Bernhard Zabel
Impact in
- Genetics top 0.1%
- Connective tissue disorders research
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genomic variations and chromosomal abnormalities
- Sensory Systems top 0.5%
Papers in
-
- Renal and related cancers 15
- Ubiquitin and proteasome pathways 10
- Genetics 93
- Connective tissue disorders research 46
- Genomic variations and chromosomal abnormalities 18
- Genetic Syndromes and Imprinting 12
- Co-authors
- Stefan Mundlos (16 shared papers)Andreas Winterpacht (40 shared papers)F Otto (2 shared papers)William G. Cole (4 shared papers)Jürgen W. Spranger (16 shared papers)Dirk Prawitt (15 shared papers)Gerd Scherer (3 shared papers)Niels Tommerup (2 shared papers)
- Journals
- Genomics (9 papers)The American Journal of Human Genetics (9 papers)Human Genetics (8 papers)European Journal of Human Genetics (7 papers)Nature Genetics (6 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Bernhard Zabel
165 papers receiving 10.8k citations
Bernhard Zabel's Hit Papers
Peers
Comparison fields: 5 of 143
- Genetics 4.4k
- Sensory Systems 460
- Molecular Biology 6.7k
- Rheumatology 1.3k
- Immunology and Allergy 539
Countries citing papers authored by Bernhard Zabel
This map shows the geographic impact of Bernhard Zabel'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 Bernhard Zabel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernhard Zabel more than expected).
Fields of papers citing papers by Bernhard Zabel
This network shows the impact of papers produced by Bernhard Zabel. 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 Bernhard Zabel. The network helps show where Bernhard Zabel may publish in the future.
Co-authors
The 25 scholars most cited alongside Bernhard Zabel, 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 167 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9 Hit paper breakdown → | 1994 | 1240 |
| 2 | Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia Hit paper breakdown → | 1997 | 1217 |
| 3 | Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome Hit paper breakdown → | 1996 | 722 |
| 4 | Nosology and classification of genetic skeletal disorders: 2010 revision Hit paper breakdown → | 2011 | 452 |
| 5 | 1999 | 379 | |
| 6 | 1998 | 344 | |
| 7 | 2003 | 285 | |
| 8 | 1993 | 268 | |
| 9 | 2000 | 244 | |
| 10 | 1983 | 237 | |
| 11 | 1992 | 202 | |
| 12 | 1996 | 196 | |
| 13 | 1994 | 178 | |
| 14 | 1994 | 155 | |
| 15 | 2001 | 141 | |
| 16 | 1999 | 126 | |
| 17 | 1993 | 122 | |
| 18 | 2011 | 120 | |
| 19 | 2002 | 117 | |
| 20 | 2005 | 108 |
About Bernhard Zabel
Bernhard Zabel is a scholar working on Molecular Biology, Genetics, Rheumatology, Immunology and Allergy and Oncology, having authored 167 papers that have together received 11.1k indexed citations. Recurring topics across this work include Connective tissue disorders research (46 papers), Cell Adhesion Molecules Research (22 papers), Genomic variations and chromosomal abnormalities (18 papers), Osteoarthritis Treatment and Mechanisms (17 papers), Renal and related cancers (15 papers), Genetic Syndromes and Imprinting (12 papers), Prenatal Screening and Diagnostics (11 papers) and Ubiquitin and proteasome pathways (10 papers). The work is most often cited by research in Genetics (4.4k citations), Sensory Systems (460 citations), Molecular Biology (6.7k citations), Rheumatology (1.3k citations) and Immunology and Allergy (539 citations). Bernhard Zabel has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Stefan Mundlos, Andreas Winterpacht, F Otto, William G. Cole, Jürgen W. Spranger, Dirk Prawitt, Gerd Scherer, Niels Tommerup, F. Dagna Bricarelli and Elisabeth Hustert. Their work appears in journals such as Genomics, The American Journal of Human Genetics, Human Genetics, European Journal of Human Genetics and Nature 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.