Ellen Magenis
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Hematology top 5%
- Chronic Myeloid Leukemia Treatments
Papers in
- Genetics 17
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
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- Genomics and Chromatin Dynamics 2
- Epigenetics and DNA Methylation 2
- Co-authors
- Leland Allen (3 shared papers)John M. Opitz (2 shared papers)Loris McGavran (1 shared paper)Ann C. M. Smith (1 shared paper)Gail Waldstein (1 shared paper)Martin B. Lahr (1 shared paper)Jacob A. Reiss (1 shared paper)James F. Reynolds (1 shared paper)
- Journals
- Human Genetics (3 papers)Cytogenetic and Genome Research (2 papers)Genomics (2 papers)Blood (1 paper)The Journal of Pediatrics (1 paper)
- Partner nations
- United StatesIrelandCanada
In The Last Decade
Ellen Magenis
30 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 89
- Genetics 815
- Genetics 245
- Hematology 215
- Immunology and Allergy 92
- Molecular Biology 694
Countries citing papers authored by Ellen Magenis
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
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-authors
The 25 scholars most cited alongside Ellen Magenis, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1986 | 292 | |
| 2 | Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype. | 1990 | 194 |
| 3 | 1986 | 119 | |
| 4 | 1981 | 109 | |
| 5 | 2002 | 104 | |
| 6 | 1994 | 70 | |
| 7 | 1988 | 66 | |
| 8 | Pregnancy and the Turner syndrome. | 1978 | 60 |
| 9 | 1987 | 54 | |
| 10 | 1996 | 43 | |
| 11 | 2007 | 38 | |
| 12 | 1982 | 35 | |
| 13 | The genes coding for human pro alpha 1(IV) collagen and pro alpha 2(IV) collagen are both located at the end of the long arm of chromosome 13. | 1988 | 33 |
| 14 | 1986 | 28 | |
| 15 | 1977 | 25 | |
| 16 | 1981 | 25 | |
| 17 | 1999 | 24 | |
| 18 | 1986 | 23 | |
| 19 | 1994 | 17 | |
| 20 | 1978 | 16 |
About Ellen Magenis
Ellen Magenis is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Hematology and Rheumatology, having authored 31 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Chromosomal and Genetic Variations (3 papers), Cell Adhesion Molecules Research (2 papers), Genomics and Chromatin Dynamics (2 papers), Epigenetics and DNA Methylation (2 papers) and Immunodeficiency and Autoimmune Disorders (2 papers). The work is most often cited by research in Genetics (815 citations), Genetics (245 citations), Hematology (215 citations), Immunology and Allergy (92 citations) and Molecular Biology (694 citations). Ellen Magenis has collaborated with scholars based in United States, Ireland and Canada. Frequent co-authors include Leland Allen, John M. Opitz, Loris McGavran, Ann C. M. Smith, Gail Waldstein, Martin B. Lahr, Jacob A. Reiss, James F. Reynolds, Julie R. Korenberg and Hiroko Kawashima. Their work appears in journals such as Human Genetics, Cytogenetic and Genome Research, Genomics, Blood and The Journal of Pediatrics.
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.