Selected PhD student publications

  • Wang et al. An exhausted phenotype of TH2 cells is primed by allergen exposure, but not reinforced by allergen-specific immunotherapy. Allergy. 2021;76:2827–2839. DOI: 10.1111/all.14896
  • Dzinovic I, Škorvánek M, Pavelekova P, Zhao C, Keren B, Whalen S, Bakhtiari S, Chih Jin S, Kruer MC, Jech R, Winkelmann J, Zech M. Variant recurrence confirms the existence of a FBXO31-related spastic-dystonic cerebral palsy syndrome. Ann Clin Transl Neurol. 2021 Apr;8(4):951-955. doi: 10.1002/acn3.51335. Epub 2021 Mar 6. PMID: 33675180; PMCID: PMC8045898.
  • Dzinovic I, Serranová T, Prouteau C, Colin E, Ziegler A, Winkelmann J, Jech R, Zech M. Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant. Neurogenetics. 2021 May;22(2):137-141. doi: 10.1007/s10048-021-00637-6. Epub 2021 Mar 6. PMID: 33677721.
  • Dzinovic I, Škorvánek M, Necpál J, Boesch S, Švantnerová J, Wagner M, Havránková P, Pavelekova P, Haň V, Janzarik WG, Berweck S, Diebold I, Kuster A, Jech R, Winkelmann J, Zech M. Dystonia as a prominent presenting feature in developmental and epileptic encephalopathies: A case series. Parkinsonism Relat Disord. 2021 Sep;90:73-78. doi: 10.1016/j.parkreldis.2021.08.007. Epub 2021 Aug 11. PMID: 34399161.
  • Anand A, Fang H-Y, Mohammad-Shahi D, Ingermann J, Baumeister T, Strangmann J, et al. Elimination of NF-κB signaling in Vimentin+ stromal cells attenuate tumorigenesis in a mouse model of Barrett’s Esophagus. Carcinogenesis. 2020.
  • Stenton, S. L., Sheremet, N. L., Catarino, C. B., Andreeva, N. A., Assouline, Z., Barboni, P., ... & Prokisch, H. (2021). Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy. The Journal of clinical investigation, 131(6).
  • Stenton, S. L., Piekutowska‐Abramczuk, D., Kulterer, L., Kopajtich, R., Claeys, K. G., Ciara, E., ... & Prokisch, H. (2021). Expanding the clinical and genetic spectrum of FDXR deficiency by functional validation of variants of uncertain significance. Human Mutation, 42(3), 310-319.
  • Stenton, S. L., Zou, Y., Cheng, H., Prokisch, H., & Fang, F. (2021). Pediatric Leigh Syndrome: Neuroimaging Features and Genetic Correlations. Annals of Neurology, 89(3), 629-631.
  • Seeger, M., Karlas, A., Soliman, D., Pelisek, J., & Ntziachristos, V. (2016). Multimodal optoacoustic and multiphoton microscopy of human carotid atheroma. Photoacoustics, 4(3), 102-111.
  • Seeger, M., Soliman, D., Aguirre, J., Diot, G., Wierzbowski, J., & Ntziachristos, V. (2020). Pushing the boundaries of optoacoustic microscopy by total impulse response characterization. Nature communications, 11(1), 1-13.
  • Seeger, M., Stiel, A. C., & Ntziachristos, V. (2021). In vitro optoacoustic flow cytometry with light scattering referencing. Scientific reports, 11(1), 1-8.
  • Seeger, M., Dehner, C., Jüstel, D., & Ntziachristos, V. (2021). Label-free concurrent 5-modal microscopy (Co5M) resolves unknown spatio-temporal processes in wound healing. Communications biology, 4(1), 1-13.

Shared-First author papers:

  • Zhou, J., Li, J., Stenton, S. L., Ren, X., Gong, S., Fang, F., & Prokisch, H. (2020). NAD (P) HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses. Brain, 143(2), e8-e8.
  • Kellnberger, S., Soliman, D., Tserevelakis, G. J., Seeger, M., Yang, H., Karlas, A., ... & Ntziachristos, V. (2018). Optoacoustic microscopy at multiple discrete frequencies. Light: Science & Applications, 7(1), 1-12.
  • Di Giosia, M., Soldà, A., Seeger, M., Cantelli, A., Arnesano, F., Nardella, M. I., ... & Ntziachristos, V. (2021). A Bio‐Conjugated Fullerene as a Subcellular‐Targeted and Multifaceted Phototheranostic Agent. Advanced Functional Materials, 31(20), 2101527.
  • Fischer, D.S., Ansari, M., Wagner, K.I. et al. Single-cell RNA sequencing reveals ex vivo signatures of SARS-CoV-2-reactive T cells through ‘reverse phenotyping’. Nat Commun 12, 4515 (2021).