Maritha Kotze
Maritha Kotze
Extraordinary Professor of Human Genetics, Stellenbosch University
Verified email at
Cited by
Cited by
The genetic structure and history of Africans and African Americans
SA Tishkoff, FA Reed, FR Friedlaender, C Ehret, A Ranciaro, A Froment, ...
science 324 (5930), 1035-1044, 2009
A third major locus for autosomal dominant hypercholesterolemia maps to 1p34. 1-p32
M Varret, JP Rabes, B Saint-Jore, A Cenarro, JC Marinoni, F Civeira, ...
The American journal of human genetics 64 (5), 1378-1387, 1999
Genetic origins of lactase persistence and the spread of pastoralism in Africa
A Ranciaro, MC Campbell, JB Hirbo, WY Ko, A Froment, P Anagnostou, ...
The American Journal of Human Genetics 94 (4), 496-510, 2014
APRI: a simple bedside marker for advanced fibrosis that can avoid liver biopsy in patients with NAFLD/NASH
FC Kruger, CR Daniels, M Kidd, G Swart, K Brundyn, C Van Rensburg, ...
South African Medical Journal 101 (7), 477-480, 2011
Phenotypic variation among familial hypercholesterolemics heterozygous for either one of two Afrikaner founder LDL receptor mutations.
MJ Kotze, WJ De Villiers, K Steyn, JA Kriek, AD Marais, E Langenhoven, ...
Arteriosclerosis and Thrombosis: A Journal of Vascular Biology 13 (10), 1460 …, 1993
The UMD‐LDLR database: additions to the software and 490 new entries to the database
L Villéger, M Abifadel, D Allard, JP Rabès, R Thiart, MJ Kotze, C Béroud, ...
Human mutation 20 (2), 81-87, 2002
LDLR Database: new additions to the database and the software, and results of the first molecular analysis
M Varret, JP Rabés, R Thiart, MJ Kotze, H Baron, A Cenarro, O Descamps, ...
Nucleic acids research 26 (1), 248-252, 1998
Inhibition of cholesterol synthesis by atorvastatin in homozygous familial hypercholesterolaemia
FJ Raal, AS Pappu, DR Illingworth, GJ Pilcher, AD Marais, JC Firth, ...
Atherosclerosis 150 (2), 421-428, 2000
The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners
MJ Kotze, E Langenhoven, L Warnich, L Plessis, AE Retief
Annals of human genetics 55 (2), 115-121, 1991
Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria
JNP de Villiers, R Hillermann, L Loubser, MJ Kotze
Human Molecular Genetics 8 (8), 1517-1522, 1999
Fat mass and obesity-associated (FTO) gene polymorphisms are associated with physical activity, food intake, eating behaviors, psychological health, and modeled change in body …
J Harbron, L Van der Merwe, MG Zaahl, MJ Kotze, M Senekal
Nutrients 6 (8), 3130-3152, 2014
Identification of three mutations and associated haplotypes in the protoporphyrinogen oxidase gene in South African families with variegate porphyria
L Warnich, MJ Kotze, IM Groenewald, JZ Groenewald, MG Van Brakel, ...
Human molecular genetics 5 (7), 981-984, 1996
Mapping of novel regions of DNA gain and loss by comparative genomic hybridization in esophageal carcinoma in the Black and Colored populations of South Africa
L Du Plessis, E Dietzsch, M Van Gele, N Van Roy, P Van Helden, ...
Cancer research 59 (8), 1877-1883, 1999
Estimation of the prevalence of familial hypercholesterolaemia in a rural Afrikaner community by direct screening for three Afrikaner founder low density lipoprotein receptor …
K Steyn, YP Goldberg, MJ Kotze, M Steyn, ASP Swanepoel, JM Fourie, ...
Human genetics 98 (4), 479-484, 1996
Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.
J Leggo, A Dalton, PJ Morrison, A Dodge, M Connarty, MJ Kotze, ...
Journal of medical genetics 34 (12), 982-985, 1997
Analysis of the NRAMP1 gene implicated in iron transport: association with multiple sclerosis and age effects
MJ Kotze, JNP de Villiers, RN Rooney, JJ Grobbelaar, EPG Mansvelt, ...
Blood Cells, Molecules, and Diseases 27 (1), 44-53, 2001
FH Afrikaner-3 LDL receptor mutation results in defective LDL receptors and causes a mild form of familial hypercholesterolemia
JFG van Roggen, DR Van der Westhuyzen, GA Coetzee, AD Marais, ...
Arteriosclerosis, thrombosis, and vascular biology 15 (6), 765-772, 1995
The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemia
MJ Kotze, E Langenhoven, L Warnich, L Du Plessis, MP Marx, ...
Health & Medical Publishing Group, 1989
Recent origin and spread of a common Lithuanian mutation, G197del LDLR, causing familial hypercholesterolemia: positive selection is not always necessary to account for disease …
R Durst, R Colombo, S Shpitzen, LB Avi, Y Friedlander, R Wexler, FJ Raal, ...
The American Journal of Human Genetics 68 (5), 1172-1188, 2001
A RFLP associated with the low-density lipoprotein receptor gene (LDLR).
MJ Kotze, E Langenhoven, E Dietzsch, AE Retief
Nucleic acids research 15 (1), 376, 1987
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