Publications

2018

Soderquist CR, Ewalt MD, Czuchlewski DR, Geyer JT, Rogers HJ, Hsi ED, et al. Myeloproliferative neoplasms with concurrent BCR-ABL1 translocation and JAK2 V617F mutation: a multi-institutional study from the bone marrow pathology group. Mod Pathol. 2018;31(5):690-704.
Legault K, Schunemann H, Hillis C, Yeung C, Akl EA, Carrier M, et al. McMaster RARE-Bestpractices clinical practice guideline on diagnosis and management of the catastrophic antiphospholipid syndrome. J Thromb Haemost. 2018.
Mechery V, Hernandez T, Mathew AT, Wanchoo R, Seshan SV, Jhaveri KD, et al. Nephropathology Education During Nephrology Fellowship Training in the United States. Kidney Int Rep. 2018;3(2):236-241.
Cheleuitte-Nieves C, Gulvik CA, Humrighouse BW, Bell ME, Villarma A, Westblade LF, et al. Draft Reference Genome Sequence of 16-1433, Isolated from a Mouse. Genome Announc. 2018;6(7).
Debnath S, Yallowitz AR, McCormick J, Lalani S, Zhang T, Xu R, et al. Discovery of a periosteal stem cell mediating intramembranous bone formation. Nature. 2018;562(7725):133-139.
Li W, Xia S, Aronova A, Min IM, Verma A, Scognamiglio T, et al. CHL1 expression differentiates Hürthle cell carcinoma from benign Hürthle cell nodules. J Surg Oncol. 2018;118(6):1042-1049.
Santo EE, Paik J. FOXO in Neural Cells and Diseases of the Nervous System. Curr Top Dev Biol. 2018;127:105-118.
Inoue K, Deng Z, Chen Y, Giannopoulou E, Xu R, Gong S, et al. Bone protection by inhibition of microRNA-182. Nat Commun. 2018;9(1):4108.
Chen H, Luthra R, Patel KP, Routbort M, Rashid A, Roy-Chowdhuri S, et al. Challenges in next generation sequencing analysis of somatic mutations in transplant patients. Cancer Genet. 2018;226-227:17-22.

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