Doctoral Researcher
(Alumni)
University of Freiburg
Center for Chronic Immunodeficiency (CCI)
| 2016 – present | PhD student in the lab of Prof. Stephan Ehl, Center for Chronic Immunodeficiency, Medical Center - University of Freiburg |
| 2007 – 2014 | Study of Biology (Diploma), University of Freiburg, Germany |
Publications based on CRC1160 funding
Ohishi Y, Ammann S, Ziaee V, Strege K, Groß M, Amos CV, Shahrooei M, Ashournia P, Razaghian A, Griffiths GM, Ehl S, Fukuda M, Parvaneh N. 2020. Griscelli Syndrome Type 2 Sine Albinism: Unraveling Differential RAB27A Effector Engagement. Front Immunol. 11:612977. doi: 10.3389/fimmu.2020.612977.
Wegehaupt, O., M. Gross, C. Wehr, R. Marks, A. Schmitt-Graeff, M. Uhl, M. Lorenz, K. Schwarz, C. Kratz, C. Niemeyer, and S. Ehl. 2020. TIM-3 deficiency presenting with two clonally unrelated episodes of mesenteric and subcutaneous panniculitis-like T-cell lymphoma and hemophagocytic lymphohistiocytosis. Pediatr Blood Cancer 67: e28302.
Thian, M., B. Hoeger, A. Kamnev, F. Poyer, S. Kostel Bal, M. Caldera, R. Jimenez-Heredia, J. Huemer, W. F. Pickl, M. Gross, S. Ehl, C. L. Lucas, J. Menche, C. Hutter, A. Attarbaschi, L. Dupre, and K. Boztug. 2020. Germline biallelic PIK3CG mutations in a multifaceted immunodeficiency with immune dysregulation. Haematologica. pii: haematol.2019.231399. doi: 10.3324/haematol.2019.231399. [Epub ahead of print]
Castro CN, Rosenzwajg M, Carapito R, Shahrooei M, Konantz M, Khan A, Miao Z, Groß M, Tranchant T, Radosavljevic M, Paul N, Stemmelen T, Pitoiset F, Hirschler A, Nespola B, Molitor A, Rolli V, Pichot A, Faletti LE, Rinaldi B, Friant S, Mednikov M, Karauzum H, Aman MJ, Carapito C, Lengerke C, Ziaee V, Eyaid W, Ehl S, Alroqi F, Parvaneh N, Bahram S. 2020. NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation. J Exp Med. 217(12):e20192275. doi: 10.1084/jem.20192275.
