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Fischer Carina |

** = Publications listed in SCI/SSCI/Pubmed

2021

Full paper/article (Journal)

** Fischer, C; Koblmüller, S; Börger, C; Michelitsch, G; Trajanoski, S; Schlötterer, C; Guelly, C; Thallinger, GG; Sturmbauer, C Genome sequences of Tropheus moorii and Petrochromis trewavasae, two eco-morphologically divergent cichlid fishes endemic to Lake Tanganyika.
Sci Rep. 2021; 11(1):4309-4309 Doi: 10.1038/s41598-021-81030-z [OPEN ACCESS]
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Abstract (Journal)

** Nonn, O; Debnath, O; Valdes, DS; Fischer, C; Secener, K; Tiesmeyer, S; Ishaque, N; Sallinger, K; El-Heliebi, A; Staff, A; Dominik, NM; Dechend, R; Gauster, M; Herse, F Unravelling Cell-specific Interactions At The Preeclamptic Maternal-foetal Interface From Early To Late Pregnancy
HYPERTENSION. 2021; 78: Doi: 10.1161/hyp.78.suppl_1.27 [Onlinepräsentation]
Web of Science FullText FullText_MUG

 

2019

Full paper/article (Journal)

** Heitzer, E; Groenewoud, A; Meditz, K; Lohberger, B; Liegl-Atzwanger, B; Prokesch, A; Kashofer, K; Behrens, D; Haybaeck, J; Kolb-Lenz, D; Koefeler, H; Riedl, S; Schaider, H; Fischer, C; Snaar-Jagalska, BE; de'Jong, D; Szuhai, K; Zweytick, D; Rinner, B Human melanoma brain metastases cell line MUG-Mel1, isolated clones and their detailed characterization.
Sci Rep. 2019; 9(1):4096-4096 Doi: 10.1038/s41598-019-40570-1 [OPEN ACCESS]
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2015

Full paper/article (Journal)

** Fischer, C; Hofmann, M; Danzer, M; Hofer, K; Kaar, J; Gabriel, C Seroprevalence and Incidence of hepatitis E in blood donors in Upper Austria.
PLoS One. 2015; 10(3):e0119576-e0119576 Doi: 10.1371/journal.pone.0119576 [OPEN ACCESS]
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** Fischer, C; Leithner, K; Wohlkoenig, C; Quehenberger, F; Bertsch, A; Olschewski, A; Olschewski, H; Hrzenjak, A Panobinostat reduces hypoxia-induced cisplatin resistance of non-small cell lung carcinoma cells via HIF-1α destabilization.
Mol Cancer. 2015; 14(8):4-4 Doi: 10.1186/1476-4598-14-4 [OPEN ACCESS]
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** Fischer, C; Scheipl, S; Zopf, A; Niklas, N; Deutsch, A; Jorgensen, M; Lohberger, B; Froehlich, EV; Leithner, A; Gabriel, C; Liegl-Atzwanger, B; Rinner, B Mutation Analysis of Nine Chordoma Specimens by Targeted Next-Generation Cancer Panel Sequencing.
J Cancer. 2015; 6(10):984-989 Doi: 10.7150/jca.11371 [OPEN ACCESS]
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2014

Abstract (Journal)

** Hrzenjak, A; Fischer, C; Leithner, K; Wohlkoenig, C; Quehenberger, F; Olschewski, A; Olschewski, H Panobinostat reduces hypoxia-related cisplatin resistance of non-small cell lung carcinoma cells via HIF-1alpha destabilization.
EUR J CANCER. 2014; 50: S203-S204. Doi: 10.1016/S0959-8049(14)50741-1 [Poster]
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** Scheipl, S; Fischer, C; Zopf, A; Deutsch, A; Jorgensen, M; Carvalho, D; Lohberger, B; Froehlich, EV; Leithner, A; Liegl, B; Rinner, B Mutation analysis of nine chordoma specimens by targeted next generation cancer panel sequencing
VIRCHOWS ARCH. 2014; 465: S326-S326. [Poster]
Web of Science

 

2013

Full paper/article (Journal)

** Rinner, B; Weinhaeusel, A; Lohberger, B; Froehlich, EV; Pulverer, W; Fischer, C; Meditz, K; Scheipl, S; Trajanoski, S; Guelly, C; Leithner, A; Liegl, B Chordoma characterization of significant changes of the DNA methylation pattern.
PLoS One. 2013; 8(3):e56609-e56609 Doi: 10.1371/journal.pone.0056609 [OPEN ACCESS]
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2012

Full paper/article (Journal)

** Beetz, C; Pieber, TR; Hertel, N; Schabhüttl, M; Fischer, C; Trajanoski, S; Graf, E; Keiner, S; Kurth, I; Wieland, T; Varga, RE; Timmerman, V; Reilly, MM; Strom, TM; Auer-Grumbach, M Exome Sequencing Identifies a REEP1 Mutation Involved in Distal Hereditary Motor Neuropathy Type V.
Am J Hum Genet. 2012; 91(1):139-145 Doi: 10.1016/j.ajhg.2012.05.007 [OPEN ACCESS]
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** Fischer, C; Trajanoski, S; Papić, L; Windpassinger, C; Bernert, G; Freilinger, M; Schabhüttl, M; Arslan-Kirchner, M; Javaher-Haghighi, P; Plecko, B; Senderek, J; Rauscher, C; Löscher, WN; Pieber, TR; Janecke, AR; Auer-Grumbach, M SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease.
J Neurol. 2012; 259(3):515-523 Doi: 10.1007/s00415-011-6213-8 [OPEN ACCESS]
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** Rinner, B; Froehlich, EV; Buerger, K; Knausz, H; Lohberger, B; Scheipl, S; Fischer, C; Leithner, A; Guelly, C; Trajanoski, S; Szuhai, K; Liegl, B Establishment and detailed functional and molecular genetic characterisation of a novel sacral chordoma cell line, MUG-Chor1.
Int J Oncol. 2012; 40(2): 443-451. Doi: 10.3892/ijo.2011.1235 [OPEN ACCESS]
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** Rinner, B; Gallè, B; Trajanoski, S; Fischer, C; Hatz, M; Maierhofer, T; Michelitsch, G; Moinfar, F; Stelzer, I; Pfragner, R; Guelly, C Molecular evidence for the bi-clonal origin of neuroendocrine tumor derived metastases.
BMC Genomics. 2012; 13(6):594-594 Doi: 10.1186/1471-2164-13-594 [OPEN ACCESS]
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2011

Short report/Letter

** Pichler, MM; Bodner, C; Fischer, C; Deutsch, AJ; Hiden, K; Beham-Schmid, C; Linkesch, W; Guelly, C; Sill, H; Wölfler, A Evaluation of mutations in the isocitrate dehydrogenase genes in therapy-related and secondary acute myeloid leukaemia identifies a patient with clonal evolution to IDH2 R172K homozygosity due to uniparental disomy.
Br J Haematol. 2011; 152(5): 669-672. Doi: 10.1111/j.1365-2141.2010.08404.x [OPEN ACCESS]
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2010

Full paper/article (Journal)

** Auer-Grumbach, M; Olschewski, A; Papić, L; Kremer, H; McEntagart, ME; Uhrig, S; Fischer, C; Fröhlich, E; Bálint, Z; Tang, B; Strohmaier, H; Lochmüller, H; Schlotter-Weigel, B; Senderek, J; Krebs, A; Dick, KJ; Petty, R; Longman, C; Anderson, NE; Padberg, GW; Schelhaas, HJ; van Ravenswaaij-Arts, CM; Pieber, TR; Crosby, AH; Guelly, C Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C.
Nat Genet. 2010; 42(2):160-164 Doi: 10.1038/ng.508 [OPEN ACCESS]
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** Papić, L; Fischer, D; Trajanoski, S; Höftberger, R; Fischer, C; Ströbel, T; Schmidt, WM; Bittner, RE; Schabhüttl, M; Gruber, K; Pieber, TR; Janecke, AR; Auer-Grumbach, M SNP-array based whole genome homozygosity mapping: a quick and powerful tool to achieve an accurate diagnosis in LGMD2 patients.
Eur J Med Genet. 2010; 54(3):214-219 Doi: 10.1016/j.ejmg.2010.12.003 [OPEN ACCESS]
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2008

Full paper/article (Journal)

** Auer-Grumbach, M; Fischer, C; Papić, L; John, E; Plecko, B; Bittner, RE; Bernert, G; Pieber, TR; Miltenberger, G; Schwarz, R; Windpassinger, C; Grill, F; Timmerman, V; Speicher, MR; Janecke, AR Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndrome.
Neuropediatrics. 2008; 39(1):33-38 Doi: 10.1055/s-2008-1077085 [OPEN ACCESS]
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2007

Full paper/article (Journal)

** Rohkamm, B; Reilly, MM; Lochmuller, H; Schlotter-Weigel, B; Barisic, N; Schols, L; Laura, M; Janecke, AR; Miltenberger-Miltenyi, G; John, E; Fischer, C; Grill, F; Wakeling, W; Davis, M; Pieber, TR; Auer-Grumbach, M; Nicholson, G; Pareyson, D Further evidence for genetic heterogeneity of distal HMN type V, CMT2 with predominant hand involvement and Silver syndrome.
J NEUROL SCI. 2007; 263(1-2): 100-106. Doi: 10.1016/j.jns.2007.06.047 [OPEN ACCESS]
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Abstract (Journal)

** Auer-Grumbach, M; Fischer, C; Duong, N; Huebner, A; John, E; Wagner, K; Speicher, M; Wehnert, M LMNA p.R644C: Pathogenic mutation of low penetrance, disease modifier or polymorphism?
NEUROMUSCULAR DISORD. 2007; 17(9-10):799-799. Doi: 10.1016/j.nmd.2007.06.129 [Poster]
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** Auer-Grumbach, M; John, E; Wallefeld, W; Fischer, C; Speicher, M; Laing, N A novel slow-skeletal myosin (MYH7) mutation in a large Austrian family presenting as late onset distal myopathy
NEUROMUSCULAR DISORD. 2007; 17(9-10):883-884. Doi: 10.1016/j.nmd.2007.06.407 [Poster]
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