Astrid Bechtold
Impact in
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- Cancer Genomics and Diagnostics
- Breast Cancer Treatment Studies
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
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- Prenatal Screening and Diagnostics 2
- Genetics 2
- BRCA gene mutations in cancer 1
- Genomic variations and chromosomal abnormalities 1
- Co-authors
- Holger Hoehn (4 shared papers)Bettina Schlehe (1 shared paper)Christoph Engel (1 shared paper)Mohammad R. Zaino (1 shared paper)Norbert Arnold (1 shared paper)Kerstin Rhiem (1 shared paper)Carolin Nestle-Kraemling (1 shared paper)Dominic Varga (1 shared paper)
- Journals
- Fetal Diagnosis and Therapy (1 paper)Journal of Clinical Oncology (1 paper)Orphanet Journal of Rare Diseases (1 paper)Immunology Letters (1 paper)Zeitschrift für Gerontologie und Geriatrie (1 paper)
- Partner nations
- GermanyDenmarkSwitzerland
In The Last Decade
Astrid Bechtold
7 papers receiving 357 citations
Peers
Comparison fields: 5 of 53
- Cancer Research 113
- Genetics 207
- Oncology 65
- Pathology and Forensic Medicine 38
- Reproductive Medicine 17
Countries citing papers authored by Astrid Bechtold
This map shows the geographic impact of Astrid Bechtold'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 Astrid Bechtold with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Astrid Bechtold more than expected).
Fields of papers citing papers by Astrid Bechtold
This network shows the impact of papers produced by Astrid Bechtold. 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 Astrid Bechtold. The network helps show where Astrid Bechtold may publish in the future.
Co-authors
The 25 scholars most cited alongside Astrid Bechtold, 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 | 2009 | 254 | |
| 2 | 2007 | 68 | |
| 3 | 2009 | 22 | |
| 4 | 2007 | 19 | |
| 5 | 2005 | 7 | |
| 6 | 2007 | 2 | |
| 7 | 2007 | 1 |
About Astrid Bechtold
Astrid Bechtold is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Immunology and Plant Science, having authored 7 papers that have together received 373 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (3 papers), Prenatal Screening and Diagnostics (2 papers), CRISPR and Genetic Engineering (1 paper), Nuclear Structure and Function (1 paper), BRCA gene mutations in cancer (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Genomics and Chromatin Dynamics (1 paper) and Immunotherapy and Immune Responses (1 paper). The work is most often cited by research in Cancer Research (113 citations), Genetics (207 citations), Oncology (65 citations), Pathology and Forensic Medicine (38 citations) and Reproductive Medicine (17 citations). Astrid Bechtold has collaborated with scholars based in Germany, Denmark and Switzerland. Frequent co-authors include Holger Hoehn, Bettina Schlehe, Christoph Engel, Mohammad R. Zaino, Norbert Arnold, Kerstin Rhiem, Carolin Nestle-Kraemling, Dominic Varga, Alfons Meindl and Rita Katharina Schmutzler. Their work appears in journals such as Fetal Diagnosis and Therapy, Journal of Clinical Oncology, Orphanet Journal of Rare Diseases, Immunology Letters and Zeitschrift für Gerontologie und Geriatrie.
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.