Javier Simón-Sánchez

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

Sonja W. Scholz, Scott Silliman, Carl D Langefeld, 2007, The Lancet Neurology.

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

David Heckerman, Lorne Zinman, Joanne Wuu, 2011, Neuron.

Pilot whole-exome sequencing of a German early-onset Alzheimer's disease cohort reveals a substantial frequency of PSEN2 variants

Florian G. Metzger, Patrizia Rizzu, Walter Maetzler, 2016, Neurobiology of Aging.

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.

Genome-wide association studies in neurological disorders

A. Singleton, J. Simón‐Sánchez, Andrew Singleton, 2008, The Lancet 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.

Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population

Jeroen van Rooij, Manu Sharma, Cornelia M. van Duijn, 2017, Neurobiology of Aging.

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.