Steffi Patzer
Impact in
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- Epilepsy research and treatment
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- Neuroscience and Neuropharmacology Research
Papers in
- Genetics 2
- Genomics and Rare Diseases 1
- Genetics and Neurodevelopmental Disorders 1
- Genomic variations and chromosomal abnormalities 1
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- RNA and protein synthesis mechanisms 1
- Co-authors
- Eric D. Marsh (1 shared paper)Ningning Hu (1 shared paper)Beth R. Shiedley (1 shared paper)Ciria C. Hernández (1 shared paper)Ethan M. Goldberg (1 shared paper)Steffen Leiz (1 shared paper)Rainer Boor (1 shared paper)Xilma R. Ortiz‐González (1 shared paper)
- Journals
- Journal of Neurology Neurosurgery & Psychiatry (1 paper)Brain (1 paper)PubMed (1 paper)
- Partner nations
- GermanyUnited StatesRussia
In The Last Decade
Steffi Patzer
3 papers receiving 97 citations
Peers
Comparison fields: 5 of 32
- Psychiatry and Mental health 41
- Cellular and Molecular Neuroscience 42
- Genetics 48
- Clinical Biochemistry 6
- Molecular Biology 48
Countries citing papers authored by Steffi Patzer
This map shows the geographic impact of Steffi Patzer'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 Steffi Patzer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Steffi Patzer more than expected).
Fields of papers citing papers by Steffi Patzer
This network shows the impact of papers produced by Steffi Patzer. 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 Steffi Patzer. The network helps show where Steffi Patzer may publish in the future.
Co-authors
The 25 scholars most cited alongside Steffi Patzer, 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 | 2016 | 78 | |
| 2 | 2023 | 13 | |
| 3 | Disturbed copper transport in humans. Part 1: mutations of the ATP7A gene lead to Menkes disease and occipital horn syndrome. | 2001 | 6 |
About Steffi Patzer
Steffi Patzer is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Developmental Biology and Clinical Biochemistry, having authored 3 papers that have together received 97 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (1 paper), Trace Elements in Health (1 paper), Genomics and Rare Diseases (1 paper), Epilepsy research and treatment (1 paper), Neuroscience and Neuropharmacology Research (1 paper), RNA and protein synthesis mechanisms (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Genomic variations and chromosomal abnormalities (1 paper). The work is most often cited by research in Psychiatry and Mental health (41 citations), Cellular and Molecular Neuroscience (42 citations), Genetics (48 citations), Clinical Biochemistry (6 citations) and Molecular Biology (48 citations). Steffi Patzer has collaborated with scholars based in Germany, United States and Russia. Frequent co-authors include Eric D. Marsh, Ningning Hu, Beth R. Shiedley, Ciria C. Hernández, Ethan M. Goldberg, Steffen Leiz, Rainer Boor, Xilma R. Ortiz‐González, Johannes R. Lemke and Dingding Shen. Their work appears in journals such as Journal of Neurology Neurosurgery & Psychiatry, Brain and PubMed.
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.