Gesa Schwanitz
Impact in
- Genetics top 2%
- 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 87
- Genomic variations and chromosomal abnormalities 71
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
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- Prenatal Screening and Diagnostics 39
- Co-authors
- Regine Schubert (22 shared papers)Thomas Eggermann (28 shared papers)Hartmut Engels (20 shared papers)Klaus Zerres (17 shared papers)Katrin van der Ven (7 shared papers)Markus H. M. Montag (5 shared papers)H.‐D. Rott (7 shared papers)Hans van der Ven (2 shared papers)
In The Last Decade
Gesa Schwanitz
137 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 95
- Genetics 1.2k
- Pediatrics, Perinatology and Child Health 703
- Developmental Biology 55
- Reproductive Medicine 129
- Plant Science 410
Countries citing papers authored by Gesa Schwanitz
This map shows the geographic impact of Gesa Schwanitz'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 Gesa Schwanitz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gesa Schwanitz more than expected).
Fields of papers citing papers by Gesa Schwanitz
This network shows the impact of papers produced by Gesa Schwanitz. 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 Gesa Schwanitz. The network helps show where Gesa Schwanitz may publish in the future.
Co-authors
The 25 scholars most cited alongside Gesa Schwanitz, 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 143 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 125 | |
| 2 | 1998 | 79 | |
| 3 | 2002 | 70 | |
| 4 | 2008 | 68 | |
| 5 | 1980 | 58 | |
| 6 | 1970 | 54 | |
| 7 | 1996 | 49 | |
| 8 | 1999 | 47 | |
| 9 | 1997 | 46 | |
| 10 | 1997 | 45 | |
| 11 | 1996 | 39 | |
| 12 | 2000 | 37 | |
| 13 | 2004 | 37 | |
| 14 | 1997 | 36 | |
| 15 | Duplication 7p de novo and literature review. | 1989 | 30 |
| 16 | 1985 | 30 | |
| 17 | 1994 | 28 | |
| 18 | Klinefelter's syndrome and mitral valve prolapse. an echocardiographic study in twenty-two patients. | 1984 | 27 |
| 19 | 1971 | 27 | |
| 20 | 1993 | 27 |
About Gesa Schwanitz
Gesa Schwanitz is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Plant Science, Developmental Biology and Molecular Biology, having authored 143 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (71 papers), Prenatal Screening and Diagnostics (39 papers), Chromosomal and Genetic Variations (37 papers), Congenital limb and hand anomalies (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Congenital Anomalies and Fetal Surgery (9 papers), Sexual Differentiation and Disorders (8 papers) and Genomics and Chromatin Dynamics (7 papers). The work is most often cited by research in Genetics (1.2k citations), Pediatrics, Perinatology and Child Health (703 citations), Developmental Biology (55 citations), Reproductive Medicine (129 citations) and Plant Science (410 citations). Gesa Schwanitz has collaborated with scholars based in Germany, Poland and Iran. Frequent co-authors include Regine Schubert, Thomas Eggermann, Hartmut Engels, Klaus Zerres, Katrin van der Ven, Markus H. M. Montag, H.‐D. Rott, Hans van der Ven, G. Lehnert and M. Hansmann. Their work appears in journals such as Human Genetics, Prenatal Diagnosis, Clinical Genetics, Human Reproduction and European Journal of Medical 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.