Manuel Belmadani
Title
Cited by
Cited by
Year
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
1052016
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
92018
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
72020
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
72019
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
42019
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), 1-16, 2020
32020
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
32016
MotifGP: DNA motif discovery using multiobjective evolution
M Belmadani
Université d'Ottawa/University of Ottawa, 2016
22016
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
12019
Data-driven approaches for improving the interpretability of patch-seq data
SJ Tripathy, L Toker, C Bomkamp, BO Mancarci, M Belmadani, P Pavlidis
bioRxiv, 298133, 2018
12018
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
Curation of over 10,000 transcriptomic studies to enable data reuse
N Lim, S Tesar, M Belmadani, G Poirier-Morency, BO Mancarci, ...
BioRxiv, 2020
2020
Systematic phenomics analysis of ASD-associated genes defines shared functions and identifies parallel genetic networks underlying hypersensitivity and impaired habituation …
TA McDiarmid, M Belmadani, J Liang, F Mieli, JB Rand, K Mizumoto, ...
2019
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
The system can't perform the operation now. Try again later.
Articles 1–16