Incorporating familial risk, lifestyle factors, and pharmacogenomic insights into personalized noncommunicable disease (NCD) reports for healthcare funder beneficiaries participating in the Open Genome Project.

Autor: De Klerk M; Health Care Leadership, University of Stellenbosch Business School, Cape Town, South Africa., Van Der Merwe N; Division of Chemical Pathology, Department of Pathology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.; FamGen Counselling, Bloemfontein, South Africa., Erasmus J; Momentum Group, Cape Town, South Africa., Whati L; Gknowmix (Pty) Ltd., Cape Town, South Africa., Moremi KE; Division of Chemical Pathology, Department of Pathology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.; Division of Chemical Pathology, Department of Pathology, National Health Laboratory Service, Tygerberg Hospital, Cape Town, South Africa., Olivier DW; Division of Chemical Pathology, Department of Pathology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa., Kotze MJ; Division of Chemical Pathology, Department of Pathology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.

Publikováno v: Annals of human genetics [Ann Hum Genet] 2024 Oct 29. Date of Electronic Publication: 2024 Oct 29.

Genetic mapping of gray leaf spot (GLS) resistance genes in maize.

Autor: Lehmensiek, A., Esterhuizen, A.M., van Staden, D., Nelson, S. W., Retief, A. E.

Publikováno v: Theoretical & Applied Genetics; Oct2001, Vol. 103 Issue 5, p797-803, 7p

Identification of Three Mutations and Associated Haplotypes in the Protoporphyrinogen Oxidase Gene in South African Families with Variegate Porphyria.

Autor: Warnich, Louise, Kotze, Maritha J., Groenewald, Ilse M., Groenewald, Johannes Z., van Brakel, Maléne G., van Heerden, Carel J., de Villiers, J. Nico P., van de Ven, Wim J. M., Schoenmakers, Eric F.P.M., Taketani, Shigeru, Retief, Andries E.

Publikováno v: Human Molecular Genetics; Jul1996, Vol. 5 Issue 7, p981-984, 4p

An exon 4 mutation identified in the majority of South African familial hypercholesterolaemics.

Autor: Kotze, M J, Warnich, L, Langenhoven, E, du Plessis, L, Retief, A E

Publikováno v: Journal of Medical Genetics; May1990, Vol. 27 Issue 5, p298-302, 5p, 2 Diagrams

Haplotype associations of three DNA polymorphisms at the human low density lipoprotein receptor gene locus in familial hypercholesterolaemia.

Autor: Kotze, M J, Langenhoven, E, Retief, A E, Steyn, K, Marais, M P, Grobbelaar, J J, Oosthuizen, C J, Weich, H F, Benadé, A J

Publikováno v: Journal of Medical Genetics; Dec1987, Vol. 24 Issue 12, p750-755, 6p, 1 Chart