Publications by Medical Specialty - Women's Health/OB/GYN
These publications were authored or co-authored by Quest Diagnostics staff.
- Clinical and Lab healthcare professionals
- Endocrinology, Diabetes & Metabolism
- Family medicine practitioners
- General Health and Wellness
- Geriatrics/Age Management
- Health Information Technology
- Infectious Disease
- Internal Medicine
- Nurse practitioners
- Pathology, Anatomic
- Pathology, Laboratory Medicine
- Physician assistants
- Sports Medicine
- Toxicology/Pain Management
- Women's Health/OB/GYN
Authors: Kushner T, Chen Z, Tressler S, Kaufman H, Feinberg J, Terrault NA.
Clin Infect Dis. 2019 Aug 26. pii: ciz841. doi: 10.1093/cid/ciz841. [Epub ahead of print]
Adrenal insufficiency in neonates undergoing cardiopulmonary bypass and postoperative hypothalamic-pituitary-adrenal function after prophylactic glucocorticoids.
Authors: Tang A, Rosenfeld CR, Mikhael M, McPhaul MJ, Koch JD.
J Perinatol. 2019 Mar; doi: 10.1038/s41372-019-0344-7. [Epub ahead of print]
Prenatal cell-free DNA screening for fetal aneuploidy in pregnant women at average or high risk: Results from a large US clinical laboratory.
Authors: Guy C, Haji-Sheikhi F, Rowland CM, Anderson B, Owen R, Lacbawan FL, Alagia DP
Mol Genet Genomic Med. 2019 Jan 31:e545. doi: 10.1002/mgg3.545. [Epub ahead of print]
Authors: Schillie SF, Canary L, Koneru A, Nelson NP, Tanico W, Kaufman HW, Hariri S, Vellozzi CJ.
Am J Prev Med. 2018 Nov;55(5):633-641.
Quality Improvement to Demonstrate the Lack of Reliability of the Human Papillomavirus mRNA Assay to Identify Women With Latent Human Papillomavirus Infections.
Authors: Kaufman HW, Hilborne LH, Alagia DP
Obstet Gynecol. 2018 Sep;132(3):778.
A multigene test could cost-effectively help extend life expectancy for women at risk of hereditary breast cancer-Reply to letter to the editor by Petelin et al.
Authors: Li Y, Devlin JJ.
Value Health. 2018 Jul;21(7):893-894. Epub 2018 Apr 5.
Effects of platforms, size filter cutoffs, and targeted regions of cytogenomic microarray on detection of copy number variants and uniparental disomy in prenatal diagnosis: Results from 5026 pregnancies.
Authors: Wang JC, Radcliff J, Coe SJ, Mahon LW.
Prenat Diagn. 2019 Feb;39(3):137-156.
Authors: Mentzel T, Kiss K
Virchows Arch. 2017 Oct 5. doi: 10.1007/s00428-017-2242-8. [Epub ahead of print]
Authors: Golisch KB, Gottesman SP, Segal RJ
Int J Womens Dermatol. 2017;3(4):231-233.
Authors: Marlise R. Luskin, Marie N. Discenza, Sarah Rae Easter, Paola Dal Cin, Renius Owen, Bernard Ilagan, Meredith Masiello, Andrew A. Lane
Blood Adv. 2017;1(19): 1491–1494.