V. Corfield

P. Brink, V. Corfield, P. Fernandez, 2004, Cardiovascular journal of South Africa : official journal for Southern Africa Cardiac Society [and] South African Society of Cardiac Practitioners.

Filamin C: a novel component of the KCNE2 interactome during hypoxia

V. Corfield, B. Loos, C. Kinnear, 2016, Cardiovascular journal of Africa.

Expression of HCM causing mutations: lessons learnt from genotype-phenotype studies of the South African founder MYH7A797T mutation

J. Moolman-Smook, P. Brink, V. Corfield, 2000, Journal of medical genetics.

A molecular approach to the characterization of an industrialBacillus amyloliquefaciens strain

V. Corfield, J. Thomson, D. Botes, 1987, Current Microbiology.

Genotype-Phenotype Correlation in the Long-QT Syndrome

G. Breithardt, S. Priori, A. Moss, 2001 .

Does pregnancy increase cardiac risk for LQT1 patients with the KCNQ1-A341V mutation?

P. Schwartz, P. Brink, V. Corfield, 2006, Journal of the American College of Cardiology.

Editorial See P 439 Clinical Perspective on P 461

Jørgen K. Kanters, E. Behr, M. Christiansen, 2022 .

Long-term follow-up of R403WMYH7 and R92WTNNT2 HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progression

J. Moolman-Smook, P. Brink, V. Corfield, 2007, Cardiovascular journal of Africa.

Abstract 1970: Genetic Causes Modifiers and Novel Candidates of Long QT Syndrome (LQTS)

M. Christiansen, V. Corfield, P. Hedley, 2009 .

Early- versus late-onset obsessive–compulsive disorder: investigating genetic and clinical correlates

D. Stein, J. Knowles, J. Moolman-Smook, 2004, Psychiatry Research.

MicroRNAs in cardiac arrhythmia: DNA sequence variation of MiR-1 and MiR-133A in long QT syndrome

Jørgen K. Kanters, E. Behr, M. Christiansen, 2014, Scandinavian journal of clinical and laboratory investigation.

Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorder

D. Stein, J. Knowles, J. Moolman-Smook, 2003, European Neuropsychopharmacology.

The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events.

J. Moolman-Smook, P. Brink, V. Corfield, 1999, American journal of human genetics.

Identification of Novel Interactions Between Domains of Myosin Binding Protein-C That Are Modulated by Hypertrophic Cardiomyopathy Missense Mutations

H. Watkins, J. Moolman-Smook, V. Corfield, 2002, Circulation research.

Corrigendum to “Gender in obsessive–compulsive disorder: clinical and genetic findings” [Eur. Neuropsychopharmacol. 14/2 (2004) 105–113]

D. Stein, J. Knowles, J. Moolman-Smook, 2004, European Neuropsychopharmacology.

Gender in obsessive–compulsive disorder: clinical and genetic findings

James A. Knowles, Dan J. Stein, Christine Lochner, 2004, European Neuropsychopharmacology.

Mutations of the Light Meromyosin Domain of the &bgr;-Myosin Heavy Chain Rod in Hypertrophic Cardiomyopathy

H. Watkins, J. Moolman-Smook, P. Brink, 2002, Circulation research.

Sudden death due to troponin T mutations.

H. Watkins, C. Seidman, P. Brink, 1997, Journal of the American College of Cardiology.

Nucleotide sequence of cytochrome oxidase (subunit III) from the mitochondrion of the tunicate Pyura stolonifera: evidence that AGR encodes glycine.

E. Harley, V. Corfield, G. Durrheim, 1993, Nucleic acids research.

Effects of cystine or glutamine restriction on human diploid fibroblasts in culture

V. Corfield, R. Hay, 1978, In Vitro.

A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3

J. Moolman-Smook, P. Brink, V. Corfield, 2005, Human Genetics.

Cluster analysis of obsessive-compulsive spectrum disorders in patients with obsessive-compulsive disorder: clinical and genetic correlates.

Christine Lochner, D. Stein, S. Seedat, 2005, Comprehensive psychiatry.

Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I.

E. Schulze-Bahr, O. Pongs, P. Brink, 2009, Journal of Clinical Investigation.

AKAP9 Is a Genetic Modifier of Congenital Long-QT Syndrome Type 1

P. Schwartz, J. Moolman-Smook, P. Brink, 2014, Circulation. Cardiovascular genetics.

AKAP 9 is a Genetic Modifier of Congenital Long-QT Syndrome Type 1 Running title

P. Schwartz, J. Moolman-Smook, P. Brink, 2014 .

The Role of CAV3 in Long–QT SyndromeClinical Perspective

Jørgen K. Kanters, E. Behr, M. Christiansen, 2013 .

The Role of CAV3 in Long–QT Syndrome: Clinical and Functional Assessment of a Caveolin-3/Kv11.1 Double Heterozygote Versus Caveolin-3 Single Heterozygote

Jørgen K. Kanters, E. Behr, M. Christiansen, 2013, Circulation. Cardiovascular genetics.

Investigating the role of the brain-derived neurotrophic factor (BDNF) val66met variant in obsessive-compulsive disorder (OCD)

D. Stein, J. Moolman-Smook, V. Corfield, 2008, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Mendelian-inherited heart disease: a gateway to understanding mechanisms in heart disease Update on work done at the University of Stellenbosch

P. Brink, V. Corfield, J. Moolman-Smook, 2009, Cardiovascular journal of Africa.

Phenotypic Variability and Unusual Clinical Severity of Congenital Long-QT Syndrome in a Founder Population

D. Roden, P. Schwartz, P. Brink, 2005, Circulation.

Molecular genetics of cardiomyopathy: changing times, shifting paradigms.

J. Moolman-Smook, P. Brink, V. Corfield, 2003, Cardiovascular journal of South Africa : official journal for Southern Africa Cardiac Society [and] South African Society of Cardiac Practitioners.

Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.

J. Moolman-Smook, P. Brink, V. Corfield, 2008, Cardiovascular research.

Association between a catechol-o-methyltransferase polymorphism and obsessive-compulsive disorder in the Afrikaner population.

D. Stein, R. Emsley, J. Knowles, 2001, Journal of affective disorders.

Identification of a new missense mutation at Arg403, a CpG mutation hotspot, in exon 13 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy.

P. Brink, V. Corfield, J. Moolman, 1993, Human molecular genetics.

Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations.

P. Brink, V. Corfield, J. Moolman, 1995, British heart journal.

Clinical andprognostic evaluation offamilial hypertrophic cardiomyopathy intwo South African families withdifferent cardiac I8myosin heavychain gene mutations

P. Brink, V. Corfield, J. Moolman, 1995 .

Gene for progressive familial heart block type I maps to chromosome 19q13.

P. Brink, V. Corfield, J. Moolman, 1995, Circulation.