Simone Heidemann
Impact in
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- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 8
- BRCA gene mutations in cancer 4
- Genomic variations and chromosomal abnormalities 4
- Congenital Ear and Nasal Anomalies 1
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- Prenatal Screening and Diagnostics 3
- Ethics and Legal Issues in Pediatric Healthcare 3
- Co-authors
- W. Jonat (3 shared papers)Almuth Caliebe (6 shared papers)Norbert Arnold (4 shared papers)Reiner Siebert (5 shared papers)Christine Fischer (2 shared papers)Christoph Engel (2 shared papers)Christel Eckmann-Scholz (3 shared papers)Susanne Bens (3 shared papers)
In The Last Decade
Simone Heidemann
14 papers receiving 137 citations
Peers
Comparison fields: 5 of 23
- Genetics 89
- Pediatrics, Perinatology and Child Health 33
- Pathology and Forensic Medicine 20
- Cancer Research 16
- Molecular Biology 57
Countries citing papers authored by Simone Heidemann
This map shows the geographic impact of Simone Heidemann'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 Simone Heidemann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simone Heidemann more than expected).
Fields of papers citing papers by Simone Heidemann
This network shows the impact of papers produced by Simone Heidemann. 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 Simone Heidemann. The network helps show where Simone Heidemann may publish in the future.
Co-authors
The 25 scholars most cited alongside Simone Heidemann, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 44 | |
| 2 | 2012 | 25 | |
| 3 | 2007 | 13 | |
| 4 | 2011 | 12 | |
| 5 | 2010 | 11 | |
| 6 | 2012 | 9 | |
| 7 | 2017 | 6 | |
| 8 | 2011 | 6 | |
| 9 | 2013 | 5 | |
| 10 | Gendiagnostikgesetz : Kommentar für die Praxis | 2011 | 5 |
| 11 | 2021 | 3 | |
| 12 | 2010 | 2 | |
| 13 | 2024 | 1 | |
| 14 | 2020 | 1 |
About Simone Heidemann
Simone Heidemann is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Pathology and Forensic Medicine and Public Health, Environmental and Occupational Health, having authored 14 papers that have together received 143 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers), Ethics and Legal Issues in Pediatric Healthcare (3 papers), Chromosomal and Genetic Variations (2 papers), Medical and Health Sciences Research (2 papers), Genetic factors in colorectal cancer (2 papers) and Congenital Ear and Nasal Anomalies (1 paper). The work is most often cited by research in Genetics (89 citations), Pediatrics, Perinatology and Child Health (33 citations), Pathology and Forensic Medicine (20 citations), Cancer Research (16 citations) and Molecular Biology (57 citations). Simone Heidemann has collaborated with scholars based in Germany, Austria and Estonia. Frequent co-authors include W. Jonat, Almuth Caliebe, Norbert Arnold, Reiner Siebert, Christine Fischer, Christoph Engel, Christel Eckmann-Scholz, Susanne Bens, Susanne Morlot and Nicola Dikow. Their work appears in journals such as Molecular Cytogenetics, Archives of Gynecology and Obstetrics, Clinical Genetics, Breast Cancer Research and Treatment and Epilepsia.
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.