Kailash P. Bhatia

Research interests

Publications

• Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria

  Movement Disorders · 2017 · https://doi.org/10.1002/mds.26987

• Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease

  Brain · 2017 · https://doi.org/10.1093/brain/awx285

• Treatable inherited rare movement disorders

  Movement Disorders · 2017 · https://doi.org/10.1002/mds.27140

• Consensus Statement on the classification of tremors. from the task force on tremor of the International Parkinson and Movement Disorder Society

  Movement Disorders · 2017 · https://doi.org/10.1002/mds.27121

• Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia

  Nature Genetics · 2016 · https://doi.org/10.1038/ng.3740

• Genetic and phenotypic characterization of complex hereditary spastic paraplegia

  Brain · 2016 · https://doi.org/10.1093/brain/aww111

• Pallidal neurostimulation in patients with medication-refractory cervical dystonia: a randomised, sham-controlled trial

  The Lancet Neurology · 2014 · https://doi.org/10.1016/s1474-4422(14)70143-7

• Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers

  Brain · 2014 · https://doi.org/10.1093/brain/awu179

• Loss of sensory attenuation in patients with functional (psychogenic) movement disorders

  Brain · 2014 · https://doi.org/10.1093/brain/awu237

• Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

  Proceedings of the National Academy of Sciences · 2014 · https://doi.org/10.1073/pnas.1318306111

• Beta-propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation

  Brain · 2013 · https://doi.org/10.1093/brain/awt095

• Phenomenology and classification of dystonia: A consensus update

  Movement Disorders · 2013 · https://doi.org/10.1002/mds.25475

• Criteria for the diagnosis of corticobasal degeneration

  Neurology · 2013 · https://doi.org/10.1212/wnl.0b013e31827f0fd1

• Mutations in the Gene PRRT2 Cause Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions

  Cell Reports · 2012 · https://doi.org/10.1016/j.celrep.2011.11.001

• Mutations in the autoregulatory domain of β‐tubulin 4a cause hereditary dystonia

  Annals of Neurology · 2012 · https://doi.org/10.1002/ana.23832

• Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA

  The American Journal of Human Genetics · 2012 · https://doi.org/10.1016/j.ajhg.2012.10.019

• Neuroimaging Features of Neurodegeneration with Brain Iron Accumulation

  American Journal of Neuroradiology · 2011 · https://doi.org/10.3174/ajnr.a2677

• Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations

  Neurobiology of Aging · 2010 · https://doi.org/10.1016/j.neurobiolaging.2010.05.009

• ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation

  Movement Disorders · 2010 · https://doi.org/10.1002/mds.22947

• Early‐onset L‐dopa‐responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations

  Movement Disorders · 2010 · https://doi.org/10.1002/mds.23221

• A common polymorphism in the brain‐derived neurotrophic factor gene ( BDNF ) modulates human cortical plasticity and the response to rTMS

  The Journal of Physiology · 2008 · https://doi.org/10.1113/jphysiol.2008.159905

• Characterization of PLA2G6 as a locus for dystonia‐parkinsonism

  Annals of Neurology · 2008 · https://doi.org/10.1002/ana.21415

• GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak

  Journal of Clinical Investigation · 2008 · https://doi.org/10.1172/jci34438

• Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

  The Lancet Neurology · 2008 · 10.1016/s1474-4422(08)70117-0

• A systematic review on the diagnosis and treatment of primary (idiopathic) dystonia and dystonia plus syndromes: report of an EFNS/MDS‐ES Task Force

  European Journal of Neurology · 2006 · https://doi.org/10.1111/j.1468-1331.2006.01537.x

• A common LRRK2 mutation in idiopathic Parkinson's disease

  The Lancet · 2005 · 10.1016/s0140-6736(05)17830-1

• Theta Burst Stimulation of the Human Motor Cortex

  Neuron · 2005 · https://doi.org/10.1016/j.neuron.2004.12.033

• SIC Task Force appraisal of clinical diagnostic criteria for parkinsonian disorders

  Movement Disorders · 2003 · 10.1002/mds.10459

• Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

  Neurology · 2001 · https://doi.org/10.1212/wnl.56.12.1702

• Autosomal Dominant Nocturnal Frontal-Lobe Epilepsy: Genetic Heterogeneity and Evidence for a Second Locus at 15q24

  The American Journal of Human Genetics · 1998 · https://doi.org/10.1086/302047

• Autosomal dominant nocturnal frontal lobe epilepsy

  Brain · 1995 · https://doi.org/10.1093/brain/118.1.61

Current projects

No projects listed.