Amanda Krause
Impact in
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- Genetic Neurodegenerative Diseases
- Genetics top 5%
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- BRCA gene mutations in cancer
- Digestive system and related health
- Genomics and Rare Diseases
- Neurogenetic and Muscular Disorders Research
Papers in
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- DNA Repair Mechanisms 8
- Mitochondrial Function and Pathology 8
- Muscle Physiology and Disorders 5
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- Genetic Neurodegenerative Diseases 26
- Co-authors
- Jennifer G.R. Kromberg (13 shared papers)T Jenkins (6 shared papers)Tina‐Marié Wessels (6 shared papers)David G. Anderson (11 shared papers)Mark Poulter (2 shared papers)Dallas M. Swallow (2 shared papers)Edward J. Hollox (2 shared papers)C. Musingwini (1 shared paper)
- Journals
- European Journal of Human Genetics (4 papers)Frontiers in Genetics (4 papers)Haemophilia (3 papers)The American Journal of Human Genetics (3 papers)Human Genetics (2 papers)
- Partner nations
- South AfricaUnited StatesUnited Kingdom
In The Last Decade
Amanda Krause
108 papers receiving 1.7k citations
Peers
Comparison fields: 5 of 131
- Cellular and Molecular Neuroscience 452
- Genetics 505
- Neurology 177
- Genetics 111
- Molecular Biology 631
Countries citing papers authored by Amanda Krause
This map shows the geographic impact of Amanda Krause'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 Amanda Krause with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amanda Krause more than expected).
Fields of papers citing papers by Amanda Krause
This network shows the impact of papers produced by Amanda Krause. 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 Amanda Krause. The network helps show where Amanda Krause may publish in the future.
Co-authors
The 25 scholars most cited alongside Amanda Krause, 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 113 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 187 | |
| 2 | 2001 | 125 | |
| 3 | 2003 | 65 | |
| 4 | 2018 | 55 | |
| 5 | 2002 | 50 | |
| 6 | 2015 | 46 | |
| 7 | 2013 | 46 | |
| 8 | 2015 | 40 | |
| 9 | 2011 | 39 | |
| 10 | Modelling open pit shovel-truck systems using the Machine Repair Model | 2007 | 34 |
| 11 | 2009 | 32 | |
| 12 | 2017 | 32 | |
| 13 | 1992 | 31 | |
| 14 | Antigenicity and accessory cell function of human articular chondrocytes. | 1991 | 30 |
| 15 | 2022 | 29 | |
| 16 | 2012 | 28 | |
| 17 | Beta-globin haplotype analysis suggests that a major source of Malagasy ancestry is derived from Bantu-speaking Negroids. | 1996 | 28 |
| 18 | 2006 | 27 | |
| 19 | 2016 | 26 | |
| 20 | Huntington's disease: genetic heterogeneity in black African patients. | 2008 | 25 |
About Amanda Krause
Amanda Krause is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Genetics, Genetics and Neurology, having authored 113 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (26 papers), DNA Repair Mechanisms (8 papers), Mitochondrial Function and Pathology (8 papers), Neurological disorders and treatments (8 papers), BRCA gene mutations in cancer (7 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (6 papers) and Muscle Physiology and Disorders (5 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (452 citations), Genetics (505 citations), Neurology (177 citations), Genetics (111 citations) and Molecular Biology (631 citations). Amanda Krause has collaborated with scholars based in South Africa, United States and United Kingdom. Frequent co-authors include Jennifer G.R. Kromberg, T Jenkins, Tina‐Marié Wessels, David G. Anderson, Mark Poulter, Dallas M. Swallow, Edward J. Hollox, C. Musingwini, Russell L. Margolis and Michèle Ramsay. Their work appears in journals such as European Journal of Human Genetics, Frontiers in Genetics, Haemophilia, The American Journal of Human Genetics and 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.