| A comprehensive analysis of 3′ end sequencing data sets reveals novel polyadenylation signals and the repressive role of heterogeneous ribonucleoprotein C on cleavage and … AJ Gruber, R Schmidt, AR Gruber, G Martin, S Ghosh, M Belmadani, ... Genome research 26 (8), 1145-1159, 2016 | 223 | 2016 |
| Systematic phenomics analysis of autism-associated genes reveals parallel networks underlying reversible impairments in habituation TA McDiarmid, M Belmadani, J Liang, F Meili, EA Mathews, GP Mullen, ... Proceedings of the National Academy of Sciences 117 (1), 656-667, 2020 | 65 | 2020 |
| Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunction KL Post, M Belmadani, P Ganguly, F Meili, R Dingwall, TA McDiarmid, ... Nature communications 11 (1), 2073, 2020 | 51 | 2020 |
| Assessing transcriptome quality in patch-seq datasets SJ Tripathy, L Toker, C Bomkamp, BO Mancarci, M Belmadani, P Pavlidis Frontiers in Molecular Neuroscience 11, 363, 2018 | 41 | 2018 |
| Curation of over 10 000 transcriptomic studies to enable data reuse N Lim, S Tesar, M Belmadani, G Poirier-Morency, BO Mancarci, ... Database 2021, baab006, 2021 | 35 | 2021 |
| VariCarta: a comprehensive database of harmonized genomic variants found in autism spectrum disorder sequencing studies M Belmadani, M Jacobson, N Holmes, M Phan, T Nguyen, P Pavlidis, ... Autism Research 12 (12), 1728-1736, 2019 | 31 | 2019 |
| Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohort DB Callaghan, S Rogic, PPC Tan, K Calli, Y Qiao, R Baldwin, M Jacobson, ... Clinical genetics 96 (3), 199-206, 2019 | 23 | 2019 |
| Interactive exploration, analysis, and visualization of complex phenome–genome datasets with ASPIREdb PPC Tan, S Rogic, A Zoubarev, C McDonald, F Lui, G Charathsandran, ... Human mutation 37 (8), 719-726, 2016 | 5 | 2016 |
| MotifGP: DNA motif discovery using multiobjective evolution M Belmadani Université d'Ottawa/University of Ottawa, 2016 | 3 | 2016 |
| VariCarta: a comprehensive database of harmonized genomic variants found in ASD sequencing studies M Belmadani, M Jacobson, N Holmes, M Phan, P Pavlidis, S Rogic bioRxiv, 608356, 2019 | 2 | 2019 |
| Motifgp: Using multi-objective evolutionary computing for mining network expressions in dna sequences M Belmadani, M Turcotte 2016 IEEE Conference on Computational Intelligence in Bioinformatics and …, 2016 | 1 | 2016 |
| Cataloging the potential functional diversity of Cacna1e splice variants using long-read sequencing S Bhuiyan, JR Tyson, M Belmadani, J Sicherman, TP Snutch, P Pavlidis bioRxiv, 2022.04. 06.487199, 2022 | | 2022 |
| SnpReportR: A Tool for Clinical Reporting of RNAseq Expression and Variants A Al Khleifat BioHackrXiv, 2021 | | 2021 |
| Systematic phenomics analysis of ASD-associated genes reveals shared functions and parallel networks underlying reversible impairments in habituation learning TA McDiarmid, M Belmadani, J Liang, F Meili, EA Mathews, GP Mullen, ... bioRxiv, 687194, 2019 | | 2019 |
| A critical assessment of single-cell transcriptomes sampled following patch-clamp electrophysiology SJ Tripathy, L Toker, C Bomkamp, BO Mancarci, M Belmadani, P Pavlidis bioRxiv, 298133, 2018 | | 2018 |
| Systematic phenomics analysis of ASD-associated genes reveals shared functions and TA McDiarmid, M Belmadani, J Liang, F Meili, EA Mathews, GP Mullen, ... Psychol. Med 25, 63-77, 1995 | | 1995 |
| Michael Smith Laboratories, University of British Columbia, Vancouver BC, Canada Department of Psychiatry, University of British Columbia, Vancouver BC, Canada Corresponding … SJ Tripathy, L Toker, C Bomkamp, BO Mancarci, M Belmadani, P Pavlidis | | |
| Multi-Model Functionalization of 106 PTEN Missense Mutations Identifies Multiple Molecular Mechanisms Underlying Protein Dysfunction K Post, M Belmadani, P Ganguly, F Meili, R Dingwall, TA McDiarmid, ... INSAR 2020 Virtual Meeting, 0 | | |
