Publications by authors named "Andy Singleton"

Claim this Profile
D
Deciphering the Genetic Architecture of Parkinson's Disease in India.
Asha Kishore, Ashwin Ashok Kumar Sreelatha, Amabel M M Tenghe, Rupam Borgohain, Divya Kalikavil Puthanveedu, Andy Singleton

medRxiv· February 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Longitudinal analyses of cerebrospinal fluid α-Synuclein in prodromal and early Parkinson's disease.
Brit Mollenhauer, Chelsea J Caspell-Garcia, Christopher S Coffey, Peggy Taylor, Andy Singleton

Mov Disord· September 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Lysosomal storage disorder gene variants in multiple system atrophy.
Lasse Pihlstrøm, Lucia Schottlaender, Viorica Chelban, , Wassilios G Meissner, Andy Singleton

Brain· July 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Longitudinal CSF biomarkers in patients with early Parkinson disease and healthy controls.
Brit Mollenhauer, Chelsea J Caspell-Garcia, Christopher S Coffey, Peggy Taylor, Leslie M Shaw, Andy Singleton

Neurology· November 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multi-infarct dementia of Swedish type is caused by a 3'UTR mutation of COL4A1.
Maija Siitonen, Anne Börjesson-Hanson, Minna Pöyhönen, Ari Ora, Petra Pasanen, Andy Singleton

Brain· May 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Erratum to "The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism" [Neurobiol. Aging 36 (2015) 1221.e1-1221.e6].
Lucia V Schottlaender, James M Polke, Helen Ling, Nicola D MacDoanld, Arianna Tucci, Andy B Singleton

Neurobiol Aging· April 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonism.
Lucia V Schottlaender, James M Polke, Helen Ling, Nicola D MacDoanld, Arianna Tucci, Andy B Singleton

Neurobiol Aging· February 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Missense variant in TREML2 protects against Alzheimer's disease.
Bruno A Benitez, Sheng Chih Jin, Rita Guerreiro, Rob Graham, Jenny Lord, Andy Singleton

Neurobiol Aging· June 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease.
Carlos Cruchaga, Celeste M Karch, Sheng Chih Jin, Bruno A Benitez, Yefei Cai, Andy Singleton

Nature· January 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis