Bernd Auber
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- BRCA gene mutations in cancer
- Genetic and Kidney Cyst Diseases
- Neurogenetic and Muscular Disorders Research
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- Amyotrophic Lateral Sclerosis Research
Papers in
-
- Congenital heart defects research 5
- DNA Repair Mechanisms 4
- Epigenetics and DNA Methylation 3
- Genetics 23
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 6
- Genetics and Neurodevelopmental Disorders 5
- BRCA gene mutations in cancer 5
- Co-authors
- Peter Burfeind (6 shared papers)Knut Brockmann (5 shared papers)Moneef Shoukier (3 shared papers)Gunnar Schmidt (11 shared papers)Brigitte Schlegelberger (11 shared papers)Doris Steinemann (9 shared papers)Barbara Zoll (4 shared papers)Sandra von Hardenberg (13 shared papers)
- Journals
- Clinical Genetics (4 papers)European Journal of Human Genetics (2 papers)Frontiers in Pediatrics (2 papers)JACC CardioOncology (1 paper)Journal of the American Medical Informatics Association (1 paper)
- Partner nations
- GermanyUnited StatesFrance
In The Last Decade
Bernd Auber
44 papers receiving 494 citations
Peers
Comparison fields: 5 of 63
- Genetics 202
- Neurology 43
- Genetics 30
- Cancer Research 35
- Immunology and Allergy 13
Countries citing papers authored by Bernd Auber
This map shows the geographic impact of Bernd Auber'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 Bernd Auber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernd Auber more than expected).
Fields of papers citing papers by Bernd Auber
This network shows the impact of papers produced by Bernd Auber. 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 Bernd Auber. The network helps show where Bernd Auber may publish in the future.
Co-authors
The 25 scholars most cited alongside Bernd Auber, 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 49 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2012 | 55 | |
| 2 | 2017 | 48 | |
| 3 | 2018 | 41 | |
| 4 | 2019 | 31 | |
| 5 | 2008 | 30 | |
| 6 | 2011 | 20 | |
| 7 | 2011 | 20 | |
| 8 | 2020 | 19 | |
| 9 | 2004 | 19 | |
| 10 | 2019 | 18 | |
| 11 | 2022 | 17 | |
| 12 | 2007 | 17 | |
| 13 | 2017 | 17 | |
| 14 | 2024 | 12 | |
| 15 | 2018 | 11 | |
| 16 | 2009 | 9 | |
| 17 | 2019 | 9 | |
| 18 | 2009 | 9 | |
| 19 | 2023 | 8 | |
| 20 | 2020 | 8 |
About Bernd Auber
Bernd Auber is a scholar working on Molecular Biology, Genetics, Surgery, Immunology and Pulmonary and Respiratory Medicine, having authored 49 papers that have together received 513 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), Immunodeficiency and Autoimmune Disorders (6 papers), Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), BRCA gene mutations in cancer (5 papers), DNA Repair Mechanisms (4 papers) and Epigenetics and DNA Methylation (3 papers). The work is most often cited by research in Genetics (202 citations), Neurology (43 citations), Genetics (30 citations), Cancer Research (35 citations) and Immunology and Allergy (13 citations). Bernd Auber has collaborated with scholars based in Germany, United States and France. Frequent co-authors include Peter Burfeind, Knut Brockmann, Moneef Shoukier, Gunnar Schmidt, Brigitte Schlegelberger, Doris Steinemann, Barbara Zoll, Sandra von Hardenberg, Susanne Petri and Alma Osmanovic. Their work appears in journals such as Clinical Genetics, European Journal of Human Genetics, Frontiers in Pediatrics, JACC CardioOncology and Journal of the American Medical Informatics Association.
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.