Yi W. Tay

Kuala Lumpur, Malaysia

Last Updated: 09/26/2026

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Found 38 publications

Optimizing participant recruitment and retention in clinical studies by hearing the voice of persons with Parkinson's.

Optimizing participant recruitment and retention in clinical studies by hearing the voice of persons with Parkinson's.

Journal: Journal of Parkinson's disease

Published: August 14, 2026

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2026

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

GCH1 p.Ser80Asn Confers Risk for Parkinson's Disease in East Asian Populations.

Journal: medRxiv : the preprint server for health sciences

Published: July 03, 2026

Multi-ancestry analysis of POLG variants in Parkinson's disease.

Multi-ancestry analysis of POLG variants in Parkinson's disease.

Journal: medRxiv : the preprint server for health sciences

Published: June 22, 2026

Groaning in Progressive Supranuclear Palsy: Insights From a Large Asian Cohort.

Groaning in Progressive Supranuclear Palsy: Insights From a Large Asian Cohort.

Journal: Movement disorders clinical practice

Published: June 12, 2026

The Global Parkinson's Genetics Program (GP2): Advancing genetic discovery and capacity building worldwide.

The Global Parkinson's Genetics Program (GP2): Advancing genetic discovery and capacity building worldwide.

Journal: Journal of Parkinson's disease

Published: May 20, 2026

Utility of the Short Cognitive and Neuropsychiatric Assessment Scale (ShoCo) in a multiethnic Asian cohort of patients with progressive supranuclear palsy.

Utility of the Short Cognitive and Neuropsychiatric Assessment Scale (ShoCo) in a multiethnic Asian cohort of patients with progressive supranuclear palsy.

Journal: Parkinsonism & related disorders

Published: March 15, 2026

Is SORL1 a common genetic target across neurodegenerative diseases? A multi-ancestry biobank study.

Is SORL1 a common genetic target across neurodegenerative diseases? A multi-ancestry biobank study.

Journal: Brain : a journal of neurology

Published: February 27, 2026

Is SORL1 a common genetic target across neurodegenerative diseases?: A multi-ancestry biobank scale assessment.

Is SORL1 a common genetic target across neurodegenerative diseases?: A multi-ancestry biobank scale assessment.

Journal: medRxiv : the preprint server for health sciences

Published: February 06, 2026

Ex Vivo LRRK2 Activation in Asian G2385R and R1628P Variant Carriers and Idiopathic Parkinson's Disease.

Ex Vivo LRRK2 Activation in Asian G2385R and R1628P Variant Carriers and Idiopathic Parkinson's Disease.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: November 17, 2025

"Subthreshold" Expansions in Individuals With Otherwise-Typical Clinicoradiological Features of GAA-FGF14-Related Cerebellar Ataxia (SCA27B).

"Subthreshold" Expansions in Individuals With Otherwise-Typical Clinicoradiological Features of GAA-FGF14-Related Cerebellar Ataxia (SCA27B).

Journal: Journal of movement disorders

Published: November 01, 2025

Validation of a Mitochondrial Polygenic Score for Parkinson's Disease.

Validation of a Mitochondrial Polygenic Score for Parkinson's Disease.

Journal: medRxiv : the preprint server for health sciences

Published: October 01, 2025

Showing 1-12 of 38

Last Updated: 09/26/2026