Clinical Heterogeneity Among LRRK2 Variants in Parkinson's Disease: A Meta-Analysis
Published 2018 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Clinical Heterogeneity Among LRRK2 Variants in Parkinson's Disease: A Meta-Analysis
Authors
Keywords
-
Journal
Frontiers in Aging Neuroscience
Volume 10, Issue -, Pages -
Publisher
Frontiers Media SA
Online
2018-09-19
DOI
10.3389/fnagi.2018.00283
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Comparison of clinical features among Parkinson's disease subtypes: A large retrospective study in a single center
- (2018) Takuya Konno et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin , PINK1 , DJ1: MDSGene Systematic Review
- (2018) Meike Kasten et al. MOVEMENT DISORDERS
- Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2 -related Parkinson's disease
- (2018) Anna De Rosa et al. PARKINSONISM & RELATED DISORDERS
- Progression in the LRRK2-Associated Parkinson Disease Population
- (2018) Rachel Saunders-Pullman et al. JAMA Neurology
- 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
- Polymorphisms of Dopamine Receptor Genes and Risk of L-Dopa–Induced Dyskinesia in Parkinson’s Disease
- (2017) Cristoforo Comi et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Parkinson’s Disease: From Pathogenesis to Pharmacogenomics
- (2017) Ramón Cacabelos INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Lack of association between LRRK2 G2385R and cognitive dysfunction in Korean patients with Parkinson’s disease
- (2017) Jeong Hoon Hong et al. JOURNAL OF CLINICAL NEUROSCIENCE
- Clinical profiles associated with LRRK2 and GBA mutations in Brazilians with Parkinson's disease
- (2017) Camilla P. da Silva et al. JOURNAL OF THE NEUROLOGICAL SCIENCES
- Levodopa: A new look at an old friend
- (2017) C. Warren Olanow et al. MOVEMENT DISORDERS
- Motor complications in Parkinson's disease: Striatal molecular and electrophysiological mechanisms of dyskinesias
- (2017) Barbara Picconi et al. MOVEMENT DISORDERS
- TMEM230 mutation analysis in Parkinson's disease in a Chinese population
- (2017) Weiqian Yan et al. NEUROBIOLOGY OF AGING
- LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease
- (2017) Ahmed Bouhouche et al. Parkinsons Disease
- Sex differences in LRRK2 G2019S and idiopathic Parkinson's Disease
- (2017) Marta San Luciano et al. Annals of Clinical and Translational Neurology
- LRRK2, GBA and SMPD1 Founder Mutations and Parkinson's Disease in Ashkenazi Jews
- (2016) Efrat Dagan et al. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
- Cerebrospinal fluid biomarkers and clinical features in leucine-rich repeat kinase 2 (LRRK2) mutation carriers
- (2016) Dolores Vilas et al. MOVEMENT DISORDERS
- Motor and nonmotor heterogeneity of LRRK2 -related and idiopathic Parkinson's disease
- (2016) Connie Marras et al. MOVEMENT DISORDERS
- Olfactory Dysfunction in Parkinson’s Disease Patients with the LRRK2 G2385R Variant
- (2016) Ming Cao et al. Neuroscience Bulletin
- Lack of association between IL-10 and IL-18 gene promoter polymorphisms and Parkinson’s disease with cognitive impairment in a Chinese population
- (2016) Zhenhua Liu et al. Scientific Reports
- Cognitive Impairments in LRRK2-Related Parkinson’s Disease: A Study in Chinese Individuals
- (2015) Yifan Zheng et al. BEHAVIOURAL NEUROLOGY
- REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers
- (2015) Rachel Saunders-Pullman et al. MOVEMENT DISORDERS
- Polygenic determinants of Parkinson's disease in a Chinese population
- (2015) Ji-Feng Guo et al. NEUROBIOLOGY OF AGING
- LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian population
- (2015) Kai Li et al. NEUROBIOLOGY OF AGING
- Greater motor progression in patients with Parkinson disease who carryLRRK2risk variants
- (2015) Linda P. Oosterveld et al. NEUROLOGY
- Age-specific penetrance ofLRRK2G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium
- (2015) Karen Marder et al. NEUROLOGY
- Clinical and imaging markers in premotor LRRK2 G2019S mutation carriers
- (2015) Dolores Vilas et al. PARKINSONISM & RELATED DISORDERS
- Cognitive and behavioral symptoms in Parkinson's disease patients with the G2019S and R1441G mutations of the LRRK2 gene
- (2015) Johanne Hatteland Somme et al. PARKINSONISM & RELATED DISORDERS
- Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's disease
- (2015) Roy N. Alcalay et al. PARKINSONISM & RELATED DISORDERS
- Clinical Correlations With Lewy Body Pathology inLRRK2-Related Parkinson Disease
- (2015) Lorraine V. Kalia et al. JAMA Neurology
- Olfactory identification inLRRK2G2019S mutation carriers: a relevant marker?
- (2015) Rachel Saunders-Pullman et al. Annals of Clinical and Translational Neurology
- Motor phenotype of LRRK2-associated Parkinson's disease: A tunisian longitudinal study
- (2014) Fatma Nabli et al. MOVEMENT DISORDERS
- Motor progression of Parkinson's disease with the leucine-rich repeat kinase 2 G2019S mutation
- (2014) Gilad Yahalom et al. MOVEMENT DISORDERS
- Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2
- (2014) A. Estanga et al. PARKINSONISM & RELATED DISORDERS
- Confirmation of the association between LRRK2 R1628P variant and susceptibility to Parkinson's disease in the Thai population
- (2014) Teeratorn Pulkes et al. PARKINSONISM & RELATED DISORDERS
- Nonmotor Symptoms in LRRK2 G2019S Associated Parkinson’s Disease
- (2014) Carles Gaig et al. PLoS One
- LRRK2 G2385R variant carriers of female Parkinson’s disease are more susceptible to motor fluctuation
- (2013) Chao Gao et al. JOURNAL OF NEUROLOGY
- Factors predictive of the development of Levodopa-induced dyskinesia and wearing-off in Parkinson's disease
- (2013) C. Warren Olanow et al. MOVEMENT DISORDERS
- Parkinson disease phenotype in Ashkenazi jews with and withoutLRRK2G2019S mutations
- (2013) Roy N. Alcalay et al. MOVEMENT DISORDERS
- Fall risk and gait in Parkinson's disease: The role of the LRRK2 G2019S mutation
- (2013) Anat Mirelman et al. MOVEMENT DISORDERS
- A comparative study of Parkinson's disease and leucine-rich repeat kinase 2 p.G2019S parkinsonism
- (2013) Joanne Trinh et al. NEUROBIOLOGY OF AGING
- Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson’s disease in a Han-Chinese population in south-eastern China
- (2013) Jiangping Cai et al. NEUROLOGICAL SCIENCES
- Olfaction and imaging biomarkers in premotor LRRK2 G2019S-associated Parkinson disease
- (2013) M. Sierra et al. NEUROLOGY
- The LRRK2 G2019S mutation in a series of Argentinean patients with Parkinson's disease: Clinical and demographic characteristics
- (2013) Emilia Mabel Gatto et al. NEUROSCIENCE LETTERS
- The LRRK2 G2019S mutation status does not affect the outcome of subthalamic stimulation in patients with Parkinson's disease
- (2013) Lior Greenbaum et al. PARKINSONISM & RELATED DISORDERS
- Autonomic dysfunction in parkinsonian LRRK2 mutation carriers
- (2013) Beatriz Tijero et al. PARKINSONISM & RELATED DISORDERS
- Correlation between LRRK2 gene G2385R polymorphisms and Parkinson’s disease
- (2012) HUIRU YAN et al. Molecular Medicine Reports
- Dyskinesias in patients with Parkinson's disease: Effect of the leucine-rich repeat kinase 2 (LRRK2) G2019S mutation
- (2012) Gilad Yahalom et al. PARKINSONISM & RELATED DISORDERS
- LRRK2 G2385R and LRRK2 R1628P increase risk of Parkinson's disease in a Han Chinese population from Southern Mainland China
- (2012) Xiaoli Fu et al. PARKINSONISM & RELATED DISORDERS
- G2019S Mutation of the Leucine-Rich Repeat Kinase 2 Gene in a Cohort of Egyptian Patients with Parkinson's Disease
- (2011) Doaa I. Hashad et al. Genetic Testing and Molecular Biomarkers
- Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's disease
- (2011) Vicki Shanker et al. MOVEMENT DISORDERS
- Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers
- (2011) C. Marras et al. NEUROLOGY
- Olfactory dysfunction in LRRK2 G2019S mutation carriers
- (2011) R. Saunders-Pullman et al. NEUROLOGY
- Gender differences in the risk of familial parkinsonism: Beyond LRRK2?
- (2011) R. Saunders-Pullman et al. NEUROSCIENCE LETTERS
- Cognitive dysfunction in Tunisian LRRK2 associated Parkinson’s disease
- (2011) Samia Ben Sassi et al. PARKINSONISM & RELATED DISORDERS
- LRRK2 G2019S mutation in Parkinson’s disease: A neuropsychological and neuropsychiatric study in a large Algerian cohort
- (2010) Soreya Belarbi et al. PARKINSONISM & RELATED DISORDERS
- Motor Phenotype of LRRK2 G2019S Carriers in Early-Onset Parkinson Disease
- (2009) Roy N. Alcalay et al. ARCHIVES OF NEUROLOGY
- LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China
- (2009) Lihua Yu et al. BRAIN RESEARCH
- LRRK2gene variation and its contribution to Parkinson disease
- (2009) Coro Paisán-Ruiz HUMAN MUTATION
- Non-motor symptoms in Parkinson’s disease
- (2009) Ariane Park et al. JOURNAL OF NEUROLOGY
- LRRK2R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China
- (2009) Zijuan Zhang et al. MOVEMENT DISORDERS
- Clinical features of LRRK2 parkinsonism
- (2009) Kristoffer Haugarvoll et al. PARKINSONISM & RELATED DISORDERS
- The LRRK2 G2385R variant is a risk factor for sporadic Parkinson's disease in the Korean population
- (2009) Jong-Min Kim et al. PARKINSONISM & RELATED DISORDERS
- The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study
- (2008) Jeanne C Latourelle et al. BMC Medicine
- LRRK2 Gly2385Arg variant is a risk factor of Parkinson’s disease among Han-Chinese from mainland China
- (2008) X.-K. An et al. EUROPEAN JOURNAL OF NEUROLOGY
- LRRK2 Gly2385Arg mutation and clinical features in a Chinese population with early-onset Parkinson’s disease compared to late-onset patients
- (2008) Daniel Kam Yin Chan et al. JOURNAL OF NEURAL TRANSMISSION
- LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic study
- (2008) Mary M Hulihan et al. LANCET NEUROLOGY
- Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
- (2008) Daniel G Healy et al. LANCET NEUROLOGY
- Clinical correlates of depressive symptoms in familial Parkinson's disease
- (2008) Nathan Pankratz et al. MOVEMENT DISORDERS
- Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?
- (2008) S. Lesage et al. NEUROLOGY
- Hyposmia in G2019S LRRK2-related parkinsonism: Clinical and pathologic data
- (2008) L. Silveira-Moriyama et al. NEUROLOGY
- Genotype-phenotype correlations between GBA mutations and Parkinson disease risk and onset
- (2008) Z. Gan-Or et al. NEUROLOGY
- LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay
- (2008) Ignacio F. Mata et al. PARKINSONISM & RELATED DISORDERS
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started