Rebecca M. Reimers

Neonatology | Obstetrics and Gynecology | Medical Genetics

3020 Children's Way
San Diego, CA 92123

Last Updated: 09/26/2026

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Found 20 publications

Novel Therapeutic Treatments in Perinatal Genetics Bridging Prenatal and Postnatal Care of Genetic Conditions.

Novel Therapeutic Treatments in Perinatal Genetics Bridging Prenatal and Postnatal Care of Genetic Conditions.

Journal: Clinical therapeutics

Published: May 28, 2026

The Fastest NICU Genome is One Completed (or at Least Coordinated) Prenatally: A Joint Perspective From United States-Based Maternal-Fetal Medicine and Neonatologist-Geneticists.

The Fastest NICU Genome is One Completed (or at Least Coordinated) Prenatally: A Joint Perspective From United States-Based Maternal-Fetal Medicine and Neonatologist-Geneticists.

Journal: Clinical therapeutics

Published: January 29, 2026

Clinical utility and cost-effectiveness of BeginNGS newborn screening by genome sequencing and standard newborn screening for severe childhood genetic diseases: an adaptive, international and comparative clinical trial.

Clinical utility and cost-effectiveness of BeginNGS newborn screening by genome sequencing and standard newborn screening for severe childhood genetic diseases: an adaptive, international and comparative clinical trial.

Journal: BMJ open

Published: November 14, 2025

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations.

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations.

Journal: Nature communications

Published: November 11, 2024

Advancing precision care in pregnancy through a treatable fetal findings list.

Advancing precision care in pregnancy through a treatable fetal findings list.

Journal: American journal of human genetics

Published: September 25, 2024

Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial.

Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial.

Journal: American journal of human genetics

Published: August 07, 2024

A Machine Learning Decision Support Tool Optimizes Whole Genome Sequencing Utilization in a Neonatal Intensive Care Unit.

A Machine Learning Decision Support Tool Optimizes Whole Genome Sequencing Utilization in a Neonatal Intensive Care Unit.

Journal: medRxiv : the preprint server for health sciences

Published: July 15, 2024

A machine learning decision support tool optimizes WGS utilization in a neonatal intensive care unit.

A machine learning decision support tool optimizes WGS utilization in a neonatal intensive care unit.

Journal: NPJ digital medicine

Published: July 05, 2024

Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection.

Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection.

Journal: American journal of human genetics

Published: June 11, 2024

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations.

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations.

Journal: bioRxiv : the preprint server for biology

Published: February 26, 2024

Unique Challenges of NIPT for Sex Chromosome Aneuploidy.

Unique Challenges of NIPT for Sex Chromosome Aneuploidy.

Journal: Clinical obstetrics and gynecology

Published: August 31, 2023

The landscape of tolerated genetic variation in humans and primates.

The landscape of tolerated genetic variation in humans and primates.

Journal: Science (New York, N.Y.)

Published: June 01, 2023

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Last Updated: 09/26/2026