Publications by Medical Specialty - Hematology/Hemostasis/Thrombosis

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

Hematology/Hemostasis/Thrombosis 

Secondary mutation (c.94_95delAG) in A -alpha(3.7) allele associated with Hb H disease in two unrelated African American individuals homozygous for the -alpha(3.7) deletion (-alpha(3.7)/-alpha(3.7T)).

Authors: Zhao P, Buller-Burckle AM, Peng M, Anderson A, Han ZJ, Gallivan MV.
Hemoglobin. 2012;36:103-107.

Specialties: Hematology/Hemostasis/Thrombosis, Pediatrics

Comparison between Langerhans cell concentration in lichen planopilaris and traction alopecia with possible immunologic implications.

Authors: Hutchens KA, Balfour EM, Smoller BR.
Am J Dermatopathol. 2011;33:277-280.

Specialties: Dermatologists, Hematology/Hemostasis/Thrombosis, Oncology, Pathologists

FMR1 premutation carrier frequency in patients undergoing routine population-based carrier screening: insights into the prevalence of fragile X syndrome, fragile X-associated tremor/ataxia syndrome, and fragile X-associated primary ovarian insufficiency in the United States.

Quest Diagnostics Authors: Strom, C
Authors: Hantash FM, Goos DM, Crossley B, Anderson B, Zhang K, Sun W.
Genet Med. 2011;13:39-45.

Specialties: Hematology/Hemostasis/Thrombosis, OB/GYNs, Oncology, PCPs

Genetic variants of F11, statin use and venous thrombosis.

Authors: Bare LA, Arellano AR, Tong CH, Bezemer I, Lijfering WM, Devlin JJ, Reitsma PH, Rosendaal FR.
J Thromb Haemost. 2011;9:1249-1251.

Specialties: Cardiology, Hematologists, Hematology/Hemostasis/Thrombosis, PCPs, Pediatrics

Gaps in diabetes screening during pregnancy and postpartum.

Quest Diagnostics Authors: Nakamoto, JM
Authors: Blatt AJ, Kaufman HW.
Obstet Gynecol. 2011;117:61-68.

Specialties: Endocrinology, Diabetes & Metabolism, Hematology/Hemostasis/Thrombosis, OB/GYNs, Oncology, PCPs

MPL mutation profile in JAK2 mutation-negative patients with myeloproliferative disorders.

Authors: Ma W, Zhang X, Wang X, Zhang Z, Yeh CH, Uyeji J, Albitar M.
Diagn Mol Pathol. 2011;20:34-39.

Specialties: Hematologists, Hematology/Hemostasis/Thrombosis, Oncologists, Pathology, Laboratory Medicine

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

Preparing for the 2011-2012 influenza season.

Authors: Lieberman JM.
MLO Med Lab Obs. 2011;43:30.

Specialties: Hematology/Hemostasis/Thrombosis, Infectious Disease, Oncology, Pathologists, PCPs

Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach.

Authors: Giardine B, Borg J, Higgs DR, Peterson KR, Philipsen S, Maglott D, Singleton BK, Anstee DJ, Basak AN, Clark B, Costa FC, Faustino P, Fedosyuk H, Felice AE, Francina A, Galanello R, Gallivan MV, Georgitsi M, Gibbons RJ, Giordano PC, Harteveld CL, Hoyer JD,
Nat Genet. 2011;43:295-301.

Specialties: Hematologists, Hematology/Hemostasis/Thrombosis, Pediatrics

The importance of beta globin deletion analysis in the evaluation of patients with beta thalassemia.

Quest Diagnostics Authors: Strom, C
Authors: Mikula M, Buller-Burckle A, Gallivan M, Sun W, Franklin CR.
Int J Lab Hematol. 2011;33:310-317.

Specialties: Hematologists, Hematology/Hemostasis/Thrombosis, Pediatricians, Women's Health/OB/GYN