J. L. Steckley

A homozygous germ-line mutation in the human MSH2 gene predisposes to hematological malignancy and multiple café-au-lait spots.

Darcy Whiteside, Ross McLeod, Gail E. Graham et al. · PubMed · 2002 · 142 citations

Multiple Café-au-lait Spots, Genetics, Pathology +16

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus

J. L. Steckley, George C. Ebers, M. Zameel Cader et al. · Neurology · 2001 · 105 citations

Mendelian Disorder, Balance Disorders, Genetic Disorder +10

Genetic analysis of vitamin D related genes in Canadian multiple sclerosis patients

J. L. Steckley, D. A. Dyment, A. Dessa Sadovnick et al. · Neurology · 2000 · 94 citations

A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia

M. Zameel Cader, J. L. Steckley, D. A. Dyment et al. · Neurology · 2005 · 73 citations

Channelopathies, Novel Episodic Ataxia, Linkage Mapping +14

No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study

David A. Dyment, J. L. Steckley, Cristen J. Willer et al. · Journal of Neuroimmunology · 2002 · 48 citations

Autoimmune Disease, Genetic Disorder, Medicine +14