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#TitleJournalYearCitations
1Genome-wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CH1Genes Chromosomes and Cancer2001159
2Demystifying chromosome preparation and the implications for the concept of chromosome condensation during mitosisCytogenetic and Genome Research2002102
3Telomeres and telomerase: biological and clinical importanceClinical Chemistry1997101
4Protein Profiling of Microdissected Pancreas Carcinoma and Identification of HSP27 as a Potential Serum MarkerClinical Chemistry200791
5Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dyeHuman Mutation200481
6Src kinase potentiates androgen receptor transactivation function and invasion of androgen-independent prostate cancer C4-2 cellsOncogene200876
7Maternal UPD 20 in a hyperactive child with severe growth retardationEuropean Journal of Human Genetics199975
8Immune Escape for Renal Cell Carcinoma: CD70 Mediates Apoptosis in LymphocytesNeoplasia200670
9Impact of Polyphenol Metabolites Produced by Colonic Microbiota on Expression of COX-2 and GSTT2 in Human Colon Cells (LT97)Nutrition and Cancer201169
10Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA librariesCytogenetic and Genome Research200263
11The DNA-Based Structure of Human Chromosome 5 in InterphaseAmerican Journal of Human Genetics200262
12Multicolor fluorescence in situ hybridization (FISH) applied to FISH-bandingCytogenetic and Genome Research200662
13Characterization of Pepsinogen C as a Potential Biomarker for Gastric Cancer Using a Histo-Proteomic ApproachJournal of Proteome Research200558
14Identification of Specific Protein Markers in Microdissected Hepatocellular CarcinomaJournal of Proteome Research200751
15Trends in overweight and obesity and changes in the distribution of body mass index in schoolchildren of Jena, East GermanyEuropean Journal of Clinical Nutrition200746
16Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20Prenatal Diagnosis200145
17Multitude multicolor chromosome banding (mMCB) – a comprehensive one-step multicolor FISH banding methodCytogenetic and Genome Research200342
18Autosomal-Dominant Microtia Linked to Five Tandem Copies of a Copy-Number-Variable Region at Chromosome 4p16American Journal of Human Genetics200842
19Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseasesArthritis Research200141
20Colon-Derived Liver Metastasis, Colorectal Carcinoma, and Hepatocellular Carcinoma Can Be Discriminated by the Ca2+-Binding Proteins S100A6 and S100A11PLoS ONE200840
21Optically controlled thermal management on the nanometer length scaleNanotechnology200838
22Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German familyHuman Genetics199635
23Epidermal growth factor receptor kinase domain mutations are rare in salivary gland carcinomasBritish Journal of Cancer200934
24The Nucleosome Assembly Activity of NAP1 Is Enhanced by AlienMolecular and Cellular Biology200733
25Chromosome variability of human multipotent mesenchymal stromal cellsBulletin of Experimental Biology and Medicine200733
26An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotypeEuropean Journal of Medical Genetics200731
27Proteomic analysis of human papillomavirus‐related oral squamous cell carcinoma: Identification of thioredoxin and epidermal‐fatty acid binding protein as upregulated protein markers in microdissected tumor tissueProteomics200931
28Telomeres and telomerase: biological and clinical importanceClinical Chemistry199731
29Microdissecting the proteomeProteomics200730
30Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemiaBritish Journal of Haematology200129
31t(11;19)(q21;p12∼p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinomaJournal of Pediatric Surgery200729
32Identification of proteins from colorectal cancer tissue by two-dimensional gel electrophoresis and SELDI mass spectrometryInternational Journal of Molecular Medicine200529
33The nature of G-bands analyzed by chromosome stretchingCytogenetic and Genome Research199727
34Genotype/phenotype analysis in a patient with pure and complete trisomy 12p200427
35Proteome Analysis of Maternal Serum Samples for Trisomy 21 Pregnancies Using ProteinChip Arrays and BioinformaticsJournal of Histochemistry and Cytochemistry200527
36Expression of EDA+ and EDB+ fibronectin splice variants in bone☆Bone200425
37Protein profiling of oral brush biopsies: S100A8 and S100A9 can differentiate between normal, premalignant, and tumor cellsProteomics - Clinical Applications200725
38Growth studies in Jena, Germany: Changes in body size and subcutaneous fat distribution between 1975 and 1995199824
39Two-Photon Multicolor FISH: A Versatile Technique to Detect Specific Sequences with in Single DNA Molecules in Cells and TissuesSingle Molecules200024
40Growth studies in Jena, Germany: Changes in sitting height, biacromial and bicristal breadth in the past decenniumsAmerican Journal of Human Biology200024
41Kabuki syndrome-like features associated with a small ring chromosome X andXIST gene expressionAmerican Journal of Medical Genetics Part A200123
42Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter ? p12.2)[10]American Journal of Medical Genetics Part A200322
43Cytogenetic, histopathologic, and immunologic studies of multifocal renal cell carcinomaCancer199721
44Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell linesJournal of Neuroscience Research199921
45Residual Chromosomal Damage after Radiochemotherapy with and without Amifostine Detected by 24-Color FISHStrahlentherapie Und Onkologie200320
46Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11->q11:)/46,XX karyotypeJournal of Medical Genetics200218
47Synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases show chromosomal aberrationsGenes Chromosomes and Cancer200318
48Molecular cytogenetic characterization of del(7q) in two uterine leiomyoma-derived cell lines199717
49Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literatureMolecular Cytogenetics200816
50Characterization of five novel large deletions causing hereditary haemorrhagic telangiectasiaClinical Genetics200816