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Archives of Neurology|October 14, 2009
Urate as a predictor of the rate of clinical decline in Parkinson diseaseAlberto Ascherio, Peter A LeWitt, Kui Xu, et al.Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2007
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin geneLorraine N Clark, Eneli Haamer, Helen Mejia-Santana, et al.Neurobiology of Aging|November 26, 2020
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's diseasePrabhjyot Saini, Uladzislau Rudakou, Eric Yu, et al.Parkinsonism & Related Disorders|March 31, 2015
Genetic markers of Restless Legs Syndrome in Parkinson diseaseZiv Gan-Or, Roy N Alcalay, Anat Bar-Shira, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 24, 2020
Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's DiseaseEric Yu, Uladzislau Rudakou, Lynne Krohn, et al.Brain : a Journal of Neurology|August 23, 2015
Closing the tau loop: the missing tau mutationAllan McCarthy, Roisin Lonergan, Diana A Olszewska, et al.Neurology. Genetics|February 12, 2020
Analysis of common and rare VPS13C variants in late-onset Parkinson diseaseUladzislau Rudakou, Jennifer A Ruskey, Lynne Krohn, et al.Neurobiology of Aging|May 7, 2020
Variants in the Niemann-Pick type C gene NPC1 are not associated with Parkinson's diseaseBouchra Ouled Amar Bencheikh, Konstantin Senkevich, Uladzislau Rudakou, et al.Medrxiv : the Preprint Server for Health Sciences|March 30, 2023
Association of rare variants in ARSA with Parkinson's diseaseKonstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2023
Association of Rare Variants in ARSA with Parkinson's DiseaseKonstantin Senkevich, Mariia Beletskaia, Aliza Dworkind, et al.Pageof 17