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JAMA Network Open|April 21, 2021
Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease ProgressionRoberto A Ortega, Cuiling Wang, Deborah Raymond, et al.
JAMA Neurology|May 31, 2017
Complex and Dynamic Chromosomal Rearrangements in a Family With Seemingly Non-Mendelian Inheritance of Dopa-Responsive DystoniaKatja Lohmann, Claire Redin, Holger Tönnies, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 27, 2015
Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 geneAnat Mirelman, Roy N Alcalay, Rachel Saunders-Pullman, et al.
JAMA Neurology|January 9, 2018
Progression in the LRRK2-Asssociated Parkinson Disease PopulationRachel Saunders-Pullman, Anat Mirelman, Roy N Alcalay, et al.
NPJ Parkinson'S Disease|December 7, 2023
Genetic risk variants in New Yorkers of Puerto Rican and Dominican Republic heritage with Parkinson's diseaseGabriel Miltenberger-Miltenyi, Roberto A Ortega, Aloysius Domingo, et al.
Annals of Clinical and Translational Neurology|January 20, 2016
Psychiatric disorders, myoclonus dystonia and SGCE: an international studyKathryn J Peall, Joke M Dijk, Rachel Saunders-Pullman, et al.
Neurology|March 29, 2013
The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson diseaseZiv Gan-Or, Laurie J Ozelius, Anat Bar-Shira, et al.
Bioinformatics (Oxford, England)|December 24, 2021
BATL: Bayesian annotations for targeted lipidomicsJustin G Chitpin, Anuradha Surendra, Thao T Nguyen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 1, 2018
Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriersAnat Mirelman, Rachel Saunders-Pullman, Roy N Alcalay, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 15, 2015
REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriersRachel Saunders-Pullman, Roy N Alcalay, Anat Mirelman, et al.
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