|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
AL Burlingame, TA Baillie, DH Russell
Analytical chemistry 64 (12), 467-502, 1992
|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
|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
|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
|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
|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
|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
|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
|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 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
|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