scispace - formally typeset
J

Jasmin Coulombe-Huntington

Researcher at Université de Montréal

Publications -  40
Citations -  4819

Jasmin Coulombe-Huntington is an academic researcher from Université de Montréal. The author has contributed to research in topics: Gene & Alternative splicing. The author has an hindex of 17, co-authored 35 publications receiving 3398 citations. Previous affiliations of Jasmin Coulombe-Huntington include McGill University & Boston University.

Papers
More filters
Journal ArticleDOI

A proteome-scale map of the human interactome network

Thomas Rolland, +80 more
- 20 Nov 2014 - 
TL;DR: The map uncovers significant interconnectivity between known and candidate cancer gene products, providing unbiased evidence for an expanded functional cancer landscape, while demonstrating how high-quality interactome models will help "connect the dots" of the genomic revolution.
Journal ArticleDOI

The BioGRID interaction database: 2019 update

TL;DR: A new dedicated aspect of BioGRID annotates genome-wide CRISPR/Cas9-based screens that report gene–phenotype and gene–gene relationships, and captures chemical interaction data, including chemical–protein interactions for human drug targets drawn from the DrugBank database and manually curated bioactive compounds reported in the literature.
Journal ArticleDOI

The BioGRID database: A comprehensive biomedical resource of curated protein, genetic, and chemical interactions.

TL;DR: The BioGRID (Biological General Repository for Interaction Datasets, thebiogrid.org) is an open‐access database resource that houses manually curated protein and genetic interactions from multiple species including yeast, worm, fly, mouse, and human.
Journal ArticleDOI

Widespread Macromolecular Interaction Perturbations in Human Genetic Disorders

TL;DR: This work functionally profile several thousand missense mutations across a spectrum of Mendelian disorders using various interaction assays, suggesting that disease-associated alleles that perturb distinct protein activities rather than grossly affecting folding and stability are relatively widespread.
Journal ArticleDOI

Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing

TL;DR: This work cloned full-length open reading frames of alternatively spliced transcripts for a large number of human genes and used protein-protein interaction profiling to functionally compare hundreds of protein isoform pairs, revealing a widespread expansion of protein interaction capabilities through alternative splicing and suggesting that many alternative "isoforms" are functionally divergent (i.e., "functional alloforms").