E. Langenhoven

748 total citations
27 papers, 631 citations indexed

About

E. Langenhoven is a scholar working on Surgery, Molecular Biology and Cancer Research. According to data from OpenAlex, E. Langenhoven has authored 27 papers receiving a total of 631 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Surgery, 7 papers in Molecular Biology and 6 papers in Cancer Research. Recurrent topics in E. Langenhoven's work include Lipoproteins and Cardiovascular Health (22 papers), RNA and protein synthesis mechanisms (6 papers) and Cancer, Lipids, and Metabolism (5 papers). E. Langenhoven is often cited by papers focused on Lipoproteins and Cardiovascular Health (22 papers), RNA and protein synthesis mechanisms (6 papers) and Cancer, Lipids, and Metabolism (5 papers). E. Langenhoven collaborates with scholars based in South Africa and Belgium. E. Langenhoven's co-authors include Maritha J. Kotze, A.E. Retief, Louise Warnich, L. du Plessis, Armand V. Peeters, A. David Marais, Krisela Steyn, Gerhard A. Coetzee, D R van der Westhuyzen and Rochelle Thiart and has published in prestigious journals such as Nucleic Acids Research, Genome Research and Arteriosclerosis Thrombosis and Vascular Biology.

In The Last Decade

E. Langenhoven

27 papers receiving 609 citations

Peers

E. Langenhoven
Raffaele Fresa Italy
Claudio Rabacchi Italy
Jorge Peter Netherlands
Margaret L. Snyder United States
Claudio Priore Oliva Italy
Michael A. Iacocca Canada
Monika Fink Germany
Riko Tsuji Japan
P Lohse Germany
A. Dhyani Italy
Raffaele Fresa Italy
E. Langenhoven
Citations per year, relative to E. Langenhoven E. Langenhoven (= 1×) peers Raffaele Fresa

Countries citing papers authored by E. Langenhoven

Since Specialization
Citations

This map shows the geographic impact of E. Langenhoven'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 E. Langenhoven with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites E. Langenhoven more than expected).

Fields of papers citing papers by E. Langenhoven

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by E. Langenhoven. 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 E. Langenhoven. The network helps show where E. Langenhoven may publish in the future.

Co-authorship network of co-authors of E. Langenhoven

This figure shows the co-authorship network connecting the top 25 collaborators of E. Langenhoven. A scholar is included among the top collaborators of E. Langenhoven 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 E. Langenhoven. E. Langenhoven is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Villiers, J. Nico P. de, et al.. (1999). High prevalence of the Cys282Tyr HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa.. PubMed. 89(3). 279–82. 13 indexed citations
3.
Kotze, Maritha J., Odell Loubser, Rochelle Thiart, et al.. (1997). CpG hotspot mutations at the LDL receptor locus are a frequent cause of familial hypercholesterolemia among South African Indians. Clinical Genetics. 51(6). 394–398. 27 indexed citations
4.
Langenhoven, E., Louise Warnich, Rochelle Thiart, et al.. (1996). Two novel point mutations causing receptor-negative familial hypercholesterolemia in a South African Indian homozygote. Atherosclerosis. 125(1). 111–119. 19 indexed citations
5.
6.
Peeters, Armand V., et al.. (1995). Two novel frameshift mutations in the low density lipoprotein receptor gene generated by endogenous sequence-directed mechanisms. Human Genetics. 96(4). 401–406. 6 indexed citations
7.
Kotze, Maritha J., et al.. (1995). A de novo duplication in the low density lipoprotein receptor gene. Human Mutation. 6(2). 181–183. 11 indexed citations
8.
Kotze, Maritha J., et al.. (1995). Recurrent LDL-receptor mutation causes familial hypercholesterolaemia in South African coloureds and Afrikaners.. PubMed. 85(5). 357–61. 7 indexed citations
9.
Rubinsztein, David C., Gerhard A. Coetzee, D R van der Westhuyzen, E. Langenhoven, & Maritha J. Kotze. (1995). Familial defective apolipoprotein-B is rare in hypercholesterolaemic South African Afrikaners, coloureds and Indians.. PubMed. 85(5). 355–7. 8 indexed citations
10.
Kotze, Maritha J., Armand V. Peeters, E. Langenhoven, J. Wauters, & Luc F. Van Gaal. (1994). Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics. Atherosclerosis. 111(2). 217–225. 26 indexed citations
11.
Kotze, Maritha J., et al.. (1994). Detection of two point mutations causing familial defective apolipoprotein B-100 by heteroduplex analysis. Molecular and Cellular Probes. 8(6). 513–518. 13 indexed citations
12.
Kotze, Maritha J., et al.. (1992). DNA screening of hyperlipidemic Afrikaners for familial hypercholesterolemia. Clinical Genetics. 42(1). 43–46. 14 indexed citations
13.
Warnich, Louise, Maritha J. Kotze, E. Langenhoven, & A.E. Retief. (1992). Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor gene. Human Genetics. 89(3). 362–362. 28 indexed citations
14.
Kotze, Maritha J., E. Langenhoven, Louise Warnich, L. du Plessis, & A.E. Retief. (1991). The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners. Annals of Human Genetics. 55(2). 115–121. 76 indexed citations
15.
Kotze, Maritha J., Louise Warnich, E. Langenhoven, L. du Plessis, & A.E. Retief. (1990). An exon 4 mutation identified in the majority of South African familial hypercholesterolaemics.. Journal of Medical Genetics. 27(5). 298–302. 12 indexed citations
16.
Kotze, Maritha J., et al.. (1989). The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemia.. PubMed. 76(8). 399–401. 42 indexed citations
17.
Kotze, Maritha J., E. Langenhoven, A.E. Retief, et al.. (1989). Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus.. Journal of Medical Genetics. 26(4). 255–259. 26 indexed citations
18.
Kotze, Maritha J., E. Langenhoven, & A.E. Retief. (1987). Improved visualization of the Bst EII RFLP of the human LDL receptor gene by co-digestion. Nucleic Acids Research. 15(23). 10067–10067. 4 indexed citations
19.
Kotze, Maritha J., E. Langenhoven, E. Dietzsch, & A.E. Retief. (1987). A RFLP associated with the low-density lipoprotein receptor gene (LDLR). Nucleic Acids Research. 15(1). 376–376. 52 indexed citations
20.
Kotze, Maritha J., E. Langenhoven, A.E. Retief, et al.. (1987). Haplotype associations of three DNA polymorphisms at the human low density lipoprotein receptor gene locus in familial hypercholesterolaemia.. Journal of Medical Genetics. 24(12). 750–755. 23 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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