Knut Brockmann
Impact in
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 45
- Genetics and Neurodevelopmental Disorders 23
- Genomics and Rare Diseases 17
- Genomic variations and chromosomal abnormalities 11
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- Epilepsy research and treatment 15
- Co-authors
- Folker A. Hanefeld (34 shared papers)Samuel Refetoff (2 shared papers)Alexandra M. Dumitrescu (2 shared papers)Jutta Gärtner (31 shared papers)Xiao-Hui Liao (1 shared paper)Jens Frahm (17 shared papers)Petra J. W. Pouwels (8 shared papers)Andreas Ohlenbusch (13 shared papers)
- Journals
- Neuropediatrics (17 papers)Neurology (12 papers)Journal of Medical Genetics (7 papers)Orphanet Journal of Rare Diseases (7 papers)The American Journal of Human Genetics (6 papers)
- Partner nations
- GermanyUnited StatesAustria
In The Last Decade
Knut Brockmann
174 papers receiving 7.8k citations
Knut Brockmann's Hit Papers
Peers
Comparison fields: 5 of 134
- Clinical Biochemistry 717
- Genetics 1.8k
- Endocrinology, Diabetes and Metabolism 752
- Molecular Biology 3.3k
- Neurology 356
Countries citing papers authored by Knut Brockmann
This map shows the geographic impact of Knut Brockmann'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 Knut Brockmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Knut Brockmann more than expected).
Fields of papers citing papers by Knut Brockmann
This network shows the impact of papers produced by Knut Brockmann. 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 Knut Brockmann. The network helps show where Knut Brockmann may publish in the future.
Co-authors
The 25 scholars most cited alongside Knut Brockmann, 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 184 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | A Mosaic Activating Mutation in AKT1 Associated with the Proteus Syndrome Hit paper breakdown → | 2011 | 670 |
| 2 | Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response Hit paper breakdown → | 2009 | 606 |
| 3 | 2004 | 584 | |
| 4 | 2008 | 295 | |
| 5 | 1999 | 266 | |
| 6 | 2019 | 218 | |
| 7 | 2008 | 207 | |
| 8 | 2012 | 201 | |
| 9 | 2009 | 190 | |
| 10 | 2010 | 184 | |
| 11 | 2001 | 144 | |
| 12 | GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture Hit paper breakdown → | 2023 | 124 |
| 13 | 2017 | 122 | |
| 14 | 2010 | 115 | |
| 15 | 2013 | 115 | |
| 16 | 2016 | 108 | |
| 17 | 2014 | 101 | |
| 18 | 2014 | 97 | |
| 19 | 2005 | 87 | |
| 20 | 2014 | 86 |
About Knut Brockmann
Knut Brockmann is a scholar working on Genetics, Psychiatry and Mental health, Molecular Biology, Pediatrics, Perinatology and Child Health and Clinical Biochemistry, having authored 184 papers that have together received 8.1k indexed citations. Recurring topics across this work include RNA regulation and disease (25 papers), Genetics and Neurodevelopmental Disorders (23 papers), Genomics and Rare Diseases (17 papers), Epilepsy research and treatment (15 papers), Metabolism and Genetic Disorders (12 papers), Traumatic Brain Injury Research (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Hereditary Neurological Disorders (10 papers). The work is most often cited by research in Clinical Biochemistry (717 citations), Genetics (1.8k citations), Endocrinology, Diabetes and Metabolism (752 citations), Molecular Biology (3.3k citations) and Neurology (356 citations). Knut Brockmann has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Folker A. Hanefeld, Samuel Refetoff, Alexandra M. Dumitrescu, Jutta Gärtner, Xiao-Hui Liao, Jens Frahm, Petra J. W. Pouwels, Andreas Ohlenbusch, Peter Dechent and Bernd Wilken. Their work appears in journals such as Neuropediatrics, Neurology, Journal of Medical Genetics, Orphanet Journal of Rare Diseases and The American 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.