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Causal Genetic Variants in Stillbirth. Reply.
Stanley KE, Wapner RJ, Goldstein DB. Stanley KE, et al. N Engl J Med. 2020 Dec 31;383(27):2687-2688. doi: 10.1056/NEJMc2032136. N Engl J Med. 2020. PMID: 33382938 No abstract available.
Causal Genetic Variants in Stillbirth.
Stanley KE, Giordano J, Thorsten V, Buchovecky C, Thomas A, Ganapathi M, Liao J, Dharmadhikari AV, Revah-Politi A, Ernst M, Lippa N, Holmes H, Povysil G, Hostyk J, Parker CB, Goldenberg R, Saade GR, Dudley DJ, Pinar H, Hogue C, Reddy UM, Silver RM, Aggarwal V, Allen AS, Wapner RJ, Goldstein DB. Stanley KE, et al. N Engl J Med. 2020 Sep 17;383(12):1107-1116. doi: 10.1056/NEJMoa1908753. Epub 2020 Aug 12. N Engl J Med. 2020. PMID: 32786180 Free PMC article.
Cell type signatures in cell-free DNA fragmentation profiles reveal disease biology.
Stanley KE, Jatsenko T, Tuveri S, Sudhakaran D, Lannoo L, Van Calsteren K, de Borre M, Van Parijs I, Van Coillie L, Van Den Bogaert K, De Almeida Toledo R, Lenaerts L, Tejpar S, Punie K, Rengifo LY, Vandenberghe P, Thienpont B, Vermeesch JR. Stanley KE, et al. Nat Commun. 2024 Mar 12;15(1):2220. doi: 10.1038/s41467-024-46435-0. Nat Commun. 2024. PMID: 38472221 Free PMC article.
Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study.
Koko M, Motelow JE, Stanley KE, Bobbili DR, Dhindsa RS, May P; Canadian Epilepsy Network; Epi4K Consortium; Epilepsy Phenome/Genome Project; EpiPGX Consortium; EuroEPINOMICS-CoGIE Consortium. Koko M, et al. Among authors: stanley ke. Epilepsia. 2022 Mar;63(3):723-735. doi: 10.1111/epi.17166. Epub 2022 Jan 15. Epilepsia. 2022. PMID: 35032048 Free PMC article.