| The genetic basis of long QT and short QT syndromes: a mutation update PL Hedley, P Jørgensen, S Schlamowitz, R Wangari, J Moolman‐Smook, ... Human mutation 30 (11), 1486-1511, 2009 | 542 | 2009 |
| Cardiac myosin binding protein C: its role in physiology and disease E Flashman, C Redwood, J Moolman-Smook, H Watkins Circulation research 94 (10), 1279-1289, 2004 | 402 | 2004 |
| Corrigendum to “Gender in obsessive–compulsive disorder: clinical and genetic findings”[Eur. Neuropsychopharmacol. 14/2 (2004) 105–113] C Lochner, SMJ Hemmings, CJ Kinnear, JC Moolman-Smook, ... European Neuropsychopharmacology 14 (5), 437-445, 2004 | 241 | 2004 |
| Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy CS Redwood, JC Moolman-Smook, H Watkins Cardiovascular research 44 (1), 20-36, 1999 | 240 | 1999 |
| The genetic basis of Brugada syndrome: a mutation update PL Hedley, P Jørgensen, S Schlamowitz, J Moolman‐Smook, JK Kanters, ... Human mutation 30 (9), 1256-1266, 2009 | 210 | 2009 |
| Hoarding in obsessive-compulsive disorder: clinical and genetic correlates C Lochner, CJ Kinnear, SMJ Hemmings, C Seller, DJH Niehaus, ... Journal of Clinical Psychiatry 66 (9), 1155-1160, 2005 | 187 | 2005 |
| Cluster analysis of obsessive-compulsive spectrum disorders in patients with obsessive-compulsive disorder: clinical and genetic correlates C Lochner, SMJ Hemmings, CJ Kinnear, DJH Niehaus, DG Nel, ... Comprehensive psychiatry 46 (1), 14-19, 2005 | 178 | 2005 |
| Early-versus late-onset obsessive–compulsive disorder: investigating genetic and clinical correlates SMJ Hemmings, CJ Kinnear, C Lochner, DJH Niehaus, JA Knowles, ... Psychiatry Research 128 (2), 175-182, 2004 | 171 | 2004 |
| Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives PS Andersen, O Havndrup, L Hougs, KM Sørensen, M Jensen, LA Larsen, ... Human mutation 30 (3), 363-370, 2009 | 155 | 2009 |
| Dissociative experiences in obsessive-compulsive disorder and trichotillomania: clinical and genetic findings C Lochner, S Seedat, SMJ Hemmings, CJ Kinnear, VA Corfield, ... Comprehensive psychiatry 45 (5), 384-391, 2004 | 150 | 2004 |
| Identification of novel interactions between domains of myosin binding protein-C that are modulated by hypertrophic cardiomyopathy missense mutations J Moolman-Smook, E Flashman, W de Lange, Z Li, V Corfield, ... Circulation research 91 (8), 704-711, 2002 | 145 | 2002 |
| The origins of hypertrophic cardiomyopathy–causing mutations in two South African subpopulations: a unique profile of both independent and founder events JC Moolman-Smook, WJ De Lange, ECD Bruwer, PA Brink, VA Corfield The American Journal of Human Genetics 65 (5), 1308-1320, 1999 | 145 | 1999 |
| Investigating the role of dopaminergic and serotonergic candidate genes in obsessive-compulsive disorder SMJ Hemmings, CJ Kinnear, DJH Niehaus, JC Moolman-Smook, ... European Neuropsychopharmacology 13 (2), 93-98, 2003 | 144 | 2003 |
| Mutations of the light meromyosin domain of the β-myosin heavy chain rod in hypertrophic cardiomyopathy E Blair, C Redwood, M de Jesus Oliveira, JC Moolman-Smook, P Brink, ... Circulation research 90 (3), 263-269, 2002 | 131 | 2002 |
| The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy DV Møller, PS Andersen, P Hedley, MK Ersbøll, H Bundgaard, ... European Journal of Human Genetics 17 (10), 1241-1249, 2009 | 104 | 2009 |
| Investigating the role of the brain-derived neurotrophic factor (BDNF) val66met variant in obsessive-compulsive disorder (OCD) SMJ Hemmings, CJ Kinnear, L Van Der Merwe, C Lochner, VA Corfield, ... The World Journal of Biological Psychiatry 9 (2), 126-134, 2008 | 102 | 2008 |
| Investigating SAPAP3 variants in the etiology of obsessive-compulsive disorder and trichotillomania in the South African white population L Boardman, L van der Merwe, C Lochner, CJ Kinnear, S Seedat, ... Comprehensive psychiatry 52 (2), 181-187, 2011 | 97 | 2011 |
| Genetics and personality traits in patients with social anxiety disorder: a case-control study in South Africa C Lochner, S Hemmings, S Seedat, C Kinnear, R Schoeman, ... European Neuropsychopharmacology 17 (5), 321-327, 2007 | 97 | 2007 |
| The role of the brain‐derived neurotrophic factor (BDNF) val66met variant in the phenotypic expression of obsessive‐compulsive disorder (OCD) H Katerberg, C Lochner, DC Cath, P de Jonge, Z Bochdanovits, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150 …, 2009 | 94 | 2009 |
| RBBP6 interacts with multifunctional protein YB-1 through its RING finger domain, leading to ubiquitination and proteosomal degradation of YB-1 M Chibi, M Meyer, A Skepu, DJG Rees, JC Moolman-Smook, DJR Pugh Journal of molecular biology 384 (4), 908-916, 2008 | 91 | 2008 |
