Meghan Ferguson

Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2.

M. Dubé, M. Matsuoka, S. Evans, 2009, American journal of human genetics.

Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia

M. Fleming, M. Matsuoka, S. Evans, 2009, Nature Genetics.

Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4.

P. Awadalla, M. Matsuoka, S. Evans, 2010, American journal of human genetics.

Clinical predictors of a positive test result in patients undergoing genetic evaluation for a hereditary kidney cancer syndrome.

M. Ferguson, J. Serrano-Lomelin, R. Rendon, 2019, Canadian Urological Association journal = Journal de l'Association des urologues du Canada.

Mutation in the Gene Encoding Ubiquitin Ligase LRSAM1 in Patients with Charcot-Marie-Tooth Disease

T. Benstead, M. Matsuoka, S. Evans, 2010, PLoS genetics.

Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome

Haiyan Jiang, Mark E Samuels, Makoto Matsuoka, 2011, Nature Genetics.

Universal access to genetic counseling for women with epithelial ovarian cancer in Nova Scotia: Evaluating a new collaborative care model

K. Kieser, L. Penney, E. Chamberlain, 2021, Journal of genetic counseling.