| Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22 LM Brzustowicz, KA Hodgkinson, EWC Chow, WG Honer, AS Bassett Science 288 (5466), 678-682, 2000 | 673 | 2000 |
| Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene ND Merner, KA Hodgkinson, AFM Haywood, S Connors, VM French, ... The American Journal of Human Genetics 82 (4), 809-821, 2008 | 583 | 2008 |
| 22q11 deletion syndrome in adults with schizophrenia AS Bassett, K Hodgkinson, EWC Chow, S Correia, LE Scutt, R Weksberg American journal of medical genetics 81 (4), 328-337, 1998 | 303 | 1998 |
| Linkage of familial schizophrenia to chromosome 13q32 LM Brzustowicz, WG Honer, EWC Chow, D Little, J Hogan, K Hodgkinson, ... The American Journal of Human Genetics 65 (4), 1096-1103, 1999 | 257 | 1999 |
| The impact of implantable cardioverter-defibrillator therapy on survival in autosomal-dominant arrhythmogenic right ventricular cardiomyopathy (ARVD5) KA Hodgkinson, PS Parfrey, AS Bassett, C Kupprion, J Drenckhahn, ... Journal of the American College of Cardiology 45 (3), 400-408, 2005 | 240 | 2005 |
| Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22 LM Brzustowicz, J Simone, P Mohseni, JE Hayter, KA Hodgkinson, ... The American Journal of Human Genetics 74 (5), 1057-1063, 2004 | 201 | 2004 |
| Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian Cardiovascular Society … MH Gollob, L Blier, R Brugada, J Champagne, V Chauhan, S Connors, ... Canadian Journal of Cardiology 27 (2), 232-245, 2011 | 184 | 2011 |
| Reproductive fitness in familial schizophrenia AS Bassett, A Bury, KA Hodgkinson, WG Honer Schizophrenia research 21 (3), 151-160, 1996 | 161 | 1996 |
| Premature death in adults with 22q11. 2 deletion syndrome AS Bassett, EWC Chow, J Husted, KA Hodgkinson, E Oechslin, L Harris, ... Journal of medical genetics 46 (5), 324-330, 2009 | 110 | 2009 |
| The natural history of a genetic subtype of arrhythmogenic right ventricular cardiomyopathy caused by a p. S358L mutation in TMEM43 KA Hodgkinson, SP Connors, N Merner, A Haywood, TL Young, ... Clinical genetics 83 (4), 321-331, 2013 | 98 | 2013 |
| Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p LM Brzustowicz, WG Honer, EWC Chow, J Hogan, K Hodgkinson, ... The American Journal of Human Genetics 61 (6), 1388-1396, 1997 | 94 | 1997 |
| Intrafamilial variability in cleidocranial dysplasia: a three generation family D Chitayat, KA Hodgkinson, EM Azouz American journal of medical genetics 42 (3), 298-303, 1992 | 78 | 1992 |
| The TMEM43 Newfoundland mutation p.S358L causing ARVC-5 was imported from Europe and increases the stiffness of the cell nucleus H Milting, B Klauke, AH Christensen, J Müsebeck, V Walhorn, ... European heart journal 36 (14), 872-881, 2015 | 77 | 2015 |
| Personal privacy, public benefits, and biobanks: a conjoint analysis of policy priorities and public perceptions D Pullman, H Etchegary, K Gallagher, K Hodgkinson, M Keough, ... Genetics in medicine 14 (2), 229-235, 2012 | 70 | 2012 |
| Genetic counselling for schizophrenia in the era of molecular genetics KA Hodgkinson, J Murphy, S O'Neill, L Brzustowicz, AS Bassett The Canadian Journal of Psychiatry 46 (2), 123-130, 2001 | 69 | 2001 |
| Mucolipidosis type IV: clinical manifestations and natural history D Chitayat, CM Meunier, KA Hodgkinson, K Silver, M Flanders, ... American journal of medical genetics 41 (3), 313-318, 1991 | 69 | 1991 |
| Elucidating the diagnostic odyssey of 22q11. 2 deletion syndrome LD Palmer, NJ Butcher, E Boot, KA Hodgkinson, T Heung, EWC Chow, ... American Journal of Medical Genetics Part A 176 (4), 936-944, 2018 | 68 | 2018 |
| Genetic knowledge and moral responsibility: ambiguity at the interface of genetic research and clinical practice D Pullman, K Hodgkinson Clinical genetics 69 (3), 199-203, 2006 | 67 | 2006 |
| Fine mapping of the schizophrenia susceptibility locus on chromosome 1q22 LM Brzustowicz, JE Hayter, KA Hodgkinson, EWC Chow, AS Bassett Human heredity 54 (4), 199-209, 2003 | 64 | 2003 |
| Adult polycystic kidney disease: knowledge, experience, and attitudes to prenatal diagnosis. KA Hodgkinson, L Kerzin-Storrar, EA Watters, R Harris Journal of medical genetics 27 (9), 552-558, 1990 | 60 | 1990 |
