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Fluorometric Assay for Testing Rifampin Susceptibility of Mycobacterium tuberculosis Complex

Journal of Clinical Microbiology, 2008-04, Vol.46 (4), p.1369-1373

2008

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Dopamine transporter binding in social anxiety disorder: the effect of treatment with escitalopram

Metabolic brain disease, 2012-06, Vol.27 (2), p.151-158

2012

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Novel mutations identified within the 3' region of the PKD1 gene in South African polycystic kidney disease patients

South African journal of science, 2006-08, Vol.102 (7-8), p.317-321

2006

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Prevalence of plakophilin 2 gene (PKP2) mutations in South African patients with arrhythmogenic right ventricular cardiomyopathy : preliminary results of the ARVC Registry of South Africa : abstract

Cardiovascular Journal of Africa, 2008-11, Vol.11 (con-1), p.21-22

2008

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Cardiac Myosin Binding Protein C: Its Role in Physiology and Disease

Circulation research, 2004-05, Vol.94 (10), p.1279-1289

2004

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Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population

PloS one, 2013-08, Vol.8 (8), p.e71904-e71904

2013

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Hoarding in obsessive-compulsive disorder: clinical and genetic correlates

The journal of clinical psychiatry, 2005-09, Vol.66 (9), p.1155-1160

2005

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Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy

Cardiovascular research, 1999-10, Vol.44 (1), p.20-36

1999

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Mutations of the Light Meromyosin Domain of the β-Myosin Heavy Chain Rod in Hypertrophic Cardiomyopathy

Circulation research, 2002-02, Vol.90 (3), p.263-269

2002

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Support for a trimeric collar of myosin binding protein C in cardiac and fast skeletal muscle, but not in slow skeletal muscle

FEBS letters, 2008-02, Vol.582 (3), p.434-438

2008

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

Comprehensive psychiatry, 2005, Vol.46 (1), p.14-19

2005

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MT‐CYB mutations in hypertrophic cardiomyopathy

Molecular genetics & genomic medicine, 2013-05, Vol.1 (1), p.54-65

2013

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Gender in obsessive–compulsive disorder: clinical and genetic findings

European neuropsychopharmacology, 2004-03, Vol.14 (2), p.105-113

2004

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

Psychiatry research, 2004-09, Vol.128 (2), p.175-182

2004

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Dissociative experiences in obsessive-compulsive disorder and trichotillomania: Clinical and genetic findings

Comprehensive psychiatry, 2004-09, Vol.45 (5), p.384-391

2004

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

Journal of affective disorders, 2001-06, Vol.65 (1), p.61-65

2001

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

Circulation research, 2002-10, Vol.91 (8), p.704-711

2002

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

European neuropsychopharmacology, 2003-03, Vol.13 (2), p.93-98

2003

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MT‐CYB mutations in hypertrophic cardiomyopathy

Molecular genetics & genomic medicine, 2013-09, Vol.1 (3), p.187-187

2013

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Violence in Male Patients with Schizophrenia: Risk Markers in a South African Population

Australian and New Zealand journal of psychiatry, 2004-04, Vol.38 (4), p.254-259

2004

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Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations

Journal of medical genetics, 2001-12, Vol.38 (12), p.e43-43

2001

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Violence in male patients with schizophrenia: risk markers in a South African population

Australian and New Zealand journal of psychiatry, 2004-04, Vol.38 (4), p.254-259

2004

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The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study

Journal of negative results in biomedicine, 2011-10, Vol.10 (1), p.12-12, Article 12

2011

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

European neuropsychopharmacology, 2004-10, Vol.14 (5), p.437-445

2004

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Obsessive–compulsive disorder and the promoter region polymorphism (5-HTTLPR) in the serotonin transporter gene (SLC6A4): a negative association study in the Afrikaner population

The international journal of neuropsychopharmacology, 2000-12, Vol.3 (4), p.327-331, Article S1461145700002054

2000

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Fluorometric Assay for Testing Rifampin Susceptibility of Mycobacterium tuberculosis Complex

Dopamine transporter binding in social anxiety disorder: the effect of treatment with escitalopram

Novel mutations identified within the 3' region of the PKD1 gene in South African polycystic kidney disease patients

Prevalence of plakophilin 2 gene (PKP2) mutations in South African patients with arrhythmogenic right ventricular cardiomyopathy : preliminary results of the ARVC Registry of South Africa : abstract

Cardiac Myosin Binding Protein C: Its Role in Physiology and Disease

Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population

Hoarding in obsessive-compulsive disorder: clinical and genetic correlates

Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy

Mutations of the Light Meromyosin Domain of the β-Myosin Heavy Chain Rod in Hypertrophic Cardiomyopathy

Support for a trimeric collar of myosin binding protein C in cardiac and fast skeletal muscle, but not in slow skeletal muscle

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

MT‐CYB mutations in hypertrophic cardiomyopathy

Gender in obsessive–compulsive disorder: clinical and genetic findings

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

Dissociative experiences in obsessive-compulsive disorder and trichotillomania: Clinical and genetic findings

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

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

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

MT‐CYB mutations in hypertrophic cardiomyopathy

Violence in Male Patients with Schizophrenia: Risk Markers in a South African Population

Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations

Violence in male patients with schizophrenia: risk markers in a South African population

The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study

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

Obsessive–compulsive disorder and the promoter region polymorphism (5-HTTLPR) in the serotonin transporter gene (SLC6A4): a negative association study in the Afrikaner population

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