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Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.
Lowther C, Valkanas E, Giordano JL, Wang HZ, Currall BB, O'Keefe K, Pierce-Hoffman E, Kurtas NE, Whelan CW, Hao SP, Weisburd B, Jalili V, Fu J, Wong I, Collins RL, Zhao X, Austin-Tse CA, Evangelista E, Lemire G, Aggarwal VS, Lucente D, Gauthier LD, Tolonen C, Sahakian N, Stevens C, An JY, Dong S, Norton ME, MacKenzie TC, Devlin B, Gilmore K, Powell BC, Brandt A, Vetrini F, DiVito M, Sanders SJ, MacArthur DG, Hodge JC, O'Donnell-Luria A, Rehm HL, Vora NL, Levy B, Brand H, Wapner RJ, Talkowski ME. Lowther C, et al. Among authors: gilmore k. Am J Hum Genet. 2023 Sep 7;110(9):1454-1469. doi: 10.1016/j.ajhg.2023.07.010. Epub 2023 Aug 17. Am J Hum Genet. 2023. PMID: 37595579 Free PMC article.
Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges.
Vora NL, Powell B, Brandt A, Strande N, Hardisty E, Gilmore K, Foreman AKM, Wilhelmsen K, Bizon C, Reilly J, Owen P, Powell CM, Skinner D, Rini C, Lyerly AD, Boggess KA, Weck K, Berg JS, Evans JP. Vora NL, et al. Among authors: gilmore k. Genet Med. 2017 Nov;19(11):1207-1216. doi: 10.1038/gim.2017.33. Epub 2017 May 18. Genet Med. 2017. PMID: 28518170 Free PMC article.
Ethical and counseling challenges in prenatal exome sequencing.
Harris S, Gilmore K, Hardisty E, Lyerly AD, Vora NL. Harris S, et al. Among authors: gilmore k. Prenat Diagn. 2018 Nov;38(12):897-903. doi: 10.1002/pd.5353. Epub 2018 Sep 11. Prenat Diagn. 2018. PMID: 30171820 Free PMC article.
How can prenatal exome sequencing inform future pregnancies?
Talati AN, Gilmore KL, Hardisty E, Vora NL. Talati AN, et al. Am J Obstet Gynecol. 2022 Jul;227(1):98-99. doi: 10.1016/j.ajog.2022.02.008. Epub 2022 Feb 12. Am J Obstet Gynecol. 2022. PMID: 35167813 Free PMC article. No abstract available.
273 results