B Wittwer
Impact in
- Ophthalmology top 5%
- Retinal Diseases and Treatments
- Cell Biology top 10%
- Cellular transport and secretion
Papers in
-
- RNA regulation and disease 2
- Retinal Development and Disorders 2
- Ubiquitin and proteasome pathways 1
- Peroxisome Proliferator-Activated Receptors 1
- Genetics 3
- Genetics and Neurodevelopmental Disorders 2
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Co-authors
- Thomas Meitinger (2 shared papers)Maria Raquel Santos Carvalho (2 shared papers)Birgit Lorenz (2 shared papers)Helene Achatz (2 shared papers)A Meindl (1 shared paper)Eberhart Zrenner (1 shared paper)Michele D’Urso (1 shared paper)Carmela Migliaccio (1 shared paper)
- Journals
- The American Journal of Human Genetics (2 papers)Clinical Genetics (1 paper)Nature Genetics (1 paper)Human Molecular Genetics (1 paper)American Journal of Medical Genetics (1 paper)
- Partner nations
- GermanyItalyUnited Kingdom
In The Last Decade
B Wittwer
6 papers receiving 506 citations
Peers
Comparison fields: 5 of 47
- Ophthalmology 128
- Cell Biology 113
- Molecular Biology 468
- Genetics 156
- Cellular and Molecular Neuroscience 61
Countries citing papers authored by B Wittwer
This map shows the geographic impact of B Wittwer'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 B Wittwer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B Wittwer more than expected).
Fields of papers citing papers by B Wittwer
This network shows the impact of papers produced by B Wittwer. 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 B Wittwer. The network helps show where B Wittwer may publish in the future.
Co-authors
The 25 scholars most cited alongside B Wittwer, 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 | 1996 | 391 | |
| 2 | 1998 | 57 | |
| 3 | 1995 | 49 | |
| 4 | 2000 | 9 | |
| 5 | 1996 | 7 | |
| 6 | Gene of a new X-linked syndrome with multiple congenital anomalies and severe mental retardation maps in Xp22-pter | 1994 | 1 |
About B Wittwer
B Wittwer is a scholar working on Molecular Biology, Genetics, Oncology, Rheumatology and Cancer Research, having authored 6 papers that have together received 514 indexed citations. Recurring topics across this work include RNA regulation and disease (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Retinal Development and Disorders (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Ubiquitin and proteasome pathways (1 paper), Photochromic and Fluorescence Chemistry (1 paper), Peroxisome Proliferator-Activated Receptors (1 paper) and Moyamoya disease diagnosis and treatment (1 paper). The work is most often cited by research in Ophthalmology (128 citations), Cell Biology (113 citations), Molecular Biology (468 citations), Genetics (156 citations) and Cellular and Molecular Neuroscience (61 citations). B Wittwer has collaborated with scholars based in Germany, Italy and United Kingdom. Frequent co-authors include Thomas Meitinger, Maria Raquel Santos Carvalho, Birgit Lorenz, Helene Achatz, A Meindl, Eberhart Zrenner, Michele D’Urso, Carmela Migliaccio, Heide Hellebrand and Katherine L. Dry. Their work appears in journals such as The American Journal of Human Genetics, Clinical Genetics, Nature Genetics, Human Molecular Genetics and American Journal of Medical Genetics.
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.