Mayada Elsabbagh

Assistant Professor
McGill University

Mayada Elsabbagh is associate professor of neurology and neurosurgery at the Montreal Neurological Institute at McGill University in Canada. Her research focuses on understanding the root causes of autism and tracing its developmental pathways. The approach combines innovative research with the mission of accelerating the translation of scientific discoveries into community impact. Elsabbagh’s contributions include the discovery of early brain-function markers for autism prior to the onset of behavioral signs. She has supported the successful launch of several collaborative research and translational networks aimed at accelerating the pace of discovery in autism. This includes the Transforming Autism Care Consortium, a Québec research network supported by the Fonds de recherche du Québec-Santé and several community partners. She is also active in global efforts to improve evidence-based practice in the community and capacity-building in low- and middle-income countries. The public value and social relevance of Elsabbagh’s research has been recognized through various awards, including the Neville Butler Memorial Prize and the British Psychological Society Neil O’Conner Prize.

From this contributor

Explore more from The Transmitter

Research image of a fiber optic implant in a mouse brain.

Bespoke photometry system captures variety of dopamine signals in mice

The tool tracks the excitation of an engineered protein that senses dopamine’s absolute levels, including fast and slow fluctuations in real time, and offers new insights into how the signals change across the brain.

By Sydney Wyatt
21 March 2025 | 5 min read
Cognitive neuroscientist Nick Turk-Browne helps an infant into an fMRI machine.

What infant fMRI is revealing about the developing mind

Cognitive neuroscientists have finally clocked how to perform task-based functional MRI experiments in awake babies—long known for their inability to lie still or take direction. Next, they aim to watch cognition take shape and settle a debate about our earliest memories—with one group publishing a big clue today.

By Calli McMurray
20 March 2025 | 12 min read
A mouse sits on a gloved hand.

Molecular changes after MECP2 loss may drive Rett syndrome traits

Knocking out the gene in adult mice triggered up- and down-regulated expression of myriad genes weeks before there were changes in neuronal function.

By Chloe Williams
20 March 2025 | 5 min read