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Author Details
Full Name
Michael J Szego
Affiliation
University of Toronto.
ORCID
Career Start Year
2003
Papers
30
H Index
14
Expertise
CM4AI Collaborator
Vardit Ravitsky (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37011345
Ethics Debriefs and Moral Distress: What are we Doing?
Am J Bioeth
2023
36368308
Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Cell
2022
34276804
Corrigendum: Parental Access to Children's Raw Genomic Data in Canada: Legal Rights and Professional Responsibility.
Front Genet
2021
33597540
Please give me a copy of my child's raw genomic data.
NPJ Genom Med
2021
33868358
Parental Access to Children's Raw Genomic Data in Canada: Legal Rights and Professional Responsibility.
Front Genet
2021
33758185
Author Correction: Please give me a copy of my child's raw genomic data.
NPJ Genom Med
2021
32036949
Response.
Gastrointest Endosc
2020
30528884
Revisiting code status in patients undergoing GI endoscopy with a "do not resuscitate" order.
Gastrointest Endosc
2019
31813827
Precision Health Resource of Control iPSC Lines for Versatile Multilineage Differentiation.
Stem Cell Reports
2019
31515274
Impact of DNA source on genetic variant detection from human whole-genome sequencing data.
J Med Genet
2019
30503855
Views from the clinic: Healthcare provider perspectives on whole genome sequencing in paediatrics.
Eur J Med Genet
2019
28771251
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.
Genet Med
2018
29431110
The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants.
CMAJ
2018
27888232
Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?
J Med Ethics
2017
28263302
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Nat Neurosci
2017
26159620
Difficult healthcare transitions: Ethical analysis and policy recommendations for unrepresented patients.
Nurs Ethics
2016
28567303
Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.
NPJ Genom Med
2016
27274747
Whole Genome Sequencing as a Genetic Test for Autism Spectrum Disorder: From Bench to Bedside and then Back Again.
J Can Acad Child Adolesc Psychiatry
2016
25046648
Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines.
Clin Genet
2015
25923536
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome.
BMC Genomics
2015
24592833
Predictive genomic testing of children for adult onset disorders: a Canadian perspective.
Am J Bioeth
2014
25512545
STAT3 promotes survival of mutant photoreceptors in inherited photoreceptor degeneration models.
Proc Natl Acad Sci U S A
2014
23469133
Endothelin-2-mediated protection of mutant photoreceptors in inherited photoreceptor degeneration.
PLoS One
2013
24223516
Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate.
PLoS Biol
2013
23926223
Building trust in 21st century genomics.
G3 (Bethesda)
2013
21851763
Organelle transplantation should be legalized in Canada.
J Obstet Gynaecol Can
2011
17988153
Overexpression of human CRB1 or related isoforms, CRB2 and CRB3, does not regulate the human presenilin complex in culture cells.
Biochemistry
2007
16959036
Generalization of DNA microarray dispersion properties: microarray equivalent of t-distribution.
Biol Direct
2006
15703187
Natural antisense transcripts associated with genes involved in eye development.
Hum Mol Genet
2005
14527271
Progress toward understanding the genetic and biochemical mechanisms of inherited photoreceptor degenerations.
Annu Rev Neurosci
2003
1 - 30 of 30
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