Myra I Roche


Ontology type: schema:Person     


Person Info

NAME

Myra I

SURNAME

Roche

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
  • JSON-LD is the canonical representation for SciGraph data.

    TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

    [
      {
        "@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
        "affiliation": [
          {
            "affiliation": {
              "id": "http://www.grid.ac/institutes/grid.10698.36", 
              "type": "Organization"
            }, 
            "isCurrent": true, 
            "type": "OrganizationRole"
          }, 
          {
            "id": "http://www.grid.ac/institutes/grid.410711.2", 
            "type": "Organization"
          }
        ], 
        "familyName": "Roche", 
        "givenName": "Myra I", 
        "id": "sg:person.01271031056.31", 
        "identifier": [
          {
            "name": "orcid_id", 
            "type": "PropertyValue", 
            "value": "0000-0001-9680-6006"
          }
        ], 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01271031056.31", 
          "https://orcid.org/0000-0001-9680-6006"
        ], 
        "sdDataset": "persons", 
        "sdDatePublished": "2021-11-01T19:33", 
        "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
        "sdPublisher": {
          "name": "Springer Nature - SN SciGraph project", 
          "type": "Organization"
        }, 
        "sdSource": "s3://com-springernature-scigraph/baseset/20211101/entities/gbq_results/person/person_968.jsonl", 
        "type": "Person"
      }
    ]
     

    Download the RDF metadata as:  json-ld nt turtle xml License info

    HOW TO GET THIS DATA PROGRAMMATICALLY:

    JSON-LD is a popular format for linked data which is fully compatible with JSON.

    curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/person.01271031056.31'

    N-Triples is a line-based linked data format ideal for batch operations.

    curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/person.01271031056.31'

    Turtle is a human-readable linked data format.

    curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/person.01271031056.31'

    RDF/XML is a standard XML format for linked data.

    curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/person.01271031056.31'


     




    Preview window. Press ESC to close (or click here)


    ...