| Functional variants of OCTN cation transporter genes are associated with Crohn disease VD Peltekova, RF Wintle, LA Rubin, CI Amos, Q Huang, X Gu, B Newman, ... Nature genetics 36 (5), 471-475, 2004 | 984 | 2004 |
| Structural variants: changing the landscape of chromosomes and design of disease studies L Feuk, CR Marshall, RF Wintle, SW Scherer Human molecular genetics 15 (suppl 1), R57-R66, 2006 | 366 | 2006 |
| FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project CL Beaulieu, J Majewski, J Schwartzentruber, ME Samuels, ... The American Journal of Human Genetics 94 (6), 809-817, 2014 | 278 | 2014 |
| Dopamine modulates the plasticity of mechanosensory responses in Caenorhabditis elegans S Sanyal, RF Wintle, KS Kindt, WM Nuttley, R Arvan, P Fitzmaurice, ... The EMBO journal 23 (2), 473-482, 2004 | 274 | 2004 |
| Association of the lymphoid tyrosine phosphatase R620W variant with rheumatoid arthritis, but not Crohn's disease, in Canadian populations M Van Oene, RF Wintle, X Liu, M Yazdanpanah, X Gu, B Newman, ... Arthritis & Rheumatism 52 (7), 1993-1998, 2005 | 183 | 2005 |
| Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications MJ Ombrello, VL Arthur, EF Remmers, A Hinks, I Tachmazidou, AA Grom, ... Annals of the rheumatic diseases 76 (5), 906-913, 2017 | 167 | 2017 |
| A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn’s disease B Newman, X Gu, R Wintle, D Cescon, M Yazdanpanah, X Liu, ... Gastroenterology 128 (2), 260-269, 2005 | 156 | 2005 |
| Clinically relevant copy number variations detected in cerebral palsy M Oskoui, MJ Gazzellone, B Thiruvahindrapuram, M Zarrei, J Andersen, ... Nature communications 6 (1), 7949, 2015 | 155 | 2015 |
| A large data resource of genomic copy number variation across neurodevelopmental disorders M Zarrei, CL Burton, W Engchuan, EJ Young, EJ Higginbotham, ... NPJ genomic medicine 4 (1), 26, 2019 | 137 | 2019 |
| Genetic or other causation should not change the clinical diagnosis of cerebral palsy AH MacLennan, S Lewis, A Moreno-De-Luca, M Fahey, RJ Leventer, ... Journal of child neurology 34 (8), 472-476, 2019 | 105 | 2019 |
| De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy M Zarrei, DL Fehlings, K Mawjee, L Switzer, B Thiruvahindrapuram, ... Genetics in Medicine 20 (2), 172-180, 2018 | 90 | 2018 |
| A high-resolution copy-number variation resource for clinical and population genetics M Uddin, B Thiruvahindrapuram, S Walker, Z Wang, P Hu, S Lamoureux, ... Genetics in medicine 17 (9), 747-752, 2015 | 85 | 2015 |
| Genomic architecture of autism from comprehensive whole-genome sequence annotation B Trost, B Thiruvahindrapuram, AJS Chan, W Engchuan, ... Cell 185 (23), 4409-4427. e18, 2022 | 81 | 2022 |
| Brief Report: The Genetic Profile of Rheumatoid Factor–Positive Polyarticular Juvenile Idiopathic Arthritis Resembles That of Adult Rheumatoid Arthritis A Hinks, MC Marion, J Cobb, ME Comeau, M Sudman, HC Ainsworth, ... Arthritis & Rheumatology 70 (6), 957-962, 2018 | 70 | 2018 |
| The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants MS Reuter, S Walker, B Thiruvahindrapuram, J Whitney, I Cohn, ... Cmaj 190 (5), E126-E136, 2018 | 64 | 2018 |
| SLC22A4 polymorphisms implicated in rheumatoid arthritis and Crohn's disease are not associated with rheumatoid arthritis in a Canadian Caucasian population B Newman, RF Wintle, M Van Oene, M Yazdanpanah, J Owen, B Johnson, ... Arthritis & Rheumatism: Official Journal of the American College of …, 2005 | 58 | 2005 |
| Dopamine signaling in Caenorhabditis elegans—potential for parkinsonism research RF Wintle, HHM Van Tol Parkinsonism & related disorders 7 (3), 177-183, 2001 | 52 | 2001 |
| Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reporting S Goobie, J Knijnenburg, D FitzPatrick, FH Sharkey, AC Lionel, ... Cytogenetic and genome research 123 (1-4), 65-78, 2009 | 51 | 2009 |
| IL1RN Variation Influences Both Disease Susceptibility and Response to Recombinant Human Interleukin‐1 Receptor Antagonist Therapy in Systemic Juvenile … VL Arthur, E Shuldiner, EF Remmers, A Hinks, AA Grom, D Foell, A Martini, ... Arthritis & Rheumatology 70 (8), 1319-1330, 2018 | 49 | 2018 |
| DLG5 variants contribute to Crohn disease risk in a Canadian population WG Newman, X Gu, RF Wintle, X Liu, M Van Oene, CI Amos, ... Human Mutation 27 (4), 353-358, 2006 | 38 | 2006 |
Scherer, Stephen W.The Hospital for Sick Children, Genetics and Genome Biology Program, University of TorontoVerified email at sickkids.ca
