Publications

Small, correlated changes in synaptic connectivity may facilitate rapid motor learning
Barbara Feulner
Raeed H. Chowdhury
Lee Miller
Juan A. Gallego
Claudia Clopath
Unified gene expression signature of novel NPM1 exon 5 mutations in acute myeloid leukemia
Véronique Lisi
Ève Blanchard
Michael Vladovsky
Éric Audemard
Albert Ferghaly
Josée Hébert
Guy Sauvageau
Vincent-Philippe Lavallee
Visual Abstract
GCNFusion: An efficient graph convolutional network based model for information diffusion
Bahare Fatemi
Soheila Mehr Molaei
Shirui Pan
Interpretable domain adaptation using unsupervised feature selection on pre-trained source models
Luxin Zhang
Yacine Kessaci
C. Biernacki
The load planning and sequencing problem for double-stack trains
Moritz Ruf
Jean-François Cordeau
QU-BraTS: MICCAI BraTS 2020 Challenge on Quantifying Uncertainty in Brain Tumor Segmentation - Analysis of Ranking Metrics and Benchmarking Results
Raghav Mehta
Angelos Filos
Ujjwal Baid
Chiharu Sako
Richard McKinley
Michael Rebsamen
Katrin Dätwyler
Raphael Meier
Piotr Radojewski
Gowtham Krishnan Murugesan
Sahil Nalawade
Chandan Ganesh
Benjamin C. Wagner
Fang Frank Yu
Baowei Fei
Ananth J. Madhuranthakam
Joseph A. Maldjian
Laura Daza
Catalina Gómez
Pablo Arbeláez … (see 72 more)
Chengliang Dai
Shuo Wang
Hadrien Reynaud
Yuanhan Mo
Elsa Angelini
Yike Guo
Wenjia Bai
Subhashis Banerjee
Linmin Pei
Murat AK
Sarahi Rosas-González
Ilyess Zemmoura
Clovis Tauber
Minh H. Vu
Tufve Nyholm
Tommy Löfstedt
Laura Mora Ballestar
Veronica Vilaplana
Hugh McHugh
Gonzalo Maso Talou
Alan Wang
Jay Patel
Ken Chang
Katharina Hoebel
Mishka Gidwani
Nishanth Arun
Sharut Gupta
Mehak Aggarwal
Praveer Singh
Elizabeth R. Gerstner
Jayashree Kalpathy-Cramer
Nicolas Boutry
Alexis Huard
Lasitha Vidyaratne
Md Monibor Rahman
Khan M. Iftekharuddin
Joseph Chazalon
Elodie Puybareau
Guillaume Tochon
Jun Ma
Mariano Cabezas
Xavier Llado
Arnau Oliver
Liliana Valencia
Sergi Valverde
Mehdi Amian
Mohammadreza Soltaninejad
Andriy Myronenko
Ali Hatamizadeh
Xue Feng
Quan Dou
Nicholas Tustison
Craig Meyer
Nisarg A. Shah
Sanjay Talbar
Marc-André Weber
Abhishek Mahajan
Andras Jakab
Roland Wiest
Hassan M. Fathallah-Shaykh
Arash Nazeri
Mikhail Milchenko
Daniel Marcus
Aikaterini Kotrotsou
Rivka R. Colen
John Freymann
Justin Kirby
Christos Davatzikos
Bjoern Menze
Spyridon Bakas
Yarin Gal
Fractal impedance for passive controllers: a framework for interaction robotics
Keyhan Kouhkiloui Babarahmati
Carlo Tiseo
Joshua Smith
M. S. Erden
Michael Nalin Mistry
GaMPEN: A Machine-learning Framework for Estimating Bayesian Posteriors of Galaxy Morphological Parameters
Aritra Ghosh
C. Urry
Amrit Rau
M. Cranmer
Kevin Schawinski
Dominic Stark
Chuan Tian
Ryan Ofman
T. Ananna
Connor Auge
Nico Cappelluti
D. Sanders
Ezequiel Treister
We introduce a novel machine-learning framework for estimating the Bayesian posteriors of morphological parameters for arbitrarily large num… (see more)bers of galaxies. The Galaxy Morphology Posterior Estimation Network (GaMPEN) estimates values and uncertainties for a galaxy’s bulge-to-total-light ratio (L B /L T ), effective radius (R e ), and flux (F). To estimate posteriors, GaMPEN uses the Monte Carlo Dropout technique and incorporates the full covariance matrix between the output parameters in its loss function. GaMPEN also uses a spatial transformer network (STN) to automatically crop input galaxy frames to an optimal size before determining their morphology. This will allow it to be applied to new data without prior knowledge of galaxy size. Training and testing GaMPEN on galaxies simulated to match z 0.25 galaxies in Hyper Suprime-Cam Wide g-band images, we demonstrate that GaMPEN achieves typical errors of 0.1 in L B /L T , 0.″17 (∼7%) in R e , and 6.3 × 104 nJy (∼1%) in F. GaMPEN's predicted uncertainties are well calibrated and accurate (5% deviation)—for regions of the parameter space with high residuals, GaMPEN correctly predicts correspondingly large uncertainties. We a
Learning Shared Neural Manifolds from Multi-Subject FMRI Data
Jessie Huang
Je-chun Huang
Erica Lindsey Busch
Tom Wallenstein
Michal Gerasimiuk
Andrew Benz
Nicholas Turk-Browne
Smita Krishnaswamy
Functional magnetic resonance imaging (fMRI) data is collected in millions of noisy, redundant dimensions. To understand how different brain… (see more)s process the same stimulus, we aim to denoise the fMRI signal via a meaningful embedding space that captures the data's intrinsic structure as shared across brains. We assume that stimulus-driven responses share latent features common across subjects that are jointly discoverable. Previous approaches to this problem have relied on linear methods like principal component analysis and shared response modeling. We propose a neural network called MRMD-AE (manifold-regularized multiple- decoder, autoencoder) that learns a common embedding from multi-subject fMRI data while retaining the ability to decode individual responses. Our latent common space represents an extensible manifold (where untrained data can be mapped) and improves classification accuracy of stimulus features of unseen timepoints, as well as cross-subject translation of fMRI signals.
Proteogenomics and Differential Ion Mobility Enable the Exploration of the Mutational Landscape in Colon Cancer Cells
Zhaoguan Wu
Eric Bonneil
Michael Belford
Cornelia Boeser
Maria-Virginia Ruiz Cuevas
Jean-Jacques Dunyach
Pierre Thibault
Stratifying the autistic phenotype using electrophysiological indices of social perception
Luke Mason
Carolin Moessnang
Christopher H. Chatham
Lindsay Ham
Julian Tillmann
Claire Ellis
Claire Leblond
Freddy Cliquet
Thomas Bourgeron
Christian Beckmann
Tony Charman
Beth Oakley
Tobias Banaschewski
Andreas Meyer-Lindenberg
Simon Baron-Cohen
Sven Bölte
Jan K. Buitelaar
Sarah Durston
Eva Loth … (see 7 more)
Bob Oranje
Antonio Persico
Flavio Dell’Acqua
Christine Ecker
Mark Johnson
Declan Murphy
Emily J. H. Jones
Autism spectrum disorder (ASD) is a neurodevelopmental condition characterized by difficulties in social communication, but also great heter… (see more)ogeneity. To offer individualized medicine approaches, we need to better target interventions by stratifying autistic people into subgroups with different biological profiles and/or prognoses. We sought to validate neural responses to faces as a potential stratification factor in ASD by measuring neural (electroencephalography) responses to faces (critical in social interaction) in N = 436 children and adults with and without ASD. The speed of early-stage face processing (N170 latency) was on average slower in ASD than in age-matched controls. In addition, N170 latency was associated with responses to faces in the fusiform gyrus, measured with functional magnetic resonance imaging, and polygenic scores for ASD. Within the ASD group, N170 latency predicted change in adaptive socialization skills over an 18-month follow-up period; data-driven clustering identified a subgroup with slower brain responses and poor social prognosis. Use of a distributional data-driven cutoff was associated with predicted improvements of power in simulated clinical trials targeting social functioning. Together, the data provide converging evidence for the utility of the N170 as a stratification factor to identify biologically and prognostically defined subgroups in ASD. Description N170 latency to faces relates to fusiform activity and ASD genetics, predicts social prognosis, and could improve power in clinical trials. Exploiting face processing in patients with ASD The heterogeneity observed in patients with autism spectrum disorder (ASD) highlights the need for better patient stratification methods. Here, Mason et al. evaluated the use of the speed of early-stage face processing (N170 latency) for patient stratification and prognosis in subjects with ASD and age-matched healthy individuals. N170 latency was slower in individuals with ASD and correlated with response to faces measured with fMRI and with polygenic risk score. Among subjects with ASD, the N170 values stratified patients according to socialization prognosis and improved power in a simulated clinical trial. The results suggest that including N170 evaluation in patient stratification might help the design and development of patient-specific therapies for ASD.
Two types of human TCR differentially regulate reactivity to self and non-self antigens
Assya Trofimov
Philippe Brouillard
Jean-David Larouche
Jonathan Séguin
Jean-Philippe Laverdure
Ann Brasey
Grégory Ehx
Denis-Claude Roy
Lambert Busque
Silvy Lachance
Claude Perreault