Gunnar Schmidt
Impact in
- Genetics top 10%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Blood disorders and treatments
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- Acute Myeloid Leukemia Research
- Platelet Disorders and Treatments
Papers in
- Genetics 17
- BRCA gene mutations in cancer 10
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 2
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- Acute Myeloid Leukemia Research 4
- Co-authors
- Bernd Auber (14 shared papers)Brigitte Schlegelberger (12 shared papers)Doris Steinemann (9 shared papers)Winfried A. Hofmann (6 shared papers)Tim Ripperger (5 shared papers)Thomas Illig (5 shared papers)Sandra v. Hardenberg (6 shared papers)Reinhold Ernst Schmidt (2 shared papers)
In The Last Decade
Gunnar Schmidt
30 papers receiving 581 citations
Gunnar Schmidt's Hit Papers
Peers
Comparison fields: 5 of 41
- Genetics 354
- Hematology 52
- Cancer Research 43
- Immunology 58
- Developmental Biology 5
Countries citing papers authored by Gunnar Schmidt
This map shows the geographic impact of Gunnar Schmidt'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 Gunnar Schmidt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gunnar Schmidt more than expected).
Fields of papers citing papers by Gunnar Schmidt
This network shows the impact of papers produced by Gunnar Schmidt. 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 Gunnar Schmidt. The network helps show where Gunnar Schmidt may publish in the future.
Co-authors
The 25 scholars most cited alongside Gunnar Schmidt, 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 32 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 137 | |
| 2 | 2018 | 95 | |
| 3 | Evidence-based recommendations for gene-specific ACMG/AMP variant classification from the ClinGen ENIGMA BRCA1 and BRCA2 Variant Curation Expert Panel Hit paper breakdown → | 2024 | 55 |
| 4 | 2017 | 47 | |
| 5 | 2018 | 47 | |
| 6 | 2022 | 26 | |
| 7 | 2020 | 22 | |
| 8 | 2019 | 19 | |
| 9 | 2022 | 16 | |
| 10 | 2018 | 13 | |
| 11 | 2023 | 12 | |
| 12 | 2019 | 10 | |
| 13 | 2022 | 10 | |
| 14 | 2022 | 9 | |
| 15 | 2018 | 8 | |
| 16 | 2021 | 8 | |
| 17 | 2023 | 8 | |
| 18 | 2020 | 7 | |
| 19 | 2023 | 6 | |
| 20 | 2019 | 5 |
About Gunnar Schmidt
Gunnar Schmidt is a scholar working on Genetics, Hematology, Immunology, Genetics and Cancer Research, having authored 32 papers that have together received 590 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (10 papers), Genomics and Rare Diseases (5 papers), Acute Myeloid Leukemia Research (4 papers), Immunodeficiency and Autoimmune Disorders (4 papers), Genomic variations and chromosomal abnormalities (2 papers), Epigenetics and DNA Methylation (1 paper), Pulmonary Hypertension Research and Treatments (1 paper) and Hereditary Neurological Disorders (1 paper). The work is most often cited by research in Genetics (354 citations), Hematology (52 citations), Cancer Research (43 citations), Immunology (58 citations) and Developmental Biology (5 citations). Gunnar Schmidt has collaborated with scholars based in Germany, France and Canada. Frequent co-authors include Bernd Auber, Brigitte Schlegelberger, Doris Steinemann, Winfried A. Hofmann, Tim Ripperger, Thomas Illig, Sandra v. Hardenberg, Reinhold Ernst Schmidt, Faranaz Atschekzei and Colin Davenport. Their work appears in journals such as Clinical Genetics, Genes Chromosomes and Cancer, Breast Cancer Research, Frontiers in Immunology and Clinical Immunology.
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.