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Search Results

Showing results 1 to 20 of 24.

Focus Area

Transformative Health Research for All

Event

2022 NCSL Maternal & Child Health Fellows Meeting 2: Policy Solutions and Innovations

June 04, 2022
Event

American Society of Human Genetics (ASHG) Annual Meeting 2024

November 05, 2024
News Release

Early Check genome sequencing study reaches milestone of over 1,000 newborns screened in North Carolina

February 26, 2024
Event

Newborn Screening World View: International Summit on Newborn Screening

June 28, 2022
Announcement

RTI International and the North Carolina State Laboratory of Public Health edit a special issue of the North Carolina Medical Journal on newborn screening

January 14, 2019
RTI In The Media

Revvity to provide genome sequencing for North Carolina newborn screening study under deal with RTI

April 25, 2024 - GenomeWeb
Announcement

Study: Children with Gene Mutation Associated with Fragile X Experience Developmental Delays in First Two Years of Life

April 30, 2021
News Release

North Carolina’s Early Check Program to Add New Muscular Dystrophy Test to Newborn Screening Panel

March 03, 2020
RTI In The Media

Pioneering studies show promise in sequencing a baby’s genome at birth

June 17, 2024 - Washington Post
RTI In The Media

Holly Peay, PhD, on keeping patient preference in focus

May 04, 2024 - CGTLive
Event

APHA Annual Meeting 2019

November 02, 2019
Insight

A Window of Opportunity to Modernize Newborn Screening

September 22, 2022
News Release

Three Babies with Spinal Muscular Atrophy Have Bright Futures Thanks in Part to North Carolina’s Early Check Program

May 27, 2021
Event

APHA Annual Meeting 2021

October 24, 2021
Announcement

Commentary recommends improving process for adding conditions to newborn screening panels

August 07, 2023
Event

APHA Annual Meeting 2020

October 24, 2020
RTI In The Media

Experts Call for Better Newborn Screening to Take Advantage of Novel Therapies

February 16, 2022 - Contemporary Pediatrics
Expert

Becca Wright

Announcement

New Paper Describes Accurate, Scalable Method for Detecting Fragile X Syndrome in Newborns

March 05, 2020