis 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.
Schlaubitz, Silke, Svetlana A. Yatsenko, Laurie D. Smith, et al.. (2007). Ovotestes and XY sex reversal in a female with an interstitial 9q33.3‐q34.1 deletion encompassing NR5A1 and LMX1B causing features of genitopatellar syndrome. American Journal of Medical Genetics Part A. 143A(10). 1071–1081. 38 indexed citations
2.
Korenberg, Julie R., Hiroko Kawashima, S. M. Pulst, et al.. (2005). Down syndrome: Toward a molecular definition of the phenotype. American Journal of Medical Genetics. 37(S7). 91–97. 13 indexed citations
3.
Palmer, Earl A., et al.. (2002). Optic disc drusen associated with trisomy 15q. Journal of American Association for Pediatric Ophthalmology and Strabismus. 6(1). 49–50. 4 indexed citations
4.
Magenis, Ellen, et al.. (1999). Blaschkolinear malformation syndrome in complex trisomy-7 mosaicism. American Journal of Medical Genetics. 87(5). 375–383. 24 indexed citations
5.
Trask, B. J., Heather C. Mefford, Ger van den Engh, et al.. (1996). Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients. Human Genetics. 98(6). 710–718. 43 indexed citations
6.
Kirschner, Marvin A., J.L. Arriza, N G Copeland, et al.. (1994). The Mouse and Human Excitatory Amino Acid Transporter Gene (EAAT1) Maps to Mouse Chromosome 15 and a Region of Syntenic Homology on Human Chromosome 5. Genomics. 22(3). 631–633. 17 indexed citations
7.
Lindsay, Elizabeth A., Giovanni Battista Ferrero, Ellen Magenis, et al.. (1994). Microphthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic, and molecular characterization. American Journal of Medical Genetics. 49(2). 229–234. 70 indexed citations
8.
Korenberg, Julie R., Hiroko Kawashima, Stefan M. Pulst, et al.. (1990). Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype.. PubMed. 47(2). 236–46. 194 indexed citations
9.
Bray, Paul F., et al.. (1988). Physical linkage of the genes for platelet membrane glycoproteins IIb and IIIa.. Proceedings of the National Academy of Sciences. 85(22). 8683–8687. 66 indexed citations
10.
Olson, Susan B., et al.. (1987). Comparison of maternal and fetal chromosome heteromorphisms to monitor maternal cell contamination in chorionic villus samples. Prenatal Diagnosis. 7(6). 413–417. 2 indexed citations
11.
MacDonald, Marcy E., Mary Anne Anderson, T. Conrad Gilliam, et al.. (1987). A somatic cell hybrid panel for localizing DNA segments near the Huntington's disease gene. Genomics. 1(1). 29–34. 54 indexed citations
12.
McDermid, Heather E., Alessandra M.V. Duncan, Klaus Brasch, et al.. (1986). Characterization of the Supernumerary Chromosome in Cat Eye Syndrome. Science. 232(4750). 646–648. 119 indexed citations
13.
Linder, David H., et al.. (1985). Translocation X;10 in a case of congenital acute monocytic leukemia. Cancer Genetics and Cytogenetics. 16(4). 357–364. 14 indexed citations
14.
15.
LaFranchi, Stephen, Ellen Magenis, & Gerald H. Prescott. (1980). Variation in pituitary-gonadal function in two adolescent boys with 46XX male syndrome. The Journal of Pediatrics. 97(6). 960–962. 7 indexed citations
16.
King, Charles R., et al.. (1980). Mosaic and hypermodal cells in amniotic fluid cell cultures. American Journal of Obstetrics and Gynecology. 136(3). 383–385. 6 indexed citations
17.
King, Charles R. & Ellen Magenis. (1978). Turner Syndrome in the Offspring of Artificially Inseminated Pregnancies. Fertility and Sterility. 30(5). 604–605. 6 indexed citations
18.
King, Charles R. & Ellen Magenis. (1978). The Marden-Walker syndrome.. Journal of Medical Genetics. 15(5). 366–369. 16 indexed citations
19.
Magenis, Ellen, et al.. (1977). Partial trisomy 22: A recognizable syndrome. Clinical Genetics. 12(1). 9–16. 25 indexed citations
20.
Meyers, Deborah A., P.M. Conneally, Frederick Hecht, et al.. (1975). Linkage group I: multipoint mapping. Cytogenetic and Genome Research. 14(3-6). 381–389.

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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