Karl Hackmann
Impact in
Papers in
- Genetics 31
- Genomic variations and chromosomal abnormalities 19
- Genetics and Neurodevelopmental Disorders 8
- BRCA gene mutations in cancer 7
- Congenital Ear and Nasal Anomalies 4
- Genetic Syndromes and Imprinting 4
- Genetic and Kidney Cyst Diseases 3
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- Congenital heart defects research 6
- Co-authors
- Evelin Schröck (42 shared papers)Andreas Rump (18 shared papers)Gregory G. Germino (3 shared papers)Feng Qian (3 shared papers)Hangxue Xu (2 shared papers)Nataliya Di Donato (19 shared papers)Barbara Klink (13 shared papers)Andreas Schlösser (1 shared paper)
- Journals
- European Journal of Medical Genetics (10 papers)Breast Cancer Research and Treatment (3 papers)PLoS ONE (2 papers)Molecular Diagnosis & Therapy (2 papers)European Journal of Human Genetics (2 papers)
- Partner nations
- GermanyUnited StatesSwitzerland
In The Last Decade
Karl Hackmann
54 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 86
- Genetics 593
- Genetics 120
- Virology 48
- Molecular Biology 728
- Pathology and Forensic Medicine 111
Countries citing papers authored by Karl Hackmann
This map shows the geographic impact of Karl Hackmann'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 Karl Hackmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Karl Hackmann more than expected).
Fields of papers citing papers by Karl Hackmann
This network shows the impact of papers produced by Karl Hackmann. 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 Karl Hackmann. The network helps show where Karl Hackmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Karl Hackmann, 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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 139 | |
| 2 | 2016 | 96 | |
| 3 | 2012 | 92 | |
| 4 | 2007 | 87 | |
| 5 | 2016 | 79 | |
| 6 | 1999 | 69 | |
| 7 | 2013 | 59 | |
| 8 | 2016 | 57 | |
| 9 | 2013 | 47 | |
| 10 | 2010 | 43 | |
| 11 | 2018 | 41 | |
| 12 | 2012 | 37 | |
| 13 | 2015 | 35 | |
| 14 | 2012 | 35 | |
| 15 | 2018 | 30 | |
| 16 | 2016 | 26 | |
| 17 | 2019 | 24 | |
| 18 | 2015 | 20 | |
| 19 | 2012 | 19 | |
| 20 | 2012 | 19 |
About Karl Hackmann
Karl Hackmann is a scholar working on Genetics, Molecular Biology, Genetics, Surgery and Pathology and Forensic Medicine, having authored 55 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Genetics and Neurodevelopmental Disorders (8 papers), BRCA gene mutations in cancer (7 papers), Congenital heart defects research (6 papers), Congenital Ear and Nasal Anomalies (4 papers), Genetic Syndromes and Imprinting (4 papers), Biomedical Research and Pathophysiology (3 papers) and Genetic and Kidney Cyst Diseases (3 papers). The work is most often cited by research in Genetics (593 citations), Genetics (120 citations), Virology (48 citations), Molecular Biology (728 citations) and Pathology and Forensic Medicine (111 citations). Karl Hackmann has collaborated with scholars based in Germany, United States and Switzerland. Frequent co-authors include Evelin Schröck, Andreas Rump, Gregory G. Germino, Feng Qian, Hangxue Xu, Nataliya Di Donato, Barbara Klink, Andreas Schlösser, Hildgund Schrempf and Sigrid Tinschert. Their work appears in journals such as European Journal of Medical Genetics, Breast Cancer Research and Treatment, PLoS ONE, Molecular Diagnosis & Therapy and European Journal of Human 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.