| Recessive mutations in DGKE cause atypical hemolytic-uremic syndrome M Lemaire, V Frémeaux-Bacchi, F Schaefer, M Choi, WH Tang, ... Nature genetics 45 (5), 531-536, 2013 | 534 | 2013 |
| Gain-of-function variants in SYK cause immune dysregulation and systemic inflammation in humans and mice L Wang, D Aschenbrenner, Z Zeng, X Cao, D Mayr, M Mehta, M Capitani, ... Nature genetics 53 (4), 500-510, 2021 | 85 | 2021 |
| The phenotypic spectrum of nephropathies associated with mutations in diacylglycerol kinase ε K Azukaitis, E Simkova, MA Majid, M Galiano, K Benz, K Amann, ... Journal of the American Society of Nephrology 28 (10), 3066-3075, 2017 | 63 | 2017 |
| Characterization of a new DGKE intronic mutation in genetically unsolved cases of familial atypical hemolytic uremic syndrome C Mele, M Lemaire, P Iatropoulos, R Piras, E Bresin, S Bettoni, D Bick, ... Clinical Journal of the American Society of Nephrology 10 (6), 1011-1019, 2015 | 59 | 2015 |
| Inherited kidney complement diseases M Lemaire, D Noone, AL Lapeyraque, C Licht, V Frémeaux-Bacchi Clinical Journal of the American Society of Nephrology 16 (6), 942-956, 2021 | 52 | 2021 |
| Diacylglycerol kinase-ε: properties and biological roles RM Epand, V So, W Jennings, B Khadka, RS Gupta, M Lemaire Frontiers in Cell and Developmental Biology 4, 112, 2016 | 44 | 2016 |
| Twitching and quivering of the tentacles during snail olfactory orientation M Lemaire, R Chase Journal of Comparative Physiology A 182, 81-87, 1997 | 42 | 1997 |
| Iron-containing micronutrient powder provided to children with moderate-to-severe malnutrition increases hemoglobin concentrations but not the risk of infectious morbidity: a … M Lemaire, QS Islam, H Shen, MA Khan, M Parveen, F Abedin, F Haseen, ... The American journal of clinical nutrition 94 (2), 585-593, 2011 | 39 | 2011 |
| A variant in a cis‐regulatory element enhances claudin‐14 expression and is associated with pediatric‐onset hypercalciuria and kidney stones ME Ure, E Heydari, W Pan, A Ramesh, S Rehman, C Morgan, M Pinsk, ... Human mutation 38 (6), 649-657, 2017 | 36 | 2017 |
| Novel Fanconi renotubular syndromes provide insights in proximal tubule pathophysiology M Lemaire American Journal of Physiology-Renal Physiology 320 (2), F145-F160, 2021 | 34 | 2021 |
| The pupil: a window on social automatic processing in autism spectrum disorder children N Aguillon‐Hernandez, Y Mofid, M Latinus, L Roché, MR Bufo, M Lemaire, ... Journal of Child Psychology and Psychiatry 61 (7), 768-778, 2020 | 34 | 2020 |
| SON haploinsufficiency causes impaired pre-mRNA splicing of CAKUT genes and heterogeneous renal phenotypes JH Kim, EY Park, D Chitayat, DL Stachura, J Schaper, K Lindstrom, ... Kidney international 95 (6), 1494-1504, 2019 | 32 | 2019 |
| Acidosis in a patient with cholera: A need to redefine concepts N Zalunardo, M Lemaire, MR Davids, ML Halperin QJM 97 (10), 681-696, 2004 | 28 | 2004 |
| Driving medical innovation through interdisciplinarity: unique opportunities and challenges F Gohar, P Maschmeyer, B Mfarrej, M Lemaire, LR Wedderburn, ... Frontiers in medicine 6, 35, 2019 | 26 | 2019 |
| Treatment of paediatric vancomycin intoxication: a case report and review of the literature M Lemaire, B Connolly, E Harvey, C Licht NDT plus 3 (3), 260-264, 2010 | 26 | 2010 |
| The Role of Complement in Kidney Disease: Conclusions From a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference M Vivarelli, J Barratt, LH Beck Jr, F Fakhouri, DP Gale, EG de Jorge, ... Kidney International, 2024 | 20 | 2024 |
| Rho-GTPase Activating Protein myosin MYO9A identified as a novel candidate gene for monogenic focal segmental glomerulosclerosis Q Li, A Gulati, M Lemaire, T Nottoli, A Bale, A Tufro Kidney international 99 (5), 1102-1117, 2021 | 18 | 2021 |
| Assessment of translocator protein density, as marker of neuroinflammation, in major depressive disorder: a pilot, multicenter, comparative, controlled, brain PET study … A Yrondi, B Aouizerate, W El-Hage, F Moliere, C Thalamas, N Delcourt, ... Frontiers in psychiatry 9, 326, 2018 | 15 | 2018 |
| The phenotypic spectrum of tuberous sclerosis complex: a Canadian cohort D Alsowat, R Whitney, S Hewson, P Jain, V Chan, N Kabir, K Amburgey, ... Child Neurology Open 8, 2329048X211012817, 2021 | 13 | 2021 |
| Opportunities and challenges for genetic studies of end-stage renal disease in Canada V Kalatharan, M Lemaire, MB Lanktree Canadian Journal of Kidney Health and Disease 5, 2054358118789368, 2018 | 13 | 2018 |
Christoph LichtThe Hospital for Sick Children - Nephrology and RI Cell & Systems Biology; University of TorontoVerified email at sickkids.ca
