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Speicher Michael |

Presentations at scientific conferences

Kroisel, PM; El Shabrawi-Caelen, L; Schwarzbraun, T; Speicher, M; Laccone, F; Wagner, K A young patient of disproportionate short stature suffering of glaucoma was diagnosed to have Weill-Marchesani 4 syndrome by WES however the cause of his additional progeroid phenotype is still unclear.
Medizinische Genetik. 2019; 31: -30. GfH Jahrestagung; MAR 6-8, 2019; Weimar, GERMANY. [Poster]
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Perakis, S; Ulz, P; Riedl, JM; Scheipner, L; Kashofer, K; Höfler, G; Geigl, JB; Speicher, MR; Heitzer, E; Gerger, A Molecular-biological tumor profiling for drug treatment selection in patients with advanced and refractory carcinoma: A prospective, two-stage phase II individualized cancer treatment study
The Next Generation of Clinical Trials in Molecularly Driven Therapy. 2019; -AACR; MAR 29-APR 3, 2019; Atlanta, Georgia, USA. [Oral Communication]

 

Ehrenfeld, S; Khan, R; Redhaber, D; Shoumariyeh, K; Veratti, P; Auer, M; Speicher, M; Duyster, J; Miething, C A new model for ALK plus large-cell anaplastic lymphoma (ALCL) based on CRISPR/Cas-mediated chromosomal engineering
ONCOL RES TREAT. 2018; 41: 272-273. [Poster]
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Moser, T; Ulz, P; Zhou, Q; Perakis, Samantha; Geigl, JB; Speicher, MR; Heitzer, E Single-stranded library preparation does not preferentially enrich circulating tumor DNA
11th International Symposium on Minimal Residual Cancer. 2018; -ISMRC; MAY 3-5, 2018; Montpellier, FRANCE. [Poster]

 

Graier, T; Auer, M; Heitzer, E; Ulz, P; Perakis, S; Speicher, MR; Geigl, JB Rapid single-cell copy-number aberration analysis using high- throughput sequencing.
EUR J CANCER. 2017; 72: S24-S24.-ECCO European Cancer Congress; JAN 27-30, 2017; Amsterdam, NETHERLANDS. [Poster]
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Heitzer, E; Ulz, P; Geigl JB; Speicher MR Circulating tumor DNA in Cancer Monitoring
European Journal of Human Genetics. 2017; -Annual Meeting ESHG; MAY 27-31, 2017; Cogenhagen, DENMARK. [Oral Communication]

 

Jelena Belic, Peter Ulz, Ellen Heitzer, Maria Smolle, Thomas Bauernhofer, Katja Fischereder, Jochen B. Geigl1, Michael R. Speicher Detection and characterization of neuroendocrine prostate cancer using whole genome-sequencing in circulating tumor DNA
3rd EACR Conference on Cancer Genomics; Jun 25-28, 2017; Cambridge, UK. 2017. [Oral Communication]
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Perakis S, Zhuo Q, Weber S, Ulz P, Geigl JB, Speicher MR and Heitzer E Diagnostic workflows for liquid biopsy approaches
http://journals.sagepub.com/doi/full/10.1177/1010428317742551. 2017; -ISOBM 2017 ; SEP 4-7, 2017; Rio de Janerio, BRASIL. [Oral Communication]
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Rupp, V; Ledam, R; Frömmel, M; Geigl, J; Wiesner, T; Ercan, E; Heitzer, E; Speicher, M Modelling the BAP1 tumor syndrome in iPSC derived melanocytes using an inducible knock-out system
Jahrestagung der Österreichischen Gesellschaft für Humangenetik; SEP 29, 2017; Graz, AUSTRIA. 2017. [Oral Communication]

 

Ulz P, Perakis S, Zhuo Q, Moser T, Speicher MR and Heitzer E Nucleosome positioning as cancer biomarker
https://doi.org/10.1177/1010428317742551 . 2017; -ISOBM; SEP 4-7, 2017; Rio de Janerio, BRASIL. [Oral Communication]
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Ulz, P; Speicher, MR; Thallinger, GG Reconstruction of Mitochondrial Genotypes from Diverse next Generation Sequencing Datasets
Proceedings of the 10th International Joint Conference on Biomedical Engineering Systems and Technologies. 2017; 3: 29-36.-10th International Joint Conference on Biomedical Engineering Systems; FEB 21-23, 2017; Porto, PORTUGAL. (ISBN: 978-989-758-214-1 ) [Oral Communication]
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Ulz, P; Thallinger, GG; Auer, M; Graf, R; Kashofer, K; Jahn, SW; Abete, L; Pristauz, G; Petru, E; Geigl, JB; Heitzer, E; Speicher, MR Nucleosome occupancy of cfDNA informs about gene expression
10th CNAPS International Symposium ; SEP 20-22, 2017; Montpellier, FRANCE. 2017. [Oral Communication]

 

Ulz, P; Thallinger, GG; Auer, M; Graf, R; Kashofer, K; Jahn, SW; Abete, L; Pristauz, G; Petru, E; Geigl, JB; Heitzer, E; Speicher, MR Inferring expressed genes by whole-genome sequencing of plasma DNA
28. Jahrestagung der Deutschen Gesellschaft für Humangenetik ; MAR 29-31, 2017; Bochum, GERMANY. 2017. [Oral Communication]

 

Ulz, P; Thallinger, GG; Auer, M; Graf, R; Kashofer, K; Jahn, SW; Abete, L; Pristauz, G; Petru, E; Geigl, JB; Heitzer, E; Speicher, MR Nucleosome association of cell-free DNA informs about gene expression
8th international Gene Quantification Event Symposium & Industrial Exhibition & Application Workshops ; APR 3-7, 2017; Freising-Weihenstephan, GERMANY. 2017. [Oral Communication]

 

Belic, J; Heitzer, E; Ulz, P; Auer, M; Fischereder, K; Bauernhofer, T; Geigl, JB; Speicher, MR Analysis of ctDNA using the mFastSeqS and plasma-Seq methods for screening and therapy monitoring in prostate cancer patients
CLIN CANCER RES. 2016; 22: -Meeting of the American-Association-for-Cancer-Research (AACR) Precision Medicine Series - Integrating Clinical Genomics and Cancer Therapy; JUN 13-16, 2015; Salt Lake, UT. [Oral Communication]
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Belic,J;Ulz,P; Graf, R; Auer, M; Fischereder, K; Hoefler, G; Bauernhofer, T, Geigl, JB; Heitzer, E; Speicher, MR Whole-genome sequencing of circulating tumor DNA reveals relevance of focal amplifications for the management of metastatic prostate cancer
Proceedings Book of the 24EACR. 2016; -EACR; JUL 9-12, 2016; Manchester, UK. [Poster]
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Jelena Belic, Peter Ulz, Ellen Heitzer, Martina Auer, Katja Fischereder, Thomas Bauernhofer, Jochen B. Geigl, Michael R. Speicher Detection of clonal shifts in metastatic prostate cancer patients using whole genome-sequencing in circulating tumor DNA
10th ISMRC International Symposium on Minimal Residual Cancer: Liquid Biopsy in Cancer Diagnostics and Treatment ; März 19-21, 2016; Hamburg, GERMANY. 2016. [Oral Communication]

 

Kroisel, PM; Schaller, G; Kau, T; Birnbacher, R; Speicher, MR; Windpassinger, C; Wagner, K; Schwarzbraun, T Identification of the first causative missense mutation of the GPSM2-gene in a patient with Chudley-McCullough syndrome (CMS).
ASHG Annual meeting 2016. 2016; -ASHG Annual Meeting; OCT 18-22, 2016; Vancouver, CANADA. [Poster]
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Kroisel, PM; Verheyen, S; Wagner, K; Speicher, MR; Schwerin-Nagel, A; Liehr, T Constitutional inverted insertion in a healthy parent as a pathogenetic cause for recurrent duplications in offsprings.
medizinische genetik. 2016; -GfH Jahrestagung 2016; MAR 16-18, 2016; Lübeck, GERMANY. [Poster]
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Schwach, G; Wizsy, NGT; Tam-Amersdorfer, C; Meier-Allard, N; Siddiqui, ZG; Hoeger, H; Haas, OA; Speicher, M; Niederle, B; Pfragner, R Medullary Thyroid Carcinoma Cell Lines - An Update
NEUROENDOCRINOLOGY. 2016; 103: 13-13. [Poster]
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Smolle, MA; Pichler, M; Roßmann, C; Samonigg, H; Heitzer, E; Belic, J; Speicher, M; Pummer, K; Bauernhofer, T Neuroendocrine transdifferentiation in castration resistant metastatic prostate cancer (mCRPC) - A case series
OeGHO & AHOP Frühjahrstagung; MAR 17 - 19, 2016; Vienna, AUSTRIA. 2016. [Poster]

 

Ulz, P; Belic, J; Graf, R; Auer, M; Lafer, I; Fischereder, K; Webersinke, G; Pummer, K; Augustin, H; Pichler, M; Hoefler, G; Bauernhofer, T; Geigl, JB; Heitzer, E; Speicher, MR; Whole-genome plasma sequencing reveals focal amplifications as driving force in metastatic prostate cancer
16. Jahrestagung der Österreichischen Gesellschaft für Humangenetik; SEP 30, 2016; Vienna, AUSTRIA. 2016. [Oral Communication]

 

Ulz, P; Graier, T; Auer, M; Geigl, JB; Speicher, MR; Heitzer, E Rapid copy-number aberration profiling of single-cells without whole-genome amplification
10th International Symposium on Minimal Residual Cancer; MAR 19-21, 2016; Hamburg, GERMANY. 2016. [Poster]

 

Ulz, P; Heitzer, E; Auer, M; Belic, J; Perakis, S; Geigl, JB; Speicher, MR; Krebsdiagnostik aus dem peripheren Blut: Zirkulierende Tumor DNA (ctDNA)
Forum Spital 2016, Update Onkologie; JUN 15-16, 2016; Vösendorf, AUSTRIA. 2016. [Oral Communication]

 

Ulz, P; Heitzer, E; Speicher, MR Co-occurrence of MYC amplification and TP53 mutations in human cancer
27. Jahrestagung der Deutschen Gesellschaft für Humangenetik; MAR 17-19, 2016; Lübeck, GERMANY. 2016. [Oral Communication]

 

Ulz, P; Thallinger, GG; Auer, M; Graf, R; Kashofer, K; Jahn, SW; Abete, L; Pristauz, G; Petru, E; Geigl, JB; Heitzer, E; Speicher, MR Inferring expressed genes by whole-genome sequencing of plasma DNA.
16. Jahrestagung der Österreichischen Gesellschaft für Humangenetik; SEP 30, 2016; Vienna, AUSTRIA. 2016. [Oral Communication]

 

Verheyen, S; Aubell, K; Emberger, W; Juch, H; Kroisel, P; Speicher, MR Overestimation of the positive predictive value of NIPT for Turner syndrome underlines the need for genetic counselling prior to NIPT
medizinische genetik, Springer, 1, 2016. 2016; -GfH Tagung 2016; MAR 16-18, 2016; Lübeck, Germany. [Poster]

 

Zhou, Q; Perakis, S; Ulz, P; Heitzer, E; Pichler,M; Gerger, A; Bauernhofer, T; Geigl, JB; Speicher, MR Monitoring targeted therapy response by cell-free circulating tumor DNA in metastatic colorectal cancer
Doctoral day; DEC 14, 2016; Graz, Austria. 2016. [Poster]

 

Belic, J; Heitzer, E; Ulz, P ; Auer, M; Fischereder, K; Bauernhofer, T; Geigl, JB; Speicher, MR Analysis of ctDNA using mFastSeqS and plasma–Seq methods for screening and therapy monitoring in prostate cancer patients
AACR Precision Medicine Series: Integrating Clinical Genomics and Cancer Therapy; June 13-16, 2015; Salt Lake City, Utah, USA. 2015. [Oral Communication]
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Belic, J; Koch, M; Ulz, P; Auer, M; Fischereder, K; Bauernhofer, T; Geigl, JB; Speicher, MR Heitzer, E Modified FAST-SeqS approach as a pre-screening method for detection of plasma samples with elevated ctDNA in prostate cancer patients
EACR CONFERENCE SERIES 2015 2ND SPECIAL CONFERENCE: CANCER GENOMICS; 28 JUNE – 1 JULY 2015; Cambridge, UK. 2015. [Poster]
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Heitzer, E; Ulz, P; Auer, M; Belic, J; Sumitra, M; Lax, S; Hoefler, G; Augustin, H; Edgar, P; Bauernhofer, T; Geigl, J; Speicher, M Clinical utility of circulating tumor DNA in human cancers: A report of more than 300 plama-Seqs
EUR J CANCER. 2015; 51: S33-S33.-European Cancer Congress; Sep 25-29, 2015; Vienna, AUSTRIA. [Poster]
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J. Belic, M. Koch, P. Ulz, M. Auer, K. Fischereder, T. Bauernhofer, J. B. Geigl, M. R. Speicher, E. Heitzer Modified FAST-SeqS approach as a pre-screening method for detection of plasma samples with elevated ctDNA in prostate cancer patients
2nd EACR Special Conference on Cancer Genomics, Churchill College; June-July 28-1, 2015; Cambridge, UK. 2015. [Poster]

 

Kroisel, PM; Speicher, MR; Windpassinger C Unusual form of congenital ichthyosiform erythroderma (CIE) in two siblings of an Austrian family. Attempts to unravel genetic basis of this disorder.
European Journal of Human Genetics. 2015; Volume 23, Supp 1: -The European Human Genetics Conference 2015; JUN 6-9, 2015; Glasgow , UK. [Poster]
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Kroisel, PM; Wagner, K; Lindner, S; Gruber, H; Bergmann, C; Speicher, MR; Windpassinger, C Identification of a potential new candidate gene region for Bardet-Biedl-syndrome at chromosome 14 by homozygosity mapping in an affected offspring of a couple of Austrian extraction.
medizinische genetik 1 · 2015. 2015; -26. Jahrestagung der Deutschen Gesellschaft für Humangenetik gemeinsam mit der Österreichischen Gesellschaft für Humangenetik und der Schweizerischen Gesellschaft für Medizinische Genetik; APR 15-17, 2015; Graz, AUSTRIA. [Poster]
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Lafer, I; Nagel, B; Köstenberger, M; Gamillscheg, A; Lax, S; Geigl, JB; Windpassinger, C; Speicher, MR; Schwarzbraun, T Molecular autopsies: should cardiovascular NGS-Panel testing be implemented in the workup of sudden unexplained death?
Medizinische Genetik. 2015; 27(1):79-109. 2015; -26. Jahrestagung der Deutschen Gesellschaft für Humangenetik gemeinsam mit der Österreichischen Gesellschaft für Humangenetik und der Schweizerischen Gesellschaft für Medizinische Genetik; APR 15-17, 2015; Graz, AUSTRIA. [Oral Communication]

 

Pfragner, R; Schwach, G; Hoeger, H; Tabrizi-Wizsy, NG; Tam-Amersdorfer, C; Leitinger, G; Bock, E; Zeitlhofer, P; Haas, OA; Beichler, C; Speicher, MR; Rinner, B; Niederle, B; Strobl, H A Novel Human Cell Line from Familial Medullary Thyroid Carcinoma
NEUROENDOCRINOLOGY. 2015; 102(1-2):86-86.-12th Annual ENETS Conference for the Diagnosis and Treatment of Neuroendocrine Tumor Disease; MAR 11-13, 2015; Barcelona, SPAIN. [Poster]
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Rupp, VM.; Hoffmann EM; Heitzer, E; Auer, M; Ulz; P, Perakis, S; Beichler, C; Geigl, JB; Speicher,MR A novel adenoviral system allows highly specific tumor cell detection in blood
Medizinische Genetik, March 2015, Volume 27, Issue 1, pp 79-196. 2015; 27(1):79-196.-26. Jahrestagung der Deutschen Gesellschaft für Humangenetik gemeinsam mit der Österreichischen Gesellschaft für Humangenetik und der Schweizerischen Gesellschaft für Medizinische Genetik; APR 15-17, 2015; Graz. [Oral Communication]
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Schenk, M; Geigl, JB; Wenninger, J; Mächler, E; Windpassinger, C; Petek, P; Speicher, MR Neuigkeiten aus der Reproduktionsmedizin
Reproduktionsmedizin und Genetik ; June 16, 2015; F.R.E.D. GmbH Am Sendergrund 11 8143 Dobl, Austria. 2015. [Oral Communication]

 

Speicher, MR; Heitzer, E; Ulz, P; Geigl, JB; Monitoring tumor evolution by whole-genome plasma sequencing
CANCER RES. 2015; 75: -106th Annual Meeting of the American-Association-for-Cancer-Research (AACR); APR 18-22, 2015; Philadelphia, PA. [Oral Communication]
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Ulz, P; Auer, M; Belic, J; Lafer I; Jahn, SW; Pristauz, G; Heidary, M; Schwarzbraun, T; Fischereder K; Gerger, A; Hoefler; G; Augustin, H; Bauernhofer, T; Petru, E; Heitzer, E; Geigl, JB; Speicher, MR Circulating tumor DNA sequencing reveals cancer driver genes and their plasticity in focal amplifications
Medizinische Genetik. 2015; 27(1):79-109.-26. Jahrestagung der Deutschen Gesellschaft für Humangenetik gemeinsam mit der Österreichischen Gesellschaft für Humangenetik und der Schweizerischen Gesellschaft für Medizinische Genetik; APR 15-17, 2015; Graz, AUSTRIA. [Oral Communication]
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Ulz, P; Heitzer, E; Belic, J; Auer, M; Geigl, JB, Speicher, MR; Analysis of cell-free DNA in metastasized cancer patients using next-generation sequencing
5th Polish Illumina Symposium; OCT 15-16, 2015; Poznan, POLAND. 2015. [Oral Communication]

 

Ulz, P; Heitzer, E; Belic, J; Lafer, I; Schwarzbraun, T; Bauernhofer, T; Eisner, F; Pichler, M; Fischereder, K; Gutschi, S; Augustin H; Pummer K; Webersinke, G; Geigl, JB; Speicher, MR; Whole-genome plasma sequencing reveals focal amplifications as driving force in metastatic prostate cancer
15. Jahrestagung der Österreichischen Gesellschaft für Humangenetik; SEP 25, 2015; Salzburg, AUSTRIA. 2015. [Oral Communication]

 

Verheyen, S; Kroisel, PM; Pfingstl, HM; Gruber-Sedlmayr, U; Sperl, M; Speicher, MR; Windpassinger, C Severe phenotype of metaphyseal dysplasia due to a novel homozygous frameshift mutation in the MMP13 gene.
European Journal of Human Genetics. Volume 23 Supplement 1.. 2015; -European Human Genetics Conference 2015; JUN 6-9, 2015; Glasgow, SCOTLAND. [Poster]

 

Auer, M; Heitzer, E; Ulz, P; Petru, E; Pristauz, G; Jahn, S; Speicher, MR; Geigl, JB Whole-genome sequencing of plasma DNA reveals frequently occurring copy number changes in patients with metastatic breast cancer
http://gfhev.de/de/kongress/GfH_Tagung_2014_Abstractbook.pdf. 2014; -25. Jahrestagung der Deutschen Gesellschaft für Humangenetik; MARCH 19-21, 2014; Essen, GERMANY. [Poster]

 

Auer, M; Heitzer, E; Ulz, P; Pristauz, G; Petru, E; Jahn, S; Speicher, MR; Geigl JB Low coverage whole-genome sequencing of plasma DNA reveals frequently occurring copy number changes in patients with metastatic breast cancer
http://eacr23.eacr.org/. 2014; -23rd Biennal Congress of the European Association of Cancer Research; JULY 4 - 8, 2014; Munich, GERMANY. [Poster]

 

Auer, M; Heitzer, E; Ulz, P; Pristauz, G; Petru, E; Jahn, S; Speicher, MR; Geigl, JB; Whole-genome sequencing of plasma DNA reveals frequently occurring copy number changes in patients with metastatic breast cancer.
EUR J CANCER. 2014; 50: S153-S153.-EACR; München. [Oral Communication]
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Heitzer, E; Mohan, S; Ulz, P; Lafer, I; Auer, M; Lax, S; Hoefler, G; Bauernhofer, T; Geigl, JB; Speicher, MR; Changes in colorectal carcinoma genomes under anti-EGFR therapy identified by whole-genome plasma DNA sequencing.
EUR J CANCER. 2014; 50: S96-S96.-EACR 2014; München. [Poster]
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Kroisel PM1, Auer M1, Roetzer KM2, Birnbacher R3, Wagner K1, Speicher MR1, Mehrjouy MM4, Bak M4, Geigl JB1, Tommerup N4. Application of array painting and next generation mate-pair sequencing (MPS) for improved mapping of chromosomal breakpoints in a familial translocation segregating with a particular phenotype
American Journal of Human Genetics. 2014; -American Society of Human Genetics Meeting 20014; OCT 18-22,2014; San Diego, USA. [Poster]
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Kroisel, P.M.1, R. Birnbacher2, K. Wagner1 , E. Petek1, S. Quasthoff3, M. R. Speicher1, C. Windpassinger1 Identification of potential causative gene loci for an autosomal recessive novel syndrome with brain anomalies, vision impairment and distinct facial dysmorphism.
Medizinische Genetik. 2014; Tagungsband: -25. Jahrestagung der Deutschen Gesellschaft für Humangenetik (GfH) gemeinsam mit der Österreichischen Gesellschaft für Humangenetik (ÖGH) und der Schweizerischen Gesellschaft für Medizinische Genetik (SGMG); MAR 19-21, 2014; Essen, GERMANY. [Poster]
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Lafer, I; Gamillscheg, A; Pieske, BM; Speicher, MR; Windpassinger, C; Schwarzbraun, T Cardiovascular NGS-Panel testing: design and first experiences
European Journal of Human Genetics. 2014; -The European Human Genetics Conference 2014 ; MAI 31 - JUN 3, 2014; Mailand, Italien. [Poster]

 

P.M. Kroisel1, V. Rupp1, R. Birnbacher2, C. Liechtenstein2, E. Petek1, M. R. Speicher1, C. Windpassinger1 In a consanguineous family with two patients showing a novel autosomal recessive inherited syndrome another patient with an unlinked autosomal nonsyndromic form of mental retardation was identified.
European Journalof Human Genetics . 2014; Volume 22 Supplement: 186--The European Human Genetics Conference 2014; May 31 - June 3, 2014; Milan, ITALY. [Poster]
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Riethdorf, S; Westphal, M; Mueller, C; Holtschmidt, J; Schulte, A; Matschke, J; Auer, M; Speicher, M; Lamszus, K; Pantel, K CIRCULATING TUMOR CELLS IN GLIOBLASTOMA
NEURO-ONCOLOGY. 2014; 16:
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Rupp VM, Khan MA, Orpinell M, Hussain MS, Altmüller J, Steinmetz MO, Enzinger C, Thiele H, Höhne W, Nürnberg G, Baig SM, Ansar M, Nürnberg P, Vincent JB, Speicher MR, Gönczy P, Windpassinger C A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family
64th Annual Meeting of the American Society of Human Genetics. 2014; -ASHG 2014; OCT 18-22, 2014; San Diego. [Poster]

 

Schulz, E; Klampfl, P; Holzapfel, S; Janecke, AR; Ulz, P; Renner, W; Kashofer, K; Najima, S; Leitner, A; Zebisch, A; Wölfler, A; Hofer, S; Gerger, A; Lax, S; Beham-Schmid, C; Steinke, V; Geigl, JB; Höfler, G; Speicher, MR; Boland, CR; Kumanogoh, A; Sill, H Germline variants in the semaphorin SEMA4A confer susceptibility to familial colorectal cancer type X
Oncol Res Treat. 2014; 37(S5):105-105.-Annual Meeting of the German, Austrian and Swiss Associations of Hematology and Medical Oncology; OCT 10-14, 2014; Hamburg, GERMANY. (ISBN: 978-3-318-02811-9 ) [Oral Communication]
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Seidel, MG; Hirschmugl, T; Schwinger, W; Gamez-Diaz, L; Serwas, N; Deutschmann, A; Gorkiewicz, G; Zenz, W; Windpassinger, C; Speicher, M; Grimbacher, B; Urban, C; Boztug, K Extended Phenotype and Allogeneic Hematopoietic Stem Cell Transplantation in Newly Identified Patients with Lipopolysaccharide Responsive Beige-like Anchor (LRBA) Deficiency
31st Annual Meeting of the API (Arbeitsgemeinschaft Pädiatrische Immunologie); May 9-11, 2014; Ittingen, Switzerland. 2014. [Oral Communication]

 

Seidel, MG; Hirschmugl, T; Schwinger, W; Gamez-Diaz, L; Serwas, N; Deutschmann, A; Gorkiewicz, G; Zenz, W; Windpassinger, C; Speicher, M; Grimbacher, B; Urban, C; Boztug, K Long-Term Continuous Remission After Allogeneic Hematopoietic Stem Cell Transplantation in ALPS/CVID Overlap Syndrome Due to Lipopolysaccharide Responsive Beige-Like Anchor Protein (LRBA) Deficiency
J CLIN IMMUNOL. 2014; 34: S226-S227.-16th Biennial Meeting of the European-Society-for-Immunodeficiencies; OCT 29-NOV 01, 2014; Prague, CZECH REPUBLIC. [Oral Communication]
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Smolle, E; Flicker, K; Moinfar, F; Speicher, M; Haybaeck, J Genomic characterization of endometrial stromal sarcomas by array CGH
VIRCHOWS ARCH. 2014; 465: S317-S317. [Poster]
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Smolle, E; Flicker, K; Moinfar, F; Speicher, M; Haybaeck, J Genomic Characterization of Endometrial Stromal Sarcomas using Array CGH.
Congress Abstracts, 9th International Congress of Anticancer Research. 2014; -9th International Congress of Anticancer Research; OCT 6-10, 2014; Porto Carras, Sithonia, GREECE. [Poster]

 

Smolle, E; Flicker, K; Moinfar, F; Speicher, M; Haybaeck J Genomic Characterization of Endometrial Stromal Sarcomas by Array CGH.
Congress Abstracts, 26th European Congress of Pathology. 2014; -26th European Congress of Pathology; AUG 30 - SEP 3, 2014; ExCel London, UNITED KINGDOM. [Poster]

 

Auer, M; Fondi, M; Heitzer, E; Pristauz, G; Petru, E; Jahn, S; Gasch, C; Pantel, K; Riethdorf, S; Speicher, MR; Geigl, JB High-resolution molecular characterization of circulating cell-free DNA and circulating tumor cells of patients with metastatic breast cancer
7. Forschungsforum der österreichsichen Fachhochschulen; APRIL 3-4, 2013; Dornbirn, AUSTRIA. 2013. [Poster]

 

Auer, M; Heitzer, E; Ulz, P; Pristauz, G; Petru, E; Jahn, S; Lafer, I; Pantel, K; Riethdorf, S; Speicher, MR; Geigl, JB Complex tumor genomes inferred from plasma DNA of patients with metastatic breast cancer by whole-genome sequencing.
http://www.ecco-org.eu. 2013; -The European Cancer Congress 2013 (ECCO17 - ESMO38 - ESTRO32) ; SEP 27 - OCT 1, 2013; Amsterdam, NETHERLANDS. [Keynote lecture]

 

Auer, M; Heitzer, E; Ulz, P; Pristauz, G; Petru, E; Jahn, S; Lafer, I; Pantel, K; Speicher, MR; Geigl, JB Complex tumor genomes inferred from plasma DNA of patients with metastatic breast cancer by whole-genome sequencing
EUR J CANCER. 2013; 49: S399-S399.-17th ECCO / 38th ESMO / 32nd ESTRO European Cancer Congress on Reinforcing Multidisciplinarity; SEP 27-OCT 01, 2013; Amsterdam, NETHERLANDS. [Oral Communication]
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Auer, M; Ulz, P; Pristauz, G; Petru, E; Jahn, S; Gasch, C; Riethdorf, S; Pantel, K; Geigl, JB; Speicher, MR; Heitzer, E High-resolution molecular characterization of circulating cell-free DNA and circulating tumor cells of patients with metastatic breast cancer.
http://gfhev.de/de/kongress/GfH_Tagung_2013_Abstractbook.pdf. 2013; -24. Jahrestagung der Deutschen Gesellschaft für Humangenetik ; MAR 20-22,2013; Dresden, GERMANY. [Keynote lecture]

 

Belic, J; Ulz, P; Heitzer, E; Gutschi, S; Fischereder, K; Pichler, M; Auer, M; Augustin, H; Hoefler, G; Geigl, JB; Speicher, MR Whole genome plasma DNA sequencing as a non-invasive tool for personalized therapy in prostate cancer patients
EMBL Conference, Cancer Genomix; Nov 3-5, 2013; Heidelberg, Germany. 2013. [Oral Communication]

 

Bettermann, K; Kuldeep Mehta, A; Lederer, E; Ernst, C; Kessler, SM; Kojima, K; Chen, X; Hoshida, Y; Bardeesy, N; Fuchs, B; Tanabe, KK; Müller, H; Svendova, V; Schimek, MG; Mach, M; Speicher, M; Divoky, C; Lipfert, A; Mahajan, V; Stumptner, C; Thüringer, A; Fröhlich, LF; Smole, C; Stojakovic, T; Scheideler, M; Nilsson, KPR; Kolbe, T; Rülicke, T; Longerich, T; Schirmacher, P; Magin, TM; Strnad, P; Fuchs, C; Trauner, M; Spilka, R; Kiemer, A; Teufel, A; Maass, T; Grabe, N; Müller, KM; Themanns, M; Moriggl, R; Campbell, J; Thorgeirsson, S; Pasparakis, M; Stauffer, J; Karin, M; Llovet, JM; Zatloukal, K; Denk, H; Lackner, C; Haybaeck, J Dysbalanced keratins drive steatohepatitis-associated liver carcinogenesis
8th European Conference of Intermediate filaments in health and disease. 2013; -8th European Conference of Intermediate filaments in health and disease; SEP 18-21, 2013; Amsterdam, Netherlands. [Poster]

 

Bettermann, K; Kuldeep Mehta, A; Lederer, EM; Ernst, C; Kessler, SM; Kojima, K; Cheng, X; Hoshida, Y; Bardessy, NM; Fuchs, BC; Tanabe, KK; Müller, HH; Svendova, V; Schimek, MG; Mach, M; Speicher, MR; Diwoky, C; Lipfert, A; Mahajan, V; Stumptner, C; Thüringer, A; Fröhlich, LF; Smole, C; Stojakovic, T; Scheideler, M; Nilsson, KPR; Kolbe, T; Rülicke, T; Longerich, T; Schirmacher, P; Magin, TM; Strnad, P; Fuchs, CD; Trauner, M; Spilka, R; Kiemer, AK; Teufel, A; Maass, T; Grabe, N; Müller, KM; Themanns, M; Moriggl, R; Campbell, JS; Thorgeirsson, S; Pasparakis, M; Stauffer, J; Karin, M; Llovet, JM; Zatloukal, K; Denk, H; Lackner, C; Haybaeck, J Dysbalanced Keratins promote Steatohepatitis-associated Liver Carcinogenesis
Der Pathologe, FP 08. 2013; 34(Issue6):591-591.-Joined Annual Meeting of the Swiss and Austrian Society for Pathology; NOV 7-9, 2013; Baden, Switzerland. [Oral Communication]

 

Bettermann, K; Mehta, AK; Lederer, E; Ernst, C; Kessler, SM; Chen, X; Hoshida, Y; Bardeesy, N; Fuchs, BC; Tanabe, KK; Müller, H; Svendova, V; Schimek, MG; Mach, M; Speicher, MR; Mahajan, V; Stumptner, C; Thueringer, A; Stojakovic, T; Longerich, T; Schirmacher, P; Magin, TM; Strnad, P; Fuchs, CD; Trauner, M; Spilka, R; Kiemer, AK; Teufel, A; Maass, T; Moriggl, R; Campbell, JS; Thorgeirsson, SS; Stauffer, J; Karin, M; Llovet, JM; Zatloukal, K; Lackner, C; Haybäck, J Steatohepatitis-associated Hepatocellular Carcinoma: Evidence of a Keratinopathy.
HEPATOLOGY. 2013; 58(S1):543A-543A.-64th Annual Meeting of the American Association for the Study of Liver Diseases (AASLD); NOV 1-5, 2013; Washington, DC, USA. [Poster]
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Geigl, JB; Pristauz, G; Ulz, P; Lafer, I; Högenauer, C; Petru, E; Speicher, MR; Heitzer, E Li-Fraumeni Syndrome and Hereditary Diffuse Gastric Cancer in one patient identified by next generation sequencing
http://gfhev.de/de/kongress/GfH_Tagung_2013_Abstractbook.pdf. 2013; -24. Jahrestagung der Deutschen Gesellschaft für Humangenetik ; MAR 20-22,2013; Dresden, GERMANY. [Poster]

 

Griewank, KG; Westekemper, H; Schilling, B; Mach, M; Murali, R; Wiesner, T; Schimming, T; Grabellus, F; Metz, C; Sucker, A; Hillen, U; Speicher, M; Woodman, S; Steuhl, K; Schadendorf, D; Oncogene and copy number analysis of a larger cohort of conjunctival melanoma.
EXP DERMATOL. 2013; 22(3):E43-E43.-40th Annual Meeting of the Association-of-Dermatological-Research; MAR 14-16, 2013; Dessau, GERMANY. [Oral Communication]
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Heitzer, E; Ulz, P; Belic, J; Gutschi, S; Quehenberger, F; Auer, M; Augustin, H; Hoefler, G; Geigl, JB; Speicher, MR Tumor associated copy number changes identified by whole-genome sequencing in the circulation of patients with prostate cancer
EUR J CANCER. 2013; 49: S98-S98.-17th ECCO / 38th ESMO / 32nd ESTRO European Cancer Congress on Reinforcing Multidisciplinarity; SEP 27-OCT 01, 2013; Amsterdam, NETHERLANDS. [Oral Communication]
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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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Kroisel, PM; Plecko, B; Brunner-Krainz, M; Speicher, MR; Windpassinger, C Lobar holoprosencephaly (HPE) associated with additional clinical anomalies in two daughters of a consanguineous couple. Comparison of SNP-array analysis results as an attempt to search for a potential causative candidate gene
Meeting abstracts http://www.ashg.org/2013meeting/abstracts/fulltext/index.shtml. 2013; -The 63rd Annual Meeting of the American Society of Human Genetics ; OCT 22-26, 2013; Boston, USA. [Poster]
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Kroisel, PM; Plecko, B; Gruber-Sedlmayr, U; Petek, E; Wagner, K; Speicher, MR A de novo 8/22 translocation with a 275 kb subtelomeric 8q microdeletion in a female patient is associated with multiple but stable white matter lesions and early onset of bilateral hearing loss.
Medizinische Genetik Abstractband. 2013; su: -24. Jahrestagung der Deutschen Gesellschaft für Humangenetik gemeinsam mit der Österreichischen Gesellschaft für Humangenetik und der Schweizerischen Gesellschaft für Medizinische Genetik; MAR 20-23. 2013; Dresden, GERMANY. [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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Mohan, S; Heitzer,E; Ulz, P; Lafer, I; Lax, S; Auer, M; Pichler,M; Eisner,F; Hoefler, G; Bauernhofer, T; Geigl, JB; Speicher, MR; Development of acquired resistance to anti-EGFR therapy in colorectal cancer identified by whole-genome plasma DNA sequencing
Doctoral Day; Dec 9, 2013; Graz. 2013. [Poster]

 

Orendi, K; Emberger, W; Hoefler, G; Speicher, M.R.; Sill, H; Wert der molekularen Zytogenetik und multiplex RT-PCR in der Risikostratifizierung der akuten myeloischen Leukämie.
Proceedings of the Annual Meeting of the Austrian Society of Haematology and Oncology, MEMO (Magazine of European Medical Oncology), Suppl 01/13. 2013; 6(1):-Frühjahrstagung 2013 der Österreichischen Gesellschaft für Hämatologie & Onkologie; APR 18-20,2013; Linz, AUSTRIA. [Oral Communication]

 

Orendi, K; Emberger, W; Hoefler, G; Speicher, MR; Sill, H; Diagnostic value of molecular cytogenetics and multiplex RT-PCR for risk stratification in acute myeloid leukemia.
European Journal of Human Genetics. 2013; 21, Supplement 2: 525-525.-European Human Genetics Conference 2013; JUNE 8-11, 2013; Paris, FRANCE.

 

Rupp, V; Ahmad Khan, M; Orpinell, M; Nürnberg, P; Steinmetz, MO, Speicher, MR; Enzinger, C; Gönczy, P.; Windpassinger, C. Mutation eines neuen Mikrozephalie Gens in einer konsanguinen, pakistanischen Familie führt zur Störung der Zentriolenduplikation
13.Tagung der Österreichischen Gesellschaft für Humangenetik; SEPT 26, 2013; Innsbruck, AUSTRIA. 2013. [Oral Communication]

 

Windpassinger, C; Kroisel, PM; Rupp, V; Speicher, MR; Birnbacher, R Eine neuartige, syndromale Form von mentaler Retardierung mit spezifischen Dysmorphien in einer konsanguiner Konstellation ist assoziiert mit einer homozgoten Splice-Site Mutation in einem Gen der Kinesin-Familie
http://www.oegh.at/. 2013; -ÖGH Jahrestagung 2013; SEP 26, 2013; Innsbruck, AUSTRIA. [Oral Communication]

 

Belic, J; Auer, M; Heitzer, E; Gutschi, S; Fischereder, K; Pichler, M; Ulz, P; Geigl, J; Augustin, H; Eisner, F; Höfler, G; Pantel, K; Riethdorf, S; Geigl, JB; Speicher, MR Characterization of circulating tumor cells and plasma DNA in patients with prostate cancer
Doctoral day; dec 7,2012; Graz, Austria. 2012. [Poster]

 

Geigl JB; Heitzer E; Wolf I; Lax S; Cerroni L; Speicher MR SUFU germline mutation in a patient with Gorlin syndrome identified by next generation sequencing.
62nd Annual Meeting of The American Society of Human Genetics; Nov 6-10, 2012; San Francisco, USA. 2012. [Poster]

 

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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Kroisel, PM; Roetzer, KM; Mach, M; Speicher, MR; Kortschak, A; Kaschnitz, W; Auer, M; Geigl, JB; Wagner, K A de novo balanced translocation that affects chromosomal bands Xp21.2 and 11q13.1 is associated with an autism spectrum disorder.
http://www.abstractsonline.com/Plan/SSResults.aspx. 2012; -European Human Genetics Conference; JUNE 23 - 26; Nürnberg, GERMANY. [Poster]
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Maritschnegg, E; Dandachi, N; Stadelmeyer, E;, Speicher, MR; Heitzer, E; Samonigg, H; Höfler, G; Pichler, M; Otte, M; Bauernhofer, T; Blood-based treatment monitoring of metastatic colorectal cancer patients by KRAS mutation analysis
Frühjahrstagung der österreichischen Gesellschaft für Hämatologie und Onkologie (ÖGHO); APR 12-14, 2012; Graz. 2012. [Poster]

 

Maritschnegg, E; Dandachi, N; Stadelmeyer, E;, Speicher, MR; Heitzer, E; Samonigg, H; Höfler, G; Pichler, M; Otte, M; Bauernhofer, T; KRAS mutation analysis using blood derived cell free tumor DNA for treatment monitoring of metastatic colorectal cancer patients
Cancer Res., . 2012; 72: 4513. : -AACR Annual Meeting; MAR 31- APR 4, 2012; Chicago, USA. [Poster]

 

Pfragner, R; Schwach, G; Ghaffari Tabrizi-Wizsy, N; Fuchs, R; Haas, HS; Tam-Amersdorfer, C; Allard, N; Hoeger, H; Ingolic, E; Behmel, A; Flicker, K; Speicher, M; Zeitlhofer, P; Haas, OA;; Niederle, B A new human cell line for study of sporadic medullary thyroid carcinoma with M918T mutation.
ÖGMBT Annual Meeting 2012; SEP 17-19,2012; Technische Universität Graz. 2012. [Poster]

 

Schulz, E; Valentin, A; Ulz, P; Beham-Schmid, C; Lind, K; Rupp, V; Lackner, H; Wolfler, A; Zebisch, A; Olipitz, W; Geigl, JB; Berghold, A; Speicher, MR; Sill, H Germ-line mutations in cancer predisposing genes BRCA1, BRCA2, BARD1 and TP53 in patients with therapy-related myeloid neoplasms.
ONKOLOGIE. Onkologie. 2012; 35: 117-117.-Annual Meeting of the German, Austrian and Swiss Associations of Hematology and Medical Oncology; OCT 19-23, 2012; Stuttgart, GERMANY. [Poster]
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Seidel, M; Schwinger, W; Lackner, H; Deutschmann, A; Gorkiewicz, G; Speicher, M; Boztug, K; Urban, C Familiäres Multiorgan-Autoimmunitäts-Syndrom mit Zytopenie, Leber- und Inselzell-Autoantikörpern - ein neues Immundysregulationssyndrom?
Monatsschrift Kinderheilkunde. 2012; 160: -50. Jahrestagung der Österreichischen Gesellschaft für Kinder- und Jugendheilkunde; 2012; Salzburg. [Poster]

 

Seidel, M; Schwinger, W; Lackner, H; Deutschmann, A; Gorkiewicz, G; Speicher, MR; Boztug, K; Urban, EC Familial multiorgan-autoimmunity syndrome with cytopenia, liver-, and islet cell autoantibodies - a novel inherited immune dysregulation syndrome?
IMMUNOLOGY. 2012; 137: 567-567. [Poster]
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Seidel, MG; Schwinger, W; Lackner, H; Deutschmann, A; Speicher, MR; Boztug, K; Urban, EC Familial Multiorgan-Autoimmunity Syndrome with Cytopenia, Liver-, and Islet Cell Autoantibodies – A Novel Inherited Immune Dysregulation Syndrome ?
29th Annual Meeting of the API (AG Pädiatrische Immunolgoie) 2012 and 3rd Meeting of the DGFI Study Group “Pädiatrische Immunolgoie”; May 18-20; Kartause Ittingen, Schweiz. 2012. [Oral Communication]

 

Sperl, D; Benesch, M; Urban, C; Lackner, H; Sovinz, P; Speicher, M; Uhrig, S; Schwarzbraun, T; Schwinger, W; zur Stadt, U; Beutel, K; Janka, G; Scarpatetti, M; Seidel, M Verschiedene klinische Manifestationen in einer XLP-1-Familie - Familienanamnese und schnelle Diagnostik können Leben retten
Monatsschrift Kinderheilkunde. 2012; 160: -50. Jahrestagung der Österreichischen Gesellschaft für Kinder- und Jugendheilkunde; Sept 27-29, 2012; Salzburg, AUSTRIA. [Oral Communication]

 

Sperl, D; Urban, C; Lackner, H; Sovinz, P; Speicher, M; Kroisel, P; Ofern-Zeigenfuß, L; Emberger, W; Schwinger, W; Benesch, M; Strenger, V; Schmidt, S; Seidel, M Lebensbedrohliche Veno-occlusive-Disease und langdauernde hepatobiliäre Transportstörung nach Carboplatin-Etoposid-Konditionierung und autologer Stammzelltransplantation - möglicherweise auf Basis einer neuen Genmutation in ABCB11.
Monatsschrift Kinderheilkunde. 2012; 160: -50. Jahrestagung der Österreichischen Gesellschaft für Kinder- und Jugendheilkunde; Sept 27-29, 2012; Salzburg. [Poster]

 

Thalhammer M; Heitzer E; Liegl-Atzwanger B; Auer M; Speicher MR; Geigl JB SDHB germline mutation in a patient with Carney-Stratakis syndrome.
European Journal of Human Genetics, Suppl. 1. 2012; 20: -European Society of Human Genetics GfH Jahrestagung; June 23-26, 2012; Nürnberg, Germany. [Poster]

 

Wiesner, T; Obenauf, AC; Murali, R; Fried, I; Griewank, KG; Ulz, P; Windpassinger, C; Wackernagel, W; Loy, S; Wolf, I; Viale, A; Lash, AE; Pirun, M; Socci, ND; Rütten, A; Palmedo, G; Abramson, D; Offit, K; Ott, A; Becker, JC; Cerroni, L; Kutzner, H, Bastian, BC; Speicher, MR Germline mutations in BAP1 predispose to melanocytic tumors.
Experimental Dermatology. 2012; 21(3):e22--39th Annual Meeting of the Arbeitsgemeinschaft Dermatologische Forschung (ADF); March 01-03, 2012; Marburg, Germany. [Poster]
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Jungwirth, E; Orendi, K; Haeusler, M; Speicher, M; Emberger, W; Evaluation of specific prenatal ultrasound abnormalities as chromosomal risk factors.
European Journal of Human Genetics. 2011; 20, Supplement 2: -European Human Genetics Conference 2011; MAY 28-31, 2011; Amsterdam, Netherlands. [Poster]

 

Jungwirth, E; Orendi, K; Häusler, M; Speicher, M; Emberger, W. Evaluation of Specific Prenatal Ultrasound Abnormalities as Chromosomal Risk Factors.
Keine. 2011; -European Human Genetics Conference (ESHG).; May 28 - 31, 2011.; Amsterdam RAI, The Netherlands.. [Oral Communication]

 

Kroisel PM, Geigl JB, Auer M, Mach M, Vallant E, Obenauf AM, Rötzer KM, Wagner K, Speicher MR, Gruber-Sedlmayr U, Kortschak A, Liechtenstein C, Birnbacher R Array Painting-eine neue Methode zur exakten Bruchpunktbestimmung bei balanzierten Translokationen
s.u.. 2011; -ÖGH Jahrestagung 2011; SEP 30,2011; Salzburg/AUSTRIA. [Oral Communication]
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Kroisel PM, Mach M, Vallant E, Rötzer KM, Obenauf AM, Wagner K, Speicher MR, Häusler M The Graz Experience - over 1000 postnatal and several prenatal aCGH analyses. Increasing evidence for a new microdeletion syndrome affecting band 3p13 with non recurrent chromosomal breakpoints.
DECIPHER SYMPOSION 2011 s.u.. 2011; -DECIPHER Symposion 2011; MAY 23-25, 2011; Cambridge/UK. [Oral Communication]
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Kroisel, PM; Rauter, L; Wagner, K; Schwarzbraun, T; Petek, E; Windpassinger, C; Mach, M; Rötzer, KM; Speicher, MR Clinical characterization of a patient with a de novo microdeletion 3p14.1-p13 of about 5.6 Mb and comparison with a previously reported case with similar chromosomal breakpoints
Medizinische Genetik2011; -Medizinische Genetik 2011, 22. Jahrestagung der Deutschen Gesellschaft für Humangenetik gemeinsam mit der Österreichischen Gesellschaft für Humangenetik und der Schweizerischen Gesellschaft für Medizinische Genetik GERMANY. ; MAR 16-18, 2011; Regensburg, GERMANY. [Poster]
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Kroisel, PM, Roetzer, KM; Mach, M; Wagner, K; Speicher, MR; Karpf, EF; Heitzer, E; Häusler, M Arthrogryposis multiplex congenita associated with a heterozygous mutation and 855 kb microduplication in 17q12 both likely affecting function of the cation channel gene ACCN1 in a male fetus.
European Journal of Human Genetics s.u.. 2011; -European Human Genetics Conference 2011; MAY 28 - 31, 2011; Amsterdam, THE NETHERLANDS. [Poster]
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Kroisel, PM; Wagner, K; Mach, M; Vallant, EM; Brunner-Hantsch, M; Speicher, MR; Roetzer, KM Familial occurrence of Asperger Syndrome associated with a 1Mb Duplication on Xq including the MCT8-Gene
American Journal of Human Genetics http://www.ichg2011.org/cgi-bin/ichg11s. 2011; s.o.: -12Th ICHG / 61st Annual Meeting of The American Society of Human Genetics; OCT 11-15, 2011; Montreal, CANADA. [Poster]
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Liegl, B; Flicker, K; Tavassoli, F; Speicher, M; Moinfar, F Molecular and Genetic Characterization of Diagnostically Challenging Uterine Smooth Muscle Neoplasms.
LAB INVEST. 2011; 91: 1084--100th Annual Meeting USCAP; FEB 26 - MAR 3, 2011; [Poster]
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Liegl, B; Flicker, K; Tavassoli, P; Speicher, M; Moinfar, F Molecular and Genetic Characterization of Diagnostically Challenging Uterine Smooth Muscle Neoplasms
MODERN PATHOL. 2011; 24: 1084 [Poster]
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Orendi, K; Sill, H; Mulabecirovic, A; Speicher, M; Emberger, W; AML/ALL: Korrelation von klinischem Verlauf, Interphase-FISH und klassischer Zytogenetik
24.Tumorzytogenetische Arbeitstagung; MAI 16-18, 2011; Bad Ischl, AUSTRIA. 2011. [Oral Communication]

 

Pfragner, R; Flicker, K; Hofer, D; Schwach, G; Fuchs, R; Haas, HS; Svejda, B; Aguiriano-Moser, V; Sturm, S; Niederle, B; Speicher, M; Establishment and application of cell lines from medullary thyroid carcinoma.
European Thyroid Journal, Launching Issue September 2011, 35th Annual Meeting of the European Thyroid Association. 2011; -35th Annual Meeting of the European Thyroid Association; SEPT 10-14, 2011; Krakow, POLAND. (ISBN: 978-3-8055-9876-9 ) [Poster]
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Roetzer, KM; Schwerin-Nagel, A; Kroisel, PM; Mach, M; Vallant, EM; Wagner, K; Speicher, MR; Plecko-Startinig, B Vermis hypoplasia as part of a contiguous gene syndrome in a girl with microdeletion 10q26
European Journal of Human Genetics. 2011; -European Human Genetics Conference; MAY 28-31, 2011; Amsterdam, THE NETHERLANDS. [Poster]

 

Schulz E, Rohn A, Hiden K, Wölfler A, Beham-Schmid C, Guelly C, Lackner H, Geigl J, Speicher M, Sill H Germ-line mutations in the DNA damage response and repair genes BRCA1, BARD1 and TP53 in patients with therapy-related myeloid neoplasms.
Haematologica 2011. 2011; 96(S2):25--Annual Meeting of the European Hematology Association; JUNE 2011; London, UK. [Poster]

 

Schulz, E; Rohn, A; Lind, K; Woelfler, A; Beham-Schmid, C; Guelly, C; Lackner, H; Geigl, J; Speicher, M; Sill, H Keimbahnmutationen in den DNA-Reparatur und Apoptose-induzierenden Genen BRCA1, BARD1 und TP53 bei Patienten mit Therapie-assoziierten myeloischen Neoplasien.
OeGHO Frühjahrstagung (Young Investigator Meeting); MAY, 5-7, 2011; Pörtschach, AUSTRIA. 2011. [Oral Communication]

 

El-Heliebi, A; Sedlmayr, P; Kroneis, T; Lackner, C; Geigl, JB; Speicher, MR; Haybäck, J; Fischereder, K; Kampel-Kettner, K; Zigeuner, R; Huppertz, B Isolation and characterization of circulating tumor cells by ISET.
Joint ZMF & Doctoral Days; Nov 5-6, 2010; Graz, AUSTRIA. 2010. [Poster]

 

El-Heliebi, A; Sedlmayr, P; Kroneis, T; Lackner, C; Geigl, JB; Speicher, MR; Haybäck, J; Fischereder, K; Kampel-Kettner, K; Zigeuner, R; Huppertz, B Isolation and characterization of circulating tumor cells from renal cell carcinoma patients.
9. Österreichischer Histologentag; DEC 10-11, 2010; Vienna, AUSTRIA. 2010. [Oral Communication]

 

Kroisel, PM; Obenauf, AC; Eichwalder, B; Gruber-Sedlmayr, U; Wagner, K; Schwarzbraun, T; Speicher, MR; Auer, M; Hoffmann, EM; Rötzer, KM; Geigl, JB Molecular characterization of translocation breakpoints in two cases with either a familial or a de novo constitutional translocation co-segregating with phenotypic anomalies as an attempt to directly identify genes involved.
Medizinische Genetik2010; 22(1):174-175.-21. Jahrestagung der Deutschen Gesellschaft für Humangenetik gemeinsam mit der Österreichischen Gesellschaft für Humangenetik und der Schweizerischen Gesellschaft für Medizinische Genetik ; 2.–4. März 2010; Hamburg, GERMANY. [Poster]
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Kroisel, PM; Obenauf, AC; Windpassinger, C; Pfeifer, D; Wagner, K; Roetzer, KM; Schwarzbraun, T; Speicher, MR; Woellner, C; Beitzke, M; Grimbacher, B Dubowitz-Syndrome associated with Hyper-IgE-Syndrome in a female patient. No evidence thus far for a common genetic basis.
European Journal of Human Genetics2010; 57(3):123-123.-European Human Genetics Conference 2010; June 12 - 15, 2010; Gothenburg, SWEDEN. [Poster]
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Mathiesen, RR; Fjelldal, R; Due, EU; Geigl, JB; Riethdorf, S; Borresen-Dale, AL; Pantel, K; Speicher, MR; Baumbusch, LO; Naume, B Genomic profiles of single tumour cells in metastatic breast cancer patients
EJC SUPPL. 2010; 8(5): 367
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Pristauz, G; Petru, E; Stacher, E; Geigl, J; Speicher, M; Winter, R; Moinfar, F Androgen receptor expression in patients with BRCA1/2-positive and BRCA1/2-negative breast cancer
GYNECOL ONCOL. 2010; 116(3):62- [Keynote lecture]
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Reinisch, A; Hofmann, N; Obenauf, A; Karl, K; Rohde, E; Schallmoser, K; Thaler, D; Fruhwirth, M; Flicker, K; Linkesch, W; Speicher, M; Strunk, D STABLE VESSEL GENERATION TROUGH APPLICATION OF BLOOD-DERIVED ENDOTHELIAL COLONY FORMING PROGENITOR CELLS (ECFCS) AND MESENCHYMAL STROMAL/STEM CELLS (MSCS)
HAEMATOL-HEMATOL J. 15th Congress of the European Hematology Association. 2010; 95(s2):0509-220.-15th Congress of the European Hematology Association. ; JUN 10-13, 2010; Barcelona, SPAIN. [Oral Communication]
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Reinisch, A; Hofmann, NA; Obenauf, A; Kashofer, K; Rohde, E; Schallmoser, K; Thaler, D; Fruhwirth, M; Flicker, K; Linkesch, W; Speicher, M; Strunk, D Sustained vessel formation through co-transplantation of endothelial colony-forming progenitor cells with mesenchymal stromal cells
BONE MARROW TRANSPLANT. 2010; 45: S52-S52. -36th Annual Meeting of the European Group for Blood and Marrow Transplantation; MAR 21-24, 2010; Vienna, AUSTRIA. [Oral Communication]
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Roetzer, KM; Kortschak, A; Mach, M; Vallant, EM; Wagner, K; Tschepper, P; Ulz, P; Speicher, MR; Emberger, W Deletions/Duplikations-Mosaik 6q bei einem Mädchen mit Entwicklungsretardierung und Dysmorphien, das mit Array-CGH nicht identifizierbar war
ÖGH-Jahrestagung; SEP 24, 2010; Vienna, AUSTRIA. 2010. [Oral Communication]

 

Roetzer, KM; Obenauf, AC; Plecko-Startinig, B; Brunner-Krainz, M; Speicher, MR Recurrent 16p11.2-p12.2 microdeletion syndrome: narrowing the minimal critical deletion region
Medizinische Genetik2010; 22(1):-GfH-Jahrestagung; MAR 2-4, 2010; Hamburg. [Poster]

 

Roetzer, KM; Obenauf, AC; Plecko-Startinig, B; Brunner-Krainz, M; Speicher, MR Narrowing down the minimal critical deletion region of recurrent 16p11.2-p12.2 microdeletion syndrome
European Journal of Human Genetics2010; -European Human Genetics Conference; JUN 12-15, 2010; Gothenburg, SWEDEN. [Poster]

 

Roetzer, KM; Obenauf, AC; Schwarzbraun, T; Uhrig, S; Emberger, W; Sodia, S; Mach, M; Vallant, E; Hauser, E; Wagner, K; Kroisel, PM; Speicher, MR Array-CGH for the identification of constitutional copy number changes
DECIPHER Symposium; MAY 19-21, 2010; Cambridge, GREAT BRITAIN. 2010. [Oral Communication]

 

Senanayake, U; Flicker, K; Obenauf, A; Speicher, M; Hoefler, G; Guertl, B Nephrogenic rests - genetic precursor lesions of nephroblastomas?
Panonnia Congress of Pathology; MARCH 3-6, 2010; Graz, AUSTRIA. 2010. [Poster]

 

Wackernagel, W; Mayer, CF; Geigl, J; Obenauf, A; Schneider, M; Langmann, G; Speicher, M Cytogenetic analysis of choroidal melanoma after radiotherapy
2010; -World Ophthalmology Congress 2010; JUN 5-9, 2010; Berlin, GERMANY. [Oral Communication]

 

Balic, M; Lin, H; Geigl, JB; Zheng, S; Langner, S; Tai, YC; Speicher, MR; Cote, RJ A novel method to capture and characterize bone marrow micrometastases in patients with breast cancer
Abstract Book2009; -7th International Symposium on Minimal Residual Cancer; 16-19 September ; Athens, Greece. [Oral Communication]

 

Baumbusch, LO; Geigl, JB; Riethdorf, S; Schneider, IJ; Mathiesen, RMR; Fjelldal, R; Borresen-Dale, AL; Pantel, K; Speicher, MR; Naume, B Molecular signatures of disseminated tumour cells in metastatic breast cancer patients
EJC SUPPL. 2009; 7(2):113-114.-34th ESMO Multidisciplinary Congress BERLIN; 20–24 SEPTEMBER 2009 ; Berlin. [Oral Communication]
Web of Science

 

Flicker, K; Strohmeier, B; Liegl, B; Stacher, E; Moinfar, F and Speicher, MR Array-CGH of Endometrial Stromal Sarcomas.
; Graz, AUSTRIA. 2009. [Poster]

 

Geigl, JB; Gangl, B; Obenauf, A; Auer, M; Hoffmann, EM; Waldispühl-Geigl, J; Schenk, M; Speicher, MR Hochauflösende Polkörperdiagnostik mit Array-CGH.
Journal für Gynäkologische Endokrinologie2009; 19(3):39--7. Jahrestagung der Österreichischen IVF-Gesellschaft; Sept 26-26, 2009; Innsbruck, Austria. [Oral Communication]

 

Geigl, JB; Obenauf, AC; Waldispuehl-Geigl, J; Trajanoski, Z; Baumbusch, LO; Speicher, MR Performance of whole genome-amplified DNA from single cells and cell pools on tiling oligo-arrays.
Tagungsband der Jahrestagung Deutsche Gesellschaft für Humangenetik2009; -20. Jahrestagung Deutsche Gesellschaft für Humangenetik; April 1-3, 2009; Aachen, Germany. [Poster]

 

Kroneis, T; Geigl, JB; Auer, M; Ulz, P; Schwarzbraun, T; Speicher, M; Sedlmayr, P Molecular genetic and cytogenetic analysis of automatically detected and laser-microdissected single cells after low-volume on-chip whole genome amplification
Abstract book (19th Annual Conference of the German Society for Cytometry)2009; -19th Annual Conference of the German Society for Cytometry; OCT 14-16, 2009; Leipzig, GERMANY. [Oral Communication]

 

Obenauf, AC; Schwarzbraun, T; Roetzer, KM; Mach, M; Vallant, E; Kroisel, PM; Uhrig, S; Geigl, JB; Wagner, K; Speicher, MR Array-CGH for the identification of constitutional copy number changes.
Abstractbook of the European Human Genetics Conference 2009; -European Human Genetics Conference; May 23-26, 2009; Vienna, Austria. [Poster]

 

Obenauf, AC; Schwarzbraun, T; Roetzer, KM; Mach, M; Vallant, E; Kroisel, PM; Uhrig, S; Geigl, JB; Wagner, K; Speicher, MR, Array CGH for the Identification of of constitutional copy number changes
Tagung der österreichischen Gesellschaft für Humangenetik; 2009. [Oral Communication]

 

Reinisch, A; Hofmann, NA; Obenauf, A; Kashofer, K; Rohde, E; Schallmoser, K; Thaler, D; Fruehwirth, M; Flicker, K; Linkesch, W; Speicher, M; Strunk, D Vascular regeneration by adult blood-derived endothelial colony-forming cells expanded under animal serum-free conditions
BONE MARROW TRANSPLANT. 35th Annual Meeting of the European Group for Blood and Marrow Transplantation2009; 43(1):S19-S20.-35th Annual Meeting of the European Group for Blood and Marrow Transplantation; MAR 29-APR 01, 2009; Goteborg, SWEDEN. [Oral Communication]
Web of Science

 

Reinisch, A; Hofmann, NA; Obenauf, A; Kashofer, K; Rohde, E; Schallmoser, K; Thaler, D; Fruehwirth, M; Flicker, K; Linkesch, W; Speicher, M; Strunk, D MESENCHYMAL STROMAL CELLS (MSC) SUPPORT VASCULAR REGENERATION BY ADULT BLOOD-DERIVED ENDOTHELIAL COLONY-FORMING CELLS (ECFC) EXPANDED UNDER ANIMAL SERUM-FREE CONDITIONS.
3rd International Workshop on Multipotent Stromal Cells (MSCs) for Regenerative Medicine and Immune Regulation; JUN 12-13, 2009; Frankfurt am Main, GERMANY. 2009. [Poster]

 

Reinisch, A; Hofmann, N.A.; Obenauf, A; Kashofer, K; Rohde, E; Schallmoser, K; Thaler, D; Fruehwirth, M; Linkesch, W; Speicher, M; Strunk, D Humanized Large-Scale Animal Serum-Free Expanded Blood-Derived Endothelial Colony-Forming Cells Function In Vitro and In Vivo.
International Society for Stem Cell Research 7th Annual Meeting; JUL 8-11, 2009; Barcelona, SPAIN. 2009. [Poster]

 

Reinisch, A; Hofmann, NA; Obenauf, AC; Kashofer, K; Rohde, E; Schallmoser, K; Flicker, K; Linkesch, W; Speicher, M; Strunk, D Therapeutic Vasculogenesis in Vivo by Co-Transplantation f Endothelial and Mesenchymal Progenitor Cells.
Gemeinsame Jahrestagung der Deutschen, Österreichischen und Schweizerischen Gesellschaften für Hämatologie und Onkologie2009; 32(4):166-167.-Deutsches Gesellschaft für Hämatologie und Onkologie; OCT 2-6, 2009; Heidelberg / Mannheim, GERMANY. (ISBN: 978-3-8055-9351-9 ) [Oral Communication]

 

Reinisch, A; Hofmann, NA; Obenauf, AC; Kashofer, K; Rohde, E; Schallmoser, K; Thaler, D; Fruehwirth, M; Flicker, K; Linkesch, W; Speicher, M; Strunk, D Stable vascular regeneration through co-application of adult blood-derived endothelial colony-forming cells (ECFCs) and mesenchymal stromal cells (MSCs).
23rd Meeting of the Austrian Society of Transplantation, Transfusion and Genetics.2009; 41(231):23-23.-23rd Meeting of the Austrian Society of Transplantation, Transfusion and Genetics.; OCT 21-23, 2009; Seefeld, AUSTRIA. [Oral Communication]

 

Reinisch, A; Hofmann, NA; Obenauf, AC; Kashofer, K; Rohde, E; Schallmoser, K; Thaler, D; Fruehwirth, M; Linkesch, W; Speicher; MR; Strunk, D Making functional Endothelial progenitors: animal serum-free humanized large-scale propagated adult blood-derived Endothelial colony-forming cells assemble stable perfused vessel in vivo.
2009 Proceedings of the Annual Meeting of the Austrian Society of Haematology and Oncology2009; 2(2):1-2.-ÖGHO Frühjahrestagung; APR 16-18, 2009; Salzburg, AUSTRIA. (ISBN: 1865-5041 ) [Oral Communication]

 

Roetzer, KM;Obenauf, AC;Schwarzbraun, T;Schoner, K;Speicher, MR; Rehder, H Complex chromosomal rearrangement in chromosome 4q causes acrofacial dysostosis and cardiovascular malformation
Abstractbook of the European Human Genetics Conference 20092009; -European Human Genetics Conference; MAY 23-26, 2009; Vienna, AUSTRIA. [Poster]

 

Scheffer, A; Yamada, NA; Ach, R; Tsang, P; Carr, E; Aleksic, K; Sampas, N; Peter, BJ; Speicher, M; Bruhn, L High-Resolution Cytogenetic Analysis Using Customized Oligonucleotide-Based Fluorescence in situ Hybridization (FISH)
J MOL DIAGN. 2009; 11(6):675-675. [Poster]
Web of Science

 

Schwarzbraun, T; Wang, L; Ulz, P; Nigg, EA; Speicher, MR Mitosis updated - PICH and the anaphase threads.
Abstractbook2009; -European Human Genetics Conference 2009 ; May 23 - 26, 2009; Vienna, AUSTRIA. [Oral Communication]

 

Schwarzbraun, T; Wang, LHC; Obenauf, AC; Ulz, P; Nigg, EA; Speicher, MR MITOSIS UPDATED - PICH AND THE ANAPHASE THREADS
CELL ONCOL. 2009; 31(2):90-91.-3rd Marie Curie-Genome Architecture in Relation to Disease Meeting (MC-GARD); APR 01-05, 2009; Edinburgh, SCOTLAND. [Oral Communication]
Web of Science

 

Thomas, W; Obenauf, AC; Speicher, MR; Cerroni, L Genomic characterisation of blastic plasmacytoid dendritic cell neoplasms by array CGH
J INVEST DERMATOL. JID2009; 129: S73-S73.-39th Annual Meeting of the ESDR; SEP 9-12, 2009; Budapest, HUNGARY. [Poster]
Web of Science

 

Wackernagel, W; Mayer CF; Schneider, M; Langmann, G; Obenauf, Anna; Geigl, J; Speicher, M Genomic profiling of uveal melanoma by array-CGH
2009; -Alpe Adria Congress of Ophtalmology; Nov 13-14, 2009; Graz. [Oral Communication]

 

Weber-Mzell, D; Lackner, H; Speicher, M; Uhrig, S; Schwarzbraun, T; Schwinger, W; Sovinz, P; Benesch, M; Moser, A; Urban, C Management einer Familie mit XR-vererbtem lymphoproliferativen Syndrom-Typ 1
Monatsschrift Kinderheilkunde 2009; 157(2):193-193.-47. Jahrestagung der Österreichischen Gesellschaft für Kinder- und Jugendheilkunde; 1.-3.10.2009; Graz. [Oral Communication]

 

Wiesner, T; Obenauf, AC; Cota, C; Fried, I; Speicher, MR; Cerroni, L Alterations of the cell cycle inhibitors p27KIP1 and p16INK4a are frequent in blastic plasmacytoid dendritic cell neoplasms
Abstractband2009; -Jahrestagung der Österreichischen Gesellschaft für Dermatologie; NOV, 2009; Salzburg, AUSTRIA. [Poster]

 

Wiesner, T; Obenauf, AC; Cota, C; Fried, I; Speicher, MR; Cerroni, L Alterations of the cell cycle inhibitors p27KIP1 and p16INK4a are frequent in blastic plasmacytoid dendritic cell neoplasms.
European Academy of Dermatology and Venereology; OCT, 2009; Berlin, Germany. 2009. [Poster]

 

Balic , M; Lin, H; Geilg, JB; Zheng, S; Langner, S; Speicher, MR; Tai, YC; Cote, RJ A novel method to capture and characterize occult bone marrow metastases in patients with breast cancer
Onkologie 20082008; 31 (4 Suplement): -Jahrestagung der österr., deutschen und schweizer Gesellschaft für Hämatologie und Onkologie; Oktober 10-14; Vienna, Austria. [Oral Communication]

 

Balic, M; Lin, H; Geigl, JB; Zheng, S;Langner, S; Speicher, MR; Tai, YC; Cote RJ A novel method to capture and characterize occult bone marrow metastases in patients with breast cancer
AACR Annual Research Meeting 20082008; -AACR Annual Meeting; April 12-16; San Diego, CA, USA. [Poster]

 

Flicker, K; Pfragner R; Speicher MR Characterisation of Genetic Changes in Medullary Thyroid Carcinoma (MTC) for Improvement of Diagnosis and Treatment.
1st Doctoral Day; OCT 18, 2008; Graz, AUSTRIA. 2008. [Poster]

 

Geigl, JB; Obenauf, AC; Waldispuehl-Geigl, J; Langer S; Schenk, MA; Hörmann, M; Speicher, MR High-resolution aneuploidy screening by array-CGH identifies polar bodies with unbalanced translocation chromosomes and their mode of meiotic segregation
8. Jahrestagung der Österreichischen Gesellschaft für Humangenetik; Sept 26, 2008; Innsbruck, Austria. 2008. [Oral Communication]

 

Geigl, JB; Obenauf AC; Waldispühl-Geigl J; Mach M; Langer S; Kastelic D; Hörmann M; Schenk MA; Speicher MR High-resolution aneuploidy screening by array-CGH identifies polar bodies with unbalanced translocation chromosomes and their mode of meiotic segregation
Konferenzband DGH2008; -19. Jahrestagung Deutsche Gesellschaft für Humangenetik; Apr 8-10, 2008; Hannover, Germany. [Oral Communication]

 

Geigl, JB; Speicher, MR Array-CGH analysis of single cells.
Genome Biology 2008; 10(1):301--1st Golden Helix Syposium; Nov 28-29, 2008; Athens, Greece. [Keynote lecture]

 

Geigl, JB; Speicher, MR Hereditäre Tumorerkrankungen
Österreichische Gesellschaft für Innere Medizin; Sept 17-20, 2008; Graz, Austria. 2008. [Oral Communication]

 

Kroneis, T; Alunni-Fabbroni, M; Johannes, T; Kofler, K; Walcher, W; Dohr, G; Petek, E; Sedlmayr, P Merging of Sample Processing, Semi-automated Detection, and Molecular Genetic Analysis for Process-like Single-cell Analysis.
Abstractband des Workshops (2008 erhältlich)2008; -Safe PHD Student Workshop/Non Invasive Prenatal Diagnosis; Feb 24-25, 2008; Bologna, ITALY. [Oral Communication]

 

Kroneis, Th; Geigl, J;Waldispühl-Geigl, J; Alunni-Fabbroni, M; Petek, E; Walcher, W; Dohr, G; Sedlmayr, P;, 2008 Contamination-free Analysis of Single Cells in Cell-based Non-invasive Prenatal Diagnosis
European Journal of Human Genetics, suppl. 2 2008; 16: -The European Human Genetics Conference 2008; May 31-3, 2008; Barcelona, SPAIN. [Oral Communication]

 

Obenauf, AC; Geigl, JB; Schwarzbraun, T; Geigl-Waldispühl, J: Hoffmann, EM; Auer, M; Duba, HC; Speicher, MR Identification of disease causing genes by array painting of microdissected chromosomes
1st Doctoral Day; OCT 18, 2008; Graz, AUSTRIA. 2008. [Oral Communication]

 

Obenauf, AC; Schwarzbraun, T; Kroisel, PM; Uhrig, S; Mach, M; Vallant, EM; Geigl, JB, Wagner, K; Speicher, MR Array CGH for the identification of constitutional copy number changes
Medizinische Genetik. 2008; -Tagung der Gesellschaft für Humangenetik; APRIL 8-10,2008 ; Hannover. [Poster]

 

Obenauf, AC; Schwarzbraun, T; Kroisel, PM; Uhrig, S; Mach, M; Vallant, EM; Geigl, JB, Wagner, K; Speicher, MR Array CGH for the identification of constitutional copy number changes.
DECIPHER Abstractbook2008; -DECIPHER meeting; MAY 19-21; 2008; Cambridge, UK. [Poster]

 

Reinisch, A; Hofmann, NA; Obenauf, A; Kashofer, K; Rohde, E; Schallmoser, K; Thaler, D; Fruehwirth, M; Linkesch, W; Speicher, M; Strunk, D Making Functional Endothelial Progenitors: Humanized Large-scale Animal Serum-free Propagated Adult Blood-derived Endothelial Colony-forming Cells Assemble Stable Perfused Vessels In vivo.
Fiftieth Annual Meeting Abstracts2008; 112(11):659-659.-American Society of Hematology 50th Annual Meeting and Exposition; DEC 6-9, 2008; San Francisco, USA. [Poster]
Web of Science

 

Reinisch, A; Hofmann, NA; Obenauf, A; Kashofer, K; Rohde, E; Schallmoser, K; Thaler, D; Fruehwirth, M; Linkesch, W; Speicher, M; Strunk, D Humanized Large-Scale Propagation of Vessel-Forming Endothelial Progenitor Cells.
ZMF Day; NOV 12, 2008; Graz, AUSTRIA. 2008. [Poster]

 

Schallmoser, K; Rohde, E; Reinisch, A; Obenauf, A; Speicher, M; Bartmann, C; Lanzer, G; Linkesch, W; Strunk, D Minimum requirements for fully humanised clinical scale propagation of multipotent mesenchymal stromal cells.
. 2008; 41(1): S314-S314. [Poster]
Web of Science

 

Sodia, S; W. Emberger, H. Zierler, M.Speicher Prenatal Diagnosis of a fetus with 44 Chromosomes and homozygous translocations (14;21)
European Journal of Human Genetics2008; 16(2):183-183.-European Human Genetics Conference 2008; May 31- June 3,2008; Barcelona , Spain. [Poster]

 

Speicher,MR Molecular cytogenetics
; Nov 27-29,2008; Athen, GRIECHENLAND. 2008. [Oral Communication]

 

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. [Poster]
Web of Science

 

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. [Poster]
Web of Science

 

Geigl, JB; Langer, S; Obenauf, A; Unger, K; Speicher, MR Generation of high-quality chromosome painting probes from single chromosomes after FISH.
Konferenzband DGH2007; -18. Jahrestagung Deutsche Gesellschaft für Humangenetik; March 7-10, 2007; Bonn, Germany. [Poster]

 

Geigl, JB; Obenauf, AC; Waldispuehl-Geigl, J; Langer, S; Speicher, MR Mikrodissektion und Array-Painting von Einzel-Chromosomen
7. Jahrestagung der Österreichischen Gesellschaft für Humangenetik; Sept 28, 2007; Graz, Austria. 2007. [Oral Communication]

 

Langer S; Geigl, JB; Clement- Sengewald A; Buchholz T; Obenauf A; Unger K; Speicher MR; Polar body testing on different array platforms
Konferenzband Jahrestagung DGH2007; -18. Jahrestagung Deutsche Gesellschaft für Humangenetik; March 7-10, 2007; Bonn. [Poster]

 

Obenauf, AC; Uhrig, S; Schwarzbraun, T; Geigl, JB; Wagner, K; Speicher, MR One year array-CGH in clinical genetics and research.
Abstractbook zur Jahrestagung der Österreichischen Gesellschaft für Humangenetik, 20072007; -Jahrestagung der Österreichischen Gesellschaft für Humangenetik; September 28, 2007; Graz, AUSTRIA. [Oral Communication]

 

Obenauf, AC; Uhrig, S; Schwarzbraun, T; Wagner, K; Speicher, MR Array-CGH for the identification of constitutional copy number changes
DECIPHER Symposium; MAY 16-18, 2007; Cambridge, United Kingdom. 2007. [Oral Communication]

 

Schipf, A; Pfleghaar, K; Speicher, M; Kirchner, T; Diebold, J Chromosomal instability (CIN) in early colorectal adenoma: A FISH analysis
PATHOL RES PRACT. 2007; 203(5):366-367. [Poster]
Web of Science

 

Schwarzbraun, T; Pfleghaar, K; Obenauf, A; Cremer, T; Cremer, M; Speicher, M The impact of CDC4 mutations and cyclin E increase on chromosomal instability
CELL ONCOL. 2007; 29(2):116-117.-MC-GARD Conference: “Molecular profiling of the genome”; Amsterdam, Netherlands. [Oral Communication]
Web of Science

 

Speicher, MR High resolution single cell analysis
CHROMOSOME RES. 2007; 15: 83-84. [Oral Communication]
Web of Science

 

Geigl, JB; Fiegler H; Langer, S; Unger K; Speicher MR Array CGH mit Einzelzell-Amplifikationsprodukten.
6. Tagung der Österreichischen Gesellschaft für Humangenetik; Sept 29, 2006; Wien, Austria. 2006. [Oral Communication]

 

Langer, S; Geigl, JB; Buchholz, T; Clement-Sengewald, A; Unger, K; Speicher, MR Polar body testing by comparative genomic hybridization.
Abstractbook 3rd arrayCGH-MC meeting. 2006; -Third arrayCGH-MC meeting; Sept 13-16; Leuven, Belgium. [Poster]

 

Langer, S; Geigl, JB; Clement-Sengewald, A; Buchholz, T; Speicher, MR Rapid polar body testing by comparative genomic hybridization.
Tagungsband Jahrestagung der Deutschen Gesellschaft für Humangenetik2006; -17. Jahrestagung Deutsche Gesellschaft für Humangenetik; March 8-11, 2006; Heidelberg, Germany. [Oral Communication]

 

Mayr, C; Schulz, C; Stilgenbauer, S; Krober, A; Dohner, H; Jager, U; Kainz, B; Hopfinger, G; Hoffmann, R; Wendtner, C; Hallek, M; Speicher, MR Occurrence of chromosomal translocations as independent prognostic factor in chronic lymphocytic leukemia.
BLOOD. 2006; 108(11): 590A-590A. [Poster]
Web of Science

 

Obenauf, AC; Geigl, JB; Speicher, MR Array CGH in routine diagnostics and research
OEGH Tagung der Österreichischen Gesellschaft für Humangenetik; Vienna, AUSTRIA. 2006. [Oral Communication]

 

Geigl, JB; Langer, S; Gangnus, R; Speicher, MR Sequential application of interphase FISH and CGH to single cells.
Tagungsband der Jahrestagung Deutsche Gesellschaft für Humangenetik2005; -16. Jahrestagung Deutsche Gesellschaft für Humangenetik; March 9-12, 2005; Halle/Saale, Germany. [Oral Communication]

 

Geigl, JB; Langer, S; Speicher, MR Generation of high-quality chromosome painting probes from single chromosomes after FISH.
Abstractbook 5th European Cytogentics Conference2005; -5th European Cytogentics Conference; June 4-7, 2005; Madrid, Spain. [Poster]

 

Langer, S; Geigl, JB; Leifheit, J; Lederer, G; Hempel, M; Daumer-Haas, C; Speicher, MR Breakpoint characterization of a 2q deletion in a young girl with epilepsy.
Tagungsband der Jahrestagung Deutsche Gesellschaft für Humangenetik2005; -16. Jahrestagung Deutsche Gesellschaft für Humangenetik; March 9-12, 2005; Halle/Saale, Germany. [Poster]

 

Langer, S; Geigl JB; Leifheit J; Lederer G; Hempel M; Daumer-Haas C; Speicher MR Breakpoint characterization of a 2q deletion in a young girl with epilepsy.
Abstractbook 5th European Cytogentics Conference2005; -5th European Cytogentics Conference; June 4-7, 2005; Madrid, Spain. [Poster]

 

Geigl, JB; Langer, S; Thalhammer, S; Heckl, WM; Speicher, MR Generation of chromosome painting probes from single chromosomes by laser microdissection and linker-adaptor PCR.
Abstractbook European Human Genetics Conference2004; -European Society of Human Genetics, European Human Genetics Conference; June 12 - 15, 2004; Munich, Germany. [Poster]

 

Langer, S; Geigl, JB; Thalhammer, S; Gangnus, R; Speicher, MR Single cell analysis by sequential application of two different approaches: multicolor interphase FISH followed by single cell CGH.
Abstractbook of the European Human Genetics Conference 2004, PO 02, Cytogenetics.2004; -European Society of Human Genetics, European Human Genetics Conference; June 12 - 15, 2004; Munich, Germany. [Poster]

 

Speicher, MR; Fiegler, H; Fauth, C; Carr, P; Kraus, J; Carter, NP Application of array CGH in clinical genetics.
AMER J HUM GENET 2003 73: 311-311.
Web of Science

 

Puttinger, R; Kronberger, G; Kraus, J; Speicher, MR; Rittinger, O Dup(3)(q26 > qter) & del(3)(pter > p25) due to paternal pericentric inv(3) but with phenotypic abnormalities not consistent with both well-known clinical syndromes - A case report
EUR J HUMAN GENET 2002 10: 119-119.
Web of Science

 

Speicher, MR; Kraus, J; Gangnus, R; Maierhofer, C; Jentsch, I; Langer, S; Lederer, G; Keri, C; Fauth, C Multicolor FISH in two and three-dimensions
EUR J HUMAN GENET 2002 10: 57-58.
Web of Science

 

Speicher, MR; Kraus, J; Bolzer, A; Gangnus, R; Maierhofer, C; Jentsch, I; Langer, S; Lederer, G; Keri, C; Fauth, C; Saracoglu, K; Eils, R Three-dimensional multicolor FISH for the single cell analysis of tumor interphase nuclei.
AMER J HUM GENET 2001 69: 231-231.
Web of Science

 

Bartels, I; Bohlander, SK; Mehraein, Y; Speicher, MR; Uhrig, S; Zoll, B Molecular cytogenetic characterization of a familiar translocation (1;4) with a breakpoint telomeric to the most distal subtelomeric single copy probe known on chromosome 4.
AMER J HUM GENET 1999 65: -.
Web of Science

 

Bolzer, A; Saracoglu, K; Eils, R; Cremer, T; Speicher, MR Repeat depleted painting probes for M-FISH in 2-and 3-dimensional applications
CYTOGENET CELL GENET 1999 85: 104-104.
Web of Science

 

Brown, J; Saracoglu, K; Uhrig, S; Knight, SJL; Lucas, SJA; Speicher, MR; Eils, R; Kearney, L Development of a multicolour FISH assay for subtelomeric chromosome rearrangements in leukaemia
CYTOGENET CELL GENET 1999 85: 10-10.
Web of Science

 

Daumer-Haas, C; Uhrig, S; Minderer, S; Fauth, C; Speicher, MR Rare structural rearrangements in prenatal diagnosis characterized by M-FISH
CYTOGENET CELL GENET 1999 85: 37-37.
Web of Science

 

Eils, R; Bolzer, A; Saracoglu, K; Kraus, J; Fauth, C; Uhrig, S; Speicher, MR High resolution analysis of chromosomes using new M-FISH strategies and multicolor bar coding.
AMER J HUM GENET 1999 65: -.
Web of Science

 

Eils, R; Bolzer, A; Uhrig, S; Fauth, C; Kraus, J; Gangnus, R; Jentsch, I; Grabowski, M; Cleve, B; Azofeifa, J; Saracoglu, K; Speicher, MR Technical advances in multiplex-FISH (M-FISH) and other multicolor-FISH approaches
CYTOGENET CELL GENET 1999 85: 9-9.
Web of Science

 

Garcia-Rostan, G; Hsue, A; Liu, S; Speicher, MR; Ward, DC; Tallini, G Chromosomal DNA unbalance is a common alteration in thyroid oncocytic (Hurthle cell) neoplasms and is independent of Ras mutations
LAB INVEST 1999 79: -.
Web of Science

 

Jurgen, K; Scheunemann, P; Grabowski, M; Bolzer, A; Hosch, S; Izbicki, JR; Witter, K; Pantel, K; Speicher, MR Analysis of micrometastatic cancer cells by advanced molecular cytogenetic tools
CYTOGENET CELL GENET 1999 85: 125-125.
Web of Science

 

Klein, CA; Schmidt-Kittler, O; Schardt, JA; Speicher, MR; Ahr, A; Schlimok, G; Riethmuller, G Whole genome analysis of single micrometastatic cells from bone marrow of cancer patients
CYTOGENET CELL GENET 1999 85: 31-31.
Web of Science

 

Kooy, RF; Reyniers, E; Uhrig, S; Schoepen, I; Golla, A; Wauters, J; Kroisel, P; Bossuyt, P; Rost, I; Jedele, K; Zierler, H; Schwab, S; Wildenauer, D; Speicher, M; Willems, PJ; Meitinger, T; Holinkski-Feder, E Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation t(3;16)(q29;p13.3).
AMER J HUM GENET 1999 65: A168-A168.
Web of Science

 

Scheunemann, P; Hosch, SB; Kraus, J; Pantel, K; Speicher, MR; Izbicki, JR Malignant cytogenetic characteristics of nodal micrometastates in esophageal cancer
GASTROENTEROLOGY 1999 116: -.
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