NSIGHT BabySeq Project

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.

O. Ceyhan-Birsoy, J. Murry, K. Machini, et al.. (2019). American journal of human genetics. Cited 264 times. https://doi.org/10.1016/j.ajhg.2018.11.016

Newborn Sequencing in Genomic Medicine and Public Health

J. Berg, P. Agrawal, D. Bailey, et al.. (2017). Pediatrics. Cited 212 times. https://doi.org/10.1542/peds.2016-2252

The BabySeq project: implementing genomic sequencing in newborns

I. Holm, P. Agrawal, O. Ceyhan-Birsoy, et al.. (2018). BMC Pediatrics. Cited 158 times. https://doi.org/10.1186/s12887-018-1200-1

Parental Interest in Genomic Sequencing of Newborns: Enrollment Experience from the BabySeq Project

C. Genetti, T. Schwartz, J. Robinson, et al.. (2018). Genetics in medicine : official journal of the American College of Medical Genetics. Cited 78 times. https://doi.org/10.1038/s41436-018-0105-6

Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project

M. Wojcik, Tian Zhang, O. Ceyhan-Birsoy, et al.. (2021). Genetics in Medicine. Cited 64 times. https://doi.org/10.1038/s41436-021-01146-5

Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial.

Stacey Pereira, H. Smith, L. Frankel, et al.. (2021). JAMA pediatrics. Cited 53 times. https://doi.org/10.1001/jamapediatrics.2021.2829

Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project

I. Holm, A. McGuire, Stacey Pereira, et al.. (2019). Pediatrics. Cited 46 times. https://doi.org/10.1542/peds.2018-1099H

Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report

J. Murry, K. Machini, O. Ceyhan-Birsoy, et al.. (2018). Cold Spring Harbor Molecular Case Studies. Cited 8 times. https://doi.org/10.1101/mcs.a002873

Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression

T. Schwartz, K. Christensen, M. Uveges, et al.. (2021). Journal of Genetic Counseling. Cited 7 times. https://doi.org/10.1002/jgc4.1475