Oana Caluseriu
Alicia Chan
Sarah Hughes A genetic model for Neurofibromatosis Type II: Identification and characterization of protein partners of the Merlin tumour suppressor protein
Alison Eaton
Stacey Hume
Shailly Jain Ghai Liver transplantation in inborn errors of metabolism and newborn screening for inborn errors of metabolism
Peter Kannu Understanding biologic pathways that affect the growth and maintenance of the skeletal system and developing therapeutic options for rare genetic disorders
Karen Niederhoffer
Melissa MacPherson
Paulo Nuin
Komudi Siriwardena
Sherryl Taylor
Anastassia Voronova Neural stem cells, neurodevelopment, regeneration, neurodevelopmental disorders, KBG syndrome, glia, remyelination, multiple sclerosis, epigenetics, cell-to-cell communication
Michael Walter Molecular genetics of glaucoma, Molecular genetics of bawl-like breast cancer
Zhixiang Wang ERBB Receptor Signaling, Cancer Cell Biology, Drug Resistance and Novel Therapy in Breast Cancer
Rachel Wevrick Genetic, molecular, and physiological basis of abnormal neurodevelopment, growth and metabolism in developmental disorders affecting children
Toshifumi Yokota Antisense technology, Genome-editing technology, Neuromuscular diseases, Musculoskeletal diseases, Neuroscience

Adjunct Faculty

Katherine Aitchison
Ted Allison
Fred Berry Bone and cartilage development, Cell differentiation, Gene regulation
Amit Bhavsar Bacterial effector proteins, Safety of childhood cancer treatments
Francois Bolduc
Deobrah Burshtyn
David Eisenstat
Monica Gibson Periodontal disease, bone biology, mineralization defects in dental tissues
Daniel Graf
Jennifer Hocking The development and maintenance of photoreceptor morphology
Glen Jickling
Ordan Lehmann
Ian MacDonald
Lesley Mitchell
Jeremy Squires
Oksana Suchowersky The genetic basis for heritable disorders such as spinocerebellar
ataxia and hereditary spastic paraparesis.
Alan Underhill

Professors Emeriti

Dr. Stephen Bamforth

Dr. Diane W Cox

Dr. Dawna Gilchrist

Dr. Martin Somerville