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Baudis Michael

Research Profile

Disorders

Procedures

Physiology

Chemicals & Drugs

DNA, Neoplasm

Genes & Molecular Sequences

Single Nucleotide Polymorphism

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Publications

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Itziar Salaverria; Carsten Schwaenen; Monika Szczepanowski; Lorenz Trümper; Swen Wessendorf; Thorsten Zenz; Norbert Arnold; Baudis Michael; Susanne Bens; Birgit Burkhardt; Africa García-Orad; Wolfram Klapper; Markus Kreuz; Jasmin Lisfeld; Idoia Martin-Guerrero; Ilske Oschlies; Michael Pfreundschuh; Reiner Siebert
High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas.
A Bluwstein; Baudis Michael; N Kumar; K Léger; J van Oostrum; Hubert Rehrauer; J Traenkle; M O Hottiger
PKC signaling prevents irradiation-induced apoptosis of primary human fibroblasts.
Sabrina Spengler; Klaus Zerres; Baudis Michael; Matthias Begemann; Peter Blümel; Bernd Denecke; Anna Jauch; Peter Michael Kroisel; Ute Moog; Barbara Oehl-Jaschkowitz; Nadina Ortiz Brüchle; Gisela Raabe-Meyer; Bernd Schulze; Christiane Spaich; Thomas Eggermann
Molecular karyotyping as a relevant diagnostic tool in children with growth retardation with Silver-Russell features.

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All Publications

2013: Itziar Salaverria; Carsten Schwaenen; Monika Szczepanowski; Lorenz Trümper; Swen Wessendorf; Thorsten Zenz; Norbert Arnold; Baudis Michael; Susanne Bens; Birgit Burkhardt; Africa García-Orad; Wolfram Klapper; Markus Kreuz; Jasmin Lisfeld; Idoia Martin-Guerrero; Ilske Oschlies; Michael Pfreundschuh; Reiner Siebert
High resolution copy number analysis of IRF4 translocation-positive diffuse large B-cell and follicular lymphomas.
Genes, chromosomes & cancer 2013;52(2):150-5.
2013: A Bluwstein; Baudis Michael; N Kumar; K Léger; J van Oostrum; Hubert Rehrauer; J Traenkle; M O Hottiger
PKC signaling prevents irradiation-induced apoptosis of primary human fibroblasts.
Cell death & disease 2013;4():e498.
2012: Sabrina Spengler; Klaus Zerres; Baudis Michael; Matthias Begemann; Peter Blümel; Bernd Denecke; Anna Jauch; Peter Michael Kroisel; Ute Moog; Barbara Oehl-Jaschkowitz; Nadina Ortiz Brüchle; Gisela Raabe-Meyer; Bernd Schulze; Christiane Spaich; Thomas Eggermann
Molecular karyotyping as a relevant diagnostic tool in children with growth retardation with Silver-Russell features.
The Journal of pediatrics 2012;161(5):933-42.
2012: Thomas Eggermann; Baudis Michael; Bernd Denecke; Sabrina Spengler; Andreas Venghaus; Klaus Zerres; Regina Ensenauer
2p21 Deletions in hypotonia-cystinuria syndrome.
European journal of medical genetics 2012;55(10):561-3.
2011: M Begemann; G Binder; Karin Buiting; Baudis Michael; S Fricke-Otto; A Haake; D Kanber; I Leisten; S Markus; R Mühlenberg; T Rupprecht; H Segerer; R Siebert; S Spengler; Thomas Eggermann
Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues.
Clinical genetics 2011;80(1):83-8.
2011: Nitin Kumar; Hubert Rehrauer; Haoyang Cai; Baudis Michael
CDCOCA: a statistical method to define complexity dependence of co-occuring chromosomal aberrations.
BMC medical genomics 2011;4():21.
2010: Ezequiel Lacunza; Baudis Michael; Andrea G Colussi; Amada Segal-Eiras; Maria V Croce; Martin Abba
MUC1 oncogene amplification correlates with protein overexpression in invasive breast carcinoma cells.
Cancer genetics and cytogenetics 2010;201(2):102-10.
2010: Thomas Eggermann; Sabrina Spengler; Nadine Bachmann; Baudis Michael; Ulrike A Mau-Holzmann; Sylke Singer; Eva Rossier
Chromosome 11p15 duplication in Silver-Russell syndrome due to a maternally inherited translocation t(11;15).
American journal of medical genetics. Part A 2010;152A(6):1484-7.
2010: Raúl Peralta; Baudis Michael; Guelaguetza Vazquez; Sergio Juárez; Rocío Ortiz; Horacio Decanini; Dulce Hernandez; Francisco Gallegos; Alejandra Valdivia; Patricia Piña; Mauricio Salcedo
Increased expression of cellular retinol-binding protein 1 in laryngeal squamous cell carcinoma.
Journal of cancer research and clinical oncology 2010;136(6):931-8.
2010: S Spengler; Nadine Schönherr; G Binder; Hartmut A Wollmann; S Fricke-Otto; R Mühlenberg; Bernd Denecke; Baudis Michael; Thomas Eggermann
Submicroscopic chromosomal imbalances in idiopathic Silver-Russell syndrome (SRS): the SRS phenotype overlaps with the 12q14 microdeletion syndrome.
Journal of medical genetics 2010;47(5):356-60.
2010: Thomas Eggermann; Nadine Schönherr; Sabrina Spengler; Susanne Jäger; Bernd Denecke; Gerhard Binder; Baudis Michael
Identification of a 21q22 duplication in a Silver-Russell syndrome patient further narrows down the Down syndrome critical region.
American journal of medical genetics. Part A 2010;152A(2):356-9.
2009: Moritz Gerstung; Baudis Michael; Holger Moch; Niko Beerenwinkel
Quantifying cancer progression with conjunctive Bayesian networks.
Bioinformatics (Oxford, England) 2009;25(21):2809-15.
2009: Jun Liu; Nirmalya Bandyopadhyay; Sanjay Ranka; Baudis Michael; Tamer Kahveci
Inferring progression models for CGH data.
Bioinformatics (Oxford, England) 2009;25(17):2208-15.
2009: Stefanie Bug; Jan Dürig; Florian Oyen; Ludger Klein-Hitpass; Jose I Martin-Subero; Lana Harder; Baudis Michael; Norbert Arnold; Uwe Kordes; Ulrich Dührsen; Reinhard Schneppenheim; Reiner Siebert
Recurrent loss, but lack of mutations, of the SMARCB1 tumor suppressor gene in T-cell prolymphocytic leukemia with TCL1A-TCRAD juxtaposition.
Cancer genetics and cytogenetics 2009;192(1):44-7.
2009: E G Boerma; Reiner Siebert; Philip M Kluin; Baudis Michael
Translocations involving 8q24 in Burkitt lymphoma and other malignant lymphomas: a historical review of cytogenetics in the light of todays knowledge.
Leukemia 2009;23(2):225-34.
2008: Verena L Bauer; Herbert Braselmann; Michael Henke; Dominik Mattern; Axel Walch; Kristian Unger; Baudis Michael; Silke Lassmann; Reinhard Huber; Johannes Wienberg; Martin Werner; Horst F Zitzelsberger
Chromosomal changes characterize head and neck cancer with poor prognosis.
Journal of molecular medicine (Berlin, Germany) 2008;86(12):1353-65.
2008: Andreas Roos; Miriam Elbracht; Baudis Michael; Jan Senderek; Nadine Schönherr; Thomas Eggermann; Herdit Schüler
A 10.7 Mb interstitial deletion of 13q21 without phenotypic effect defines a further non-pathogenic euchromatic variant.
American journal of medical genetics. Part A 2008;146A(18):2417-20.
2008: Alexander Hoischen; Marion Ehrler; Jana Fassunke; Matthias Simon; Baudis Michael; Christina Landwehr; Bernhard Radlwimmer; Peter Lichter; Johannes Schramm; Albert J Becker; Ruthild G Weber
Comprehensive characterization of genomic aberrations in gangliogliomas by CGH, array-based CGH and interphase FISH.
Brain pathology (Zurich, Switzerland) 2008;18(3):326-37.
2008: Inga Nieländer; José I Martín-Subero; Florian Wagner; Baudis Michael; Stefan Gesk; Lana Harder; Dirk Hasenclever; Wolfram Klapper; Markus Kreuz; Christiane Pott; José A Martinez-Climent; Martin Dreyling; Norbert Arnold; Reiner Siebert
Recurrent loss of the Y chromosome and homozygous deletions within the pseudoautosomal region 1: association with male predominance in mantle cell lymphoma.
Haematologica 2008;93(6):949-50.
2007: Jan Dürig; S Bug; Ludger Klein-Hitpass; Tanja Boes; T Jöns; Jose I Martin-Subero; Lana Harder; Baudis Michael; Ulrich Dührsen; R Siebert
Combined single nucleotide polymorphism-based genomic mapping and global gene expression profiling identifies novel chromosomal imbalances, mechanisms and candidate genes important in the pathogenesis of T-cell prolymphocytic leukemia with inv(14)(q11q32).
Leukemia 2007;21(10):2153-63.
2007: Baudis Michael
Genomic imbalances in 5918 malignant epithelial tumors: an explorative meta-analysis of chromosomal CGH data.
BMC cancer 2007;7():226.
2006: Baudis Michael; Victor Prima; Yoon Han Tung; Stephen P Hunger
ABCB1 over-expression and drug-efflux in acute lymphoblastic leukemia cell lines with t(17;19) and E2A-HLF expression.
Pediatric blood & cancer 2006;47(6):757-64.
2006: Jun Liu; Jaaved Mohammed; James Carter; Sanjay Ranka; Tamer Kahveci; Baudis Michael
Distance-based clustering of CGH data.
Bioinformatics (Oxford, England) 2006;22(16):1971-8.
2006: Xin Mao; Rifat A Hamoudi; Ian C Talbot; Baudis Michael
Allele-specific loss of heterozygosity in multiple colorectal adenomas: toward an integrated molecular cytogenetic map II.
Cancer genetics and cytogenetics 2006;167(1):1-14.
2006: Baudis Michael
Online database and bioinformatics toolbox to support data mining in cancer cytogenetics.
BioTechniques 2006;40(3):269-70, 272.
2005: Xin Mao; Rifat A Hamoudi; Po Zhao; Baudis Michael
Genetic losses in breast cancer: toward an integrated molecular cytogenetic map.
Cancer genetics and cytogenetics 2005;160(2):141-51.
2005: Jo Vandesompele; Baudis Michael; Katleen De Preter; Nadine Van Roy; Peter F Ambros; Nick Bown; Christian Brinkschmidt; Holger Christiansen; Valérie Combaret; Maria Lastowska; James Nicholson; Anne O'Meara; Dominique Plantaz; Raymond L Stallings; Bénédicte Brichard; Caroline Van den Broecke; Sylvia De Bie; Anne De Paepe; Geneviève Laureys; Frank Speleman
Unequivocal delineation of clinicogenetic subgroups and development of a new model for improved outcome prediction in neuroblastoma.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2005;23(10):2280-99.
2005: Alfredo Hidalgo; Baudis Michael; Iver Petersen; Hugo Arreola; Patricia Piña; Guelaguetza Vázquez-Ortiz; Dulce Hernández; José González; Minerva Lazos; Ricardo López; Carlos Pérez; José García; Karla Vázquez; Brenda Alatorre; Alfredo Hidalgo-Miranda
Microarray comparative genomic hybridization detection of chromosomal imbalances in uterine cervix carcinoma.
BMC cancer 2005;5():77.
2002: Ulrich Kaiser; Irmgard Uebelacker; Ulrich Abel; Josef Birkmann; Lorenz Trümper; Harald Schmalenberg; Tunca Karakas; Bernd Metzner; Dieter K Hossfeld; Helge G Bischoff; Astrid Franke; Marcel Reiser; Peter Müller; Luisa Mantovani; Marc Grundeis; Frank Rothmann; Cay-Uwe von Seydewitz; Rolf M Mesters; Ernst U Steinhauer; Dorothea Krahl; Kurt Schumacher; Michael Kneba; Baudis Michael; Norbert Schmitz; Rüdiger Pfab; Hubert Köppler; Reza Parwaresch; Michael Pfreundschuh; Klaus Havemann
Randomized study to evaluate the use of high-dose therapy as part of primary treatment for "aggressive" lymphoma.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2002;20(22):4413-9.
2001: Baudis Michael; M L Cleary
Progenetix.net: an online repository for molecular cytogenetic aberration data.
Bioinformatics (Oxford, England) 2001;17(12):1228-9.
2001: Martin Bentz; Thomas F E Barth; Silke Brüderlein; D Bock; Michael J Schwerer; Baudis Michael; Stefan Joos; Andreas Viardot; A C Feller; Hans Konrad Müller-Hermelink; Peter Lichter; Hartmut Döhner; Peter Möller
Gain of chromosome arm 9p is characteristic of primary mediastinal B-cell lymphoma (MBL): comprehensive molecular cytogenetic analysis and presentation of a novel MBL cell line.
Genes, chromosomes & cancer 2001;30(4):393-401.
2001: Baudis Michael; M Bentz
Comparative genomic hybridization for the analysis of leukemias and lymphomas.
Methods in molecular medicine 2001;55():43-64.
2001: Swen Wessendorf; Peter Lichter; C Schwänen; Björn Fritz; Baudis Michael; K Walenta; Marita Kloess; Hartmut Döhner; Martin Bentz
Potential of chromosomal and matrix-based comparative genomic hybridization for molecular diagnostics in lymphomas.
Annals of hematology 2001;80 Suppl 3():B35-7.
2000: Martin Bentz; A Plesch; Lars Bullinger; Stephan Stilgenbauer; German Ott; Hans Konrad Müller-Hermelink; Baudis Michael; Thomas F E Barth; Peter Möller; Peter Lichter; Hartmut Döhner
t(11;14)-positive mantle cell lymphomas exhibit complex karyotypes and share similarities with B-cell chronic lymphocytic leukemia.
Genes, chromosomes & cancer 2000;27(3):285-94.
1997: Ruthild G Weber; J Boström; Marietta Wolter; Baudis Michael; V P Collins; Guido Reifenberger; Peter Lichter
Analysis of genomic alterations in benign, atypical, and anaplastic meningiomas: toward a genetic model of meningioma progression.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(26):14719-24.
1997: CA Werner; Hartmut Döhner; Stefan Joos; L H Trümper; Baudis Michael; Thomas F E Barth; German Ott; Peter Möller; Peter Lichter; Martin Bentz
High-level DNA amplifications are common genetic aberrations in B-cell neoplasms.
The American journal of pathology 1997;151(2):335-42.
1996: Peter Lichter; K Fischer; Stefan Joos; T Fink; Baudis Michael; R K Potkul; Sibylle Ohl; S Solinas-Toldo; R Weber; Stephan Stilgenbauer; Martin Bentz; Hartmut Döhner
Efficacy of current molecular cytogenetic protocols for the diagnosis of chromosome aberrations in tumor specimens.
Cytokines and molecular therapy 1996;2(3):163-9.
1996: Martin Bentz; Ulf Bergerheim; C Li; Stefan Joos; C A Werner; Baudis Michael; J Gnarra; M J Merino; B Zbar; W M Linehan; Peter Lichter
Chromosome imbalances in papillary renal cell carcinoma and first cytogenetic data of familial cases analyzed by comparative genomic hybridization.
Cytogenetics and cell genetics 1996;75(1):17-21.
1995: Martin Bentz; Hartmut Döhner; C A Werner; K Huck; Baudis Michael; Stefan Joos; Brigitte Schlegelberger; L H Trümper; A C Feller; M Pfreundschuh
Identification of genetic imbalances in malignant lymphoma using comparative genomic hybridization.
Stem cells (Dayton, Ohio) 1995;13 Suppl 3():83-7.