Publications by Category - Genetics
These publications were authored or co-authored by Quest Diagnostics staff.
Interstitial Chromosome 3p14.1 Deletion due to a Maternal Insertion: Phenotype and Association with Balanced Parental Rearrangement.Authors: Hajek C, Wang J, Mahon L, Martinez A, Saitta SC.
Mol Syndromol. 2016;7:43-48
Am J Hum Genet. 2016;98:667-679
A novel method for simultaneous quantification of alpha-aminoadipic semialdehyde/piperideine-6-carboxylate and pipecolic acid in plasma and urine.Authors: Yuzyuk T, Liu A, Thomas A, Wilson JE, De Biase I, Pasquali M.
J Chromatogr B Analyt Technol Biomed Life Sci. 2016;1017-1018:145-52
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
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.
Clin Chem. 2016;62:70-76