Our Publications Selected recent publications from our team include: General genomics A model to implement genomic medicine in the neonatal intensive care unit. Wojcik MH, D'Gama AM, Agrawal PB. J Perinatol 2023 Feb; 43(2):248-252. Integrating rapid exome sequencing into NICU clinical care after a pilot research study. D’Gama AM; et al. NPJ Genom Med 2022 Sep 5; 7(1):51. Perspectives of United States neonatologists on genetic testing practices. Wojcik MH; et al. Genet Med 2022 Jun; 24(6):1372-1377. Further Considerations on the Value of Whole-Genome Sequencing in Critically Ill Infants. Wojcik MH, Fraiman YS. JAMA Pediatr 2022 Apr 1; 176(4):420-421. Condition-specific Trisomy 13: Survival beyond the NICU. Hu RS; et al. Neoreviews 2023 Jan 1; 24(1):51-56. Association of Potentially Damaging De Novo Gene Variants With Neurologic Outcomes in Congenital Heart Disease. Morton SU; et al. JAMA Network Open 2023 Jan 3; 6(1):e2253191. The Genetics of Neurodevelopment in Congenital Heart Disease. Patt E, Singhania A, Roberts AE, Morton SU. Can J Cardiol 2023 Feb; 39(2):97-114. Premature Infants Have Normal Maturation of the T Cell Receptor Repertoire at Term. Morton SU; et al. Front Immunol 2022 May 30; 13:854414. Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era: A Review. Morton SU; et al. JAMA Neurol 2022 Apr 1; 79(4):405-413.
