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Children (Basel, Switzerland)
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May 27, 2026
Resource Use and Costs of Nurse Navigator Support for Parents of High-Risk Infants After Discharge from a Neonatal Intensive Care Unit
Vercancy Wu, Myla E Moretti, Kayla Esser, et al.
Clinical Therapeutics
|
July 15, 2023
Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions
Wendy J Ungar, Robin Z Hayeems, Christian R Marshall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 25, 2025
A Microcosting and Cost Consequence Analysis from a Randomized Controlled Trial Comparing Genome Sequencing to Exome Sequencing for Genetic Diagnosis
Wendy J Ungar, Vercancy Wu, Christian R Marshall, et al.
BMJ Open
|
March 27, 2026
Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study
Daniel Assamad, Abigail Hansen, Katharine Fooks, et al.
Journal of Genetic Counseling
|
May 5, 2026
Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencing
Abigail Hansen, Stephanie Luca, Olivia Moran, et al.
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Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Children (Basel, Switzerland)
|
May 27, 2026
Resource Use and Costs of Nurse Navigator Support for Parents of High-Risk Infants After Discharge from a Neonatal Intensive Care Unit
Vercancy Wu, Myla E Moretti, Kayla Esser, et al.
Clinical Therapeutics
|
July 15, 2023
Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions
Wendy J Ungar, Robin Z Hayeems, Christian R Marshall, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 25, 2025
A Microcosting and Cost Consequence Analysis from a Randomized Controlled Trial Comparing Genome Sequencing to Exome Sequencing for Genetic Diagnosis
Wendy J Ungar, Vercancy Wu, Christian R Marshall, et al.
BMJ Open
|
March 27, 2026
Understanding the impact of genomic secondary findings on clinical care and patient experience: a protocol for a prospective observational study
Daniel Assamad, Abigail Hansen, Katharine Fooks, et al.
Journal of Genetic Counseling
|
May 5, 2026
Understanding the decision of parents to opt-out of medically actionable secondary findings offered through genome sequencing
Abigail Hansen, Stephanie Luca, Olivia Moran, et al.
Page
of 1