E. Langenhoven

748 citations

27 papers · 631 indexed · h-index 14

Surgery top 10%
Cancer Research top 10%
Molecular Biology
Endocrinology, Diabetes and Metabolism top 10%
Cardiology and Cardiovascular Medicine

Co-authors: Maritha J. Kotze A.E. Retief Louise Warnich L. du Plessis Armand V. Peeters A. David Marais Krisela Steyn Gerhard A. Coetzee
Topics: Lipoproteins and Cardiovascular Health (22 papers)RNA and protein synthesis mechanisms (6 papers)Cancer, Lipids, and Metabolism (5 papers)
Cited by: Surgery Cancer Research Endocrinology, Diabetes and Metabolism
Journals: Nucleic Acids Research Genome Research Arteriosclerosis Thrombosis and Vascular Biology
Partner nations: South Africa Belgium

In The Last Decade

E. Langenhoven

27 papers receiving 609 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Intrafamilial variability in the clinical expression of familial hypercholesterolemia: importance of risk factor determination for genetic counselling 2008 ·Clinical Genetics ·Maritha J. Kotze,(unknown),S. Bissbort,E. Langenhoven,(unknown),(unknown)	6
2	High prevalence of the Cys282Tyr HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa. 1999 ·PubMed ·J. Nico P. de Villiers,(unknown),Greetje de Jong,E. Langenhoven,(unknown),(unknown),Maritha J. Kotze	13
3	CpG hotspot mutations at the LDL receptor locus are a frequent cause of familial hypercholesterolemia among South African Indians 1997 ·Clinical Genetics ·Maritha J. Kotze,Odell Loubser,Rochelle Thiart,J. Nico P. de Villiers,E. Langenhoven,(unknown),Krisela Steyn,A. David Marais,Frederick J. Raal	27
4	Two novel point mutations causing receptor-negative familial hypercholesterolemia in a South African Indian homozygote 1996 ·Atherosclerosis ·E. Langenhoven,Louise Warnich,Rochelle Thiart,David C. Rubinsztein,Deneys R. van der Westhuyzen,A. David Marais,Maritha J. Kotze	19
5	Nonradioactive multiplex PCR screening strategy for the simultaneous detection of multiple low-density lipoprotein receptor gene mutations. 1995 ·Genome Research ·Maritha J. Kotze,(unknown),(unknown),Armand V. Peeters,Rochelle Thiart,E. Langenhoven	45
6	Two novel frameshift mutations in the low density lipoprotein receptor gene generated by endogenous sequence-directed mechanisms 1995 ·Human Genetics ·Armand V. Peeters,Luc F. Van Gaal,(unknown),E. Langenhoven,Maritha J. Kotze	6
7	A de novo duplication in the low density lipoprotein receptor gene 1995 ·Human Mutation ·Maritha J. Kotze,(unknown),Armand V. Peeters,E. Langenhoven	11
8	Recurrent LDL-receptor mutation causes familial hypercholesterolaemia in South African coloureds and Afrikaners. 1995 ·PubMed ·Maritha J. Kotze,E. Langenhoven,(unknown),Odell Loubser,(unknown),(unknown)	7
9	Familial defective apolipoprotein-B is rare in hypercholesterolaemic South African Afrikaners, coloureds and Indians. 1995 ·PubMed ·David C. Rubinsztein,Gerhard A. Coetzee,D R van der Westhuyzen,E. Langenhoven,Maritha J. Kotze	8
10	Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics 1994 ·Atherosclerosis ·Maritha J. Kotze,Armand V. Peeters,E. Langenhoven,J. Wauters,Luc F. Van Gaal	26
11	Detection of two point mutations causing familial defective apolipoprotein B-100 by heteroduplex analysis 1994 ·Molecular and Cellular Probes ·Maritha J. Kotze,E. Langenhoven,Armand V. Peeters,(unknown),(unknown)	13
12	DNA screening of hyperlipidemic Afrikaners for familial hypercholesterolemia 1992 ·Clinical Genetics ·Maritha J. Kotze,E. Langenhoven,(unknown),(unknown),A.E. Retief	14
13	Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor gene 1992 ·Human Genetics ·Louise Warnich,Maritha J. Kotze,E. Langenhoven,A.E. Retief	28
14	The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners 1991 ·Annals of Human Genetics ·Maritha J. Kotze,E. Langenhoven,Louise Warnich,L. du Plessis,A.E. Retief	76
15	An exon 4 mutation identified in the majority of South African familial hypercholesterolaemics. 1990 ·Journal of Medical Genetics ·Maritha J. Kotze,Louise Warnich,E. Langenhoven,L. du Plessis,A.E. Retief	12
16	The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemia. 1989 ·PubMed ·Maritha J. Kotze,E. Langenhoven,Louise Warnich,L. du Plessis,(unknown),(unknown),A.E. Retief	42
17	Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus. 1989 ·Journal of Medical Genetics ·Maritha J. Kotze,E. Langenhoven,A.E. Retief,H C Seftel,Howard Henderson,H. F. H. Weich	26
18	Improved visualization of the Bst EII RFLP of the human LDL receptor gene by co-digestion 1987 ·Nucleic Acids Research ·Maritha J. Kotze,E. Langenhoven,A.E. Retief	4
19	A RFLP associated with the low-density lipoprotein receptor gene (LDLR) 1987 ·Nucleic Acids Research ·Maritha J. Kotze,E. Langenhoven,E. Dietzsch,A.E. Retief	52
20	Haplotype associations of three DNA polymorphisms at the human low density lipoprotein receptor gene locus in familial hypercholesterolaemia. 1987 ·Journal of Medical Genetics ·Maritha J. Kotze,E. Langenhoven,A.E. Retief,Krisela Steyn,(unknown),(unknown),(unknown),H. F. H. Weich,A. J. S. Benadé	23

About E. Langenhoven

E. Langenhoven is a scholar working on Surgery, Cancer Research and Pathology and Forensic Medicine, having authored 27 papers that have together received 631 indexed citations. Recurring topics across this work include Lipoproteins and Cardiovascular Health (22 papers), RNA and protein synthesis mechanisms (6 papers) and Cancer, Lipids, and Metabolism (5 papers). The work is most often cited by research in Surgery (526 citations), Cancer Research (166 citations) and Endocrinology, Diabetes and Metabolism (152 citations). E. Langenhoven has collaborated with scholars based in South Africa and Belgium. Frequent 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. Their work appears in journals such as Nucleic Acids Research, Genome Research and Arteriosclerosis Thrombosis and Vascular Biology.

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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