Portrait of Julien Cohen-Adad

Julien Cohen-Adad

Associate Academic Member
Associate Professor, Polytechnique Montréal, Electrical Engineering Department
Adjunct Professor, Université de Montréal, Department of Neuroscience
Research Topics
Medical Machine Learning

Biography

Julien Cohen-Adad is a professor at Polytechnique Montréal and the associate director of the Neuroimaging Functional Unit at Université de Montréal. He is also the Canada Research Chair in Quantitative Magnetic Resonance Imaging.

His research focuses on advancing neuroimaging methods with the help of AI. Some examples of projects are:

- Multi-modal training for medical imaging tasks (segmentation of pathologies, diagnosis, etc.)

- Adding prior from MRI physics to improve model generalization

- Incorporating uncertainty measures to deal with inter-rater variability

- Continuous learning strategies when data sharing is restricted

- Bringing AI methods into clinical radiology routine via user-friendly software solutions

Cohen-Adad also leads multiple open-source software projects that are benefiting the research and clinical community (see neuro.polymtl.ca/software.html). In short, he loves MRI with strong magnets, neuroimaging, programming and open science!

Current Students

PhD - Polytechnique Montréal
Master's Research - Polytechnique Montréal
Master's Research - Polytechnique Montréal
PhD - Polytechnique Montréal

Publications

Microscopy-BIDS: An Extension to the Brain Imaging Data Structure for Microscopy Data
Marie-Hélène Bourget
Lee Kamentsky
Satrajit S. Ghosh
Giacomo Mazzamuto
Alberto Lazari
Christopher J. Markiewicz
Robert Oostenveld
Guiomar Niso
Yaroslav O. Halchenko
Ilona Lipp
Sylvain Takerkart
Paule-Joanne Toussaint
Ali R. Khan
Gustav Nilsonne
Filippo Maria Castelli
Stefan Ross Eric Franklin Anthony Rémi Christopher J. Taylor Appelhoff
The Brain Imaging Data Structure (BIDS) is a specification for organizing, sharing, and archiving neuroimaging data and metadata in a reusab… (see more)le way. First developed for magnetic resonance imaging (MRI) datasets, the community-led specification evolved rapidly to include other modalities such as magnetoencephalography, positron emission tomography, and quantitative MRI (qMRI). In this work, we present an extension to BIDS for microscopy imaging data, along with example datasets. Microscopy-BIDS supports common imaging methods, including 2D/3D, ex/in vivo, micro-CT, and optical and electron microscopy. Microscopy-BIDS also includes comprehensible metadata definitions for hardware, image acquisition, and sample properties. This extension will facilitate future harmonization efforts in the context of multi-modal, multi-scale imaging such as the characterization of tissue microstructure with qMRI.
Rapid, automated nerve histomorphometry through open-source artificial intelligence
Simeon Christian Daeschler
Marie-Hélène Bourget
Dorsa Derakhshan
Vasudev Sharma
Stoyan Ivaylov Asenov
Tessa Gordon
Gregory Howard Borschel
We aimed to develop and validate a deep learning model for automated segmentation and histomorphometry of myelinated peripheral nerve fibers… (see more) from light microscopic images. A convolutional neural network integrated in the AxonDeepSeg framework was trained for automated axon/myelin segmentation using a dataset of light-microscopic cross-sectional images of osmium tetroxide-stained rat nerves including various axonal regeneration stages. In a second dataset, accuracy of automated segmentation was determined against manual axon/myelin labels. Automated morphometry results, including axon diameter, myelin sheath thickness and g-ratio were compared against manual straight-line measurements and morphometrics extracted from manual labels with AxonDeepSeg as a reference standard. The neural network achieved high pixel-wise accuracy for nerve fiber segmentations with a mean (± standard deviation) ground truth overlap of 0.93 (± 0.03) for axons and 0.99 (± 0.01) for myelin sheaths, respectively. Nerve fibers were identified with a sensitivity of 0.99 and a precision of 0.97. For each nerve fiber, the myelin thickness, axon diameter, g-ratio, solidity, eccentricity, orientation, and individual x -and y-coordinates were determined automatically. Compared to manual morphometry, automated histomorphometry showed superior agreement with the reference standard while reducing the analysis time to below 2.5% of the time needed for manual morphometry. This open-source convolutional neural network provides rapid and accurate morphometry of entire peripheral nerve cross-sections. Given its easy applicability, it could contribute to significant time savings in biomedical research while extracting unprecedented amounts of objective morphologic information from large image datasets.
Comparison of multi-center MRI protocols for visualizing the spinal cord gray matter
Eva Alonso-Ortiz
Stephanie Alley
Maria Marcella Laganà
Francesca Baglio
Signe Johanna Vannesjo
Haleh Karbasforoushan
Maryam Seif
Alan C. Seifert
Junqian Xu
Joo-Won Kim
René Labounek
Lubomír Vojtíšek
Marek Dostál
Rebecca S. Samson
Francesco Grussu
Marco Battiston
Claudia A. M. Gandini Wheeler-Kingshott
Marios C. Yiannakas … (see 4 more)
Guillaume Gilbert
Torben Schneider
Brian Johnson
Ferrán Prados
We propose quality assessment criteria and metrics for gray‐matter visualization and apply them to different protocols. The proposed crite… (see more)ria and metrics, the analyzed protocols, and our open‐source code can serve as a benchmark for future optimization of spinal cord gray‐matter imaging protocols.
Reproducibility and Evolution of Diffusion Mri Measurements Within the Cervical Spinal Cord in Multiple Sclerosis
Haykel Snoussi
Emmanuel Caruyer
Benoit Combes
Olivier Commowick
Élise Bannier
Anne Kerbrat
Christian Barillot
In Multiple Sclerosis (MS), there is a large discrepancy between the clinical observations and how the pathology is exhibited on brain image… (see more)s, this is known as the clinical-radiological paradox. One of the hypotheses is that the clinical deficit may be more related to the spinal cord damage than the number or location of lesions in the brain. Therefore, investigating how the spinal cord is damaged becomes an acute challenge to better understand and overcome this paradox. Diffusion MRI is known to provide quantitative figures of neuronal degeneration and axonal loss, in the brain as well as in the spinal cord. In this paper, we propose to investigate how diffusion MRI metrics vary in the different cervical regions with the progression of the disease. We first study the reproducibility of diffusion MRI on healthy volunteers with a test-retest procedure using both standard diffusion tensor imaging (DTI) and multi-compartment Ball-and-Stick models. Then, based on the test re-test quantitative calibration, we provide quantitative figures of pathology evolution between M0 and M12 in the cervical spine on a set of 31 MS patients, exhibiting how the pathology damage spans in the cervical spinal cord.
Medical Image Segmentation on MRI Images with Missing Modalities: A Review
Reza Azad
Nika Khosravi
Mohammad Dehghanmanshadi
Dorit Merhof
Quantitative electrophysiological assessments as predictive markers of lower limb motor recovery after spinal cord injury: a pilot study with an adaptive trial design
Yin Nan Huang
El-Mehdi Meftah
Charlotte H. Pion
Jean-Marc Mac-Thiong
Dorothy Barthélemy
Observational, cohort study. (1) Determine the feasibility and relevance of assessing corticospinal, sensory, and spinal pathways early aft… (see more)er traumatic spinal cord injury (SCI) in a rehabilitation setting. (2) Validate whether electrophysiological and magnetic resonance imaging (MRI) measures taken early after SCI could identify preserved neural pathways, which could then guide therapy. Intensive functional rehabilitation hospital (IFR). Five individuals with traumatic SCI and eight controls were recruited. The lower extremity motor score (LEMS), electrical perceptual threshold (EPT) at the S2 dermatome, soleus (SOL) H-reflex, and motor evoked potentials (MEPs) in the tibialis anterior (TA) muscle were assessed during the stay in IFR and in the chronic stage (>6 months post-SCI). Control participants were only assessed once. Feasibility criteria included the absence of adverse events, adequate experimental session duration, and complete dataset gathering. The relationship between electrophysiological data collected in IFR and LEMS in the chronic phase was studied. The admission MRI was used to calculate the maximal spinal cord compression (MSCC). No adverse events occurred, but a complete dataset could not be collected for all subjects due to set-up configuration limitations and time constraints. EPT measured at IFR correlated with LEMS in the chronic phases (r = −0.67), whereas SOL H/M ratio, H latency, MEPs and MSCC did not. Adjustments are necessary to implement electrophysiological assessments in an IFR setting. Combining MRI and electrophysiological measures may lead to better assessment of neuronal deficits early after SCI.
Advanced Diffusion MR Imaging for Multiple Sclerosis in the Brain and Spinal Cord
Masaaki Hori
Tomoko Maekawa
Kouhei Kamiya
Akifumi Hagiwara
Masami Goto
Mariko Yoshida Takemura
Shohei Fujita
Christina Andica
Koji Kamagata
Shigeki Aoki
Diffusion tensor imaging (DTI) has been established its usefulness in evaluating normal-appearing white matter (NAWM) and other lesions that… (see more) are difficult to evaluate with routine clinical MRI in the evaluation of the brain and spinal cord lesions in multiple sclerosis (MS), a demyelinating disease. With the recent advances in the software and hardware of MRI systems, increasingly complex and sophisticated MRI and analysis methods, such as q-space imaging, diffusional kurtosis imaging, neurite orientation dispersion and density imaging, white matter tract integrity, and multiple diffusion encoding, referred to as advanced diffusion MRI, have been proposed. These are capable of capturing in vivo microstructural changes in the brain and spinal cord in normal and pathological states in greater detail than DTI. This paper reviews the current status of recent advanced diffusion MRI for assessing MS in vivo as part of an issue celebrating two decades of magnetic resonance in medical sciences (MRMS), an official journal of the Japanese Society of Magnetic Resonance in Medicine.
Erratum to: Rapid simultaneous acquisition of macromolecular tissue volume, susceptibility, and relaxometry maps (Magn Reson Med. 2022;87:781‐790.)
Fang Frank Yu
Susie Yi Huang
Ashwin Kumar
Thomas Witzel
Congyu Liao
Tanguy Duval
Berkin Bilgic
Brain-spinal cord interaction in long-term motor sequence learning in human: An fMRI study
Ali Khatibi
Shahabeddin Vahdat
Ovidiu Lungu
Jürgen Finsterbusch
Christian Büchel
Veronique Marchand-Pauvert
Julien Doyon
Titre: Title: Comparison of Myelin Imaging Techniques in Ex Vivo Spinal Cord Auteur:
Nikola Stikov
Manh-Tung Vuong
Vuong Manh Tung
Myelin is a dielectric material that wraps around the axons of nerve fibers to enable fast conduction of signals throughout the nervous syst… (see more)em. Loss of myelin can cause anywhere from minor interruption to complete disruption of nerve impulses in a range of neurodegenerative diseases such as multiple sclerosis and Parkinson’s disease. There is an ongoing debate in the myelin imaging community about which biomarker based on Magnetic Resonance Imaging (MRI) is more correlated with myelin. In this work, we implemented and compared several MRI-based myelin imaging techniques (quantitative magnetization transfer imaging, myelin water imaging, and proton density imaging) by evaluating their repeatability and their relation to large-scale histology in the ex vivo spinal cords of a rat, a dog, and a human. While there are studies investigating the relationship between pairs of them as well as with histology, to the best of our knowledge, this is the first study that implemented and compared all those methods at the same time to evaluate their reproducibility and their correlation with myelin. Qualitatively the contrasts were similar, and all techniques had comparable scan-rescan and correlations with histology. Surprisingly, the voxel-wise correlations between the various myelin measures were almost as high as the scan-rescan correlations. The correlations decreased when only white matter was considered, which could be due to the small dynamic range of the measurement, or due to artifacts related to the preparation and panoramic scanning of the tissue. We conclude that the myelin imaging techniques explored in this thesis exhibit similar specificity to myelin, yet the histological correlations suggest that more work is needed to determine the optimal myelin imaging protocol. The study also pointed out some potential miscalibrations during acquisitions as well as data processing that may lead to anywhere from minor to major impact on the accuracy of the results. These include B1 mapping, insufficient spoiling and variation of the predelay time. We have also standardized the data processing routines by upgrading qMTLab to qMRLab which adds several quantitative MR methods to the toolbox, such as standard T1 mapping and field mapping. In addition, the data of the dog spinal cord in this study will be published together with the analysis scripts to help the interested reader to reproduce the findings from this thesis.
The Myelin-Weighted Connectome in Parkinson's Disease
Tommy Boshkovski
Bratislav Misic
Isabelle Arnulf
Jean-Christophe Corvol
Marie Vidailhet
Stéphane Lehéricy
Nikola Stikov
Matteo Mancini
Even though Parkinson's disease (PD) is typically viewed as largely affecting gray matter, there is growing evidence that there are also str… (see more)uctural changes in the white matter. Traditional connectomics methods that study PD may not be specific to underlying microstructural changes, such as myelin loss. The primary objective of this study is to investigate the PD‐induced changes in myelin content in the connections emerging from the basal ganglia and the brainstem. For the weighting of the connectome, we used the longitudinal relaxation rate as a biologically grounded myelin‐sensitive metric. We computed the myelin‐weighted connectome in 35 healthy control subjects and 81 patients with PD. We used partial least squares to highlight the differences between patients with PD and healthy control subjects. Then, a ring analysis was performed on selected brainstem and subcortical regions to evaluate each node's potential role as an epicenter for disease propagation. Then, we used behavioral partial least squares to relate the myelin alterations with clinical scores. Most connections (~80%) emerging from the basal ganglia showed a reduced myelin content. The connections emerging from potential epicentral nodes (substantia nigra, nucleus basalis of Meynert, amygdala, hippocampus, and midbrain) showed significant decrease in the longitudinal relaxation rate (P  0.05). This effect was not seen for the medulla and the pons. The myelin‐weighted connectome was able to identify alteration of the m
Reduced Axon Calibre in the Associative Striatum of the Sapap3 Knockout Mouse
Eliana Lopes Rio da Silva Lousada
Mathieu Boudreau
Julien Cohen‐Adad
Brahim Nait‐Oumesmar
Eric Burguière
Christiane Schreiweis
Pathological repetitive behaviors are a common feature of different neuropsychiatric disorders such as obsessive-compulsive disorder or Gill… (see more)es de la Tourette syndrome. The Sapap3 knockout mouse (Sapap3-KO) is the current reference model used in translational psychiatry to study co-morbid repetitive behaviors, presenting both compulsive-like as well as tic-like behaviors. Consistent with clinical and fundamental research literature relating compulsive-like symptoms to associative cortico-striatal dysfunctions and tic-like symptoms to sensorimotor cortico-striatal dysfunctions, abnormalities comprising both circuits have been described in this mouse model. Findings reported on these mice point towards not only macro-, but also micro-circuitry deficits, both of which can be affected by neuronal structural changes. As such, in the present study, we aimed to investigate structural changes in associative and sensorimotor striatal areas that could affect information conduction. We used AxonDeepSeg, an open-source software to automatically segment and measure myelin thickness and axon caliber, and found that axon caliber, the main contributor for changes in conduction speed, is specifically reduced in the associative but not the sensorimotor striatum of the Sapap3-KO mouse. This smaller axon caliber in Sapap3-KO mice is not a general neuronal feature of this region, but specific to a subpopulation of axons with large caliber. These results point to a primary structural deficit in the associative striatum, affecting signal conduction and consequent connectivity.