Myra I Roche

Ontology type: schema:Person     

Person Info


Myra I



Publications in SciGraph latest 50 shown

  • 2021-06-14 Evaluating the clinical utility of early exome sequencing in diverse pediatric outpatient populations in the North Carolina Clinical Genomic Evaluation of Next-generation Exome Sequencing (NCGENES) 2 study: a randomized controlled trial in TRIALS
  • 2020-05-18 Parental Views on Newborn Next Generation Sequencing: Implications for Decision Support in MATERNAL AND CHILD HEALTH JOURNAL
  • 2019-07-25 Correction: Genomic knowledge in the context of diagnostic exome sequencing: changes over time, persistent subgroup differences, and associations with psychological sequencing outcomes in GENETICS IN MEDICINE
  • 2019-07-17 Genomic Knowledge in the Context of Diagnostic Exome Sequencing: Changes over Time, Persistent Subgroup Differences, and Associations with Psychological Sequencing Outcomes in GENETICS IN MEDICINE
  • 2018-09-21 Factors influencing NCGENES research participants’ requests for non-medically actionable secondary findings in GENETICS IN MEDICINE
  • 2018-07-06 Developing a Conceptual, Reproducible, Rubric-Based Approach to Consent and Result Disclosure for Genetic Testing by Clinicians with Minimal Genetics Background in GENETICS IN MEDICINE
  • 2018-06-28 Evaluating parents’ decisions about next-generation sequencing for their child in the NC NEXUS (North Carolina Newborn Exome Sequencing for Universal Screening) study: a randomized controlled trial protocol in TRIALS
  • 2018-03-01 Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium in JOURNAL OF GENETIC COUNSELING
  • 2017-10-26 The who, what and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study in GENETICS IN MEDICINE
  • 2017-10-02 “Possibly positive or certainly uncertain?”: Participants’ responses to uncertain diagnostic results from exome sequencing in GENETICS IN MEDICINE
  • 2017-08-03 Parental preferences toward genomic sequencing for non-medically actionable conditions in children: a discrete choice experiment in GENETICS IN MEDICINE
  • 2016-04-07 It’s time to ramp up genetic counseling training in GENETICS IN MEDICINE
  • 2015-08-25 Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice in CURRENT GENETIC MEDICINE REPORTS
  • 2015-08-13 A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing in GENETICS IN MEDICINE
  • 2014-08-01 Next Generation Genetic Counseling: Introduction to the Special Issue in JOURNAL OF GENETIC COUNSELING
  • 2014-02-08 GCH1 heterozygous mutation identified by whole-exome sequencing as a treatable condition in a patient presenting with progressive spastic paraplegia in JOURNAL OF NEUROLOGY
  • 2013-02-01 Design and Evaluation of a Decision Aid for Inviting Parents to Participate in a Fragile X Newborn Screening Pilot Study in JOURNAL OF GENETIC COUNSELING
  • 2012-10-25 Can a decision aid enable informed decisions in neonatal nursery recruitment for a fragile X newborn screening study? in GENETICS IN MEDICINE
  • 2012-07-12 Moving toward NextGenetic Counseling in GENETICS IN MEDICINE
  • 2008-05-14 A case of genetic counselling for Dr Watson in NATURE
  • 2006 Genetic Counseling Considerations in Molecular Diagnosis in MOLECULAR DIAGNOSTICS
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