Author: Kailash P Bhatia

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Preprints

Whole genome sequencing for diagnosis of neurological repeat expansion disorders

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Non-invasive Amelioration of Essential Tremor via Phase-Locked Disruption of its Temporal Coherence

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  • In neuroscience: 8,653
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Transcriptomic analysis of dystonia-associated genes reveals functional convergence within specific cell types and shared neurobiology with psychiatric disorders

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  • In genetics: 3,252
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Bi-allelic variants in TSPOAP1, encoding the active zone protein RIMBP1, cause autosomal recessive dystonia

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  • In genetics: 3,301
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Lysosomal enzyme deficiency and GBA mutations in Dystonia

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