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You searched for: Author/Creator Singleton, Andrew B.

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1. A 7.5‐Mb duplication at chromosome 11q21‐11q22.3 is associated with a novel spastic ataxia syndrome. Issue 2 (27th December 2014)

2. A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory Study. (7th March 2019)

3. A comprehensive analysis of SNCA‐related genetic risk in sporadic parkinson disease. Issue 1 (26th August 2018)

4. A genome-wide association study in multiple system atrophy. (11th October 2016)

6. A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking. (29th August 2016)

7. Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource. Issue 8 (7th May 2021)

8. Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance. (18th October 2016)

9. Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+). (February 2018)

10. Arguing against the proposed definition changes of PD. Issue 11 (5th August 2016)