Matthias Kohn
Impact in
- Genetics top 10%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Neurofibromatosis and Schwannoma Cases
Papers in
- Genetics 10
- Genetics and Neurodevelopmental Disorders 5
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
- Genome Rearrangement Algorithms 2
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- Genomics and Phylogenetic Studies 2
- Ubiquitin and proteasome pathways 2
- Co-authors
- Hildegard Kehrer‐Sawatzki (9 shared papers)H. Hameister (11 shared papers)Jennifer A. Marshall Graves (4 shared papers)Walther Vogel (1 shared paper)Lan Kluwe (1 shared paper)Victor‐Felix Mautner (1 shared paper)I. Hansmann (1 shared paper)Katharina Wimmer (1 shared paper)
- Journals
- Chromosome Research (2 papers)Cytogenetic and Genome Research (2 papers)The American Journal of Human Genetics (1 paper)European Journal of Human Genetics (1 paper)PLoS Genetics (1 paper)
- Partner nations
- GermanyAustraliaUnited States
In The Last Decade
Matthias Kohn
14 papers receiving 365 citations
Peers
Comparison fields: 5 of 65
- Genetics 226
- Neurology 63
- Molecular Biology 224
- Plant Science 115
- Rheumatology 27
Countries citing papers authored by Matthias Kohn
This map shows the geographic impact of Matthias Kohn'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 Matthias Kohn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Matthias Kohn more than expected).
Fields of papers citing papers by Matthias Kohn
This network shows the impact of papers produced by Matthias Kohn. 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 Matthias Kohn. The network helps show where Matthias Kohn may publish in the future.
Co-authors
The 25 scholars most cited alongside Matthias Kohn, 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 | 2004 | 107 | |
| 2 | 2006 | 67 | |
| 3 | 2004 | 63 | |
| 4 | 2009 | 44 | |
| 5 | 2003 | 21 | |
| 6 | 2003 | 16 | |
| 7 | 2005 | 14 | |
| 8 | 2009 | 9 | |
| 9 | 2007 | 8 | |
| 10 | 2009 | 8 | |
| 11 | 2006 | 8 | |
| 12 | 2004 | 3 | |
| 13 | 2007 | 2 | |
| 14 | 2024 | 1 |
About Matthias Kohn
Matthias Kohn is a scholar working on Genetics, Molecular Biology, Plant Science, Dermatology and Neurology, having authored 14 papers that have together received 371 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (6 papers), Genetics and Neurodevelopmental Disorders (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Genomics and Phylogenetic Studies (2 papers), Ubiquitin and proteasome pathways (2 papers), Genome Rearrangement Algorithms (2 papers), interferon and immune responses (1 paper) and Soft tissue tumor case studies (1 paper). The work is most often cited by research in Genetics (226 citations), Neurology (63 citations), Molecular Biology (224 citations), Plant Science (115 citations) and Rheumatology (27 citations). Matthias Kohn has collaborated with scholars based in Germany, Australia and United States. Frequent co-authors include Hildegard Kehrer‐Sawatzki, H. Hameister, Jennifer A. Marshall Graves, Walther Vogel, Lan Kluwe, Victor‐Felix Mautner, I. Hansmann, Katharina Wimmer, Andreas Peyrl and Dieter E. Jenne. Their work appears in journals such as Chromosome Research, Cytogenetic and Genome Research, The American Journal of Human Genetics, European Journal of Human Genetics and PLoS Genetics.
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.