ID
44953
Description
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000089.v3.p2 Epidemiological studies have estimated a cumulative prevalence of PD of greater than 1 per thousand. When prevalence is limited to senior populations, this proportion increases nearly 10-fold. The estimated genetic risk ratio for PD is approximately 1.7 (70% increased risk for PD if a sibling has PD) for all ages, and increases over 7-fold for those under age 66 years. The role for genes contributing to the risk of PD is therefore significant. This study utilized the well characterized collection of North American Caucasians with Parkinson's disease, and neurologically normal controls from the sample population which are banked in the National Institute of Neurological Disorders and Stroke (NINDS Repository) collection for a first stage whole genome analysis. Genome-wide, single nucleotide polymorphism (SNP) genotyping of these publicly available samples was originally done in 267 Parkinson's disease patients and 270 controls, and this has been extended to include genome wide genotyping in 939 Parkinson's disease cases and 802 controls. The NINDS repository was established in 10-2001 towards the goal of developing standardized, broadly useful diagnostic and other clinical data and a collection of DNA and cell line samples to further advances in gene discovery of neurological disorders. All samples, phenotypic, and genotypic data are available to the research community including to academics and industry scientists. In addition, well characterized neurologically normal control subjects are a part of the collection. This collection formed the basis of this first stage study by Fung et al., and the expanded study by Simon-Sanchez et al. The genotyping data was generated and provided by the laboratory of Dr. Andrew Singleton NIA, and Dr. John Hardy NIA (NIH Intramural, funding from NIA and NINDS). *Important links to apply for individual-level data* - Data Use Certification Requirements (DUC) - Apply here for controlled access to individual level data - Participant Protection Policy FAQ
Link
https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000089.v3.p2
Keywords
Versions (2)
- 5/13/22 5/13/22 - Martin Dugas
- 6/3/22 6/3/22 - Dr. Christian Niklas
Copyright Holder
Hong-Chung Fung, National Institute of Aging, National Institutes of Health, Bethesda, MD, USA, Chang Gung Memorial Hospital, Taiwan, and University College London, UK
Uploaded on
May 13, 2022
DOI
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License
Creative Commons BY 4.0
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dbGaP phs000089 NINDS Parkinson's Disease
Diagnostic interview of neurologically healthy subjects
- StudyEvent: SEV1
- Diagnostic interview of neurologically healthy subjects
- Diagnostic interview of subjects affected with Parkinson disease
- Subject ID, subject source, consent group, and affection status of subjects affected or not affected with Parkinson disease
- Sample ID and subject ID of subjects affected or not affected with Parkinson disease
Similar models
Diagnostic interview of neurologically healthy subjects
- StudyEvent: SEV1
- Diagnostic interview of neurologically healthy subjects
- Diagnostic interview of subjects affected with Parkinson disease
- Subject ID, subject source, consent group, and affection status of subjects affected or not affected with Parkinson disease
- Sample ID and subject ID of subjects affected or not affected with Parkinson disease