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Pischler Carina |

Presentations at scientific and public conferences

Pischler, C; Beichler, C; Pristauz, G; Trapp, EK; Peintinger, F; Weirather, C; Siebenhofer, C; Petru,E; Geigl, J; Heitzer, E; Speicher, M Identification of biomarkers from plasma-DNA from patients with ovarian cancer
Doctoral Day 2021; FEB 12, 2021; Virtual Congress, Graz, AUSTRIA. 2021. [Onlinepräsentation]

Murali, R; van de Nes, J; Gessi, M; Sucker, A; Moeller, I; Stiller, M; Horn, S; Scholz, S; Pischler, C; Stadler, N; Schilling, B; Zimmer, L; Hillen, U; Scolyer, RA; Buckland, M; Lauriola, L; Pietsch, T; Waha, A; Schadendorf, D; Griewank, K Targeted Next Generation Sequencing Reveals Unique Mutation Profile of Primary Melanocytic Tumors of the Central Nervous System
LAB INVEST. .. 2016; 96: 434A-434A.-105th Annual Meeting of the United-States-and-Canadian-Academy-of-Pathology; MAR 12-18, 2016; Seattle, WA. [Poster]
Web of Science

Murali, R; van de Nes, J; Gessi, M; Sucker, A; Moeller, I; Stiller, M; Horn, S; Scholz, S; Pischler, C; Stadler, N; Schilling, B; Zimmer, L; Hillen, U; Scolyer, RA; Buckland, M; Lauriola, L; Pietsch, T; Waha, A; Schadendorf, D; Griewank, K Targeted Next Generation Sequencing Reveals Unique Mutation Profile of Primary Melanocytic Tumors of the Central Nervous System
MODERN PATHOL. .. 2016; 29: 434A-434A.-105th Annual Meeting of the United-States-and-Canadian-Academy-of-Pathology; MAR 12-18, 2016; Seattle, WA. [Poster]
Web of Science

Kroisel, PM; Pichler, U; Kuchernig, D; Mach, M; Pischler, C; Schwarzbraun, T; Wagner, K; Speicher, MR West syndrome, general psychomotor retardation and dysmorphic features in a female patient due to a 2.92 Mb microdeletion leading to a haploinsufficiency of the CDKL5 gene and several additional flanking genes
https://www.eshg.org/programme2013.0.html www.nature.com/ejhg. 2013; -European Human Genetics Conference 2013; JUN 8-11, 2013; Paris, FRANCE. [Poster]
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Lafer, I; Geigl, JB; Mach, M; Pischler, C; Vallant, E; Speicher, MR; Wagner, K; Kroisel, PM Microdeletion of 831 kb in a young woman leads to haploinsufficiency of more than 30 genes at 17q including a copy of the BRCA1-gene. Consequences for genetic and clinical management.
http://www.gfhev.de/kongress_archiv/2013%20de/kongress/GfH-Tagung_Abstractband_2013.pdf. 2013; -24. Jahrestagung der Deutschen Gesellschaft für Humangenetik gemeinsam mit der Österreichischen Gesellschaft für Humangenetik und der Schweizerischen Gesellschaft für Medizinische Genetik; MAR 20-22, 2013; Dresden, GERMANY. [Poster]
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Kroisel, PM; Geigl, JB; Mach, M; Pischler, C; Vallant, E; Speicher, MR; Wagner, K A microdeletion of about 831 kb in a young woman causes a loss of more than 30 genes on the long arm of chromosome 17 including a copy of the BRCA1-gene. Implications for genetic counselling and clinical management.(3116F)
http://abstracts.ashg.org/cgi-bin/2012/ashg12s. 2012; -American Society of Human Genetics, Annuak Meeting; NOV 6-10, 2012; San Francisco, USA. [Poster]
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