Karin Panzer
Impact in
- Neurology top 10%
- Neurofibromatosis and Schwannoma Cases
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- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
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- Neurofibromatosis and Schwannoma Cases 3
- Genetics 3
- Genomics and Rare Diseases 3
- Genetics and Neurodevelopmental Disorders 2
- Co-authors
- Amanda L. Bergner (1 shared paper)Heather B. Radtke (1 shared paper)Ashley D. Cannon (1 shared paper)Allison L. Goetsch (1 shared paper)Caroline McGowan (1 shared paper)Osayame A. Ekhaguere (1 shared paper)Jennifer Cook (1 shared paper)Benjamin W. Darbro (1 shared paper)
- Journals
- Annals of Clinical and Translational Neurology (1 paper)The American Journal of Human Genetics (1 paper)Clinical Genetics (1 paper)JCI Insight (1 paper)Human Mutation (1 paper)
- Partner nations
- United StatesAustraliaPoland
In The Last Decade
Karin Panzer
9 papers receiving 719 citations
Karin Panzer's Hit Papers
Peers
Comparison fields: 5 of 107
- Neurology 139
- Genetics 174
- Cancer Research 73
- Molecular Biology 309
- Endocrinology 13
Countries citing papers authored by Karin Panzer
This map shows the geographic impact of Karin Panzer'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 Karin Panzer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karin Panzer more than expected).
Fields of papers citing papers by Karin Panzer
This network shows the impact of papers produced by Karin Panzer. 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 Karin Panzer. The network helps show where Karin Panzer may publish in the future.
Co-authors
The 22 scholars most cited alongside Karin Panzer, 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 | An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge Hit paper breakdown → | 2014 | 406 |
| 2 | 2015 | 127 | |
| 3 | 2019 | 100 | |
| 4 | 2018 | 45 | |
| 5 | 2018 | 19 | |
| 6 | 2020 | 18 | |
| 7 | 2016 | 6 | |
| 8 | 2021 | 5 | |
| 9 | 2019 | 4 |
About Karin Panzer
Karin Panzer is a scholar working on Neurology, Genetics, Molecular Biology, Pulmonary and Respiratory Medicine and Rheumatology, having authored 9 papers that have together received 730 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Neurofibromatosis and Schwannoma Cases (3 papers), RNA modifications and cancer (2 papers), Mitochondrial Function and Pathology (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Sarcoma Diagnosis and Treatment (1 paper), Tuberous Sclerosis Complex Research (1 paper) and Soft tissue tumor case studies (1 paper). The work is most often cited by research in Neurology (139 citations), Genetics (174 citations), Cancer Research (73 citations), Molecular Biology (309 citations) and Endocrinology (13 citations). Karin Panzer has collaborated with scholars based in United States, Australia and Poland. Frequent co-authors include Amanda L. Bergner, Heather B. Radtke, Ashley D. Cannon, Allison L. Goetsch, Caroline McGowan, Osayame A. Ekhaguere, Jennifer Cook, Benjamin W. Darbro, Oleg A. Shchelochkov and Patrick E. Lantz. Their work appears in journals such as Annals of Clinical and Translational Neurology, The American Journal of Human Genetics, Clinical Genetics, JCI Insight and Human Mutation.
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.