University of Utah

University / College

Salt Lake City, UT, United States (USA)

Research projects with FAU researchers

Iterative Solvers for Inverse Bioelectric Field Problems
Prof. Dr. Ulrich Rüde
(01/10/2001 - 30/09/2004)

Publications in cooperation with FAU scientists

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Cheung, A.K., Chang, T.I., Cushman, W.C., Furth, S.L., Ix, J.H., Pecoits-Filho, R.,... Williamson, J.D. (2019). Blood pressure in chronic kidney disease: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney International, 95(5), 1027-1036.
Wright, J.T., Fete, M., Schneider, H., Zinser, M., Koster, M.I., Clarke, A.J.,... Morasso, M.I. (2019). Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway. American Journal of Medical Genetics Part A, 179(3), 442-447.
Haase, V., Stierstorfer, K., Hahn, K., Schöndube, H., Maier, A., & Noo, F. (2019). Exploring the space between smoothed and non-smooth total variation for 3D iterative CT reconstruction. In Hilde Bosmans, Guang-Hong Chen, Taly Gilat Schmidt (Eds.), Progress in Biomedical Optics and Imaging - Proceedings of SPIE. San Diego, CA, US: SPIE.
Yang, Y., Wu, L., Shu, X., Lu, Y., Shu, X.-O., Cai, Q.,... Long, J. (2019). Genetic Data from Nearly 63,000 Women of European Descent Predicts DNA Methylation Biomarkers and Epithelial Ovarian Cancer Risk. Cancer Research, 79(3).
Hotter, D., Bosso, M., Jønsson, K.L., Krapp, C., Stürzel, C.M., Das, A.,... Kirchhoff, F. (2019). IFI16 Targets the Transcription Factor Sp1 to Suppress HIV-1 Transcription and Latency Reactivation. Cell Host & Microbe, 25(6), 858-872.e13.
Gong, B., Zhang, H., Huang, L., Chen, Y., Shi, Y., Tam, P.O.S.,... Yang, Z. (2019). Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis. Genetics in Medicine.
Greiner, J., Sankarankutty, A.C., Seemann, G., Seidel, T., & Sachse, F.B. (2018). Confocal Microscopy-Based Estimation of Parameters for Computational Modeling of Electrical Conduction in the Normal and Infarcted Heart. Frontiers in Physiology, 9.
Azizi, M., Schmieder, R., Mahfoud, F., Weber, M.A., Daemen, J., Davies, J.,... Mauri, L. (2018). Endovascular ultrasound renal denervation to treat hypertension (RADIANCE-HTN SOLO): a multicentre, international, single-blind, randomised, sham-controlled trial. Lancet.
Scharfman, H.E., Kanner, A.M., Friedman, A., Blümcke, I., Crocker, C.E., Cendes, F.,... Pohlmann-Eden, B. (2018). Epilepsy as a Network Disorder (2): What can we learn from other network disorders such as dementia and schizophrenia, and what are the implications for translational research? Epilepsy and Behavior, 78, 302-312.
Song, J., Paul, S.S., Caetano, M.J.D., Smith, S., Dibble, L.E., Love, R.,... Allen, N.E. (2018). Home-based step training using videogame technology in people with Parkinson's disease: a single-blinded randomised controlled trial. Clinical Rehabilitation, 32(3), 299-311.
O'Mara, T.A., Glubb, D.M., Amant, F., Annibali, D., Ashton, K., Attia, J.,... Thompson, D.J. (2018). Identification of nine new susceptibility loci for endometrial cancer. Nature Communications, 9(1).
Major-Monfried, H., Renteria, A.S., Pawarode, A., Reddy, P., Ayuk, F., Holler, E.,... Levine, J.E. (2018). MAGIC biomarkers predict long term outcomes for steroid-resistant acute GVHD. Blood.
Anderson, N.D., De Borja, R., Young, M.D., Fuligni, F., Rosic, A., Roberts, N.D.,... Shlien, A. (2018). Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors. Science, 361(6405).
Kelemen, L.E., Earp, M., Fridley, B.L., Chenevix-Trench, G., Fasching, P., Beckmann, M.,... Berchuck, A. (2018). rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology. International Journal of Molecular Sciences, 19(9).
Shimelis, H., Mesman, R.L.S., Von Nicolai, C., Ehlen, A., Guidugli, L., Martin, C.,... Couch, F.J. (2017). BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer. Cancer Research, 77(11), 2789-2799.
Dikow, N., Granzow, M., Graul-Neumann, L.M., Karch, S., Hinderhofer, K., Paramasivam, N.,... Moog, U. (2017). DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome. American Journal of Medical Genetics Part A, 173(5), 1369-1373.
Pelaz, B., Alexiou, C., Alvarez -Puebla, R.A., Alves, F., Andrews, A.M., Ashraf, S.,... Parak, W.J. (2017). Diverse Applications of Nanomedicine. Acs Nano, 11(3), 2313-2381.
Dand, N., Mucha, S., Tsoi, L.C., Mahil, S.K., Stuart, P.E., Arnold, A.,... Barker, J.N. (2017). Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signalling. Human Molecular Genetics, 26(21), 4301-4313.
Tsoi, L.C., Stuart, P.E., Tian, C., Gudjonsson, J.E., Das, S., Zawistowski, M.,... Elder, J.T. (2017). Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants. Nature Communications, 8, 15382.
Johnson, S., Soowamber, M., Fransen, J., Khanna, D., Van Den Hoogen, F., Baron, M.,... Pope, J. (2017). There is a need for new systemic sclerosis subset criteria. A content analytic approach. Scandinavian Journal of Rheumatology, 1-9.

Last updated on 2013-02-07 at 12:11