Markus Zweier
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
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- Chromatin Remodeling and Cancer
- Congenital heart defects research
- Genomics and Chromatin Dynamics
Papers in
- Genetics 13
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 6
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- Chromatin Remodeling and Cancer 4
- Protein Tyrosine Phosphatases 2
- Co-authors
- Anita Rauch (17 shared papers)André Reis (7 shared papers)Christiane Zweier (7 shared papers)Arif B. Ekici (6 shared papers)Emilia K. Bijlsma (2 shared papers)Eiko K. de Jong (1 shared paper)Annette Schenck (1 shared paper)Lilian Bomme Ousager (1 shared paper)
- Journals
- European Journal of Human Genetics (2 papers)Human Mutation (2 papers)The American Journal of Human Genetics (2 papers)Swiss Medical Weekly (2 papers)npj Genomic Medicine (1 paper)
- Partner nations
- SwitzerlandGermanyUnited States
In The Last Decade
Markus Zweier
22 papers receiving 923 citations
Peers
Comparison fields: 5 of 78
- Genetics 547
- Molecular Biology 582
- Cognitive Neuroscience 138
- Clinical Biochemistry 40
- Developmental Neuroscience 24
Countries citing papers authored by Markus Zweier
This map shows the geographic impact of Markus Zweier'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 Markus Zweier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Markus Zweier more than expected).
Fields of papers citing papers by Markus Zweier
This network shows the impact of papers produced by Markus Zweier. 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 Markus Zweier. The network helps show where Markus Zweier may publish in the future.
Co-authors
The 25 scholars most cited alongside Markus Zweier, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 244 | |
| 2 | 2012 | 173 | |
| 3 | 2010 | 114 | |
| 4 | 2011 | 63 | |
| 5 | 2017 | 58 | |
| 6 | 2011 | 46 | |
| 7 | 2011 | 45 | |
| 8 | 2019 | 39 | |
| 9 | 2017 | 32 | |
| 10 | 2021 | 27 | |
| 11 | 2019 | 19 | |
| 12 | 2019 | 16 | |
| 13 | 2023 | 10 | |
| 14 | 2013 | 9 | |
| 15 | 2020 | 9 | |
| 16 | 2018 | 8 | |
| 17 | 2023 | 6 | |
| 18 | 2019 | 5 | |
| 19 | 2016 | 5 | |
| 20 | 2022 | 4 |
About Markus Zweier
Markus Zweier is a scholar working on Genetics, Molecular Biology, Rheumatology, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, having authored 23 papers that have together received 937 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Chromatin Remodeling and Cancer (4 papers), Protein Tyrosine Phosphatases (2 papers), Prenatal Screening and Diagnostics (2 papers), Pancreatic function and diabetes (1 paper) and Pediatric Urology and Nephrology Studies (1 paper). The work is most often cited by research in Genetics (547 citations), Molecular Biology (582 citations), Cognitive Neuroscience (138 citations), Clinical Biochemistry (40 citations) and Developmental Neuroscience (24 citations). Markus Zweier has collaborated with scholars based in Switzerland, Germany and United States. Frequent co-authors include Anita Rauch, André Reis, Christiane Zweier, Arif B. Ekici, Emilia K. Bijlsma, Eiko K. de Jong, Annette Schenck, Lilian Bomme Ousager, Amanda Collins and Merel A.W. Oortveld. Their work appears in journals such as European Journal of Human Genetics, Human Mutation, The American Journal of Human Genetics, Swiss Medical Weekly and npj Genomic Medicine.
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.