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Publications by Henry Houlden

Towards a Complete Resolution of the Genetic Architecture of Disease

Trends in Genetics

English

Mutations in XRCC1 Cause Cerebellar Ataxia and Peripheral Neuropathy

Journal of Neurology, Neurosurgery and Psychiatry

English

Practical Approach to the Diagnosis of Adult-Onset Leukodystrophies: An Updated Guide in the Genomic Era

Journal of Neurology, Neurosurgery and Psychiatry

English

Adult Leukodystrophy: Multi-Disciplinary Structured Approach

Journal of Neurology, Neurosurgery and Psychiatry

English

Truncating Mutations inSPASTpatients Are Associated With a High Rate of Psychiatric Comorbidities in Hereditary Spastic Paraplegia

Journal of Neurology, Neurosurgery and Psychiatry

English

Investigation of Somatic CNVs in Brains of Synucleinopathy Cases Using Targeted SNCA Analysis and Single Cell Sequencing

Acta neuropathologica communications

Forensic Medicine

Molecular Neuroscience

English

Hereditary Sensory Neuropathy Type 1 Is Caused by the Accumulation of Two Neurotoxic Sphingolipids

Journal of Biological Chemistry

Molecular Biology

English

NeuroChip, an Updated Version of the NeuroX Genotyping Platform to Rapidly Screen for Variants Associated With Neurological Diseases

Neurobiology of Aging

Developmental Biology

English

Multiple System Atrophy Is Not Caused by C9orf72 Hexanucleotide Repeat Expansions

Neurobiology of Aging

Developmental Biology

English

Familial Childhood-Onset Progressive Cerebellar Syndrome Associated With theATP1A3mutation

Neurology: Genetics

English