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Professor Andrew Sharp seminar

10 June 2025, 3:00 pm–4:00 pm

UK DRI at UCL

Phenome-wide association studies to study the role of tandem repeats in human disease

Event Information

Open to

All

Organiser

Jessica Tingle

Location

Gilliatt Lecture Theatre
Queen Square House
Queen Square
London
WC1N 3RX
United Kingdom

Host: UK Dementia Research Institute at UCL

 

 

About the Speaker

Professor Andrew Sharp

Andy completed his PhD with Pat Jacobs in 2003 at The Wessex Regional Genetics Lab in Salisbury, then spent 4 years as a Postdoc in the laboratory of Evan Eichler in Seattle, USA before moving to the University of Geneva, Switzerland where he was a Marie Curie Fellow. For the past 15 years he has run a human genomics research lab at the Icahn School of Medicine at Mount Sinai in New York where he is a Professor of Genetics. Andy’s work has included some of the seminal work on structural genome variation, including discovery and characterization of many recurrent microdeletion/duplication syndromes, such as those at 1q21, 15q13, and 17q21, in addition to the use of epigenome profiling as a tool to study the human genome. More recently his lab has focused on characterizing the role of tandem repeat variation in the human genome. Fun fact: Despite running a successful bioinformatics lab, he has never written a line of code in his life!