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Author Details
Full Name
Lauren Chad
Affiliation
Hospital for Sick Children, Canada University of Toronto
ORCID
Career Start Year
2008
Papers
28
H Index
8
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37924259
Evaluation of the diagnostic accuracy of exome sequencing and its impact on diagnostic thinking for patients with rare disease in a publicly funded health care system: A prospective cohort study.
Genet Med
2024
37962958
Spliceosome malfunction causes neurodevelopmental disorders with overlapping features.
J Clin Invest
2024
37932018
Next generation of free? Points to consider when navigating sponsored genetic testing.
J Med Genet
2024
36353900
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing data.
Clin Genet
2023
37516567
Assessing the Performance of the Clinician-reported Genetic Testing Utility InDEx (C-GUIDE): Further Evidence of Inter-rater Reliability.
Clin Ther
2023
36959498
Equity implications of patient-initiated recontact and follow-up in clinical genetics.
Eur J Hum Genet
2023
33199447
Canadian College of Medical Geneticists (CCMG) points to consider: resuming genetic services in a pandemic-a summary.
J Med Genet
2022
35361921
DNA methylation signature associated with Bohring-Opitz syndrome: a new tool for functional classification of variants in ASXL genes.
Eur J Hum Genet
2022
35859676
Bioethics at the bedside.
Paediatr Child Health
2022
36195708
Applying the Clinician-reported Genetic testing Utility InDEx (C-GUIDE) to genome sequencing: further evidence of validity.
Eur J Hum Genet
2022
36161483
Rapid Genetic Testing in Pediatric and Neonatal Critical Care: A Scoping Review of Emerging Ethical Issues.
Hosp Pediatr
2022
35043535
The utility of DNA methylation signatures in directing genome sequencing workflow: Kabuki syndrome and CDK13-related disorder.
Am J Med Genet A
2022
34906486
The Clinician-reported Genetic testing Utility InDEx (C-GUIDE): Preliminary evidence of validity and reliability.
Genet Med
2022
33244863
The point-of-care use of a facial phenotyping tool in the genetics clinic: An ethics tête-a-tête.
Am J Med Genet A
2021
35599679
A 5-year-old girl with abdominal pain, headache, and cracked lips.
Paediatr Child Health
2021
33597540
Please give me a copy of my child's raw genomic data.
NPJ Genom Med
2021
33758185
Author Correction: Please give me a copy of my child's raw genomic data.
NPJ Genom Med
2021
33554457
The point-of-care use of a facial phenotyping tool in the genetics clinic: Enhancing diagnosis and education with machine learning.
Am J Med Genet A
2021
35273666
Understanding genetic variants of uncertain significance.
Paediatr Child Health
2021
34481766
Screening for facial differences worldwide: equity and ethics.
Lancet Digit Health
2021
31363181
The development of the Clinician-reported Genetic testing Utility InDEx (C-GUIDE): a novel strategy for measuring the clinical utility of genetic testing.
Genet Med
2020
31740736
Response to Rubanovich et al.
Genet Med
2020
28567303
Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.
NPJ Genom Med
2016
23766044
Update on antidepressant use during breastfeeding.
Can Fam Physician
2013
24410784
A majority of parents of children with peanut allergy fear using the epinephrine auto-injector.
Allergy
2013
22901051
Postmortem vascular pathology in PHACES syndrome: a case report.
Pediatr Dev Pathol
2012
18216865
Association of LY9 in UK and Canadian SLE families.
Genes Immun
2008
18682749
Germline EPHB2 receptor variants in familial colorectal cancer.
PLoS One
2008
1 - 28 of 28
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Leslie G Biesecker
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Mildred K Cho
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E Clayton
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Ingrid A Holm
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Marc S Williams
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Wylie Burke
The Heart Institute, Cincinnati Children's Hospital Medical Center
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Joann Bodurtha
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row(s) 1 - 30 of 30
Collaborators
Wendy J Ungar
The Hospital for Sick Children
Co-authored papers
5
Kym M Boycott
Children's Hospital of Eastern Ontario
Co-authored papers
3
Michael J Szego
University of Toronto.
Co-authored papers
3
Alexandre Montpetit
McGill University and Genome Quebec Innovation Centre
Co-authored papers
2
Thomas J Hudson
Ontario Institute for Cancer Research
Co-authored papers
2
Melissa D McCradden
University of Adelaide
Co-authored papers
2
Anna C E Hurst
Co-authored papers
2
Stephen W Scherer
The Hospital for Sick Children
Co-authored papers
2
Julie Richer
University of Ottawa, Canada Children's Hospital of Eastern Ontario
Co-authored papers
2
Taila Hartley
Children's Hospital of Eastern Ontario Research Institute
Co-authored papers
2
Christian R Marshall
Co-authored papers
2
Pierre Lepage
Co-authored papers
1
Lijia Huang
Children's Hospital of Eastern Ontario (CHEO)
Co-authored papers
1
Asif Doja
University of Ottawa
Co-authored papers
1
Elaine H Zackai
Children's Hospital of Philadelphia
Co-authored papers
1
John M Greally
Co-authored papers
1
Rulan S Parekh
Co-authored papers
1
Vandana Shashi
Duke University School of Medicine
Co-authored papers
1
Joan E Wither
Schroeder Arthritis Institute, Krembil Research Institute, University Health Network
Co-authored papers
1
Ryan K C Yuen
Co-authored papers
1
Ela Patel
College of Medicine, University of Kentucky
Co-authored papers
1
Marta Girdea
DATA Team and Techna Institute, University Health Network
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1
Brendan J Frey
University of Toronto
Co-authored papers
1
Paul R Fortin
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Mark A Tarnopolsky
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