Publications

These publications were authored or co-authored by Quest Diagnostics staff.

Maternal medium-chain acyl-CoA dehydrogenase deficiency identified by newborn screening.

Authors: Leydiker KB, Neidich JA, Lorey F, Barr EM, Puckett RL, Lobo RM, Abdenur JE.
Mol Genet Metab. 2011;103:92-95.

Specialties: Hematology/Hemostasis/Thrombosis, OB/GYNs, Pathology, Laboratory Medicine, Pediatricians

Genetic variants in the apolipoprotein(a) gene and coronary heart disease.

Authors: Li Y, Luke MM, Shiffman D, Devlin JJ.
Circ Cardiovasc Genet. 2011;4:565-573.

Specialties: Cardiology, Infectious Disease, Pathology, Laboratory Medicine, PCPs

Analysis of single nucleotide polymorphisms in case-control studies.

Authors: Li Y, Shiffman D, Oberbauer R.
Methods Mol Biol. 2011;719:219-234.

Specialties: Pathology, Laboratory Medicine

Polymorphisms and noncardioembolic stroke in three case-control studies.

Authors: Luke MM, Berger K, Rowland CM, Catanese JJ, Tong CH, Ross DA, Garcia V, Kuhlenbaeumer G, Ringelstein EB, Pullinger CR, Malloy MJ, Deedwania P, Ellis SG, Kane JP, Devlin JJ, Lalouschek W, Mannhalter C.
Cerebrovasc Dis. 2012;33:80-85.

Specialties: Cardiology, Neurologists, Oncology, Pathology, Laboratory Medicine

Three novel alternative splicing mutations in BCR-ABL1 detected in CML patients with resistance to kinase inhibitors.

Authors: Ma W, Giles F, Zhang X, Wang X, Zhang Z, Lee TS, Yeh CH, Albitar M.
Int J Lab Hematol. 2011;33:326-331.

Specialties: Hematology/Hemostasis/Thrombosis, Oncology