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Neurology|June 12, 2015
Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 ConsortiumKaren Marder, Yuanjia Wang, Roy N Alcalay, et al.
Genomics|January 25, 2000
The TOR1A (DYT1) gene family and its role in early onset torsion dystoniaL J Ozelius, C E Page, C Klein, et al.
Annals of Clinical and Translational Neurology|December 11, 2014
Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?Rachel Saunders-Pullman, Anat Mirelman, Cuiling Wang, et al.
Frontiers in Neurology|March 15, 2021
Cognitive Functioning of Glucocerebrosidase (<i>GBA</i>) Non-manifesting CarriersEileen E Moran, Susan B Bressman, Roberto A Ortega, et al.
The European Journal of Neuroscience|November 5, 2015
Intact working memory in non-manifesting LRRK2 carriers--an fMRI studyAvner Thaler, Rick C Helmich, Ayelet Or-Borichev, et al.
JAMA Neurology|November 18, 2014
Higher frequency of certain cancers in LRRK2 G2019S mutation carriers with Parkinson disease: a pooled analysisIlir Agalliu, Marta San Luciano, Anat Mirelman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 8, 2013
Phenomenology and classification of dystonia: a consensus updateAlberto Albanese, Kailash Bhatia, Susan B Bressman, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 1, 2014
A voxel-based morphometry and diffusion tensor imaging analysis of asymptomatic Parkinson's disease-related G2019S LRRK2 mutation carriersAvner Thaler, Moran Artzi, Anat Mirelman, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|February 10, 2016
Glucocerebrosidase enzyme activity in GBA mutation Parkinson's diseaseRoberto A Ortega, Paola A Torres, Matthew Swan, et al.
Journal of Genetic Counseling|August 17, 2014
Interest in genetic testing in Ashkenazi Jewish Parkinson's disease patients and their unaffected relativesManisha Gupte, Roy N Alcalay, Helen Mejia-Santana, et al.
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