Michaela Müller
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
Papers in
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- Genomics and Phylogenetic Studies 1
- RNA Research and Splicing 1
- RNA and protein synthesis mechanisms 1
- Genetics 1
- Genomics and Rare Diseases 1
- Genomic variations and chromosomal abnormalities 1
- Co-authors
- Vicente A. Yépez (2 shared papers)Julien Gagneur (2 shared papers)Christian Mertes (1 shared paper)Mirjana Gušić (1 shared paper)Leonhard Wachutka (1 shared paper)Laure Frésard (1 shared paper)Ines F. Scheller (1 shared paper)Holger Prokisch (1 shared paper)
- Partner nations
- United StatesGermanyPoland
In The Last Decade
Michaela Müller
2 papers receiving 167 citations
Peers
Comparison fields: 5 of 38
- Genetics 103
- Clinical Biochemistry 10
- Molecular Biology 101
- Cancer Research 19
- Genetics 9
Countries citing papers authored by Michaela Müller
This map shows the geographic impact of Michaela Müller'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 Michaela Müller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michaela Müller more than expected).
Fields of papers citing papers by Michaela Müller
This network shows the impact of papers produced by Michaela Müller. 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 Michaela Müller. The network helps show where Michaela Müller may publish in the future.
Co-authors
The 23 scholars most cited alongside Michaela Müller, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
About Michaela Müller
Michaela Müller is a scholar working on Molecular Biology, Genetics, Cancer Research, Infectious Diseases and Organic Chemistry, having authored 2 papers that have together received 168 indexed citations. Recurring topics across this work include Genomics and Phylogenetic Studies (1 paper), Genomics and Rare Diseases (1 paper), Genomic variations and chromosomal abnormalities (1 paper), Cancer Genomics and Diagnostics (1 paper), RNA Research and Splicing (1 paper) and RNA and protein synthesis mechanisms (1 paper). The work is most often cited by research in Genetics (103 citations), Clinical Biochemistry (10 citations), Molecular Biology (101 citations), Cancer Research (19 citations) and Genetics (9 citations). Michaela Müller has collaborated with scholars based in United States, Germany and Poland. Frequent co-authors include Vicente A. Yépez, Julien Gagneur, Christian Mertes, Mirjana Gušić, Leonhard Wachutka, Laure Frésard, Ines F. Scheller, Holger Prokisch, Pengfei Liu and Hsiao‐Tuan Chao. Their work appears in journals such as Nature Protocols and Journal of Clinical Investigation.
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.