Markus Zweier
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
-
- Chromatin Remodeling and Cancer
- Congenital heart defects research
- Genomics and Chromatin Dynamics
Papers in
-
- Chromatin Remodeling and Cancer 4
- Protein Tyrosine Phosphatases 2
- RNA modifications and cancer 2
- Genetics 11
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 4
- Co-authors
- Anita Rauch (18 shared papers)André Reis (7 shared papers)Christiane Zweier (7 shared papers)Arif B. Ekici (6 shared papers)Emilia K. Bijlsma (2 shared papers)Alfredo Orrico (1 shared paper)Amanda Collins (1 shared paper)Eiko K. de Jong (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)European Journal of Human Genetics (2 papers)Swiss Medical Weekly (2 papers)Human Mutation (2 papers)npj Genomic Medicine (1 paper)
- Partner nations
- SwitzerlandGermanyUnited States
In The Last Decade
Markus Zweier
23 papers receiving 989 citations
Peers
Comparison fields: 5 of 74
- Genetics 527
- Molecular Biology 572
- Cognitive Neuroscience 131
- Clinical Biochemistry 43
- Developmental Neuroscience 23
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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 266 | |
| 2 | 2012 | 179 | |
| 3 | 2010 | 123 | |
| 4 | 2011 | 66 | |
| 5 | 2017 | 63 | |
| 6 | 2011 | 49 | |
| 7 | 2011 | 46 | |
| 8 | 2019 | 40 | |
| 9 | 2017 | 33 | |
| 10 | 2021 | 32 | |
| 11 | 2019 | 21 | |
| 12 | 2019 | 18 | |
| 13 | 2021 | 11 | |
| 14 | 2023 | 11 | |
| 15 | 2013 | 10 | |
| 16 | 2020 | 9 | |
| 17 | 2018 | 8 | |
| 18 | 2023 | 6 | |
| 19 | 2019 | 5 | |
| 20 | 2016 | 5 |
About Markus Zweier
Markus Zweier is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Rheumatology and Pulmonary and Respiratory Medicine, having authored 24 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Chromatin Remodeling and Cancer (4 papers), Protein Tyrosine Phosphatases (2 papers), Prenatal Screening and Diagnostics (2 papers), RNA modifications and cancer (2 papers) and Folate and B Vitamins Research (1 paper). The work is most often cited by research in Genetics (527 citations), Molecular Biology (572 citations), Cognitive Neuroscience (131 citations), Clinical Biochemistry (43 citations) and Developmental Neuroscience (23 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, Alfredo Orrico, Amanda Collins, Eiko K. de Jong, Lilian Bomme Ousager and Merel A.W. Oortveld. Their work appears in journals such as The American Journal of Human Genetics, European Journal of Human Genetics, Swiss Medical Weekly, Human Mutation 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.