selected scholarly activity
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conferences
- COMPARISON OF NEXT GENERATION SEQUENCING VERSUS SINGLE ANALYTE TESTS FOR SOMATIC MUTATION DETECTION IN ACUTE MYELOID LEUKEMIA, MYELOPROLIFERATIVE NEOPLASM AND SOLID TUMORS. International Journal of Laboratory Hematology. 72-72. 2017
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journal articles
- Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR). Genetics in Medicine. 20:294-302. 2018
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Changes in expression of the
CD 200 tolerance‐signaling molecule and its receptor (CD 200R) by villus trophoblasts during first trimester missed abortion and in chronic histiocytic intervillositis. American Journal of Reproductive Immunology. 78. 2017 - Advances in Pediatric Genetic Testing. Journal of Pediatric Genetics. 06:001-002. 2017
- Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors. Journal of Pediatric Genetics. 06:030-041. 2017
- Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression. Genetics in Medicine. 19:53-61. 2017
- Prader–Willi syndrome and Tay–Sachs disease in association with mixed maternal uniparental isodisomy and heterodisomy 15 in a girl who also had isochromosome Xq. American Journal of Medical Genetics, Part A. 167:180-184. 2015
- HLA-DRnegative, CD34negative Hypergranular Acute Myeloid Leukemia With Trisomy 6 and del(5)(q22q33). Journal of Pediatric Hematology/Oncology. 33:e289-e295. 2011
- Age- and Schooling-Related Effects on Executive Functions in Young Children: A Natural Experiment. Child Neuropsychology. 14:510-524. 2008