Andrew B Singleton

Thomas G Schulze, Francis J McMahon, Sven Cichon, 2014, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Genetic diversity is a predictor of mortality in humans

Luigi Ferrucci, Alexander Teumer, Vilmundur Gudnason, 2014, BMC Genetics.

Genetic risk and age in Parkinson's disease: Continuum not stratum

Valentina Escott-Price, Nigel M Williams, Andrew B Singleton, 2015, Movement disorders : official journal of the Movement Disorder Society.

Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.

Kewei Chen, Eric M Reiman, Wendy Lee, 2010, Human molecular genetics.

The genetic architecture of Parkinson's disease

Andrew B Singleton, Cornelis Blauwendraat, M. Nalls, 2020, The Lancet Neurology.

Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association

Luigi Ferrucci, Anna Murray, Hanieh Yaghootkar, 2011, Human molecular genetics.

Distinct DNA methylation changes highly correlated with chronological age in the human brain.

Mark R Cookson, Andrew B Singleton, D. Hernandez, 2011, Human molecular genetics.

Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

Margaret Sutherland, John P A Ioannidis, Daniel Weintraub, 2015, The Lancet Neurology.

Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.

Sudha Seshadri, Deborah A Nickerson, Wei-Min Chen, 2015, JAMA neurology.

Genetic comorbidities in Parkinson's disease.

Mohamad Saad, Anette Schrag, Thomas Gasser, 2014, Human molecular genetics.

The genetics of Parkinson's disease: Progress and therapeutic implications

Vincenzo Bonifati, Andrew B Singleton, A. Singleton, 2013, Movement disorders : official journal of the Movement Disorder Society.

Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance

Andrew B Singleton, D. Hernandez, A. Singleton, 2016, Journal of neurochemistry.

Exome sequencing: a transformative technology

Andrew B Singleton, A. Singleton, 2011, The Lancet Neurology.

Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk.

Peter Holmans, Alexandra Durr, Manu Sharma, 2013, JAMA neurology.

Use of support vector machines for disease risk prediction in genome‐wide association studies: Concerns and opportunities

Andreas Zell, Andreas Jahn, Mohamad Saad, 2012, Human mutation.

Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans

Paola Giunti, Sonja W. Scholz, Elsdon Storey, 2007, PLoS genetics.

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease.

Mohamad Saad, Peter Holmans, Nicholas W Wood, 2013, Human molecular genetics.

Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders

Claude Bouchard, William Wheeler, Peter Kraft, 2014 .

Novel Loci Associated With PR Interval in a Genome-Wide Association Study of 10 African American Cohorts

Wei Chen, Luigi Ferrucci, Yun Li, 2012, Circulation. Cardiovascular genetics.

Epigenetic Signatures of Cigarette Smoking

Paolo Vineis, Allan C Just, Luigi Ferrucci, 2016, Circulation. Cardiovascular genetics.

Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.

Xiaofeng Zhu, Todd L Edwards, Wei Guo, 2013, American journal of human genetics.