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Page 1
Preimplantation genetic testing for aneuploidy versus morphology as selection criteria for single frozen-thawed embryo transfer in good-prognosis patients: a multicenter randomized clinical trial.
Munné S, Kaplan B, Frattarelli JL, Child T, Nakhuda G, Shamma FN, Silverberg K, Kalista T, Handyside AH, Katz-Jaffe M, Wells D, Gordon T, Stock-Myer S, Willman S; STAR Study Group. Munné S, et al. Among authors: stock myer s. Fertil Steril. 2019 Dec;112(6):1071-1079.e7. doi: 10.1016/j.fertnstert.2019.07.1346. Epub 2019 Sep 21. Fertil Steril. 2019. PMID: 31551155 Free article. Clinical Trial.
Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro.
Natesan SA, Bladon AJ, Coskun S, Qubbaj W, Prates R, Munne S, Coonen E, Dreesen JC, Stevens SJ, Paulussen AD, Stock-Myer SE, Wilton LJ, Jaroudi S, Wells D, Brown AP, Handyside AH. Natesan SA, et al. Among authors: stock myer se. Genet Med. 2014 Nov;16(11):838-45. doi: 10.1038/gim.2014.45. Epub 2014 May 8. Genet Med. 2014. PMID: 24810687 Free PMC article.
A big step forward for PGT-M?
Stock-Myer S, Johnson M. Stock-Myer S, et al. Reprod Biomed Online. 2018 Aug;37(2):126-127. doi: 10.1016/j.rbmo.2018.06.017. Reprod Biomed Online. 2018. PMID: 30075839 No abstract available.
The Effect of Assisted Reproductive Technologies on Human Sex Ratios.
Georgiou EX, Mizrachi Y, Kelley R, Stock-Myer S, Stevens J, Gardner DK, Polyakov A. Georgiou EX, et al. Among authors: stock myer s. Aust N Z J Obstet Gynaecol. 2025 Jan 26. doi: 10.1111/ajo.13940. Online ahead of print. Aust N Z J Obstet Gynaecol. 2025. PMID: 39865443
Nationwide, Couple-Based Genetic Carrier Screening.
Kirk EP, Delatycki MB, Archibald AD, Tutty E, Caruana J, Halliday JL, Lewis S, McClaren BJ, Newson AJ, Dive L, Best S, Long JC, Braithwaite J, Downes MJ, Scuffham PA, Massie J, Barlow-Stewart K, Kulkarni A, Ruscigno A, Kanga-Parabia A, Rodrigues B, Bennetts BH, Ebzery C, Hunt C, Cliffe CC, Lee C, Azmanov D, King EA, Madelli EO, Zhang F, Ho G, Danos I, Liebelt J, Fletcher J, Kennedy J, Beilby J, Emery JD, McGaughran J, Marum JE, Scarff K, Fisk K, Harrison K, Boggs K, Giameos L, Fitzgerald L, Thomas L, Burnett L, Freeman L, Harris M, Berbic M, Davis MR, Cifuentes Ochoa M, Wallis M, Wall M, Chow MTM, Ferrie MM, Pachter N, Quayum N, Lang N, Kasi Pandy P, Casella R, Allcock RJN, Ong R, Edwards S, Sundercombe S, Jelenich S, Righetti S, Lunke S, Kaur S, Stock-Myer S, Eggers S, Walker SP, Theodorou T, Catchpool T, Clinch T, Roscioli T, Hardy T, Zhu Y, Fehlberg Z, Boughtwood TF, Laing NG; Mackenzie’s Mission Investigators; Mackenzie's Mission Investigators. Kirk EP, et al. Among authors: stock myer s. N Engl J Med. 2024 Nov 21;391(20):1877-1889. doi: 10.1056/NEJMoa2314768. N Engl J Med. 2024. PMID: 39565987
Three Mendelian disorders (chronic granulomatous disease, retinitis pigmentosa, ornithine transcarbamylase deficiency) in a young woman with an X chromosome deletion, del(X)(p11.4p21.1).
Coman D, Yaplito-Lee J, La P, Nasioulas S, Bruno D, Slater HR, Stock-Myer SE, Lynch EL, Gardner RJ. Coman D, et al. Among authors: stock myer se. Mol Genet Metab. 2010 Mar;99(3):329. doi: 10.1016/j.ymgme.2009.11.006. Epub 2009 Nov 27. Mol Genet Metab. 2010. PMID: 20036594 No abstract available.