Publications

2019

Oh H, Paik J. Genetic Ablation of FOXO in Mice to Investigate Its Physiological Role. Methods Mol Biol. 2019;1890:239-248.
Hirsch Y, Zeevi DA, Lam BL, Scher SY, Bringer R, Cherki B, et al. A founder deletion in the TRPM1 gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews. Hum Genome Var. 2019;6:45.
Farooq A, Goyal A, Giorgadze T, Scherr G, Evans JJ, Hartley CP. Cytomorphological features of glomus tumors arising in the stomach: A series of two cases diagnosed on FNA. Ann Diagn Pathol. 2019;42:42-47.
Cushing MM, Asmis LM, Harris RM, DeSimone RA, Hill S, Ivascu N, et al. Efficacy of a new pathogen-reduced cryoprecipitate stored 5 days after thawing to correct dilutional coagulopathy in vitro. Transfusion. 2019;59(5):1818-1826.
Kyriakides K, Selkin G, Selkin B, Iwenofu H, Magro CM. Chronic Fibrosing Vasculitis in the Setting of Still Disease. J Clin Rheumatol. 2019;25(7):e127-e130.
DeSimone RA, Ong SJ, Crowley KM, Vasovic LV, Senaldi E, Kessler DA, et al. Hereditary elliptocytosis of donor red blood cell unit detected during Coombs crossmatch. Transfusion. 2019;59(2):446-447.
Frost EL, Mockus TE, Ren HM, Toprak M, Lauver MD, Netherby-Winslow CS, et al. PD-1 Dynamically Regulates Inflammation and Development of Brain-Resident Memory CD8 T Cells During Persistent Viral Encephalitis. Front Immunol. 2019;10:783.
Marshall CH, Imada EL, Tang Z, Marchionni L, Antonarakis ES. CDK12 inactivation across solid tumors: an actionable genetic subtype. Oncoscience. 2019;6(5-6):312-316.

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