I. Chudoba

发表

High resolution multicolor-banding: a new technique for refined FISH analysis of human chromosomes

T. Lörch, G. Senger, I. Chudoba, 1999, Cytogenetic and Genome Research.

The DNA-based structure of human chromosome 5 in interphase.

T. Liehr, K. Sperling, P. Muehlig, 2002, American journal of human genetics.

Induced aneuploidy disrupts MCF10A acini formation and CCND1 expression

C. Conrad, R. Eils, A. Jauch, 2019, bioRxiv.

Maternally inherited duplication of chromosome 7, dup(7)(p11.2p12), associated with mild cognitive deficit without features of Silver–Russell syndrome

S. Weremowicz, L. Holmes, N. Leach, 2007, American journal of medical genetics. Part A.

Losses of Both Products of the Cdkn2a/Arf Locus Contribute to Asbestos-Induced Mesothelioma Development and Cooperate to Accelerate Tumorigenesis

J. Testa, Jinfei Xu, M. Carbone, 2011, PloS one.

Detailed characterization of 7q deletions by multicolor banding (mBAND) in marginal zone cell lymphoma.

G. Salles, F. Berger, J. Magaud, 2007, Cancer genetics and cytogenetics.

Two different del(5q) clones in a patient with myelodysplastic syndrome

T. Liehr, I. Chudoba, D. Haase, 2011, Leukemia & lymphoma.

Cryptic t(X;18), ins(6;18), and SYT-SSX2 gene fusion in a case of intraneural monophasic synovial sarcoma.

P. Sorensen, D. Horsman, W. Lam, 2002, Cancer genetics and cytogenetics.

Overrepresentation of 7q31 and 17q in renal cell carcinomas

A. Bernheim, M. Terrier-Lacombe, I. Chudoba, 1998, Genes, chromosomes & cancer.

Investigations of chorionic villi after chorionic villus sampling (CVS)

J. Rüschoff, I. Chudoba, A. Köhler, 1989, Human Genetics.

Mapping of the 7q31 subregion common to the small chromosome 7 derivatives from two sporadic papillary renal cell carcinomas: increased copy number and overexpression of the MET proto-oncogene

A. Bernheim, G. Danglot, I. Chudoba, 2000, Oncogene.

Analysis of X-ray-induced aberrations in human chromosome 5 using high-resolution multicolour banding FISH (mBAND)

I. Chudoba, G. Obe, C. Johannes, 2004, Chromosome Research.

Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage–fusion–bridge cycle

C. Harrison, A. Moorman, I. Chudoba, 2007, Genes, chromosomes & cancer.

Rearrangements of the telomeric region of mouse chromosome 11 in Pre-B ABL/MYC cells revealed by mBANDing, spectral karyotyping, and fluorescence in-situ hybridization with a subtelomeric probe

G. Klein, S. Mai, I. Chudoba, 2005, Chromosome Research.

A de novo complex karyotype with two independent balanced translocations and a double inversion of chromosome 6 presenting with multiple congenital anomalies

C. Griffin, A. Kline, A. Hawkins, 2004, American journal of medical genetics. Part A.

PRENATAL DIAGNOSIS OF A HALF‐CRYPTIC TRANSLOCATION USING CHROMOSOME MICRODISSECTION

N. Tommerup, G. Senger, I. Chudoba, 1997, Prenatal diagnosis.

A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature

T. Liehr, F. Zintl, G. Senger, 2003, European Journal of Pediatrics.

Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review

A. Hübler, M. Rocchi, T. Liehr, 2000, Journal of medical genetics.

Maternal UPD 20 in a hyperactive child with severe growth retardation

G. Senger, I. Hansmann, I. Chudoba, 1999, European Journal of Human Genetics.

A FISH comparison of variant derivatives of the recurrent dic(17;20) of myelodysplastic syndromes and acute myeloid leukemia: Obligatory retention of genes on 17p and 20q may explain the formation of dicentric chromosomes

L. Campbell, I. Chudoba, Crisoula Patsouris, 2007, Genes, chromosomes & cancer.

Chromosome Intrachanges and Interchanges Detected by Multicolor Banding in Lymphocytes: Searching for Clastogen Signatures in the Human Genome

M. Durante, I. Chudoba, G. Obe, 2004, Radiation research.

Cytogenetic Evolution of Human Ovarian Cell Lines Associated with Chemoresistance and Loss of Tumorigenicity

P. Cornillet‐Lefèbvre, I. Chudoba, S. Struski, 2003, Analytical cellular pathology : the journal of the European Society for Analytical Cellular Pathology.

Microdissection and reverse painting reveals a microdeletion 6(q26qter) in a de novo r(6) chromosome.

M. König, O. Haas, W. Schnedl, 2001, Annales de genetique.

FISH studies on the telomeric regions of the T-cell acute lymphoblastic leukemia cell line CCRF-CEM

T. Efferth, B. Lausen, I. Chudoba, 2005, Cytogenetic and Genome Research.

De novo complete trisomy 5p: clinical report and FISH studies.

I. Chudoba, J. Lemke, U. Claussen, 1999, American journal of medical genetics.

Multicolor-FICTION: expanding the possibilities of combined morphologic, immunophenotypic, and genetic single cell analyses.

R. Siebert, J. Martín-Subero, M. Calasanz, 2002, The American journal of pathology.

Partial trisomy 9p12p21.3 with a normal phenotype

P. Wieacker, M. Volleth, I. Chudoba, 2002, Journal of medical genetics.

mBAND: a high resolution multicolor banding technique for the detection of complex intrachromosomal aberrations

A. Jauch, G. Senger, I. Chudoba, 2004, Cytogenetic and Genome Research.

Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics

R. Wegner, I. Chudoba, H. Tönnies, 2001, Cytogenetic and Genome Research.

Immense random colocalization, revealed by automated high content image cytometry, seriously questions FISH as gold standard for detecting EML4‐ALK fusion

I. Chudoba, B. Kajtár, L. Pajor, 2018, Cytometry. Part A : the journal of the International Society for Analytical Cytology.

Constitutional tetrasomy 18p.

I. Chudoba, S. Bakshi, P. Trivedi, 2006, Indian pediatrics.

Improved definition of chromosomal breakpoints using high-resolution multicolour banding

G. Senger, I. Chudoba, J. Lemke, 2001, Human Genetics.

Cytogenetic abnormalities in a rare case of giant cell osteogenic sarcoma.

H. Schwartz, M. Butler, I. Chudoba, 1992, Cancer genetics and cytogenetics.

Identification of a dup(5)(p15.3) by multicolor banding

I. Chudoba, J. Brown, D. Riordan, 2002, Clinical genetics.

Improved detection of chromosome 16 rearrangements in acute myeloid leukemias using 16p and 16q specific microdissection DNA libraries.

G. Senger, I. Chudoba, U. Claussen, 1996, Oncology reports.

Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias.

T. Liehr, G. Senger, I. Chudoba, 2000, International Journal of Oncology.

CBFB/MYH11 fusion in a patient with AML‐M4Eo and cytogenetically normal chromosomes 16

M. König, O. Haas, U. Jäger, 2000, Genes, chromosomes & cancer.