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The Lancet. Neurology|September 24, 2011
Exome sequencing: a transformative technologyAndrew B Singleton
Neuron|April 30, 2013
Finding risk in all the right placesAndrew B Singleton
Acta Neuropathologica|July 19, 2012
The genetics and neuropathology of Parkinson's diseaseHenry Houlden, Andrew B Singleton
Current Genetic Medicine Reports|March 19, 2013
A prognostic view on the application of individualized genomics in Parkinson's diseaseOwen A Ross
Human Molecular Genetics|March 28, 2008
Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controlsJavier Simón-Sánchez, Andrew B Singleton
Neuro-Degenerative Diseases|November 30, 2011
Using DNA methylation to understand biological consequences of genetic variabilityDena G Hernandez, Andrew B Singleton
Neuron|October 20, 2010
Nature versus nurture: death of a dogma, and the road aheadBryan J Traynor, Andrew B Singleton
Parkinsonism & Related Disorders|July 9, 2014
Chromosome 22q11.2 deletion may contain a locus for recessive early-onset Parkinson's diseaseKotaro Ogaki, Owen A Ross
Genome Medicine|September 11, 2010
Copy number variation in Parkinson's diseaseMathias Toft, Owen A Ross
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