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Clinical experience with single-nucleotide polymorphism-based non-invasive prenatal screening for 22q11.2 deletion syndrome.
Gross SJ, Stosic M, McDonald-McGinn DM, Bassett AS, Norvez A, Dhamankar R, Kobara K, Kirkizlar E, Zimmermann B, Wayham N, Babiarz JE, Ryan A, Jinnett KN, Demko Z, Benn P. Gross SJ, et al. Among authors: jinnett kn. Ultrasound Obstet Gynecol. 2016 Feb;47(2):177-83. doi: 10.1002/uog.15754. Epub 2016 Jan 5. Ultrasound Obstet Gynecol. 2016. PMID: 26396068 Free PMC article.
Detection of Clonal and Subclonal Copy-Number Variants in Cell-Free DNA from Patients with Breast Cancer Using a Massively Multiplexed PCR Methodology.
Kirkizlar E, Zimmermann B, Constantin T, Swenerton R, Hoang B, Wayham N, Babiarz JE, Demko Z, Pelham RJ, Kareht S, Simon AL, Jinnett KN, Rabinowitz M, Sigurjonsson S, Hill M. Kirkizlar E, et al. Among authors: jinnett kn. Transl Oncol. 2015 Oct;8(5):407-416. doi: 10.1016/j.tranon.2015.08.004. Transl Oncol. 2015. PMID: 26500031 Free PMC article.
Cell-Free DNA Analysis of Fetal Aneuploidies in Early Pregnancy Loss.
Kutteh WH, Miller CE, Park JK, Corey V, Chavez M, Racicot K, Alagia DP 3rd, Jinnett KN, Curnow K, Dalton K, Bhatt S, Keefe DL. Kutteh WH, et al. Among authors: jinnett kn. J Clin Med. 2024 Jul 23;13(15):4283. doi: 10.3390/jcm13154283. J Clin Med. 2024. PMID: 39124551 Free PMC article.