| De Novo Mutations in Moderate or Severe Intellectual Disability FF Hamdan, M Srour, JM Capo-Chichi, H Daoud, C Nassif, L Patry, ... PLoS genetics 10 (10), e1004772, 2014 | 450 | 2014 |
| Methylation of BDNF in women with bulimic eating syndromes: associations with childhood abuse and borderline personality disorder L Thaler, L Gauvin, R Joober, P Groleau, R de Guzman, A Ambalavanan, ... Progress in Neuro-Psychopharmacology and Biological Psychiatry 54, 43-49, 2014 | 126 | 2014 |
| SMPD1 mutations, activity, and α‐synuclein accumulation in Parkinson's disease RN Alcalay, V Mallett, B Vanderperre, O Tavassoly, Y Dauvilliers, RYJ Wu, ... Movement Disorders 34 (4), 526-535, 2019 | 114 | 2019 |
| GBA p.T369M substitution in Parkinson disease: Polymorphism or association? A meta-analysis V Mallett, JP Ross, RN Alcalay, A Ambalavanan, E Sidransky, PA Dion, ... Neurology: Genetics 2 (5), e104, 2016 | 110 | 2016 |
| De novo variants in sporadic cases of childhood onset schizophrenia A Ambalavanan, SL Girard, K Ahn, S Zhou, A Dionne-Laporte, ... European Journal of Human Genetics 24 (6), 944-948, 2016 | 100 | 2016 |
| RNF213 is associated with intracranial aneurysms in the French-Canadian population S Zhou, A Ambalavanan, D Rochefort, P Xie, CV Bourassa, P Hince, ... The American Journal of Human Genetics 99 (5), 1072-1085, 2016 | 74 | 2016 |
| Family-based exome-sequencing approach identifies rare susceptibility variants for lithium-responsive bipolar disorder C Cruceanu, A Ambalavanan, D Spiegelman, J Gauthier, RG Lafrenière, ... Genome 56 (10), 634-640, 2013 | 63 | 2013 |
| Paternal Age Explains a Major Portion of De Novo Germline Mutation Rate Variability in Healthy Individuals SL Girard, CV Bourassa, LP Lemieux Perreault, MA Legault, A Barhdadi, ... PLoS One 11 (10), e0164212, 2016 | 56 | 2016 |
| Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease JP Ross, N Dupre, Y Dauvilliers, S Strong, A Ambalavanan, ... Neurobiology of aging 45, 212. e13-212. e17, 2016 | 55 | 2016 |
| Wheeze trajectories: Determinants and outcomes in the CHILD Cohort Study R Dai, K Miliku, S Gaddipati, J Choi, A Ambalavanan, MM Tran, M Reyna, ... Journal of Allergy and Clinical Immunology 149 (6), 2153-2165, 2022 | 48 | 2022 |
| Missense variants in ATP1A3 and FXYD gene family are associated with childhood-onset schizophrenia B Chaumette, V Ferrafiat, A Ambalavanan, A Goldenberg, ... Molecular psychiatry 25 (4), 821-830, 2020 | 47 | 2020 |
| Rare susceptibility variants for bipolar disorder suggest a role for G protein-coupled receptors C Cruceanu, JF Schmouth, SG Torres-Platas, JP Lopez, A Ambalavanan, ... Molecular psychiatry 23 (10), 2050-2056, 2018 | 40 | 2018 |
| Full sequencing and haplotype analysis of MAPT in Parkinson's disease and rapid eye movement sleep behavior disorder J Li, JA Ruskey, I Arnulf, Y Dauvilliers, MTM Hu, B Högl, CS Leblond, ... Movement Disorders 33 (6), 1016-1020, 2018 | 39 | 2018 |
| Novel VPS13B Mutations in Three Large Pakistani Cohen Syndrome Families Suggests a Baloch Variant with Autistic-Like Features MA Rafiq, CS Leblond, MAN Saqib, AK Vincent, A Ambalavanan, ... BMC medical genetics 16, 1-10, 2015 | 35 | 2015 |
| A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population B Wang, S Bao, Z Zhang, X Zhou, J Wang, Y Fan, Y Zhang, Y Li, L Chen, ... Neurobiology of aging 68, 160. e1-160. e7, 2018 | 33 | 2018 |
| Family-based association study of common variants, rare mutation study and epistatic interaction detection in HDAC genes in schizophrenia O Kebir, B Chaumette, M Fatjo-Vilas, A Ambalavanan, N Ramoz, L Xiong, ... Schizophrenia research 160 (1-3), 97-103, 2014 | 30 | 2014 |
| Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome Z Gan-Or, S Zhou, A Ambalavanan, CS Leblond, P Xie, A Johnson, ... Sleep medicine 16 (9), 1151-1155, 2015 | 28 | 2015 |
| Genetic architecture and adaptations of Nunavik Inuit S Zhou, P Xie, A Quoibion, A Ambalavanan, A Dionne-Laporte, ... Proceedings of the National Academy of Sciences 116 (32), 16012-16017, 2019 | 27 | 2019 |
| Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population S Zhou, L Xiong, P Xie, A Ambalavanan, CV Bourassa, A Dionne-Laporte, ... PloS one 10 (5), e0128255, 2015 | 27 | 2015 |
| Investigation of rare variants in LRP1, KPNA1, ALS2CL and ZNF480 genes in schizophrenia patients reflects genetic heterogeneity of the disease L Jouan, SL Girard, S Dobrzeniecka, A Ambalavanan, MO Krebs, ... Behavioral and Brain Functions 9, 1-5, 2013 | 25 | 2013 |