Speaker - Stephen Scherer

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Stephen W. Scherer, PhD, DSc, FRSC is known for contributions to discovering the phenomena of global copy number variation (CNVs) of DNA and genes as the most abundant type of genetic variation in the human genome, Dr. Scherer leads one of Canada's busiest laboratories. His group has discovered numerous disease susceptibility genes and most recently has defined CNV and other genetic factors underlying autism. He collaborated with Craig Venter's team to decode human chromosome 7 and to generate the first genome sequence of an individual. Some 300 scientific papers document his work (cited >20,000 times). Professor Scherer holds the GlaxoSmithKline-Canadian Institutes of Health Research Chair in Genetics and Genomics at The Hospital for Sick Children and University of Toronto.

1 Program

Introducing the Canadian Personal Genome Project

04.25.13 | 00:50:41 min | 0 comments