Paul Eberlé
Impact in
- Developmental Neuroscience top 5%
- Williams Syndrome Research
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- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 16
- Genomic variations and chromosomal abnormalities 8
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
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- Chromosomal and Genetic Variations 11
- Co-authors
- A. J. Beuren (1 shared paper)Jürgen Apitz (1 shared paper)Dietrich Harmjanz (1 shared paper)Friedrich Oehlkers (1 shared paper)WERNER HUNSTEIN (3 shared papers)Theo W. J. Hustinx (1 shared paper)Peter Emil Becker (3 shared papers)H Leuner (1 shared paper)
- Journals
- Chromosoma (4 papers)Human Genetics (4 papers)The Lancet (1 paper)Journal of Molecular Medicine (1 paper)The American Journal of Cardiology (1 paper)
- Partner nations
- Germany
In The Last Decade
Paul Eberlé
30 papers receiving 403 citations
Peers
Comparison fields: 5 of 55
- Developmental Neuroscience 99
- Genetics 117
- Epidemiology 119
- Cardiology and Cardiovascular Medicine 77
- Developmental Biology 6
Countries citing papers authored by Paul Eberlé
This map shows the geographic impact of Paul Eberlé'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 Paul Eberlé with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paul Eberlé more than expected).
Fields of papers citing papers by Paul Eberlé
This network shows the impact of papers produced by Paul Eberlé. 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 Paul Eberlé. The network helps show where Paul Eberlé may publish in the future.
Co-authors
The 19 scholars most cited alongside Paul Eberlé, 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1964 | 237 | |
| 2 | 1961 | 57 | |
| 3 | 1968 | 34 | |
| 4 | 1963 | 30 | |
| 5 | 1956 | 28 | |
| 6 | 1956 | 24 | |
| 7 | Die Chromosomenstruktur des Menschen in mitosis and meiosis : Vergleichende zytogenetische Untersuchungen in verschiedenen Geweben und Kernphasen des Menschen, einiger Säugetiere und Insekten sowie bei Melandrium album | 1966 | 13 |
| 8 | 1956 | 11 | |
| 9 | 1963 | 10 | |
| 10 | 1964 | 8 | |
| 11 | 1969 | 8 | |
| 12 | 1956 | 7 | |
| 13 | 1977 | 7 | |
| 14 | 1970 | 5 | |
| 15 | 1973 | 5 | |
| 16 | Zur Variabilitt des weiblichen Turner-Syndroms: Chromosomenanalysen und klinische Befunde bei 17 typischen und atypischen Fllen | 1973 | 5 |
| 17 | 1964 | 4 | |
| 18 | 1964 | 4 | |
| 19 | 1968 | 4 | |
| 20 | 1975 | 4 |
About Paul Eberlé
Paul Eberlé is a scholar working on Genetics, Plant Science, Pediatrics, Perinatology and Child Health, Cancer Research and Biophysics, having authored 34 papers that have together received 520 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (11 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Carcinogens and Genotoxicity Assessment (3 papers), Muscle Physiology and Disorders (3 papers), Pharmacological Effects and Toxicity Studies (2 papers), Psychedelics and Drug Studies (2 papers) and Cardiac Valve Diseases and Treatments (2 papers). The work is most often cited by research in Developmental Neuroscience (99 citations), Genetics (117 citations), Epidemiology (119 citations), Cardiology and Cardiovascular Medicine (77 citations) and Developmental Biology (6 citations). Paul Eberlé has collaborated with scholars based in Germany. Frequent co-authors include A. J. Beuren, Jürgen Apitz, Dietrich Harmjanz, Friedrich Oehlkers, WERNER HUNSTEIN, Theo W. J. Hustinx, Peter Emil Becker, H Leuner, H. W. Stuhlsatz and Robert L. Schmidt. Their work appears in journals such as Chromosoma, Human Genetics, The Lancet, Journal of Molecular Medicine and The American Journal of Cardiology.
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.