Kathryn Peall

23PUBLICATIONS
51CO-AUTHORS
Neurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)Infant and child healthPharmacogenomicsEpigenetics (incl. genome methylation and epigenomics)
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Publications (23)

|Oct 05, 2026
Defining the Clinical Phenotypic Ground Truth: Expert Interrater Agreement in Hyperkinetic Movement Disorders.

|Dec 16, 2025
Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia.

Darren Cameron, Nicholas E Clifton, Daniel Cabezas de la Fuente

|Oct 17, 2025
Nonmotor Symptom Scales in Children With Movement Disorders: A Scoping Review.

Clément Desjardins, Christelle Nilles, Hortensia Gimeno

|Sep 11, 2025
Mapping the distribution of neurotransmitters to resting-state functional connectivity in Parkinson's disease.

Weihua Li, Nicholas P Lao-Kaim, Runtian Li

|Jul 25, 2025
Transcriptomic disruption and hypoactivity in DYT-SGCE medial ganglionic eminence-patterned inhibitory neurons.

Zongze Li, Laura Abram, Maria Cruz-Santos

|Sep 27, 2024
Deciphering the Pathophysiological Mechanisms Underpinning Myoclonus Dystonia Using Pluripotent Stem Cell-Derived Cellular Models.

Zongze Li, Laura Abram, Kathryn J Peall

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Frequent Collaborators

3 joint publications

Marina Tijssen

3 joint publications

Grace A Bailey

3 joint publications

Emmanuel Roze

3 joint publications

Clément Desjardins