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Evaluating the Modified American Academy of Pediatrics Screening Algorithm for Critical Congenital Heart Disease.

Hoff H, Quary S, Keesari R, Oster ME. Hoff H, et al. Among authors: quary s. Am J Perinatol. 2024 Oct 15. doi: 10.1055/a-2416-5637. Online ahead of print. Am J Perinatol. 2024. PMID: 39288909

A Modified Algorithm for Critical Congenital Heart Disease Screening Using Pulse Oximetry.

Diller CL, Kelleman MS, Kupke KG, Quary SC, Kochilas LK, Oster ME. Diller CL, et al. Among authors: quary sc. Pediatrics. 2018 May;141(5):e20174065. doi: 10.1542/peds.2017-4065. Pediatrics. 2018. PMID: 29691284

Clinic-based infant screening for duchenne muscular dystrophy: a feasibility study.

Cyrus A, Street N, Quary S, Kable J, Kenneson A, Fernhoff P. Cyrus A, et al. Among authors: quary s. PLoS Curr. 2012 May 2;4:e4f99c5654147a. doi: 10.1371/4f99c5654147a. PLoS Curr. 2012. PMID: 22866242 Free PMC article.

Biotinidase deficiency: novel mutations and their biochemical and clinical correlates.

Wolf B, Jensen KP, Barshop B, Blitzer M, Carlson M, Goudie DR, Gokcay GH, Demirkol M, Baykal T, Demir F, Quary S, Shih LY, Pedro HF, Chen TH, Slonim AE. Wolf B, et al. Among authors: quary s. Hum Mutat. 2005 Apr;25(4):413. doi: 10.1002/humu.9329. Hum Mutat. 2005. PMID: 15776412

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