Heide Seidel
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
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- Congenital heart defects research
- Protein Tyrosine Phosphatases
Papers in
- Genetics 17
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
- Genomic variations and chromosomal abnormalities 5
- Connective tissue disorders research 4
- Genetics and Neurodevelopmental Disorders 3
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- Protein Tyrosine Phosphatases 3
- Sexual Differentiation and Disorders 3
- Congenital heart defects research 3
- Co-authors
- H. Zankl (3 shared papers)Thomas Meitinger (3 shared papers)Simone Schuffenhauer (3 shared papers)K. D. Zang (2 shared papers)Tim M. Strom (2 shared papers)Kerstin Kutsche (3 shared papers)Jan Murken (2 shared papers)Maja Hempel (1 shared paper)
In The Last Decade
Heide Seidel
23 papers receiving 319 citations
Peers
Comparison fields: 5 of 45
- Genetics 192
- Molecular Biology 182
- Cardiology and Cardiovascular Medicine 48
- Immunology 42
- Developmental Biology 4
Countries citing papers authored by Heide Seidel
This map shows the geographic impact of Heide Seidel'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 Heide Seidel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heide Seidel more than expected).
Fields of papers citing papers by Heide Seidel
This network shows the impact of papers produced by Heide Seidel. 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 Heide Seidel. The network helps show where Heide Seidel may publish in the future.
Co-authors
The 25 scholars most cited alongside Heide Seidel, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 40 | |
| 2 | 2012 | 24 | |
| 3 | DiGeorge syndrome and partial monosomy 10p: case report and review. | 1995 | 23 |
| 4 | 2017 | 20 | |
| 5 | 1998 | 20 | |
| 6 | 1996 | 18 | |
| 7 | 2019 | 18 | |
| 8 | 2007 | 17 | |
| 9 | 2019 | 16 | |
| 10 | 2017 | 16 | |
| 11 | Cytological and cytogenetical studies on brain tumors. V. Preferential loss of sex chromosomes in human meningiomas. | 1975 | 16 |
| 12 | 1987 | 15 | |
| 13 | 1975 | 13 | |
| 14 | 2013 | 13 | |
| 15 | 1992 | 12 | |
| 16 | 1993 | 12 | |
| 17 | 1975 | 11 | |
| 18 | 2005 | 10 | |
| 19 | 1981 | 9 | |
| 20 | 2019 | 7 |
About Heide Seidel
Heide Seidel is a scholar working on Genetics, Molecular Biology, Cardiology and Cardiovascular Medicine, Pulmonary and Respiratory Medicine and Epidemiology, having authored 24 papers that have together received 337 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Connective tissue disorders research (4 papers), Protein Tyrosine Phosphatases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Sexual Differentiation and Disorders (3 papers), Congenital heart defects research (3 papers) and Cardiac Valve Diseases and Treatments (3 papers). The work is most often cited by research in Genetics (192 citations), Molecular Biology (182 citations), Cardiology and Cardiovascular Medicine (48 citations), Immunology (42 citations) and Developmental Biology (4 citations). Heide Seidel has collaborated with scholars based in Germany, Australia and Taiwan. Frequent co-authors include H. Zankl, Thomas Meitinger, Simone Schuffenhauer, K. D. Zang, Tim M. Strom, Kerstin Kutsche, Jan Murken, Maja Hempel, Martin Zenker and Janine Wagenstaller. Their work appears in journals such as Human Genetics, Clinical Genetics, Cardiovascular Pathology, Gene and Journal of Clinical Medicine.
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.