M. Albert Basson

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Professor of Neuroscience and Epigenetic

University of Exeter

United Kingdom

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About

Professor M. Albert Basson is a faculty member in the Department of Neuroscience and Epigenetics at the University of Exeter, UK. His research primarily focuses on neurodevelopmental disorders, including the role of various genes in memory consolidation and neuronal health. Recent publications highlight his work on the implications of chromatin remodeling factors in neurological conditions and the development of animal models for autism spectrum disorders.

Recent Grants

Grant: Close

Linking genotype to phenotype in autism: mechanisms of cell-type specific presynaptic dysfunction in Chd8 haploinsufficiency

Open Date: 2023-02-01

Close Date: 2026-01-01

Grant: Open

The role of cerebellar inhibitory interneurons in neurodevelopmental disorders

Open Date: 2022-07-01

Close Date: 2027-06-01

Grant: Close

Identifying Epigenetic Drivers of Neuro-Immune Abnormalities Which Influence Hippocampal Ageing

Open Date: 2021-10-01

Close Date: 2024-09-01

Grant: Close

Can learning deficits in neurodevelopmental disorders be reversed by restoring gene function in the adult brain?

Open Date: 2021-09-30

Close Date: 2023-09-29

Grant: Close

Targeting histonedemethylation to reverse age-relatedcognitive decline

Open Date: 2021-09-30

Close Date: 2025-09-29

Articles (13)

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2024

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2024

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2024

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2023

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2022

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2021

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2021

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2021

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2021

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2021

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2021

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2021

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2021

Collaborators (22)

Cathy Fernandes

King’s College London

UNITED KINGDOM

M. Albert Basson

Research Interests

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About

Recent Grants

Articles (13)

The intellectual disability risk gene Kdm5b regulates long term memory consolidation in the hippocampus

Neurodevelopmental functions of CHD8: new insights and questions

The intellectual disability risk gene Kdm5b regulates long term memory consolidation in the hippocampus

Pervasive cortical and white matter anomalies in a mouse model for CHARGE syndrome

CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicing

A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia

Inositol treatment inhibits medulloblastoma through suppression of epigenetic-driven metabolic adaptation

Effects of Low-Dose Gestational TCDD Exposure on Behavior and on Hippocampal Neuron Morphology and Gene Expression in Mice

ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder

Distinct, dosage-sensitive requirements for the autism-associated factor CHD8 during cortical development

Brain mapping across 16 autism mouse models reveals a spectrum of functional connectivity subtypes

Cell-type-specific synaptic imbalance and disrupted homeostatic plasticity in cortical circuits of ASD-associated Chd8 haploinsufficient mice

The chromatin remodelling factor Chd7 protects auditory neurons and sensory hair cells from stress-induced degeneration

Collaborators (22)

Cathy Fernandes

Hywel Williams

Takshashila Tripathi

Steven Pollard

Alessio Delogu

Yau Mun Lim

ANTONELLA LETTIERI

Jeremy Green

Lorcan Browne

Sebastian Brandner

Maria Victoria Niklison Chirou

James Cain

Michela Matteoli

Karen Low

Olivier Brock

Silvia Marino

Davide Pozzi

Marta Biagioli

Erik Dassi

Laura Andreae

Valerio Zerbi

Richard Ewald Rosch

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