Elke Back
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Connective tissue disorders research
- Genomics and Rare Diseases
- Developmental Biology top 10%
Papers in
- Genetics 35
- Genomic variations and chromosomal abnormalities 29
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Genomics and Rare Diseases 3
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- Chromosomal and Genetic Variations 5
- Co-authors
- K. D. Zang (4 shared papers)G. Wolff (9 shared papers)Gerd Scherer (3 shared papers)W. Schempp (7 shared papers)Ralf Kist (1 shared paper)Ken Dewar G (1 shared paper)Bruce W. Birren (1 shared paper)Eric S. Lander (1 shared paper)
In The Last Decade
Elke Back
35 papers receiving 751 citations
Peers
Comparison fields: 5 of 44
- Genetics 604
- Developmental Biology 25
- Pediatrics, Perinatology and Child Health 70
- Plant Science 141
- Molecular Biology 115
Countries citing papers authored by Elke Back
This map shows the geographic impact of Elke Back'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 Elke Back with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elke Back more than expected).
Fields of papers citing papers by Elke Back
This network shows the impact of papers produced by Elke Back. 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 Elke Back. The network helps show where Elke Back may publish in the future.
Co-authors
The 25 scholars most cited alongside Elke Back, 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 36 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 173 | |
| 2 | Quantitative studies on the arrangement of human metaphase chromosomes. I. Individual features in the association pattern of the acrocentric chromosomes of normal males and females. | 1968 | 77 |
| 3 | 1998 | 76 | |
| 4 | 1968 | 65 | |
| 5 | 1986 | 42 | |
| 6 | 1981 | 41 | |
| 7 | 1987 | 39 | |
| 8 | 1989 | 38 | |
| 9 | 1987 | 27 | |
| 10 | Quantitative studies on the arrangement of human metaphase chromosomes. II. Influence of the preparation technique on the association pattern of the acrocentric chromosomes. | 1969 | 26 |
| 11 | 1978 | 25 | |
| 12 | 1992 | 23 | |
| 13 | 1996 | 23 | |
| 14 | 1989 | 18 | |
| 15 | 1967 | 14 | |
| 16 | 1978 | 14 | |
| 17 | Partial monosomy 22pter leads to q11 in a newborn with the clinical features of trisomy 13 syndrome. | 1980 | 12 |
| 18 | 1994 | 12 | |
| 19 | 1995 | 12 | |
| 20 | Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies. | 1977 | 10 |
About Elke Back
Elke Back is a scholar working on Genetics, Plant Science, Pediatrics, Perinatology and Child Health, Developmental Biology and Nephrology, having authored 36 papers that have together received 829 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (29 papers), Chromosomal and Genetic Variations (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Genomics and Rare Diseases (3 papers), Down syndrome and intellectual disability research (2 papers), Congenital limb and hand anomalies (1 paper), Renal Diseases and Glomerulopathies (1 paper) and Fetal and Pediatric Neurological Disorders (1 paper). The work is most often cited by research in Genetics (604 citations), Developmental Biology (25 citations), Pediatrics, Perinatology and Child Health (70 citations), Plant Science (141 citations) and Molecular Biology (115 citations). Elke Back has collaborated with scholars based in Germany, France and Italy. Frequent co-authors include K. D. Zang, G. Wolff, Gerd Scherer, W. Schempp, Ralf Kist, Ken Dewar G, Bruce W. Birren, Eric S. Lander, Lech Korniszewski and Dietmar Pfeifer. Their work appears in journals such as Human Genetics, Clinical Genetics, The Lancet, European Journal of Human Genetics and The American Journal of Human Genetics.
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.