Joseph Porrmann
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- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 3
- Genomics and Rare Diseases 2
- BRCA gene mutations in cancer 1
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- RNA modifications and cancer 1
- CRISPR and Genetic Engineering 1
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- Cancer-related Molecular Pathways 2
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- Corneal Surgery and Treatments 1
Joseph Porrmann
9 papers receiving 109 citations
Peers
Comparison fields: 5 of 40
- Genetics 56
- Molecular Biology 69
- Cancer Research 15
- Clinical Biochemistry 5
- Developmental Neuroscience 3
Countries citing papers authored by Joseph Porrmann
This map shows the geographic impact of Joseph Porrmann'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 Joseph Porrmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joseph Porrmann more than expected).
Fields of papers citing papers by Joseph Porrmann
This network shows the impact of papers produced by Joseph Porrmann. 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 Joseph Porrmann. The network helps show where Joseph Porrmann may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Joseph Porrmann, 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 | 2025 | 1 | |
| 2 | 2021 | 16 | |
| 3 | 2019 | 24 | |
| 4 | 2018 | 6 | |
| 5 | 2018 | 1 | |
| 6 | 2018 | 29 | |
| 7 | 2017 | 11 | |
| 8 | 2017 | 13 | |
| 9 | 2015 | 9 |
About Joseph Porrmann
Joseph Porrmann is a scholar working on Genetics, Molecular Biology and Oncology, having authored 9 papers that have together received 110 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (2 papers), Cancer-related Molecular Pathways (2 papers), RNA modifications and cancer (1 paper), Corneal Surgery and Treatments (1 paper), BRCA gene mutations in cancer (1 paper) and CRISPR and Genetic Engineering (1 paper). The work is most often cited by research in Genetics (56 citations), Molecular Biology (69 citations) and Cancer Research (15 citations). Joseph Porrmann has collaborated with scholars based in Germany, United States and Sweden. Frequent co-authors include Nataliya Di Donato, Evelin Schröck, Andreas Rump, Anne‐Karin Kahlert, Andreas Tzschach, Karl Hackmann, Jens Schallner, Laura Gieldon, Barbara Klink and Johannes Maximilian Wagner. Their work appears in journals such as Ophthalmic Genetics, BMC Cancer, European Journal of Medical Genetics, npj Genomic Medicine and PLoS ONE.
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.