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Valerie Corfield

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South Africa

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Marshall Heradien; Miriam Revera; Lize van der Merwe; Althea Goosen; Valerie A Corfield; Paul A Brink; Bongani M Mayosi; Johanna C Moolman-Smook
Abnormal blood pressure response to exercise occurs more frequently in hypertrophic cardiomyopathy patients with the R92W troponin T mutation than in those with myosin mutations.
Paul A Brink; Johanna C Moolman-Smook; Valerie A Corfield
Mendelian-inherited heart disease: a gateway to understanding mechanisms in heart disease Update on work done at the University of Stellenbosch.
Miriam Revera; Lize van der Merwe; Marshall Heradien; Althea Goosen; Valerie A Corfield; Paul A Brink; Johanna C Moolman-Smook
Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.

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All Publications

2009: Marshall Heradien; Miriam Revera; Lize van der Merwe; Althea Goosen; Valerie A Corfield; Paul A Brink; Bongani M Mayosi; Johanna C Moolman-Smook
Abnormal blood pressure response to exercise occurs more frequently in hypertrophic cardiomyopathy patients with the R92W troponin T mutation than in those with myosin mutations.
Heart rhythm : the official journal of the Heart Rhythm Society 2009;6(11 Suppl):S18-24.
2009: Paul A Brink; Johanna C Moolman-Smook; Valerie A Corfield
Mendelian-inherited heart disease: a gateway to understanding mechanisms in heart disease Update on work done at the University of Stellenbosch.
Cardiovascular journal of Africa 2009;20(1):57-63.
2008: Miriam Revera; Lize van der Merwe; Marshall Heradien; Althea Goosen; Valerie A Corfield; Paul A Brink; Johanna C Moolman-Smook
Troponin T and beta-myosin mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.
Cardiovascular research 2008;77(4):687-94.
2008: Sîan M J Hemmings; Craig J Kinnear; Lize van der Merwe; Christine Lochner; Valerie A Corfield; Johanna C Moolman-Smook; Dan Stein
Investigating the role of the brain-derived neurotrophic factor (BDNF) val66met variant in obsessive-compulsive disorder (OCD).
The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry 2008;9(2):126-34.
2007: Miriam Revera; Lize van der Merwe; Marshall Heradien; Althea Goosen; Valerie A Corfield; Paul A Brink; Johanna C Moolman-Smook
Long-term follow-up of R403WMYH7 and R92WTNNT2 HCM families: mutations determine left ventricular dimensions but not wall thickness during disease progression.
Cardiovascular journal of Africa 2007;18(3):146-53.
2007: J A Carr; P E van der Walt; J Nakayama; Y-H Fu; Valerie A Corfield; Paul Brink; Louis J Ptacek
FAME 3: a novel form of progressive myoclonus and epilepsy.
Neurology 2007;68(17):1382-9.
2006: Marshall Heradien; Althea Goosen; Lia Crotti; Glenda Durrheim; Valerie A Corfield; Paul A Brink; Peter J Schwartz
Does pregnancy increase cardiac risk for LQT1 patients with the KCNQ1-A341V mutation?
Journal of the American College of Cardiology 2006;48(7):1410-5.
2006: Sian M J Hemmings; Craig J Kinnear; Christine Lochner; Soraya Seedat; Valerie A Corfield; Johanna C Moolman-Smook; Dan Stein
Genetic correlates in trichotillomania--A case-control association study in the South African Caucasian population.
The Israel journal of psychiatry and related sciences 2006;43(2):93-101.
2005: Paul A Brink; Lia Crotti; Valerie A Corfield; Althea Goosen; Glenda Durrheim; Paula Hedley; Marshall Heradien; Gerhard Geldenhuys; Emilio Vanoli; Sara Bacchini; Carla Spazzolini; Andrew L Lundquist; Dan Mark Roden; Alfred L George; Peter J Schwartz
Phenotypic variability and unusual clinical severity of congenital long-QT syndrome in a founder population.
Circulation 2005;112(17):2602-10.
2005: Pedro Fernandez; Johanna C Moolman-Smook; Paul Brink; Valerie A Corfield
A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3.
Human genetics 2005;118(1):133-7.
2005: Christine Lochner; Sian M J Hemmings; Craig J Kinnear; Dana J H Niehaus; Daniel G Nel; Valerie A Corfield; Johanna C Moolman-Smook; Soraya Seedat; Dan Stein
Cluster analysis of obsessive-compulsive spectrum disorders in patients with obsessive-compulsive disorder: clinical and genetic correlates.
Comprehensive psychiatry 2005;46(1):14-9.
2004: Christine Lochner; Sian M J Hemmings; Craig J Kinnear; Johanna C Moolman-Smook; Valerie A Corfield; James A Knowles; Dana J H Niehaus; Dan Stein
Corrigendum to "gender in obsessive-compulsive disorder: clinical and genetic findings" [Eur. Neuropsychopharmacol. 14 (2004) 105-113].
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2004;14(5):437-45.
2004: Sian M J Hemmings; Craig J Kinnear; Christine Lochner; Dana J H Niehaus; James A Knowles; Johanna C Moolman-Smook; Valerie A Corfield; Dan Stein
Early- versus late-onset obsessive-compulsive disorder: investigating genetic and clinical correlates.
Psychiatry research 2004;128(2):175-82.
2004: Christine Lochner; Soraya Seedat; Sian M J Hemmings; Craig J Kinnear; Valerie A Corfield; Dana J H Niehaus; Johanna C Moolman-Smook; Dan Stein
Dissociative experiences in obsessive-compulsive disorder and trichotillomania: clinical and genetic findings.
Comprehensive psychiatry 2004;45(5):384-91.
2004: P Fernandez; Valerie A Corfield; Paul A Brink
Progressive familial heart block type II (PFHBII): a clinical profile from 1977 to 2003.
Cardiovascular journal of South Africa : official journal for Southern Africa Cardiac Society [and] South African Society of Cardiac Practitioners 2004;15(3):129-32.
2004: Liezl Koen; Craig J Kinnear; Valerie A Corfield; Robin Emsley; Esme Renette Jordaan; Natasha Keyter; Johanna C Moolman-Smook; Dan Stein; Dana J H Niehaus
Violence in male patients with schizophrenia: risk markers in a South African population.
The Australian and New Zealand journal of psychiatry 2004;38(4):254-9.
2004: Christine Lochner; Sian M J Hemmings; Craig J Kinnear; Johanna C Moolman-Smook; Valerie A Corfield; James A Knowles; Dana J H Niehaus; Dan Stein
Gender in obsessive-compulsive disorder: clinical and genetic findings.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2004;14(2):105-13.
2003: Johanna C Moolman-Smook; Bongani M Mayosi; Paul A Brink; Valerie A Corfield
Molecular genetics of cardiomyopathy: changing times, shifting paradigms.
Cardiovascular journal of South Africa : official journal for Southern Africa Cardiac Society [and] South African Society of Cardiac Practitioners 2003;14(3):145-55.
2003: Sian M J Hemmings; Craig J Kinnear; Dana J H Niehaus; Johanna C Moolman-Smook; Christine Lochner; James A Knowles; Valerie A Corfield; Dan Stein
Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorder.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2003;13(2):93-8.
2002: Johanna C Moolman-Smook; Emily Flashman; Willem de Lange; Zhili Li; Valerie A Corfield; Charles Redwood; Hugh Watkins
Identification of novel interactions between domains of Myosin binding protein-C that are modulated by hypertrophic cardiomyopathy missense mutations.
Circulation research 2002;91(8):704-11.
2002: Valerie A Corfield; Paul A Brink
Case:control association studies of complex disease: is the search for genetic determinants a fishing expedition?
Cardiovascular journal of South Africa : official journal for Southern Africa Cardiac Society [and] South African Society of Cardiac Practitioners 2002;13(3):93-5.
2002: Edward Blair; Charles Redwood; Marisa de Jesus Oliveira; Johanna C Moolman-Smook; Paul Brink; Valerie A Corfield; Ingegerd Ostman-Smith; Hugh Watkins
Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy.
Circulation research 2002;90(3):263-9.
2002: Soraya Bardien-Kruger; Heike Wulff; Zainu Arieff; Paul Brink; K George Chandy; Valerie A Corfield
Characterisation of the human voltage-gated potassium channel gene, KCNA7, a candidate gene for inherited cardiac disorders, and its exclusion as cause of progressive familial heart block I (PFHBI).
European journal of human genetics : EJHG 2002;10(1):36-43.
2001: Paal Skytt Andersen; Ole Havndrup; Henning Bundgaard; Johanna C Moolman-Smook; Lars Larsen; Jens Mogensen; Paul A Brink; Anders D Børglum; Valerie A Corfield; Keld Kjeldsen; Jens Vuust; Michael Christiansen
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.
Journal of medical genetics 2001;38(12):E43.
2001: Craig J Kinnear; Dana J H Niehaus; Soraya Seedat; Johanna C Moolman-Smook; Valerie A Corfield; G Malherbe; A Potgieter; C Lombard; Dan Stein
Obsessive-compulsive disorder and a novel polymorphism adjacent to the oestrogen response element (ERE 6) upstream from the COMT gene.
Psychiatric genetics 2001;11(2):85-7.
2001: Dana J H Niehaus; Craig J Kinnear; Valerie A Corfield; Pieter L du Toit; Jeanine van Kradenburg; Johanna C Moolman-Smook; Jakobus weyers; A Potgieter; Soraya Seedat; Robin Emsley; James A Knowles; Paul A Brink; Dan Stein
Association between a catechol-o-methyltransferase polymorphism and obsessive-compulsive disorder in the Afrikaner population.
Journal of affective disorders 2001;65(1):61-5.
2001: Peter J Schwartz; silvia priori; Carla Spazzolini; Arthur J Moss; G Michael Vincent; Carlo Napolitano; Isabelle Denjoy; P Guicheney; Günter Breithardt; Mark T Keating; J A Towbin; Alan H Beggs; Paul Brink; Arthur A M Wilde; Lauri Toivonen; W Zareba; J L Robinson; Katherine W Timothy; Valerie A Corfield; Duangrurdee Wattanasirichaigoon; C Corbett; W Haverkamp; Eric Schulze-Bahr; Michael H Lehmann; K Schwartz; P Coumel; Raffaella Bloise
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.
Circulation 2001;103(1):89-95.
2000: Johanna C Moolman-Smook; Willem de Lange; Valerie A Corfield; Paul Brink
Expression of HCM causing mutations: lessons learnt from genotype-phenotype studies of the South African founder MYH7 A797T mutation.
Journal of medical genetics 2000;37(12):951-6.
1999: Johanna C Moolman-Smook; Willem de Lange; E C Bruwer; Paul A Brink; Valerie A Corfield
The origins of hypertrophic cardiomyopathy-causing mutations in two South African subpopulations: a unique profile of both independent and founder events.
American journal of human genetics 1999;65(5):1308-20.
1998: Johanna C Moolman-Smook; Bongani M Mayosi; P Brink; Valerie A Corfield
Identification of a new missense mutation in MyBP-C associated with hypertrophic cardiomyopathy.
Journal of medical genetics 1998;35(3):253-4.
1997: J C Moolman; Valerie A Corfield; B Posen; K Ngumbela; C Seidman; Paul A Brink; Hugh Watkins
Sudden death due to troponin T mutations.
Journal of the American College of Cardiology 1997;29(3):549-55.
1996: T de Jager; C H Corbett; J C Badenhorst; Paul A Brink; Valerie A Corfield
Evidence of a long QT founder gene with varying phenotypic expression in South African families.
Journal of medical genetics 1996;33(7):567-73.
1995: B M Posen; J C Moolman; Valerie A Corfield; Paul A Brink
Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac beta myosin heavy chain gene mutations.
British heart journal 1995;74(1):40-6.
1995: Paul A Brink; A Ferreira; J C Moolman; H W Weymar; PL van der Merwe; Valerie A Corfield
Gene for progressive familial heart block type I maps to chromosome 19q13.
Circulation 1995;91(6):1633-40.
1995: J C Moolman; Paul A Brink; Valerie A Corfield
Identification of a novel Ala797Thr mutation in exon 21 of the beta-myosin heavy chain gene in hypertrophic cardiomyopathy.
Human mutation 1995;6(2):197-8.
1993: J C Moolman; Paul A Brink; Valerie A Corfield
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.
Human molecular genetics 1993;2(10):1731-2.
1993: G A Durrheim; Valerie A Corfield; Eric Harley; M H Ricketts
Nucleotide sequence of cytochrome oxidase (subunit III) from the mitochondrion of the tunicate Pyura stolonifera: evidence that AGR encodes glycine.
Nucleic acids research 1993;21(15):3587-8.
1993: Valerie A Corfield; J C Moolman; R Martell; Paul A Brink
Polymerase chain reaction-based detection of MN blood group-specific sequences in the human genome.
Transfusion 1993;33(2):119-24.
1991: J C Moolman; Valerie A Corfield; G Stevens
PCR-based detection of a polymorphic HaeIII site in intron VII of the human albumin (ALB) gene.
Nucleic acids research 1991;19(24):6972.