Odell Loubser

2.5k total citations
14 papers, 562 citations indexed

About

Odell Loubser is a scholar working on Surgery, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Odell Loubser has authored 14 papers receiving a total of 562 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Surgery, 7 papers in Molecular Biology and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Odell Loubser's work include Lipoproteins and Cardiovascular Health (10 papers), RNA and protein synthesis mechanisms (3 papers) and Cholesterol and Lipid Metabolism (2 papers). Odell Loubser is often cited by papers focused on Lipoproteins and Cardiovascular Health (10 papers), RNA and protein synthesis mechanisms (3 papers) and Cholesterol and Lipid Metabolism (2 papers). Odell Loubser collaborates with scholars based in South Africa, Canada and Costa Rica. Odell Loubser's co-authors include Michael R. Hayden, Roshni R. Singaraja, Lisa Ellerby, Claire‐Anne Gutekunst, Rona K. Graham, Blair R. Leavitt, Sophie Roy, Donald W. Nicholson, Simon C. Warby and Dale E. Bredesen and has published in prestigious journals such as Journal of Neuroscience, Journal of Medical Genetics and Human Mutation.

In The Last Decade

Odell Loubser

14 papers receiving 551 citations

Peers

Countries citing papers authored by Odell Loubser

Since Specialization

Citations

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

Fields of papers citing papers by Odell Loubser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Odell Loubser

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

All Works

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

#	Work	Indexed citations
1	ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels 2002 ·Clinical Genetics ·(unknown), Susanne M. Clee, (unknown), James C. Engert, Roshni R. Singaraja, Odell Loubser, E. James, Kirsten Roomp, Thomas J. Hudson, J. Wouter Jukema, JJP Kastelein, Michael R. Hayden	87
2	Caspase Cleavage of Mutant Huntingtin Precedes Neurodegeneration in Huntington's Disease 2002 ·Journal of Neuroscience ·Cheryl L. Wellington, Lisa Ellerby, Claire‐Anne Gutekunst, Danny H. Rogers, Simon C. Warby, Rona K. Graham, Odell Loubser, Jeremy M. Van Raamsdonk, Roshni R. Singaraja, Yuzhou Yang, Juliette Gafni, Dale E. Bredesen, Steven M. Hersch, Blair R. Leavitt, Sophie Roy, Donald W. Nicholson, Michael R. Hayden	303
3	The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease 2001 ·Clinical Genetics ·Susanne M. Clee, Odell Loubser, Jennifer A. Collins, JJP Kastelein, Michael R. Hayden	47
4	Mutation analysis in a small cohort of New Zealand patients originating from the United Kingdom demonstrates genetic heterogeneity in familial hypercholesterolemia 2000 ·Molecular and Cellular Probes ·Rochelle Thiart, Mathilde Varret, (unknown), Russell Scott, Odell Loubser, L. du Plessis, (unknown), Cathérine Boileau, Maritha J. Kotze	5
5	Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry 1999 ·Clinical Genetics ·Odell Loubser, A. David Marais, Maritha J. Kotze, (unknown), Rochelle Thiart, (unknown), J. Nico P. de Villiers, Renate Hillermann, Jean Firth, H. F. H. Weich, Frans Maritz, (unknown), Deneys R. van der Westhuyzen	25
6	Molecular analysis reveals a high mutation frequency in the first untranslated exon of the PPOX gene and largely excludes variegate porphyria in a subset of clinically affected Afrikaner families 1998 ·Molecular and Cellular Probes ·Maritha J. Kotze, J. Nico P. de Villiers, J.Z. Groenewald, (unknown), Odell Loubser, Rochelle Thiart, (unknown), (unknown), (unknown), A.E. Retief, Louise Warnich	10
7	Two novel and two known low-density lipoprotein receptor gene mutations in German patients with familial hypercholesterolemia 1998 ·Human Mutation ·Rochelle Thiart, Odell Loubser, J. Nico P. de Villiers, (unknown), (unknown), Frederick J. Raal, Maritha J. Kotze	4
8	Familial hypercholesterolemia: potential diagnostic value of mutation screening in a pediatric population of South Africa 1998 ·Clinical Genetics ·Maritha J. Kotze, Armand V. Peeters, Odell Loubser, (unknown), (unknown), Vanessa M. Hayes, Greetje de Jong, J. Nico P. de Villiers, Carl Lombard, Peter S. Hansen, Frederick J. Raal	9
9	A double mutant LDL receptor allele in a Cypriot family with heterozygous familial hypercholesterolemia 1997 ·Human Genetics ·Maritha J. Kotze, J. Nico P. de Villiers, Odell Loubser, Rochelle Thiart, (unknown), Frederick J. Raal	15
10	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
11	Novel stop mutation causing familial hypercholesterolemia in a Costa Rican family 1997 ·Molecular and Cellular Probes ·Rochelle Thiart, Odell Loubser, J. Nico P. de Villiers, Maria João Santos, Maritha J. Kotze	4
12	Mutation analysis reveals an insertional hotspot in exon 4 of the LDL receptor gene 1996 ·Human Genetics ·Maritha J. Kotze, Rochelle Thiart, Odell Loubser, J. Nico P. de Villiers, Maria João Santos, (unknown), Armand V. Peeters	8
13	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
14	Screening for mutations in exon 4 of the LDL receptor gene: identification of a new deletion mutation. 1995 ·Journal of Medical Genetics ·(unknown), Maritha J. Kotze, E. Langenhoven, Odell Loubser, Armand V. Peeters, C.J. Lintott, Russell Scott	11

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.

Explore authors with similar magnitude of impact