Regine Schubert
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 18
- Genomic variations and chromosomal abnormalities 11
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genetic Syndromes and Imprinting 2
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- Sexual Differentiation and Disorders 4
- Co-authors
- Gesa Schwanitz (19 shared papers)Thomas Eggermann (9 shared papers)H. van der Ven (3 shared papers)Markus Montag (2 shared papers)Katrin van der Ven (3 shared papers)Hartmut Engels (6 shared papers)M. Hansmann (3 shared papers)Michael Schmid (2 shared papers)
In The Last Decade
Regine Schubert
22 papers receiving 495 citations
Peers
Comparison fields: 5 of 52
- Genetics 389
- Pediatrics, Perinatology and Child Health 185
- Reproductive Medicine 81
- Pharmaceutical Science 20
- Plant Science 107
Countries citing papers authored by Regine Schubert
This map shows the geographic impact of Regine Schubert'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 Regine Schubert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Regine Schubert more than expected).
Fields of papers citing papers by Regine Schubert
This network shows the impact of papers produced by Regine Schubert. 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 Regine Schubert. The network helps show where Regine Schubert may publish in the future.
Co-authors
The 25 scholars most cited alongside Regine Schubert, 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 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 120 | |
| 2 | 2002 | 56 | |
| 3 | 1998 | 52 | |
| 4 | 2008 | 45 | |
| 5 | 2016 | 44 | |
| 6 | 1999 | 42 | |
| 7 | 1997 | 38 | |
| 8 | 1999 | 23 | |
| 9 | 2006 | 19 | |
| 10 | 1999 | 18 | |
| 11 | 2002 | 16 | |
| 12 | Sperm analyses, genetic counselling and therapy in an infertile carrier of a supernumerary marker chromosome 15. | 2006 | 15 |
| 13 | Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature. | 1999 | 12 |
| 14 | 1997 | 11 | |
| 15 | 2008 | 10 | |
| 16 | 2002 | 6 | |
| 17 | 2000 | 6 | |
| 18 | 1998 | 5 | |
| 19 | 2004 | 5 | |
| 20 | 2013 | 3 |
About Regine Schubert
Regine Schubert is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Reproductive Medicine, having authored 23 papers that have together received 551 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Chromosomal and Genetic Variations (10 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Prenatal Screening and Diagnostics (5 papers), Sexual Differentiation and Disorders (4 papers), Sperm and Testicular Function (3 papers), Genetic Syndromes and Imprinting (2 papers) and Urological Disorders and Treatments (2 papers). The work is most often cited by research in Genetics (389 citations), Pediatrics, Perinatology and Child Health (185 citations), Reproductive Medicine (81 citations), Pharmaceutical Science (20 citations) and Plant Science (107 citations). Regine Schubert has collaborated with scholars based in Germany, Poland and Hungary. Frequent co-authors include Gesa Schwanitz, Thomas Eggermann, H. van der Ven, Markus Montag, Katrin van der Ven, Hartmut Engels, M. Hansmann, Michael Schmid, Martina Guttenbach and Peter Propping. Their work appears in journals such as Clinical Genetics, Prenatal Diagnosis, Fertility and Sterility, The Journal of Urology and Human Reproduction.
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.