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Paula Marques

Assistant Professor

McMaster University

Canada

Research Interests

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About

Paula Marques is an Assistant Professor at McMaster University in Canada. Her research focuses on genetic epilepsy, neurodevelopmental disorders, and the implications of genetic variants on surgical outcomes in drug-resistant epilepsy. Recent articles include investigations into Dravet syndrome and the developmental and epileptic encephalopathies associated with genetic variations. Dr. Marques also studies the broader impacts of functional impairment in neurological conditions.

Articles (17)

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2025

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2020

Collaborators (10)

Roland Krause

Research Scientist

University of Luxembourg

LUXEMBOURG

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Ilakkiah Chandran

University of Toronto

CANADA

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Lara Marcuse

Professor

Icahn School of Medicine at Mount Sinai

UNITED STATES

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Caroline Cusick

Broad Institute

UNITED STATES

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Allan Bayat

University of Southern Denmark

DENMARK

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Robyn Whitney

McMaster University

CANADA

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Andreas Brunklaus

University of Glasgow

UNITED KINGDOM

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Toshimitsu Suzuki

Lecturer

Nagoya University

JAPAN

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Kazuhiro Yamakawa

Professor

Nagoya University

JAPAN

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Danielle M. Andrade

UNITED STATES

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Paula Marques

Research Interests

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About

Articles (17)

Evidence demands action: An invitation to share the burden of proof

Dravet syndrome: From neurodevelopmental to neurodegenerative disease?

Variants in ATP6V0C are associated with Dravet‐like developmental and epileptic encephalopathy

Women With Genetic Epilepsies

Severe Epilepsy in an Individual with a TSC2 R905Q Variant Prompting Late Diagnosis in Affected Family Members

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Do germline genetic variants influence surgical outcomes in drug-resistant epilepsy?

Transition in epilepsy – A pilot study with patients in and outside of academic centers

Functional impairment and post-stroke depression: a 6-month longitudinal study

Teaching NeuroImage: Ictal Pouting Associated With Focal Cortical Dysplasia and Frontal Seizures on Stereotactic Depth Electrode EEG

Progressive Worsening of Gait and Motor Abnormalities in Older Adults With Dravet Syndrome

Hyperammonemic Encephalopathy Associated with Perampanel: Case Report and Discussion

A systematic review of adults with Dravet syndrome

Genome sequencing identifies rare tandem repeat expansions and copy number variants in Lennox-Gastaut Syndrome

Starting stiripentol in adults with Dravet syndrome? Watch for ammonia and carnitine

Localized sporotrichosis during natalizumab treatment in Multiple Sclerosis

Metronidazole neurotoxicity in late liver transplantation

Collaborators (10)

Roland Krause

Ilakkiah Chandran

Lara Marcuse

Caroline Cusick

Allan Bayat

Robyn Whitney

Andreas Brunklaus

Toshimitsu Suzuki

Kazuhiro Yamakawa

Danielle M. Andrade

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