Moritz Meins
Impact in
- Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
-
- RNA regulation and disease 7
- RNA Research and Splicing 6
- RNA and protein synthesis mechanisms 3
- Genomics and Chromatin Dynamics 3
- Connexins and lens biology 3
- Genetics 9
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- F. Hanefeld (5 shared papers)Franco Laccone (4 shared papers)Peter Huppke (2 shared papers)Ralf Ulrich Trappe (4 shared papers)Wolfgang Engel (2 shared papers)Joana Cobilanschi (1 shared paper)Jane C. Sowden (2 shared papers)Eckart Apfelstedt-Sylla (4 shared papers)
- Journals
- Human Mutation (6 papers)Cytogenetic and Genome Research (4 papers)Journal of Medical Genetics (2 papers)Neuropediatrics (2 papers)Electrophoresis (1 paper)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Moritz Meins
27 papers receiving 866 citations
Peers
Comparison fields: 5 of 66
- Sensory Systems 105
- Genetics 377
- Molecular Biology 537
- Cognitive Neuroscience 146
- Neurology 49
Countries citing papers authored by Moritz Meins
This map shows the geographic impact of Moritz Meins'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 Moritz Meins with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Moritz Meins more than expected).
Fields of papers citing papers by Moritz Meins
This network shows the impact of papers produced by Moritz Meins. 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 Moritz Meins. The network helps show where Moritz Meins may publish in the future.
Co-authors
The 25 scholars most cited alongside Moritz Meins, 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 27 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2001 | 189 | |
| 2 | 2001 | 66 | |
| 3 | 2009 | 62 | |
| 4 | 2006 | 55 | |
| 5 | 1999 | 51 | |
| 6 | 2000 | 42 | |
| 7 | 2003 | 39 | |
| 8 | 2002 | 37 | |
| 9 | 2000 | 33 | |
| 10 | Expression of Drosophila omb-related T-box genes in the developing human and mouse neural retina. | 2001 | 33 |
| 11 | 2003 | 32 | |
| 12 | 1993 | 30 | |
| 13 | 1994 | 29 | |
| 14 | 2009 | 27 | |
| 15 | 2002 | 25 | |
| 16 | 2007 | 22 | |
| 17 | 2003 | 19 | |
| 18 | 2002 | 16 | |
| 19 | 2006 | 16 | |
| 20 | 2004 | 15 |
About Moritz Meins
Moritz Meins is a scholar working on Molecular Biology, Genetics, Plant Science, Sensory Systems and Genetics, having authored 27 papers that have together received 897 indexed citations. Recurring topics across this work include RNA regulation and disease (7 papers), Genomic variations and chromosomal abnormalities (6 papers), RNA Research and Splicing (6 papers), Chromosomal and Genetic Variations (5 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers), RNA and protein synthesis mechanisms (3 papers), Genomics and Chromatin Dynamics (3 papers) and Connexins and lens biology (3 papers). The work is most often cited by research in Sensory Systems (105 citations), Genetics (377 citations), Molecular Biology (537 citations), Cognitive Neuroscience (146 citations) and Neurology (49 citations). Moritz Meins has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include F. Hanefeld, Franco Laccone, Peter Huppke, Ralf Ulrich Trappe, Wolfgang Engel, Joana Cobilanschi, Jane C. Sowden, Eckart Apfelstedt-Sylla, Andreas Gal and Jörg T. Epplen. Their work appears in journals such as Human Mutation, Cytogenetic and Genome Research, Journal of Medical Genetics, Neuropediatrics and Electrophoresis.
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.