Article

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

2020-11-17

Abstract excerpt

<title>Abstract</title> <p>BackgroundIncreasingly, genomics is informing clinical practice, but challenges remain for medical professionals lacking genetics expertise, and in access to and clinical utility of genomic testing for minority and underrepresented populations. The latter is a particularly pernicious problem due to the historical lack of inclusion of racially and ethnically diverse populations in genomi...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 40f1f019-2320-5f8f-a17c-6a8a86b801a6
DOI: 10.21203/rs.3.rs-64844/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City childrenDOI 10.21203/rs.3.rs-64844/v1Read

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City childrenSemantic proximity Read

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse familiesSemantic proximity Read

Reducing Time to Diagnosis of Rare Genetic Diseases in a Medically Underserved Hispanic Population- Lessons Learned for Meaningful EngagementSemantic proximity Read

Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program.Semantic proximity Read

Genomic sequencing in diverse and underserved pediatric populations: Parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of resultsSemantic proximity Read

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 trialSemantic proximity Read

An algorithm to identify patients with rare genetic disorders and its real-world data applicationSemantic proximity Read

Advancing Understanding of Inequities in Rare Disease GenomicsSemantic proximity Read

Diagnostic yield of genetic screening in a diverse, community-ascertained cohortSemantic proximity Read

Genome screening, reporting, and genetic counseling for healthy populations.Semantic proximity Read

Clinical whole genome sequencing as a first-tier test at a resource-limited dysmorphology clinic in MexicoSemantic proximity Read

Building a Vertically-Integrated Genomic Learning Health System: The Colorado Center for Personalized Medicine BiobankSemantic proximity Read