Yehani Wedatilake

Guilford Street
London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 17 publications

Artificial intelligence in drug development for delirium and Alzheimer's disease.

Artificial intelligence in drug development for delirium and Alzheimer's disease.

Journal: Acta pharmaceutica Sinica. B

Published: November 25, 2024

Female Reproductive Factors and Risk of Mild Cognitive Impairment and Dementia: The HUNT Study.

Female Reproductive Factors and Risk of Mild Cognitive Impairment and Dementia: The HUNT Study.

Journal: The journal of prevention of Alzheimer's disease

Published: July 24, 2024

A brain DNA co-methylation network analysis of psychosis in Alzheimer's disease.

A brain DNA co-methylation network analysis of psychosis in Alzheimer's disease.

Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association

Published: May 28, 2024

Number of children and dementia risk: a causal mediation analysis using data from the HUNT study linked with national registries in Norway.

Number of children and dementia risk: a causal mediation analysis using data from the HUNT study linked with national registries in Norway.

Journal: BMC neurology

Published: February 14, 2024

Genetic associations with psychosis and affective disturbance in Alzheimer's disease.

Genetic associations with psychosis and affective disturbance in Alzheimer's disease.

Journal: Alzheimer's & dementia (New York, N. Y.)

Published: April 27, 2023

Blood pressure trajectories over 35 years and dementia risk: A retrospective study: The HUNT study.

Blood pressure trajectories over 35 years and dementia risk: A retrospective study: The HUNT study.

Journal: Frontiers in aging neuroscience

Published: April 29, 2022

Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations.

Outcome of adult patients with X-linked hypophosphatemia caused by PHEX gene mutations.

Journal: Journal of inherited metabolic disease

Published: October 01, 2017

Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases.

Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases.

Journal: Annals of neurology

Published: June 13, 2017

Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.

Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.

Journal: Brain : a journal of neurology

Published: April 22, 2016

TRNT1 deficiency: clinical, biochemical and molecular genetic features.

TRNT1 deficiency: clinical, biochemical and molecular genetic features.

Journal: Orphanet journal of rare diseases

Published: March 09, 2016

Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease.

Neurophysiological profile of peripheral neuropathy associated with childhood mitochondrial disease.

Journal: Mitochondrion

Published: January 25, 2016

Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fission.

Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fission.

Journal: Brain : a journal of neurology

Published: January 28, 2015

Showing 1-12 of 17

Last Updated: 09/26/2026