Charlotte L. Scholtz

Author

Stellenbosch University

Also Known As

C L Scholtz, C.L Scholtz, C.L. Scholtz, Charlotte L Scholtz, Charlotte L. Scholtz

Publications

150

Citations

H-Index

Concepts

All Affiliations

Stellenbosch University Tygerberg Hospital University of Cape Town

About

Charlotte L. Scholtz is an author at Stellenbosch University specializing in medicine, atherosclerosis, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	73
2	Public Health	1	1	17
3	Epidemiology	1	1	17
4	Global Health	1	1	17
5	Molecular Genetics	1	1	41

Charlotte L. Scholtz

Publications

138

Citations

H-Index

Page 1

	Year	Citations
Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction G. Gebhardt, Charlotte L. Scholtz, Renate Hillermann, European Journal of Obstetrics & Gynecology and Reproductive Biology Developmental BiologyPlacental DevelopmentGenetic DisorderGeneticsMethylenetetrahydrofolate Reductase	2001	41
Founder mutations in the LDL receptor gene contribute significantly to the familial hypercholesterolemia phenotype in the indigenous South African population of mixed ancestry Odell Loubser, A. David Marais, Maritha J. Kotze, Clinical Genetics	1999	33
Analysis of two mutations in the MTHFR gene associated with mild hyperhomocysteinaemia--heterogeneous distribution in the South African population. Charlotte L. Scholtz, Hein J. Odendaal, Rochelle Thiart, PubMed	2002	20
Simultaneous Detection of Multiple Familial Hypercholesterolemia Mutations Facilitates an Improved Diagnostic Service in South African Patients at High Risk of Cardiovascular Disease Maritha J. Kotze, Gernot Kriegshäuser, Rochelle Thiart, Molecular Diagnosis Genetic TestingCardiovascular DiseaseSouth African PatientsGlobal HealthGenetic Epidemiology	2003	17
A double mutant LDL receptor allele in a Cypriot family with heterozygous familial hypercholesterolemia Maritha J. Kotze, J. Nico P. de Villiers, Odell Loubser, Human Genetics Lipid DisorderAllelic VariantHeterozygous Familial HypercholesterolemiaGeneticsInherited Metabolic Disease	1997	15
A 3-basepair deletion in repeat 1 of the LDL receptor promoter reduces transcriptional activity in a South African Pedi Armand V. Peeters, Maritha J. Kotze, Charlotte L. Scholtz, Journal of Lipid Research	1998	12

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