Identification of GBA mutations among Neurodegenerative disease Patients from eastern India

Novel and reported variants in Parkinson's disease genes confer high disease burden among Indians

(2020) Sumeet Kumar et al.   PARKINSONISM & RELATED DISORDERS

The SPID-GBA study

(2020) Letizia Straniero et al.   Neurology-Genetics

Clinical and radiological profile of posterior cortical atrophy and comparison with a group of typical Alzheimer disease and amnestic mild cognitive impairment

(2020) Gautam Das et al.   ACTA NEUROLOGICA BELGICA

Glucocerebrosidase and Parkinson Disease: Molecular, Clinical, and Therapeutic Implications

(2018) Roberta Balestrino et al.   NEUROSCIENTIST

Integrated Genetic Analysis of Racial Differences of Common GBA Variants in Parkinson's Disease: A Meta-Analysis

(2018) Yuan Zhang et al.   Frontiers in Molecular Neuroscience

Lysosomal Dysfunction and α-Synuclein Aggregation in Parkinson's Disease: Diagnostic Links

(2016) Tim Moors et al.   MOVEMENT DISORDERS

Advances in GBA-associated Parkinson's disease – Pathology, presentation and therapies

(2016) Melinda Barkhuizen et al.   NEUROCHEMISTRY INTERNATIONAL

Effect ofGBAMutations on Phenotype of Parkinson’s Disease: A Study on Chinese Population and aMeta-Analysis

(2015) Yuan Zhang et al.   Parkinsons Disease

Dementia and Cognitive Impairment in Patients With Parkinson’s Disease From India

(2014) Jaya Sanyal et al.   American Journal of Alzheimers Disease and Other Dementias

The neurobiological basis of cognitive impairment in Parkinson's disease

(2014) Glenda M. Halliday et al.   MOVEMENT DISORDERS

Parkin-mediated ubiquitination of mutant glucocerebrosidase leads to competition with its substrates PARIS and ARTS

(2014) Inna Bendikov-Bar et al.   Orphanet Journal of Rare Diseases

Glucocerebrosidase mutations in primary parkinsonism

(2014) Rosanna Asselta et al.   PARKINSONISM & RELATED DISORDERS

Glucocerebrosidase mutations in Thai patients with Parkinson's disease

(2014) Teeratorn Pulkes et al.   PARKINSONISM & RELATED DISORDERS

Glucocerebrosidase Gene Mutations Associated with Parkinson's Disease: A Meta-Analysis in a Chinese population

(2014) Jia Chen et al.   PLoS One

Glucocerebrosidase mutations influence the natural history of Parkinson’s disease in a community-based incident cohort

(2013) Sophie E. Winder-Rhodes et al.   BRAIN

No association ofGBAmutations and multiple system atrophy

(2013) K. Srulijes et al.   EUROPEAN JOURNAL OF NEUROLOGY

Tau pathology and neurodegeneration

(2013) Maria Grazia Spillantini et al.   LANCET NEUROLOGY

A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy Bodies

(2013) Michael A. Nalls et al.   JAMA Neurology

Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China

(2012) Qi-ying Sun et al.   JOURNAL OF CLINICAL NEUROSCIENCE

The Role of Glia in Alpha-Synucleinopathies

(2012) Lisa Fellner et al.   MOLECULAR NEUROBIOLOGY

GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology

(2012) D. Tsuang et al.   NEUROLOGY

Association of mutations in the glucocerebrosidase gene with Parkinson disease in a Korean population

(2012) Jung Mi Choi et al.   NEUROSCIENCE LETTERS

Gaucher Disease Glucocerebrosidase and α-Synuclein Form a Bidirectional Pathogenic Loop in Synucleinopathies

(2011) Joseph R. Mazzulli et al.   CELL

Subtypes of Dementia: A Study from a Memory Clinic in India

(2011) Suvarna Alladi et al.   DEMENTIA AND GERIATRIC COGNITIVE DISORDERS

Contribution of glucocerebrosidase mutation in a large cohort of sporadic Parkinson’s disease in Taiwan

(2011) C.-L. Huang et al.   EUROPEAN JOURNAL OF NEUROLOGY

CNS expression of glucocerebrosidase corrects  -synuclein pathology and memory in a mouse model of Gaucher-related synucleinopathy

(2011) S. P. Sardi et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease

(2010) Suzanne Lesage et al.   HUMAN MOLECULAR GENETICS

Glucocerebrosidase Gene L444P mutation is a risk factor for Parkinson's disease in Chinese population

(2010) Qi-Ying Sun et al.   MOVEMENT DISORDERS

Glucocerebrosidase mutations in diffuse Lewy body disease

(2010) Kenya Nishioka et al.   PARKINSONISM & RELATED DISORDERS

Association of Glucocerebrosidase Mutations With Dementia With Lewy Bodies

(2009) Lorraine N. Clark et al.   ARCHIVES OF NEUROLOGY

Association between GBA L444P mutation and sporadic Parkinson's disease from Mainland China

(2009) X.-Y. Mao et al.   NEUROSCIENCE LETTERS