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Publications by Mina Ryten

Rare Coding Variants in the Phospholipase D3 Gene Confer Risk for Alzheimer’s Disease

Nature
Multidisciplinary
2013English

LRP10 in Α-Synucleinopathies

The Lancet Neurology
Neurology
2018English

Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome

American Journal of Human Genetics
Genetics
2015English

Variation at the TRIM11 Locus Modifies Progressive Supranuclear Palsy Phenotype

Annals of Neurology
Neurology
2018English

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

Neurobiology of Aging
AgingGerontologyDevelopmental BiologyGeriatricsNeuroscienceNeurology
2017English

Analysis of Brain Atrophy and Local Gene Expression Implicates Astrocytes in Frontotemporal Dementia

2019English

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