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Manuel Belmadani
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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
2002016
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
552020
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
432020
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
382018
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
262019
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
212019
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
192021
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
52016
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
22019
MotifGP: DNA motif discovery using multiobjective evolution
M Belmadani
Université d'Ottawa/University of Ottawa, 2016
22016
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
12016
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, J Smith, B Blobner, S Miller, K Pagel, A Nadkarni, M Gainey, ...
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
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Articles 1–18