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Disparities in access to reproductive genetic services associated with geographic location of residence and maternal race and ethnicity.

Autor: Talati AN; Division of Maternal Fetal Medicine and Reproductive Genetics, University Of North Carolina At Chapel Hill, Chapel Hill, NC, 27599. Electronic address: asha_talati@med.unc.edu., Mallampati DP; Division of Maternal Fetal Medicine, University of California San Francisco, San Francisco, CA., Hardisty EE; Division of Maternal Fetal Medicine and Reproductive Genetics, University Of North Carolina At Chapel Hill, Chapel Hill, NC, 27599., Gilmore KL; Division of Maternal Fetal Medicine and Reproductive Genetics, University Of North Carolina At Chapel Hill, Chapel Hill, NC, 27599., Vora NL; Division of Maternal Fetal Medicine and Reproductive Genetics, University Of North Carolina At Chapel Hill, Chapel Hill, NC, 27599.

Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2024 Nov; Vol. 26 (11), pp. 101221. Date of Electronic Publication: 2024 Jul 20.

The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease.

Autor: Zhao E; Department of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Bomback M; Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA., Khan A; Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA., Krishna Murthy S; Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA., Solowiejczyk D; Department of Pediatrics, Columbia University Irving Medical Center, New York, New York, USA., Vora NL; Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, School of Medicine, Chapel Hill, North Carolina, USA., Gilmore KL; Department of Obstetrics and Gynecology, University of North Carolina at Chapel Hill, School of Medicine, Chapel Hill, North Carolina, USA., Giordano JL; Department of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, New York, USA., Wapner RJ; Department of Obstetrics and Gynecology, Columbia University Irving Medical Center, New York, New York, USA., Sanna-Cherchi S; Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA., Lyford A; Department of Mathematics and Statistics, Middlebury College, Middlebury, Vermont, USA., Jelin AC; Department of Gynecology and Obstetrics, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA., Gharavi AG; Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA., Hays T; Department of Pediatrics, Columbia University Irving Medical Center, New York, New York, USA.

Publikováno v: Prenatal diagnosis [Prenat Diagn] 2024 Mar; Vol. 44 (3), pp. 343-351. Date of Electronic Publication: 2024 Jan 29.

Association of deep phenotyping with diagnostic yield of prenatal exome sequencing for fetal brain abnormalities.

Autor: Drexler KA; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC. Electronic address: kathleen.drexler@unchealth.unc.edu., Talati AN; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC., Gilmore KL; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC., Veazey RV; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC., Powell BC; Department of Pediatrics, Division of Genetics and Metabolism, University of North Carolina at Chapel Hill, Chapel Hill, NC., Weck KE; Department of Genetics, Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC., Davis EE; Department of Pediatrics, Department of Cell and Developmental Biology, Feinberg School of Medicine, Stanley Manne Children's Research Institute, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University, Chicago, IL., Vora NL; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.

Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2023 Oct; Vol. 25 (10), pp. 100915. Date of Electronic Publication: 2023 Jun 13.

Diagnostic yield and psychological outcomes among women pursuing trio-exome sequencing: Do women with recurrent anomalous fetal phenotypes experience more negative psychological outcomes?

Autor: Talati AN; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA., Gilmore KL; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA., Hardisty EE; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA., Lyerly AD; Department of Social Medicine and Center for Bioethics, University of North Carolina, Chapel Hill, North Carolina, USA., Rini C; Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine and the Robert H. Lurie Comprehensive Cancer Center of Northwestern University, Evanston, Illinois, USA., Vora NL; Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, University of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.

Publikováno v: Prenatal diagnosis [Prenat Diagn] 2023 May; Vol. 43 (5), pp. 569-578. Date of Electronic Publication: 2023 Feb 02.