| Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects B Christensen, L Arbour, P Tran, D Leclerc, N Sabbaghian, R Platt, ... American journal of medical genetics 84 (2), 151-157, 1999 | 404 | 1999 |
| Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation JM Friedman, Á Baross, AD Delaney, A Ally, L Arbour, J Asano, DK Bailey, ... The American Journal of Human Genetics 79 (3), 500-513, 2006 | 360 | 2006 |
| Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosis S Hanks, S Adams, J Douglas, L Arbour, DJ Atherton, S Balci, H Bode, ... The American Journal of Human Genetics 73 (4), 791-800, 2003 | 247 | 2003 |
| Rights, interests and expectations: Indigenous perspectives on unrestricted access to genomic data M Hudson, G Nanibaa’A, R Sterling, NR Caron, K Fox, J Yracheta, ... Nature Reviews Genetics, 1-8, 2020 | 213 | 2020 |
| DNA on loan: issues to consider when carrying out genetic research with aboriginal families and communities L Arbour, D Cook Public Health Genomics 9 (3), 153-160, 2006 | 184 | 2006 |
| Evidence for a familial Wilms' tumour gene (FWT1) on chromosome 17q12–q21 N Rahman, L Arbour, P Tonin, J Renshaw, J Pelletier, S Baruchel, ... Nature genetics 13 (4), 461-463, 1996 | 184 | 1996 |
| Genomic research through an indigenous lens: understanding the expectations G Nanibaa’A, M Hudson, LL Ballantyne, I Garba, A Martinez, M Taualii, ... Annual review of genomics and human genetics 20, 2019 | 172 | 2019 |
| Association between preeclampsia and congenital heart defects N Auger, WD Fraser, J Healy-Profitós, L Arbour Jama 314 (15), 1588-1598, 2015 | 164 | 2015 |
| Race and ancestry in biomedical research: exploring the challenges T Caulfield, SM Fullerton, SE Ali-Khan, L Arbour, EG Burchard, ... Genome medicine 1 (1), 1-8, 2009 | 155 | 2009 |
| Submicroscopic deletions and duplications in individuals with intellectual disability detected by array‐CGH C Tyson, C Harvard, R Locker, JM Friedman, S Langlois, MES Lewis, ... American Journal of Medical Genetics Part A 139 (3), 173-185, 2005 | 131 | 2005 |
| The shared pathoetiological effects of particulate air pollution and the social environment on fetal-placental development AC Erickson, L Arbour Journal of environmental and public health 2014, 2014 | 103 | 2014 |
| Heavy smoking during pregnancy as a marker for other risk factors of adverse birth outcomes: a population-based study in British Columbia, Canada AC Erickson, LT Arbour BMC Public Health 12 (1), 102, 2012 | 101 | 2012 |
| Genetic Testing in the Evaluation of Unexplained Cardiac Arrest G Mellor, ZWM Laksman, R Tadros, JD Roberts, B Gerull, CS Simpson, ... Circulation 2017 (136), 871-876, 2017 | 89* | 2017 |
| Genetic testing in the evaluation of unexplained cardiac arrest: from the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry) G Mellor, ZWM Laksman, R Tadros, JD Roberts, B Gerull, CS Simpson, ... Circulation: Cardiovascular Genetics 10 (3), e001686, 2017 | 89 | 2017 |
| The gene for juvenile hyaline fibromatosis maps to chromosome 4q21 N Rahman, M Dunstan, MD Teare, S Hanks, SJ Edkins, J Hughes, ... The American Journal of Human Genetics 71 (4), 975-980, 2002 | 87 | 2002 |
| Changes in frequencies of select congenital anomalies since the onset of folic acid fortification in a Canadian birth defect registry KA Godwin, B Sibbald, T Bedard, B Kuzeljevic, RB Lowry, L Arbour Canadian journal of public health 99 (4), 271-275, 2008 | 83 | 2008 |
| Carnitine palmitoyltransferase 1A (CPT1A) P479L prevalence in live newborns in Yukon, Northwest Territories, and Nunavut SA Collins, G Sinclair, S McIntosh, F Bamforth, R Thompson, I Sobol, ... Molecular genetics and metabolism 101 (2-3), 200-204, 2010 | 81 | 2010 |
| Maternal risk factors for gastroschisis in Canada ED Skarsgard, C Meaney, K Bassil, M Brindle, L Arbour, R Moineddin, ... Birth Defects Research Part A: Clinical and Molecular Teratology 103 (2 …, 2015 | 77 | 2015 |
| An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus A Kukuvitis, C Deal, L Arbour, C Polychronakos The Journal of Clinical Endocrinology & Metabolism 82 (4), 1192-1194, 1997 | 76 | 1997 |
| Hypomorphic temperature-sensitive alleles of NSDHL cause CK syndrome KW McLarren, TM Severson, C du Souich, DW Stockton, LE Kratz, ... The American Journal of Human Genetics 87 (6), 905-914, 2010 | 73 | 2010 |
