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Autism Research : Official Journal of the International Society for Autism Research|November 10, 2019
VariCarta: A Comprehensive Database of Harmonized Genomic Variants Found in Autism Spectrum Disorder Sequencing StudiesManuel Belmadani, Matthew Jacobson, Nathan Holmes, et al.
Frontiers in Molecular Neuroscience|October 24, 2018
Assessing Transcriptome Quality in Patch-Seq DatasetsShreejoy J Tripathy, Lilah Toker, Claire Bomkamp, et al.
BMC Genomics|September 27, 2025
Cataloging the potential functional diversity of Cacna1e splice variants using long-read sequencingShamsuddin A Bhuiyan, John R Tyson, Manuel Belmadani, et al.
Genome Research|July 7, 2016
A comprehensive analysis of 3' end sequencing data sets reveals novel polyadenylation signals and the repressive role of heterogeneous ribonucleoprotein C on cleavage and polyadenylationAndreas J Gruber, Ralf Schmidt, Andreas R Gruber, et al.
Database : the Journal of Biological Databases and Curation|February 18, 2021
Curation of over 10 000 transcriptomic studies to enable data reuseNathaniel Lim, Stepan Tesar, Manuel Belmadani, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 23, 2019
Systematic phenomics analysis of autism-associated genes reveals parallel networks underlying reversible impairments in habituationTroy A McDiarmid, Manuel Belmadani, Joseph Liang, et al.
Human Mutation|May 10, 2016
Interactive Exploration, Analysis, and Visualization of Complex Phenome-Genome Datasets with ASPIREdbPowell Patrick Cheng Tan, Sanja Rogic, Anton Zoubarev, et al.
Nature Communications|May 1, 2020
Multi-model functionalization of disease-associated PTEN missense mutations identifies multiple molecular mechanisms underlying protein dysfunctionKathryn L Post, Manuel Belmadani, Payel Ganguly, et al.
Clinical Genetics|May 1, 2019
Whole genome sequencing and variant discovery in the ASPIRE autism spectrum disorder cohortDaniel Benjamin Callaghan, Sanja Rogic, Powell Patrick Cheng Tan, et al.
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