PIPages
Labs

Sabrina Malone Jenkins

University of Utah, UT·Medicine & Clinical Research·Early-career

Rapid whole genome sequencing reads a baby's entire DNA within days. Studies show it speeds diagnosis and life-saving treatment for critically ill newborns, and current guidelines recommend it as standard care.

Fields

Medicine & Clinical Research

Public Health & Epidemiology

Genetics

Topics

rapid whole genome sequencing

rWGS

genomic medicine

Grants
1 known grant, through Aug 2028

What they work on

  1. Build logic models mapping barriers and facilitators to adopting rapid whole genome sequencing in Level 4 (metropolitan, well-resourced) and Level 3 (rural, lower-resourced) NICUs.
  2. Develop implementation strategies tailored to each NICU level that address the barriers identified to using rapid genome sequencing for critically ill newborns.
  3. Test these strategies in a small-scale demonstration project to see whether they improve uptake of rapid whole genome sequencing in neonatal intensive care.

More about the research

Yet many neonatal intensive care units (NICUs) still do not use it. This gap delays answers for families, and it is wider in rural hospitals with fewer resources, where healthcare inequities already exist.

Why it matters

Closing the gap between guidelines and practice could bring faster genetic diagnoses and earlier treatment to critically ill newborns. The benefit could be largest in rural, lower-resourced NICUs, where adoption lags most. The strategies may help reduce healthcare inequities in neonatal genomic medicine.

Known grants

From NIH and NSF research grants. Labs often have other funding we can't see.

Addressing the research-practice gap in the implementation of rapid whole genome sequencing in the NICU

NIH · Sep 2023 – Aug 2028

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The school

University of Utah: 58 labs on PI Pages, $789M a year on research, 366 research doctorates a year.

More about University of Utah

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