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Brain Research. Molecular Brain Research|May 15, 2002
Molecular cloning and expression of rat torsinA in the normal and genetically dystonic (dt) ratPhilipp Ziefer, Joanne Leung, Tara Razzano, et al.
Cell Reports|July 19, 2018
Molecular Deconvolution Platform to Establish Disease Mechanisms by Surveying GPCR SignalingIkuo Masuho, Sreenivas Chavali, Brian S Muntean, et al.
Parkinsonism & Related Disorders|April 27, 2012
New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonismRichard L Barbano, Deborah F Hill, Beverly M Snively, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 11, 2013
The endophenotype and the phenotype: temporal discrimination and adult-onset dystoniaMichael Hutchinson, Okka Kimmich, Anna Molloy, et al.
Parkinsonism & Related Disorders|December 2, 2014
Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's diseaseRoy N Alcalay, Helen Mejia-Santana, Anat Mirelman, et al.
Neurology|August 31, 2012
Psychiatric disorders in rapid-onset dystonia-parkinsonismAllison Brashear, Jared F Cook, Deborah F Hill, et al.
American Journal of Human Genetics|November 22, 2002
Evidence that paternal expression of the epsilon-sarcoglycan gene accounts for reduced penetrance in myoclonus-dystoniaBirgitt Müller, Katja Hedrich, Norman Kock, et al.
BMC Medical Genetics|May 10, 2011
Evaluation of 22 genetic variants with Crohn's disease risk in the Ashkenazi Jewish population: a case-control studyInga Peter, Adele A Mitchell, Laurie Ozelius, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 15, 2010
Gaucher disease ascertained through a Parkinson's center: imaging and clinical characterizationRachel Saunders-Pullman, Johann Hagenah, Vijay Dhawan, et al.
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.
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