Program Director, WRHA Program of Genetics and Metabolism
Assistant Professor, Department of Paediatrics and Child Health
Assistant Professor, Department of Biochemistry and Medical Genetics

2005 PhD, University of Manitoba
1992 MS, University of Cincinnati
1990 BSc(Hons), Queen’s University

Limb malformations
Split Hand Foot Malformation
Skeletal Dysplasias
Congenital anomalies

2007, MICH Summer Student (Co-supervisor with Dr. Albert Chudley)
2008-2009, Honours Genetics Project Student

Faivre L.*, Cormier-Daire V.*, Elliott A.M., Field F., Munnich A., Maroteaux P., Le Merrer M. and Lachman R.S. Desbuquois Dysplasia, a re-evaluation with abnormal and “normal” hands: Radiographic manifestations. Am J Med Genet 2004 124:48-53

Elliott A.M., Evans J.A., Chudley A.E. and Reed M.H. The duplicated longitudinal epiphysis or “kissing delta phalanx” – evolution and variation in three different disorders. Skeletal Radiol 2004 33:345-351.

Elliott A.M., Reed M.H., Evans J.A., Cross H.G. and Chudley A.E. Cenani-Lenz Syndactyly in a Patient with Features of Kabuki Syndrome. Clin Dys 2004 13:143-150.

Elliott A.M., Field FM, Rimoin DL, and Lachman RS. Hand Involvement in Schmid Metaphyseal Chondrodysplasia. Am J Med Genet 2005 132A: 191-193.

Elliott A.M., Reed, M.H., Roscioli T. and Evans J.A. Discrepancies in Upper and Lower Limb Patterns in Split Hand Foot Malformation (SFHM) Clin Genet 2005 68:408-423.

Elliott A.M., Evans J.A. and Chudley A.E. Split Hand Foot Malformation. Clin Genet 2005 68:501-505.

Elliott A.M. and Evans J.A. Fibular Aplasia, Tibial Campomelia and Oligodactyly. (Letter to the Editor). Am J Med Genet 2006 140A:1127.

Elliott A.M. and Evans J.A. Genotype Phenotype Correlations in Split Hand Foot Malformation (SHFM). Am J Med Genet 2006 140A: 1419-1427.

Elliott A.M., Reed M.H., Chudley A.E., Chodirker, B.N. and Evans J.A. Clinical and Epidemiological Findings of Patients with Central Ray Deficiency: Split Hand Foot Malformation (SHFM) in Manitoba, Canada. Am J Med Genet 2006 140A: 1428-1439.

Elliott A.M., Wilcox W.R., Spear G.S., Field F.M., Steffensen T.S., Friedman B.D., Rimoin D.L. and Lachman R.S. Osteocraniostenosis - Skull configuration mimicking kleeblattschädel (Cloverleaf skull) with gracile bones. Four New Cases with Distinctive Chondro-osseous morphology. Am J Med Genet 2006 140A: 1553-1563.

Elliott A.M., Reed M.H. and Evans J.A. Triphalangeal Thumb in Association with Split Hand/Foot-A Phenotypic Marker for SHFM3? Birth Defects Research Part A: Clinical and Molecular Teratology 2007 79:58-61.

Elliott A.M. and Evans J.A. The Association of Split Hand Foot Malformation (SHFM) and Congenital Heart Defects. Birth Defects Research Part A: Clinical and Molecular Teratology 2008 82:425-434.

Elliott A.M., Reed M.H. and Evans J.A. Central Ray Deficiency with Extensive Syndactyly: A Dilemma for Classification. Gen Couns 2009 20:27-43.

Friedman T, Reed MH, Elliott AM. The Carpal Bones in Poland Syndrome. Skel Rad 2009 38: 585-591.

Elliott A.M., Kibria, L. and Reed M.H. The developmental spectrum of proximal radioulnar synostosis. Skel Rad 2010 39:49-54.