McLaughlin Centre, University of Toronto - 2015 Accelerator Grants

McLaughlin Centre, University of Toronto - 2015 Accelerator Grants

Anne Bassett

Centre for Addiction and Mental Health

Department of Psychiatry

Genomic screening as a window on the developing fetus, newborn and beyond

Daniel De Carvalho

UHN - Princess Margaret Hospital

Department of Medical Biophysics

Pilot study to develop a cost-effective gene panel to detect pancreatic cancer-specific cfDNA methylation suitable for clinical use

Claudia dos Santos

St. Michael's Hospital

Department of Medicine

Epigenetic Profiling in Severe Sepsis – (EPSIS)

Alfonso Fasano

UHN - Toronto Western Hospital

Department of Medicine

Surgicogenomics in Parkinson’s disease: towards an understanding of the genetic contributors of outcome variability after deep brain stimulation surgery

Meredith Irwin

Hospital for Sick Children

Department of Paediatrics

Translating the discovery of novel neuroblastoma

Peter Kannu

Hospital for Sick Children

Department of Paediatrics

Next Generation Sequencing a Cohort of Unique and Unclassified Lethal Skeletal Dysplasias

Shaf Keshavjee

UHN - Toronto General Hospital

Department of Surgery

A genomics-based rapid diagnostic tool for the treatment and repair of donor lungs during ex vivo lung perfusion

Stephen Lye

Mount Sinai Hospital

Department of Obstetrics & Gynecology

Host-microbe genomic approaches to understanding obesity and diabetes in pregnancy

Berge Minassian

Hospital for Sick Children

Department of Paediatrics

Identifying Genetic Bases of Intractability in Epilepsy

Lucy Osborne

Campus

Department of Medicine

The epigenetic landscape in neurons from 7q11.23 deletion and duplication syndromes

Samir Patel

Public Health Ontario

Department of Laboratory Medicine & Pathobiology

An integrated genomic solution for managing bacterial outbreaks and transmission in the health care system

Jim Stavropoulos

Hospital for Sick Children

Department of Laboratory Medicine & Pathobiology

Development of a multi-centre clinical database to promote standardized reporting of genomic copy number variants for prenatal and postnatal diagnostics

Michael Taylor

Hospital for Sick Children

Department of Surgery

Validation of Structural Variants in Medulloblastoma Using Long Read Sequencing Technology

Rosanna Weksberg

Hospital for Sick Children

Department of Paediatrics

Application of a novel reduced representation bisulfite sequencing technology for the epigenetic study of autism

Jay Wunder

Mount Sinai Hospital

Department of Surgery

Investigation of Genetic Alterations and Drug Sensitivities in Undifferentiated Pleomorphic Sarcomas and Corresponding Clinical Characteristics

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