These publications were authored or co-authored by Quest Diagnostics staff.
Utilization of polarized microscopy to differentiate deep penetrating nevus from equine type melanomas.Authors: Cleaver N, Parikh K, Kazlouskaya V, Elston D.
J Cutan Pathol. 2016;43:362-366
Use of an Acetyl Derivative to Improve GC-MS Determination of Norbuprenorphine in the Presence of High Concentrations of Buprenorphine in Urine.Authors: Gervais JR, Hobbs GA.
J Anal Toxicol. 2016;40:208-212
Antibiotic Resistance among Urinary Isolates from Female Outpatients in the United States in 2003 and 2012.Authors: Sanchez GV, Babiker A, Master RN, Luu T, Mathur A, Bordon J.
Antimicrob Agents Chemother. 2016;60:2680-2683
Case Rep Pathol. 2016;2016:8068513
Mutational Analysis in Pediatric Thyroid Cancer and Correlations with Age, Ethnicity, and Clinical Presentation.Authors: Nikita ME, Jiang W, Cheng SM, Hantash FM, McPhaul MJ, Newbury RO, Phillips SA, Reitz RE, Waldman FM, Newfield RS
Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history.Authors: Tada H, Melander O, Louie JZ, Catanese JJ, Rowland CM, Devlin JJ, Kathiresan S, Shiffman D.
Eur Heart J. 2016;37:561-567
Clin Chem. 2016;62:408-409
Hepatic Steatosis and Insulin Resistance, But Not Steatohepatitis, Promote Atherogenic Dyslipidemia in NAFLD.Authors: Bril F, Sninsky JJ, Baca AM, Superko HR, Portillo Sanchez P, Biernacki D, Maximos M, Lomonaco R, Orsak B,Suman A, Weber MH, McPhaul MJ, Cusi K.
J Clin Endocrinol Metab. 2016;101:644-652
Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.Authors: Akinbami AO, Campbell AD, Han ZJ, Luo HY, Chui DH, Steinberg MH.