Browse All

Current Filters

CLEAR FILTER x

TITLE

Identification of candidate Parkinson’s disease predisposition genes in high-risk pedigrees

Author:Moretti, Paolo   Figueroa, Karla   Pulst, stefan   Dotti, Alessandro   Stevens, Jeff   Allen-Brady, Kristina   Cannon-Albright, Lisa   

Session Name:S42: Movement Disorders: Genetics and Risk Modifiers  

Topic:Movement Disorders  

Program Number:S42.001  

Author Institution:University of Utah, Salt Lake City, UT  Midwestern University, Downers Grove, IL  

Frequency of Known Genetic Variants for Parkinson’s Disease in the PD GENEration Study Cohort

Author:Beck, James   Ghosh Galvelis, Kamalini   Nance, Martha   Naito, Anna   Mencacci, Niccolo   Mata, Ignacio   Hall, Anne   Schulze, Jeanine   Hodges, Rayza Priscila   Wills, Anne Marie   Schwarzschild, Michael   Marder, Karen   Simuni, Tanya   Miller, Mandy   Verbrugge, Jennifer   Cook, Lola   Heathers, Laura   Totten, Michelle   Foroud, Tatiana   Alcalay, Roy   

Session Name:S42: Movement Disorders: Genetics and Risk Modifiers  

Topic:Movement Disorders  

Program Number:S42.002  

Author Institution:Parkinson's Foundation, New York, NY  Park Nicollet Clinic, Golden Valley, MN  Parkinson's Foundation, Miami, FL  Northwestern University, Chicago, IL  Cleveland Clinic Foundation, Cleveland, OH  Parkinson's Foundation, Walnut, CA  Indiana University School of Medicine, Indianapolis, IN  Indiana University, Indianapolis, IN  MGH, Boston, MA  Massachusetts General Hospital, Boston, MA  Columbia University, New York, NY  Northwestern University Feinberg School of Medicien, Chicago, IL  

Understanding how GBA mutations influence Parkinson’s disease progression

Author:Khera, Arnav   Fish, Sarah   Estes, Raja   Yu, Selina   Pallanck, Leo   Young, Jessica   Davis, Marie   

Session Name:S42: Movement Disorders: Genetics and Risk Modifiers  

Topic:Movement Disorders  

Program Number:S42.003  

Author Institution:VA Puget Sound, Sammamish, WA  VA Puget Sound, Seattle, WA  VA Puget Sound Health Care System , Seattle, WA  Department of Genome Sciences, University of Washington, Seattle, WA  Institute for Stem Cell Regenerative Medicine, University of Washington, Seattle, WA  

Expanding the genotype-phenotype landscape of PDE10A- associated movement disorders

Author:Bohlega, Saeed   Al- Qahtani, Zainah   Guzmán-Vega, Francisco J.   Ramakrishnan, Reshmi   Abusrair, Ali   Aldosari, Haya   AlDakheel, Amaal   Al-Qahtani, Salma   Monies, Dorota   Arold, Stefan   

Session Name:S42: Movement Disorders: Genetics and Risk Modifiers  

Topic:Movement Disorders  

Program Number:S42.004  

Author Institution:King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia  King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia  University of Calgary, Calgary, AB, Canada  

Correlation Between Motor Progression and Structural Connectivity in GBA, LRRK2, and sporadic Parkinson’s Disease

Author:Yu, Cherry   Wilson, Sandra   Rodriguez-Porcel, Federico   Cooper, Christine   

Session Name:S42: Movement Disorders: Genetics and Risk Modifiers  

Topic:Movement Disorders  

Program Number:S42.005  

Author Institution:Medical University of South Carolina, Charleston, SC