Amanda Krause

3.7k total citations
111 papers, 1.5k citations indexed

About

Amanda Krause is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Amanda Krause has authored 111 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 27 papers in Cellular and Molecular Neuroscience and 27 papers in Genetics. Recurrent topics in Amanda Krause's work include Genetic Neurodegenerative Diseases (27 papers), Mitochondrial Function and Pathology (16 papers) and Neurological disorders and treatments (14 papers). Amanda Krause is often cited by papers focused on Genetic Neurodegenerative Diseases (27 papers), Mitochondrial Function and Pathology (16 papers) and Neurological disorders and treatments (14 papers). Amanda Krause collaborates with scholars based in South Africa, United States and United Kingdom. Amanda Krause's co-authors include Jennifer G.R. Kromberg, T Jenkins, David G. Anderson, Tina‐Marié Wessels, Dallas M. Swallow, Mark Poulter, Edward J. Hollox, C. Musingwini, Michèle Ramsay and Russell L. Margolis and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

In The Last Decade

Amanda Krause

106 papers receiving 1.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Amanda Krause South Africa	23	668	443	410	242	117	111	1.5k
Asbjørg Stray‐Pedersen Norway	22	516 0.8×	229 0.5×	371 0.9×	73 0.3×	164 1.4×	55	1.9k
Masaaki Niino Japan	30	661 1.0×	172 0.4×	206 0.5×	623 2.6×	73 0.6×	140	3.3k
Sarah L. Davies United Kingdom	22	926 1.4×	187 0.4×	285 0.7×	87 0.4×	77 0.7×	63	2.5k
Christopher Brown United States	22	747 1.1×	132 0.3×	230 0.6×	208 0.9×	77 0.7×	40	1.8k
Michel Weber France	28	1.1k 1.6×	226 0.5×	520 1.3×	85 0.4×	21 0.2×	111	2.5k
Benjamin P. Fairfax United Kingdom	24	1.1k 1.6×	229 0.5×	637 1.6×	47 0.2×	53 0.5×	54	2.8k
Ahmad Abou Tayoun United Arab Emirates	23	892 1.3×	117 0.3×	838 2.0×	97 0.4×	87 0.7×	81	2.0k
Nicholas C. Wong Australia	30	2.0k 3.0×	162 0.4×	432 1.1×	71 0.3×	109 0.9×	72	3.0k
Amy Tang United States	27	1.1k 1.7×	202 0.5×	291 0.7×	34 0.1×	101 0.9×	90	2.2k
James Bateman United States	19	561 0.8×	98 0.2×	251 0.6×	86 0.4×	45 0.4×	75	1.3k

Countries citing papers authored by Amanda Krause

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Amanda Krause

This figure shows the co-authorship network connecting the top 25 collaborators of Amanda Krause. A scholar is included among the top collaborators of Amanda Krause based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Amanda Krause. Amanda Krause is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Guttman, Mark, et al.. (2024). Atypical Presentations of Huntington Disease‐like 2 in South African Individuals. Movement Disorders Clinical Practice. 11(7). 850–854.

Cissé, Lassana, et al.. (2024). The First Case of Huntington’s Disease like 2 in Mali, West Africa. Tremor and Other Hyperkinetic Movements. 14(1). 15–15. 1 indexed citations

Naicker, Thirona, et al.. (2024). STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European Journal of Human Genetics. 33(1). 14–23. 2 indexed citations

Macaulay, Shelley, et al.. (2023). Identifying the genetic causes of developmental disorders and intellectual disability in Africa: a systematic literature review. Frontiers in Genetics. 14. 1137922–1137922. 3 indexed citations

Tsabedze, Nqoba, et al.. (2023). The genetic basis for adult-onset idiopathic dilated cardiomyopathy in people of African descent. Heart Failure Reviews. 28(4). 879–892. 1 indexed citations

Coovadia, Ashraf, et al.. (2023). The implementation and utility of clinical exome sequencing in a South African infant cohort. Frontiers in Genetics. 14. 1277948–1277948. 1 indexed citations

Krause, Amanda, et al.. (2022). QF-PCR: a valuable first-line prenatal and postnatal test for common aneuploidies in South Africa. Journal of Community Genetics. 13(3). 355–363. 3 indexed citations

Krause, Amanda, et al.. (2020). Five years of screening for galactosaemia in South Africa: Pitfalls of using Benedict’s test and thin layer chromatography to screen for galactosaemia in a developing country. Clinica Chimica Acta. 505. 73–77.

Krause, Amanda, et al.. (2019). Review of 10 years of preimplantation genetic diagnosis in South Africa: implications for a low-to-middle-income country. Journal of Assisted Reproduction and Genetics. 36(9). 1909–1916. 6 indexed citations

10.

Anderson, David G., et al.. (2019). The neuropsychological deficits and dissociations in Huntington Disease-Like 2: A series of case-control studies. Neuropsychologia. 136. 107238–107238. 9 indexed citations

11.

Macaulay, Shelley, et al.. (2018). The first two confirmed sub-Saharan African families with germline TP53 mutations causing Li-Fraumeni syndrome. Familial Cancer. 17(4). 607–613. 4 indexed citations

12.

Macaulay, Shelley, et al.. (2016). Breast cancer in high-risk Afrikaner families: Is BRCA founder mutation testing sufficient?. South African Medical Journal. 106(3). 264–264. 9 indexed citations

13.

Kromberg, Jennifer G.R., et al.. (2015). An unusual case of Trisomy 13. South African Journal of Child Health. 9(2). 61–62.

14.

Wessels, Tina‐Marié & Amanda Krause. (2012). Genetic counselling in primary immunodeficiency disorders : review article. 25(4). 199–203. 2 indexed citations

15.

Wessels, Tina‐Marié, et al.. (2011). The Utilization and Outcome of Diagnostic, Predictive, and Prenatal Genetic Testing for Huntington Disease in Johannesburg, South Africa. Genetic Testing and Molecular Biomarkers. 16(1). 58–62. 19 indexed citations

16.

Krause, Amanda & C. Musingwini. (2007). Modelling open pit shovel-truck systems using the Machine Repair Model. Journal of the Southern African Institute of Mining and Metallurgy. 107(8). 469–476. 34 indexed citations

17.

Labrum, Robyn, et al.. (2007). The molecular basis of Spinal Muscular Atrophy (SMA) in South African black patients. Neuromuscular Disorders. 17(9-10). 684–692. 20 indexed citations

18.

Kromberg, Jennifer G.R., Amanda Krause, Amanda B. Spurdle, et al.. (1999). Utilisation of predictive, prenatal and diagnostic testing for Huntington's disease in Johannesburg.. PubMed. 89(7). 774–8. 6 indexed citations

19.

Manga, Prashiela, et al.. (1997). Feasibility of prenatal diagnosis and carrier detection in South African haemophilia A patients. British Journal of Haematology. 97(3). 558–560. 8 indexed citations

20.

Krause, Amanda. (1982). Pflanzliche und tierische Fette in ihrer Wirkung auf Mikroorganismen in biologischen Kläranlagen. Fette Seifen Anstrichmittel. 84(S1). 536–543. 2 indexed citations

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.

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