Lauren Chad
St. Paul's Hospital
Vancouver, BC, Canada
Vancouver, BC, Canada
Last Updated: 09/26/2026
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Found 48 publications
First-Line Genetic Testing in Patients with Cleft Palate Only: The Role of Chromosomal Microarray Analysis.
Journal: Plastic and reconstructive surgery
Published: August 05, 2026
Correction: The development and usability of 'The Genetics Navigator': a digital solution for adult and paediatric clinical genetics services.
Journal: European journal of human genetics : EJHG
Published: April 02, 2026
Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study.
Journal: BMJ open
Published: March 27, 2026
The Patient-reported Genetic testing Utility InDEx (P-GUIDE): A novel measure of personal utility.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: December 16, 2025
Experiencing acute genomic care: perspectives from parents in the neonatal and paediatric intensive care units towards rapid genomic sequencing.
Journal: European journal of human genetics : EJHG
Published: August 06, 2025
Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencing.
Journal: Journal of genetic counseling
Published: July 11, 2025
How does personal utility depend on clinical setting? Evidence from 3 cohorts.
Journal: Genetics in medicine open
Published: May 13, 2025
Artificial Intelligence Software Changes Rare Disease Testing Strategy in Real Time: An International Case Series Using Face2Gene.
Journal: American journal of medical genetics. Part A
Published: April 29, 2025
The Clinician-reported Genetic Testing Utility InDEx for Neonatal Intensive Care (C-GUIDE NICU): Quantifying genome-wide sequencing utility in the NICU.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: January 22, 2025
Canadian College of Medical Geneticists (CCMG) position statement on the storage of patient genetic and genomic information in electronic health records.
Journal: Journal of medical genetics
Published: January 09, 2025
Rectifying or Reinforcing? The (In)Equity Implications of Recontacting Practices in Genomic Medicine.
Journal: The Hastings Center report
Published: December 21, 2024
Functional consequence of pathogenic GABRA3 variants determines whether X-linked inheritance is dominant or recessive.
Journal: The Journal of clinical investigation
Published: December 17, 2024
Last Updated: 09/26/2026