Harvard University

Detection of aryl hydrocarbon receptor agonists in human samples (2018) Rothhammer V, Borucki DM, Kenison JE, Hewson P, Wang Z, Bakshi R, Sherr DH, Quintana FJ Journal article Photochemical Creation of Covalent Organic 2D Monolayer Objects in Defined Shapes via a Lithographic 2D Polymerization (2018) Servalli M, Celebi K, Payamyar P, Zheng L, Polozij M, Lowe B, Kuc A, et al. Journal article Mutations in WDR4 as a new cause of Galloway–Mowat syndrome (2018) Braun DA, Shril S, Sinha A, Schneider R, Tan W, Ashraf S, Hermle T, et al. Journal article GRADING CONSIDERATIONS FOR MENINGEAL SOLITARY FIBROUS TUMOR/HEMANGIOPERICYTOMA (2018) Fritchie K, Jensch K, Jenkins S, Link M, Brown PD, Rodriguez F, Guajardo A, et al. Conference contribution Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome (2018) Braun DA, Lovric S, Schapiro D, Schneider R, Marquez J, Asif M, Hussain MS, et al. Journal article ISLES 2016 and 2017-benchmarking ischemic stroke lesion outcome prediction based on multispectral MRI (2018) Winzeck S, Hakim A, Mckinley R, Pinto JAADSR, Alves V, Silva C, Pisov M, et al. Journal article Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract (2018) Van Der Ven AT, Connaughton DM, Ityel H, Mann N, Nakayama M, Chen J, Vivante A, et al. Journal article Reflection Spectroscopy of the Black Hole Binary XTE J1752-223 in Its Long-stable Hard State (2018) Garcia JA, Steiner JF, Grinberg V, Dauser T, Connors RMT, Mcclintock JE, Remillard RA, et al. Journal article Identification of novel mutational drivers reveals oncogene dependencies in multiple myeloma (2018) Walker BA, Mavrommatis K, Wardell CP, Ashby TC, Bauer M, Davies FE, Rosenthal A, et al. Journal article GAPVD1 and ANKFY1 mutations implicate RAB5 regulation in nephrotic syndrome (2018) Hermle T, Schneider R, Schapiro D, Braun DA, Van Der Ven AT, Warejko JK, Daga A, et al. Journal article