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Author Details

Michael J Szego
University of Toronto.
2003
30
14
Vardit Ravitsky (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
37011345Ethics Debriefs and Moral Distress: What are we Doing?Am J Bioeth2023
36368308Genomic architecture of autism from comprehensive whole-genome sequence annotation.Cell2022
34276804Corrigendum: Parental Access to Children's Raw Genomic Data in Canada: Legal Rights and Professional Responsibility.Front Genet2021
33597540Please give me a copy of my child's raw genomic data.NPJ Genom Med2021
33868358Parental Access to Children's Raw Genomic Data in Canada: Legal Rights and Professional Responsibility.Front Genet2021
33758185Author Correction: Please give me a copy of my child's raw genomic data.NPJ Genom Med2021
32036949Response.Gastrointest Endosc2020
30528884Revisiting code status in patients undergoing GI endoscopy with a "do not resuscitate" order.Gastrointest Endosc2019
31813827Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation.Stem Cell Reports2019
31515274Impact of DNA source on genetic variant detection from human whole-genome sequencing data.J Med Genet2019
30503855Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatrics.Eur J Med Genet2019
28771251Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.Genet Med2018
29431110The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.CMAJ2018
27888232Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?J Med Ethics2017
28263302Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.Nat Neurosci2017
26159620Difficult healthcare transitions: Ethical analysis and policy recommendations for unrepresented patients.Nurs Ethics2016
28567303Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.NPJ Genom Med2016
27274747Whole Genome Sequencing as a Genetic Test for Autism Spectrum Disorder: From Bench to Bedside and then Back Again.J Can Acad Child Adolesc Psychiatry2016
25046648Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines.Clin Genet2015
25923536Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome.BMC Genomics2015
24592833Predictive genomic testing of children for adult onset disorders: a Canadian perspective.Am J Bioeth2014
25512545STAT3 promotes survival of mutant photoreceptors in inherited photoreceptor degeneration models.Proc Natl Acad Sci U S A2014
23469133Endothelin-2-mediated protection of mutant photoreceptors in inherited photoreceptor degeneration.PLoS One2013
24223516Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate.PLoS Biol2013
23926223Building trust in 21st century genomics.G3 (Bethesda)2013
21851763Organelle transplantation should be legalized in Canada.J Obstet Gynaecol Can2011
17988153Overexpression of human CRB1 or related isoforms, CRB2 and CRB3, does not regulate the human presenilin complex in culture cells.Biochemistry2007
16959036Generalization of DNA microarray dispersion properties: microarray equivalent of t-distribution.Biol Direct2006
15703187Natural antisense transcripts associated with genes involved in eye development.Hum Mol Genet2005
14527271Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations.Annu Rev Neurosci2003
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Dalla Lana School of Public Health, University of Toronto.
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