Robert Weißmann
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 7
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 2
- Genomic variations and chromosomal abnormalities 2
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- Microtubule and mitosis dynamics 1
- Co-authors
- Andreas Walter Kuss (9 shared papers)Hossein Najmabadi (2 shared papers)Sahar Esmaeeli (2 shared papers)M. Mahdi Motazacker (2 shared papers)Kimia Kahrizi (2 shared papers)Hans‐Hilger Ropers (2 shared papers)Andreas Tzschach (2 shared papers)Stephan J. Sigrist (1 shared paper)
In The Last Decade
Robert Weißmann
12 papers receiving 1.3k citations
Robert Weißmann's Hit Papers
Peers
Comparison fields: 5 of 71
- Genetics 538
- Developmental Neuroscience 26
- Molecular Biology 447
- Cellular and Molecular Neuroscience 89
- Physiology 110
Countries citing papers authored by Robert Weißmann
This map shows the geographic impact of Robert Weißmann'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 Robert Weißmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Robert Weißmann more than expected).
Fields of papers citing papers by Robert Weißmann
This network shows the impact of papers produced by Robert Weißmann. 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 Robert Weißmann. The network helps show where Robert Weißmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Robert Weißmann, 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 | Deep sequencing reveals 50 novel genes for recessive cognitive disorders Hit paper breakdown → | 2011 | 809 |
| 2 | 2012 | 241 | |
| 3 | 2014 | 77 | |
| 4 | 2014 | 52 | |
| 5 | 2010 | 45 | |
| 6 | 2014 | 32 | |
| 7 | 2016 | 29 | |
| 8 | 2016 | 15 | |
| 9 | 2016 | 7 | |
| 10 | 2014 | 5 | |
| 11 | 2014 | 3 | |
| 12 | 2014 | 1 | |
| 13 | 2010 | 0 |
About Robert Weißmann
Robert Weißmann is a scholar working on Genetics, Cell Biology, Sensory Systems, Physiology and Public Health, Environmental and Occupational Health, having authored 13 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Alzheimer's disease research and treatments (2 papers), Genomics and Phylogenetic Studies (2 papers), Down syndrome and intellectual disability research (1 paper), Pluripotent Stem Cells Research (1 paper) and Microtubule and mitosis dynamics (1 paper). The work is most often cited by research in Genetics (538 citations), Developmental Neuroscience (26 citations), Molecular Biology (447 citations), Cellular and Molecular Neuroscience (89 citations) and Physiology (110 citations). Robert Weißmann has collaborated with scholars based in Germany, Iran and Austria. Frequent co-authors include Andreas Walter Kuss, Hossein Najmabadi, Sahar Esmaeeli, M. Mahdi Motazacker, Kimia Kahrizi, Hans‐Hilger Ropers, Andreas Tzschach, Stephan J. Sigrist, Sara Mertel and Lia Abbasi Moheb. Their work appears in journals such as Frontiers in Aging Neuroscience, Journal of Alzheimer s Disease, The American Journal of Human Genetics, European Journal Of Haematology and PLoS ONE.
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.