Publications by authors named "Elizabeth McCready"

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Genetic modifiers and ascertainment drive variable expressivity of complex disorders.
Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Jiawan Sun, Elizabeth McCready

Cell· December 2025

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Early Mixed Donor Chimerism is a Strong Negative Prognostic Indicator in Allogeneic Stem Cell Transplant for AML and MDS.
Michael Radford, Alejandro Garcia-Horton, Rohail Badami, Elaine Jin, Nida Usmani, Elizabeth McCready

Transplant Cell Ther· February 2025

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Duplication of chromosome 1q32.1q44: presented with ventriculomegaly and transient myeloproliferative disorder of the newborn.
Medha Goyal, Malgorzata Joanna Nowaczyk, Vicky Breakey, Elizabeth McCready, Ipsita Goswami

Case Rep Perinat Med· January 2025

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Genetic modifiers and ascertainment drive variable expressivity of complex disorders.
Matthew Jensen, Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Deepro Banerjee, Elizabeth McCready

medRxiv· August 2024

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Concurrent and core binding factor beta rearrangement in de novo acute myeloid leukemia: A case report and review of literature.
Brittany Salter, Sarah Ge, Amy Tam, Suzanne Demczuk, Darci Butcher, Elizabeth McCready

EJHaem· June 2024

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Genetic and metabolic investigations for neurodevelopmental disorders: position statement of the Canadian College of Medical Geneticists (CCMG).
Melissa T Carter, Myriam Srour, Ping-Yee Billie Au, Daniela Buhas, Sarah Dyack, Elizabeth McCready

J Med Genet· June 2023

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Impaired OTUD7A-dependent Ankyrin regulation mediates neuronal dysfunction in mouse and human models of the 15q13.3 microdeletion syndrome.
Brianna K Unda, Leon Chalil, Sehyoun Yoon, Savannah Kilpatrick, Courtney Irwin, Elizabeth McCready

Mol Psychiatry· April 2023

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Further characterization of the 9q31 microdeletion phenotype; delineation of a common region of overlap containing ZNF462.
Lauren Brady, Mark Ballantyne, John Duck, Thomas Fisker, Ryan Kleefman, Elizabeth McCready

Mol Genet Genomic Med· March 2023

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Evaluation of DNA Methylation Array for Glioma Tumor Profiling and Description of a Novel Epi-Signature to Distinguish IDH1/IDH2 Mutant and Wild-Type Tumors.
Laila C Schenkel, Joseph Mathew, Hal Hirte, John Provias, Guillaume Paré, Elizabeth McCready

Genes (Basel)· November 2022

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Practice guidelines for tumour testing in ovarian cancer.
Daria Grafodatskaya, Darren D O'Rielly, Karine Bedard, Darci T Butcher, Christopher J Howlett, Elizabeth McCready

J Med Genet· August 2022

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The spectrum of epilepsy in children with 15q13.3 microdeletion syndrome.
Robyn Whitney, Arjun Nair, Elizabeth McCready, Anne E Keller, Ishita Siddiq Adil

Seizure· November 2021

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A Pan-Canadian Validation Study for the Detection of T790M Mutation Using Circulating Tumor DNA From Peripheral Blood.
Shamini Selvarajah, Sophie Plante, Marsha Speevak, Andrea Vaags, Darren Hamelinck, Elizabeth McCready

JTO Clin Res Rep· August 2021

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Practice patterns of prenatal and perinatal testing in Canadian cytogenetics laboratories.
Tamara Ashfield, Elizabeth McCready, Mary Shago, Hong Wang, Elizabeth Sinclair-Bourque

Prenat Diagn· June 2021

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Consensus Recommendations for MRD Testing in Adult B-Cell Acute Lymphoblastic Leukemia in Ontario.
Anne Tierens, Tracy L Stockley, Clinton Campbell, Jill Fulcher, Brian Leber, Elizabeth McCready

Curr Oncol· March 2021

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Twin pregnancy with metastatic complete molar pregnancy and coexisting live fetus.
Devang Odedra, Kelsey MacEachern, Lorraine Elit, Sarab Mohamed, Elizabeth McCready

Radiol Case Rep· March 2020

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ATM whole gene deletion in an Italian family with hereditary pancreatic cancer: Challenges to cancer risk prediction associated with an 11q22.3 microdeletion.
Heleen H Arts, Lorrie Lynch, Daria Grafodatskaya, Barry Eng, Lesley Malloy, Elizabeth McCready

Cancer Genet· January 2020

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CCMG practice guideline: laboratory guidelines for next-generation sequencing.
Stacey Hume, Tanya N Nelson, Marsha Speevak, Elizabeth McCready, Ron Agatep

J Med Genet· December 2019

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Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A Rosenfeld, Katrin Mannik, Elizabeth McCready

Genet Med· April 2019

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Trophoblast CD200 expression in successful human pregancies and missed abortions.
David A Clark, M Elizabeth McCready, Kate Harris, Leslie Malloy, Jorge L Arredondo

J Reprod Immunol· June 2018

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Müllerian Agenesis in Cat Eye Syndrome and 22q11 Chromosome Abnormalities: A Case Report and Literature Review.
Abdulmajeed AlSubaihin, John VanderMeulen, Kate Harris, John Duck, Elizabeth McCready

J Pediatr Adolesc Gynecol· April 2018

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Data sharing as a national quality improvement program: reporting on BRCA1 and BRCA2 variant-interpretation comparisons through the Canadian Open Genetics Repository (COGR).
Matthew S Lebo, Kathleen-Rose Zakoor, Kathy Chun, Marsha D Speevak, John S Waye, Elizabeth McCready

Genet Med· March 2018

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Changes in expression of the CD200 tolerance-signaling molecule and its receptor (CD200R) by villus trophoblasts during first trimester missed abortion and in chronic histiocytic intervillositis.
David A Clark, Jennifer M Dmetrichuk, Elizabeth McCready, Sukhbinder Dhesy-Thind, Jorge L Arredondo

Am J Reprod Immunol· July 2017

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Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors.
Laila C Schenkel, David Rodenhiser, Victoria Siu, Elizabeth McCready, Peter Ainsworth

J Pediatr Genet· March 2017

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Advances in Pediatric Genetic Testing.
Elizabeth McCready

J Pediatr Genet· March 2017

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Molecular characterization of NRXN1 deletions from 19,263 clinical microarray cases identifies exons important for neurodevelopmental disease expression.
Chelsea Lowther, Marsha Speevak, Christine M Armour, Elaine S Goh, Gail E Graham, Elizabeth McCready

Genet Med· January 2017

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