Talia Schwartz, MD

Pediatric endoscopic ultrasound-guided liver biopsy: 3-year experience. Schwartz, TS; Mouzaki, M; Berklite, L; Lopez-Nunez, OF; Miethke, A; Xanthakos, SA; Vitale, DS. Journal of Pediatric Gastroenterology and Nutrition. 2025; 80(5):920-925.

Su2029 INTERVENTIONAL RADIOLOGY VS. ENDOSCOPIC ULTRASOUND GUIDED LIVER BIOPSIES IN PEDIATRIC MASLD. Schwartz, TS; Mouzaki, M; Berklite, L; Lopez-Nunez, O; Miethke, A; Xanthakos, S; Vitale, DS. Gastroenterology. 2024; 166(5):s-898.

Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project. Green, RC; Shah, N; Genetti, CA; Yu, T; Zettler, B; Uveges, MK; Ceyhan-Birsoy, O; Lebo, MS; Pereira, S; Agrawal, PB; Schwartz, TS; Rehm, HL; Holm, IA; Beggs, AH. American Journal of Human Genetics. 2023; 110(7):1034-1045.

Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression. Schwartz, TS; Christensen, KD; Uveges, MK; Waisbren, SE; Mcguire, AL; Pereira, S; Robinson, JO; Beggs, AH; Green, RC; Bachmann, GA; Rabson, AB; Holm, IA. Journal of Genetic Counseling. 2022; 31(1):218-229.

Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project: A Randomized Clinical Trial. Pereira, S; Smith, HS; Frankel, LA; Christensen, KD; Islam, R; Robinson, JO; Genetti, CA; Blout Zawatsky, CL; Zettler, B; Parad, RB; Waisbren, SE; Beggs, AH; Green, RC; Holm, IA; Mcguire, AL. JAMA pediatrics. 2021; 175(11):1132-1141.

Discordant results between conventional newborn screening and genomic sequencing in the BabySeq Project. Wojcik, MH; Zhang, T; Ceyhan-Birsoy, O; Genetti, CA; Lebo, MS; Yu, TW; Parad, RB; Holm, IA; Rehm, HL; Beggs, AH; Green, RC; Agrawal, PB. Genetics in Medicine. 2021; 23(7):1372-1375.

Infant mortality: the contribution of genetic disorders. Wojcik, MH; Schwartz, TS; Thiele, KE; Paterson, H; Stadelmaier, R; Mullen, TE; Vannoy, GE; Genetti, CA; Madden, JA; Gubbels, CS; Yu, TW; Tan, W-H; Agrawal, PB. Journal of Perinatology. 2019; 39(12):1611-1619.

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, WN; Yu, TW; Green, RC; Beggs, AH; Parad, RB. Genetics in Medicine. 2019; 21(3):622-630.

Expanding the phenotypic spectrum associated with OPHN1 variants. Schwartz, TS; Wojcik, MH; Pelletier, RC; Edward, HL; Picker, JD; Holm, IA; Towne, MC; Beggs, AH; Agrawal, PB. European Journal of Medical Genetics. 2019; 62(2):137-143.

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project. Ceyhan-Birsoy, O; Murry, JB; Machini, K; Lebo, MS; Yu, TW; Fayer, S; Genetti, CA; Schwartz, TS; Agrawal, PB; Parad, RB; Holm, IA; Mcguire, AL; Green, RC; Rehm, HL; Beggs, AH. American Journal of Human Genetics. 2019; 104(1):76-93.