Publications with Key Summaries

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

Group IIA Secretory Phospholipase A2, Vascular Inflammation, and Incident Cardiovascular Disease.

Authors: Akinkuolie AO, Lawler PR, Chu AY, Caulfield M, Mu J, Ding B, Nyberg F, Glynn RJ, Ridker PM, Hurt-Camejo E, Chasman DI, Mora S.
Arterioscler Thromb Vasc Biol. 2019 Jun;39:1182-1190

Specialties: Cardiology

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Erythrocyte ion content and dehydration modulate maximal Gardos channel activity in KCNN4 V282M/+ Hereditary Xerocytosis (HX) red cells.

Authors: Rivera A, Vandorpe DH, Shmukler BE, Andolfo I, Iolascon A, Archer NM, Shabani E, Auerbach M, Hamerschlak N, Morton J, Wohlgemuth JG, Brugnara C, Snyder LM, Alper SL.
Am J Physiol Cell Physiol. 2019 May 15. doi: 10.1152/ajpcell.00074.2019. [Epub ahead of print]

Specialties: General Health and Wellness, Genetics

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Laboratory Blood-Based Testing for Lyme Disease at a National Reference Laboratory

Authors: Lee-Lewandrowski E, Chen Z, Branda J, Baron J, Kaufman HW
Am J Clin Pathol. 2019 Apr 15. doi: 10.1093/ajcp/aqz030. [Epub ahead of print]

Specialties: Infectious Disease, Laboratory

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Self-Insured Employer Health Benefits Strategy Established a Negative Cost Trend While Improving Performance.

Authors: Goldberg SE, Fragala MS, Wohlgemuth JG.
Popul Health Manag. 2019 Mar;doi: 10.1089/pop.2018.0184. [Epub ahead of print]

Specialties: General Health and Wellness

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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]

Specialties: Genetics, Women's Health/OB/GYN

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Hepatitis C Virus in Women of Childbearing Age, Pregnant Women, and Children.

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.

Specialties: Infectious Disease, Pediatrics, Women's Health/OB/GYN

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Frequency of frontotemporal dementia gene variants in C9ORF72, MAPT, and GRN in academic versus commercial laboratory cohorts

Authors: Rabinowitz NZ, Yokoyama JS, Bright AR, Lee SE, Fong JC, Karydas A, Bonham LW, Karbassi ID, Pribadi M, Meservey MA, Gallen M, Ramos EM, Liaquat K, Hoffman C, Krasner M, Dodge W, Rosen HJ, Boxer AL, Geschwind MD, Rankin KP, Coppola G, Miller BL, Higgins JJ
Adv Genomics Genet. 2018 Oct 25 vol 8:23–33

Specialties: Genetics, Geriatrics/Age Management, Neurology

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