J. Nico P. de Villiers

Author

Also Known As

J N de Villiers, J Nico P De Villiers, J Nico P de Villiers, J. N. P. de Villiers, J. Nico P. De Villiers, J. Nico P. de Villiers, J.N. P. DE VILLIERS, J.N.P De Villiers, J.N.P de Villiers, J.N.P. de Villiers

Publications

489

Citations

H-Index

Concepts

All Affiliations

Stellenbosch University Tygerberg Hospital University of the Witwatersrand University of Cape Town National Health Laboratory Service

About

J. Nico P. de Villiers is an author at Stellenbosch University specializing in medicine, genetics, and atherosclerosis.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	239
2	Public Health	3	3	67
3	Natural Sciences	2	2	24
4	Health Sciences	1	1	26
5	Biology	1	1	13

J. Nico P. de Villiers

Publications

430

Citations

H-Index

Page 1

	Year	Citations
Spectrum of Mutations in the HFE Gene Implicated in Haemochromatosis and Porphyria J. Nico P. de Villiers, Renate Hillermann, L. Loubser, Human Molecular Genetics	1999	84
Analysis of the NRAMP1 Gene Implicated in Iron Transport: Association with Multiple Sclerosis and Age Effects Maritha J. Kotze, J. Nico P. de Villiers, Roberta N. Rooney, Blood Cells Molecules and Diseases Neurodegenerative DiseasesDisease MechanismNeurological DisorderIron MetabolismPhysiology	2001	73
A Reverse-Hybridization Assay for the Rapid and Simultaneous Detection of Nine <i>HFE</i> Gene Mutations Christian Oberkanins, Anne Moritz, J. Nico P. de Villiers, Genetic Testing	2000	55
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
CpG hotspot mutations at the LDL receptor locus are a frequent cause of familial hypercholesterolemia among South African Indians Maritha J. Kotze, Odell Loubser, Rochelle Thiart, Clinical Genetics South African IndiansGeneticsGenetic EpidemiologyHuman PolymorphismHyperlipidemia	1997	28
Analysis of viral and genetic factors in South African patients with multiple sclerosis J. Nico P. de Villiers, Florette K. Treurnicht, Louise Warnich, Metabolic Brain Disease Disease SusceptibilityAutoimmune DiseaseSouth African PatientsMedicineNeurological Disorder	2006	26
Earlier Age of Onset of Alzheimer's Disease in Patients with Both the Transferrin C2 and Apolipoprotein E‐ɛ4 Alleles Susan J. van Rensburg, Felix Potocnik, J. Nico P. de Villiers, Annals of the New York Academy of Sciences GeneticsNeurochemical BiomarkersAlzheimer's DiseaseNeurologyAging-associated Disease	2000	26
Lack of clinical manifestation of hereditary haemochromatosis in South African patients with multiple sclerosis Maritha J. Kotze, J. Nico P. de Villiers, Louise Warnich, Metabolic Brain Disease Bone Marrow FailureAutoimmune DiseaseSouth African PatientsNeurological DisorderInherited Metabolic Disease	2006	21
High prevalence of the Cys282Tyr HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa. J. Nico P. de Villiers, R. Hillerman, Greetje de Jong, PubMed	1999	19
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

Page 1