Bonnie Nijhof

Mutations in DDHD2, encoding an intracellular phospholipase A(1), cause a recessive form of complex hereditary spastic paraplegia.

Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.

CEP89 is required for mitochondrial metabolism and neuronal function in man and fly.

GATAD2B loss-of-function mutations cause a recognisable syndrome with intellectual disability and are associated with learning deficits and synaptic undergrowth in Drosophila.

Human intellectual disability genes form conserved functional modules in Drosophila.

Ubiquitin ligase HUWE1 regulates axon branching through the Wnt/β-catenin pathway in a Drosophila model for intellectual disability.

Drosophila models of early onset cognitive disorders and their clinical applications.

Age-related decreased inhibitory vs. excitatory gene expression in the adult autistic brain.

Converging evidence does not support GIT1 as an ADHD risk gene.

Systematic Phenomics Analysis Deconvolutes Genes Mutated in Intellectual Disability into Biologically Coherent Modules.

A New Fiji-Based Algorithm That Systematically Quantifies Nine Synaptic Parameters Provides Insights into Drosophila NMJ Morphometry.

BOD1 Is Required for Cognitive Function in Humans and Drosophila.

A homozygous FITM2 mutation causes a deafness-dystonia syndrome with motor regression and signs of ichthyosis and sensory neuropathy.