To cure Parkinson’s disease new therapeutics and diagnostics are needed. We look at a global view of gene activity in human Parkinson’s disease to discover disease genes, drug targets, and molecular biomarkers. While the number of human genes has shrunken to an estimated ~22,000, the recent discovery of a hidden universe of an ever-increasing number of >100,000 unique transcripts is revolutionizing our thinking about gene-RNA-protein interactions. Complex genetic diseases such as Parkinson’s disease are caused by combinatorial effects of environmental, epigenetic, and genetic contributions that exert their disease-causing effects largely through cis- and trans-acting regulation of transcript abundance and specific post-transcriptional processing. Our laboratory specializes in translational transcriptomics and decodes the Parkinson’s transcriptome using RNA-Seq, microarray, and microfluidic platforms, combined with advanced computational biology. We translate our transcriptional targets into new therapies using high-throughput drug screens. Our longitudinal Harvard NeuroDiscovery Center Biomarker Study of more than 1,500 participants serves as a unique incubator for biomarkers and a future personalized neurology.
Genomic dark matter and personalized medicine
Source: NINDS PDBP
Biomarker for Huntington's disease identified
Harvard Gazette, October 3, 2011 »more
Study: Brain energy crisis may spark Parkinson's
The Washington Post, November 2, 2010 »more
Clemens Scherzer on cutting-edge Parkinson’s research
EarthSky, November 29, 2010 »more
Study links Parkinson’s to brain’s tiny power factories
Boston Globe,
November 2, 2010 »more
Damaged cell powerhouses linked to Parkinson's
Nature, October 6, 2010 »more
Transcriptional regulation of α-synuclein: insights from blood?
Future Neurology, March 2009 »more
Interview - Searching for biomarkers in Parkinson's disease
Biomarkers in Medicine, April, 2009 »more