Tri-Institutional MD-PhD Program

Alumni Publications

2019

Bendriem RM, Singh S, Aleem AAbdel, Antonetti DA, M Ross E. 2019. Tight junction protein occludin regulates progenitor Self-Renewal and survival in developing cortex.. Elife. 8

Meyer HC, Odriozola P, Cohodes EM, Mandell JD, Li A, Yang R, Hall BS, Haberman JT, Zacharek SJ, Liston C et al.. 2019. Ventral hippocampus interacts with prelimbic cortex during inhibition of threat response via learned safety in both mice and humans.. Proc Natl Acad Sci U S A.

Chu C, Murdock MH, Jing D, Won THyung, Chung H, Kressel AM, Tsaava T, Addorisio ME, Putzel GG, Zhou L et al.. 2019. The microbiota regulate neuronal function and fear extinction learning.. Nature. 574(7779):543-548.

Wolujewicz P, M Ross E. 2019. The search for genetic determinants of human neural tube defects.. Curr Opin Pediatr. 31(6):739-746.

Holst JM, Plesner TL, Pedersen MB, Frederiksen H, Møller MB, Clausen MR, Hansen MC, Hamilton-Dutoit SJacques, Nørgaard P, Johansen P et al.. 2019. Myeloproliferative and lymphoproliferative malignancies occurring in the same patient: a nationwide discovery cohort.. Haematologica.

Ruan J. 2019. Molecular profiling and management of mantle cell lymphoma.. Hematology Am Soc Hematol Educ Program. 2019(1):30-40.

2018

Czarnowicki T, He HY, Wen H-C, Hashim PW, Nia JK, Malik K, Estrada Y, Kimmel GW, Taliercio M, Krueger JG et al.. 2018. Alopecia areata is characterized by expansion of circulating Th2/Tc2/Th22, within the skin-homing and systemic T-cell populations.. Allergy. 73(3):713-723.

Pullabhatla V, Roberts AL, Lewis MJ, Mauro D, Morris DL, Odhams CA, Tombleson P, Liljedahl U, Vyse S, Simpson MA et al.. 2018. De novo mutations implicate novel genes in systemic lupus erythematosus.. Hum Mol Genet. 27(3):421-429.

Packer RJ, Fisher MJ, Cutter G, Cole-Plourde K, Korf BR. 2018. Neurofibromatosis Clinical Trial Consortium.. J Child Neurol. 33(1):82-91.

Koczkowska M, Chen Y, Callens T, Gomes A, Sharp A, Johnson S, Hsiao M-C, Chen Z, Balasubramanian M, Barnett CP et al.. 2018. Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848.. Am J Hum Genet. 102(1):69-87.