Fiorella Schischlik, PhD
Fiorella Schischlik, PhD
Boehringer Ingelheim, Vienna, Austria
E-mailová adresa ověřena na: - Domovská stránka
Somatic mutations of calreticulin in myeloproliferative neoplasms
T Klampfl, H Gisslinger, AS Harutyunyan, H Nivarthi, E Rumi, JD Milosevic, ...
New England Journal of Medicine 369 (25), 2379-2390, 2013
LZTR1 is a regulator of RAS ubiquitination and signaling
JW Bigenzahn, GM Collu, F Kartnig, M Pieraks, GI Vladimer, LX Heinz, ...
Science 362 (6419), 1171-1177, 2018
A reversible gene trap collection empowers haploid genetics in human cells
T Bürckstümmer, C Banning, P Hainzl, R Schobesberger, C Kerzendorfer, ...
Nature methods 10 (10), 965-971, 2013
Characterization of HLH-like manifestations as a CRS variant in patients receiving CD22 CAR T cells
DA Lichtenstein, F Schischlik, L Shao, SM Steinberg, B Yates, HW Wang, ...
Blood 138 (24), 2469-2484, 2021
MTHFD1 interaction with BRD4 links folate metabolism to transcriptional regulation
S Sdelci, AF Rendeiro, P Rathert, W You, JMG Lin, A Ringler, G Hofstätter, ...
Nature genetics 51 (6), 990-998, 2019
Mutational landscape of the transcriptome offers putative targets for immunotherapy of myeloproliferative neoplasms
F Schischlik, R Jäger, F Rosebrock, E Hug, M Schuster, R Holly, E Fuchs, ...
Blood, The Journal of the American Society of Hematology 134 (2), 199-210, 2019
Cooperation of germ line JAK2 mutations E846D and R1063H in hereditary erythrocytosis with megakaryocytic atypia
K Kapralova, M Horvathova, C Pecquet, J Fialova Kucerova, ...
Blood, The Journal of the American Society of Hematology 128 (10), 1418-1423, 2016
Mutations in myeloproliferative neoplasms–their significance and clinical use
F Schischlik, R Kralovics
Expert Review of Hematology 10 (11), 961-973, 2017
Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia
M Moder, G Velimezi, M Owusu, A Mazouzi, M Wiedner, ...
Nature communications 8 (1), 1238, 2017
Systematic genetic mapping of necroptosis identifies SLC39A7 as modulator of death receptor trafficking
A Fauster, M Rebsamen, KL Willmann, A César-Razquin, E Girardi, ...
Cell Death & Differentiation 26 (6), 1138-1155, 2019
Deconvolving Clinically Relevant Cellular Immune Cross-talk from Bulk Gene Expression Using CODEFACS and LIRICS Stratifies Patients with Melanoma to Anti–PD-1 Therapy
K Wang, S Patkar, JS Lee, EM Gertz, W Robinson, F Schischlik, ...
Cancer discovery 12 (4), 1088-1105, 2022
Germline genetic factors influence the outcome of interferon-α therapy in polycythemia vera
R Jäger, H Gisslinger, E Fuchs, E Bogner, JD Milosevic Feenstra, ...
Blood 137 (3), 387-391, 2021
The landscape of receptor-mediated precision cancer combination therapy via a single-cell perspective
S Ahmadi, P Sukprasert, R Vegesna, S Sinha, F Schischlik, N Artzi, ...
Nature communications 13 (1), 1613, 2022
PD‐L1 overexpression correlates with JAK2‐V617F mutational burden and is associated with 9p uniparental disomy in myeloproliferative neoplasms
JD Milosevic Feenstra, R Jäger, F Schischlik, D Ivanov, G Eisenwort, ...
American Journal of Hematology 97 (4), 390-400, 2022
scRNA-seq analysis of colon and esophageal tumors uncovers abundant microbial reads in myeloid cells undergoing proinflammatory transcriptional alterations
W Robinson, JK Stone, F Schischlik, B Gasmi, MC Kelly, C Seibert, ...
bioRxiv, 2020.05. 14.096230, 2020
Synthetic lethality-based prediction of anti-SARS-CoV-2 targets
LR Pal, K Cheng, NU Nair, L Martin-Sancho, S Sinha, Y Pu, L Riva, X Yin, ...
Iscience 25 (5), 104311, 2022
Myelomonocytic skewing in vitro discriminates subgroups of patients with myelofibrosis with a different phenotype, a different mutational profile and different prognosis
K Geissler, B Gisslinger, E Jäger, R Jäger, AI Schiefer, E Bogner, E Fuchs, ...
Cancers 12 (8), 2291, 2020
Frequent mutations in the calreticulin gene CALR in myeloproliferative neoplasms
K Thorsten, H Gisslinger, AS Harutyunyan, H Nivarthi, E Rumi, ...
Blood 122 (21), LBA-1, 2013
Deconvolving clinically relevant cellular immune crosstalk from bulk gene expression using CODEFACS and LIRICS
K Wang, S Patkar, JS Lee, EM Gertz, W Robinson, F Schischlik, ...
bioRxiv, 2021.01. 20.427515, 2021
Overexpression of PD-L1 correlates with JAK2-V617F mutational burden and is associated with chromosome 9p uniparental disomy in MPN
JDM Feenstra, F Schischlik, R Jäger, D Ivanov, G Eisenwort, A Keller, ...
Blood 136, 24, 2020
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Články 1–20