Publications and Literature
A collection of relevant articles and studies
Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing
Mallory J. Owen, MB, ChB1,2; Meredith S. Wright, PhD1; Sergey Batalov, MS1; et al
JAMA Network | February 2023
Moving away from one disease at a time: Screening, trial design, and regulatory implications of novel platform technologies
Lekstrom-Himes J, Brooks PJ, Koeberl DD, Brower A, Goldenberg A, Green RC, Morris JA, Orsini JJ, Yu TW, Augustine EF
American Journal of Medical Genetics | January 2023
Parents’ decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project
Pereira S, Gutierrez AM, Robinson JO, Christensen KD, Genetti CA, Zawatsky CLB, Hsu RL, Zettler B, Uveges MK, Parad RB, Beggs AH, Holm IA, Green RC, McGuire AL for The BabySeq Project Team
Genetics in Medicine | December 2022
Parental interest in genomic sequencing of newborns: Enrollment experience from the BabySeq Project
Genetti CA, Schwartz TS, Robinson JO, VanNoy GE, Petersen D, Pereira S, Fayer S, Peoples HA, Agrawal PB, Betting WB, Holm IA, McGuire AL, Waisbren SE, Yu TW, Green RC, Beggs AH, Parad RB
Genetics in Medicine | March 2018
Newborn sequencing in genomic medicine and public health (NSIGHT)
Berg JS, Agrawal PB, Bailey DB, Beggs AH, Brenner SE, Brower AM, Butler I, Caciki J, Birsoy O, Chan K, Chen F, Currier RJ, Duchovny D, Green RC, Harris-Wai J, Holm IA, Iglesias B, Joseph G, Kingsmore SF, Koenig BA, Kwok P, Lantos J, Leeder J, Lewis MA, McGuire AL, Milko LV, Mooney SD, Veeraraghaven N, Parad RB, Pereira S, Petrikin J, Powell BC, Powell CM, Puck JM, Rehm HL, Risch N, Roche M, Shieh JT, Watson MS, Willig L, Yu TW, Urv T, Wise AL
Pediatrics | February 2017
Disclosing secondary findings from pediatric sequencing to families: Considering the benefit to families
Wilfond BS, Fernandez CV, Green RC
The Journal of Law | October 2015