# Kailash P. Bhatia

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/kailash-p-bhatia/

## Facts

| Field | Value |
| --- | --- |
| Citations | 62,194 |
| Field | Neurological disorders and treatments |
| h-index | 117 |
| i10-index | 617 |
| Last Known Institution | Queen Mary University of London |
| OpenAlex ID | https://openalex.org/A5103157576 |
| ORCID iD | https://orcid.org/0000-0001-8185-286X |
| Works | 1,597 |

## Researcher papers

- [Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria](https://scholariq.org/papers/clinical-diagnosis-of-progressive-supranuclear-palsy-the-movement-disorder/)
- [Criteria for the diagnosis of corticobasal degeneration](https://scholariq.org/papers/criteria-for-the-diagnosis-of-corticobasal-degeneration/)
- [Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study](https://scholariq.org/papers/phenotype-genotype-and-worldwide-genetic-penetrance-of-lrrk2-associated/)
- [Consensus Statement on the classification of tremors. from the task force on tremor of the International Parkinson and Movement Disorder Society](https://scholariq.org/papers/consensus-statement-on-the-classification-of-tremors-from-the-task-force-on/)
- [Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease](https://scholariq.org/papers/excessive-burden-of-lysosomal-storage-disorder-gene-variants-in-parkinson-s/)
- [Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease](https://scholariq.org/papers/unbiased-screen-for-interactors-of-leucine-rich-repeat-kinase-2-supports-a/)
- [Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions](https://scholariq.org/papers/mutations-in-the-gene-prrt2-cause-paroxysmal-kinesigenic-dyskinesia-with/)
- [Genetic and phenotypic characterization of complex hereditary spastic paraplegia](https://scholariq.org/papers/genetic-and-phenotypic-characterization-of-complex-hereditary-spastic-paraplegia/)
- [Complex movement disorders at disease onset in childhood narcolepsy with cataplexy](https://scholariq.org/papers/complex-movement-disorders-at-disease-onset-in-childhood-narcolepsy-with/)
- [Which ante mortem clinical features predict progressive supranuclear palsy pathology?](https://scholariq.org/papers/which-ante-mortem-clinical-features-predict-progressive-supranuclear-palsy/)

## Researcher topics

- [Neurological disorders and treatments](https://scholariq.org/topics/neurological-disorders-and-treatments/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Botulinum Toxin and Related Neurological Disorders](https://scholariq.org/topics/botulinum-toxin-and-related-neurological-disorders/)
- [Glycogen Storage Diseases and Myoclonus](https://scholariq.org/topics/glycogen-storage-diseases-and-myoclonus/)

## Researcher university

- [Queen Mary University of London](https://scholariq.org/institutions/queen-mary-university-of-london/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.