2004

Boehm D, Herold S, Kuechler A, Liehr T, Laccone F. Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye. Hum Mutat 2004, 23:368-378.
Camps J, Mrasek K, Prat E, Weise A, Starke H, Egozcue J, Miro R, Liehr T. Molecular cytogenetic characterisation of the colorectal cancer cell line SW480. Oncol Rep 2004, 11:1215-1218.
Codina-Pascual M, Oliver-Bonet M, Navarro J, Starke H, Liehr T, Gutierrez-Mateo C, Sanchez-Garcia JF, Arango O, Egozcue J, Benet J. FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic male. Am J Med Genet 2004, 127A:302-306.
Gebhart E, Ries J, Wiltfang J, Liehr T, Efferth T. Genomic gain of the epidermal growth factor receptor harboring band 7p12 is part of a complex pattern of genomic imbalances in oral squamous cell carcinomas. Arch Med Res 2004, 35:385-394.
Heller A, Loncarevic IF, G laser M, Gebhart E, Trautmann U, Claussen U, Liehr T. Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpoints.Int J Oncol 2004, 24:127-136.
Heller A, Fricke HJ, Starke H, Loncarevic IF, Claussen U, Liehr T. Characterization of a highly aberrant plasma cell leukemia karyotype: A case report. Oncol Rep 2004, 11:89-92.
Jaeger U, Zellner K, Kromeyer-Hauschild K. Body composition and type of body shape in schoolchildren from Jena/Germany. In: Bodzsár, Č. B., and Susanne, C.: Physique and body composition. Variability and sources of variations. Biennial Books of EAA, Vol. 3. Eötvös Loránd Univ. Press, Budapest 2004:53-64.
Jaeger U, Finke L, Zellner K. Säkulare Trends bei demographischen Parametern. Anthrop Anz 2004, 62:347-362.
Keller U, Kuechler A, Liehr T, Muller E, Grabenbauer G, Sauer R, Distel L. Impact of Various Parameters in Detecting Chromosomal Aberrations by FISH to Describe Radiosensitivity. Strahlenther Onkol 2004, 180:289-296.
Korsten-Reck U, Kromeyer-Hauschild K, Korsten K, Bjarnason-Wehrens B, Dickhuth HH, Berg A. Bedeutung des Freizeit- und Ernährungsverhaltens und der Sozialanamnese in der Therapie der Adipositas bei Kindern. Perfusion 2004, 17:458-464.
Kromeyer-Hauschild K. Aktuelle Aspekte der Gewichtsentwicklung bei Kindern und Jugendlichen. Pädiatrische Praxis 2004, 64:371-378.
Kuechler A, Liehr T. FISH - Detection of individual radiosensitivity. In: Encyclopedia of Diagnostic Genomics and Proteomics. Eds: J Fuchs; M Podda. ISBN: 0824747941 and 0824755642:474-477.
Keller U, Grabenbauer G, Kuechler A, Sauer R, Distel L. Technical report. Radiation sensitivity testing by fluorescence in-situ hybridization: how many metaphases have to be analysed? Int J Radiat Biol 2004, 80:615-620.
Lehrer H, Weise A, Michel S, Starke H, Mrasek K, Heller A, Kuechler A, Claussen U, Liehr T. The hierarchically organized splitting of chromosomal bands into sub-bands analyzed by multicolor banding (MCB). Cytogenet Genome Res 2004, 105:25-28.
Liehr T. FISH-Banding Methods and their Clinical Applications. In: Encyclopedia of Diagnostic Genomics and Proteomics. Eds: J Fuchs; M Podda. pp 457- 460ISBN: 0824747941 and 0824755642:457-460.
Liehr T. FISH - Centromere specific multicolor FISH (CenM-FISH) - a versatile tool for characterization of small supernumerary
marker chromosomes. In: Encyclopedia of Diagnostic Genomics and Proteomics. Eds: J Fuchs; M Podda. ISBN: 0824747941 and 0824755642:468-470.
Liehr T, Hickmann G, Kozlowski P, Claussen U, Starke U. Molecular-cytogenetic characterization of the origin andpresence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs). Chromosome Res 2004, 12:239-244.
Liehr T, Starke H, Weise A, Lehrer H, Claussen U. Multicolor FISH probe sets and their applications. Histol Histopathol 2004, 19:229-237.
Liehr T, Mrasek K, Weise A, Kuechler A, von Eggeling F, Claussen U, Starke H. Characterization of small supernumerary marker chromosomes (sSMC) in human. Current Genomics 2004, 5:279-286.
Liehr T, Claussen U, Starke H. Small supernumerary marker chromosomes (sSMC) in humans. Cytogenet Genome Res 2004, 107:55-67.
Liehr T, Heller A, Eichhorn KH, Beensen V, Schulze E, Starke H, Claussen U, Schreyer I. Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2). Prenat Diagn 2004, 24:1022-1024.
Melle C, Kaufmann R, Hommann M, Bleul A, Driesch D, Ernst G, von Eggeling F. Proteomic profiling in microdissected hepatocellular carcinoma tissue using ProteinChip technology. Int J Oncol 2004, 24:885-891.
Melle C, Ernst G, Schimmel B, Bleul A, Koscielny S, Wiesner A, Bogumil R, Moller U, Osterloh D, Halbhuber KJ, von Eggeling F. A technical triade for proteomic identification and characterization of cancer biomarkers. Cancer Res 2004, 64:4099-4104.
Nazlican H, Zeschnigk M, Claussen U, Michel S, Boehringer S, Gillessen-Kaesbach G, Buiting K, Horsthemke B. Somatic mosaicism in patients with Angelman syndrome and an imprinting defect. Hum Mol Genet. 2004, 13:2547-2555.
Opitz F, Melle C, Schenke-Layland K, Degenkolbe I, Martin DP, Von Eggeling F, Wahlers T, Stock UA. ProteinChip system technology: a powerful tool to analyze expression differences in tissue-engineered blood vessels. Tissue Eng 2004, 10:611-620.
Polityko A, Maltseva O, Rumyantseva N, Khurs O, Seidel J, Claussen U, Weise A, Liehr T, Starke H. Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3. Int J Mol Med 2004, 14:977-979.
Rudolph C, Steinemann D, Von Neuhoff N, Gadzicki D, Ripperger T, Drexler HG, Mrasek K, Liehr T, Claussen U, Emura M, Schröck E, Schlegelberger B. Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519. Cancer Genet Cytogenet 2004, 153:144-150.
Sun F, Oliver-Bonet M, Liehr T, Starke H, Ko E, Rademaker A, Navarro J, Benet J, Martin RH. Human male recombination maps for individual chromosomes. Am J Hum Genet 2004, 74:521-531.
Taudien S, Galgoczy P, Huse K, Reichwald K, Schilhabel M, Szafranski K, Shimizu A, Asakawa S, Frankish A, Loncarevic IF, Shimizu N, Siddiqui R, Platzer M. Polymorphic segmental duplications at 8p23.1 challenge the determination of individual defensin gene repertoires and the assembly of a contiguous human reference sequence. BMC Genomics 2004, 5:92.
Weise A, Starke H, Mrasek K, Claussen U, Liehr T. New insights into the evolution of chromosome 1. Cytogenet Genome Res 2005, 108:217-222.
Zellner K, Jaeger U, Kromeyer-HauschildK. Height, weight and BMI of schoolchildren in Jena, Germany - are the secular changes levelling off? Economics and Hum Biol 2004, 2:281-294.
Zumkeller W, Volleth M, Muschke P, Tönnies H, Heller A, Liehr T, Wieacker P, Stumm M. Genotype/phenotype analysis in a patient with pure and complete trisomy 12p. Am J Med Genet 2004, 129A:261-264.