RTI GenOmics, Bioinformatics, and Translational Research Center

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Public Health and Well-Being

Rare Disease Leaders Announce Collaboration to Modernize Newborn Screening

New laboratory screening test for fragile X syndrome shortly after birth now ready for pivotal North Carolina Early Check clinical study

New NC-Based Study to Advance Research Through Free and Expanded Health Screening for Newborn Babies

Integrated Database and Registry for Angelman and Dup15q Syndromes Aims to Improve Patient Care and Treatment

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

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

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

New NIH-funded research center to leverage multiple omics to better understand and treat opioid addiction

Supplement in Pediatrics synthesizes research on fragile X

You can get your baby tested for two rare genetic disorders - for free

Researchers Find Vitamin D Does Not Impact Risks Associated with COVID-19 or Severity of the Virus

RTI, UNC to Play Key Roles in $170M NIH Study on Nutrition

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

RTI International collaborates on multiple publications on Red Blood Cell-Omics Study

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

New Study Provides Insights into the Mystery of Restless Legs Syndrome

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

SMA Added to North Carolina’s Newborn Screening Program

Publication Finds That Modernization of U.S. Newborn Screening System is Necessary, Identifies Strategies for Change

Reimagining the Newborn Screening System: Q&A with Don Bailey