PubRank

Uwe Claussen

Author PubWeight™ 46.44‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Microdissection based high resolution multicolor banding for all 24 human chromosomes. Int J Mol Med 2002 2.74
2 Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set. J Histochem Cytochem 2008 1.71
3 Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification. Hum Genet 2003 1.57
4 Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones. Int J Oncol 2010 1.33
5 Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements. Eur J Hum Genet 2002 1.19
6 Current developments in human molecular cytogenetic techniques. Curr Mol Med 2002 1.15
7 Protein profiling of microdissected pancreas carcinoma and identification of HSP27 as a potential serum marker. Clin Chem 2007 1.12
8 Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding. Int J Mol Med 2003 1.12
9 Discovery and identification of alpha-defensins as low abundant, tumor-derived serum markers in colorectal cancer. Gastroenterology 2005 1.03
10 Identification of specific protein markers in microdissected hepatocellular carcinoma. J Proteome Res 2007 1.01
11 Suspension (S)-FISH, a new technique for interphase nuclei. J Histochem Cytochem 2002 0.99
12 Somatic mosaicism in patients with Angelman syndrome and an imprinting defect. Hum Mol Genet 2004 0.97
13 The DNA-based structure of human chromosome 5 in interphase. Am J Hum Genet 2002 0.97
14 Ten years follow up of a boy with a complex chromosomal rearrangement: going from a > 5 to 15-breakpoint CCR. Am J Med Genet A 2003 0.92
15 The gut fermentation product butyrate, a chemopreventive agent, suppresses glutathione S-transferase theta (hGSTT1) and cell growth more in human colon adenoma (LT97) than tumor (HT29) cells. J Cancer Res Clin Oncol 2005 0.90
16 Proteome analysis of maternal serum samples for trisomy 21 pregnancies using ProteinChip arrays and bioinformatics. J Histochem Cytochem 2005 0.89
17 FISH banding methods: applications in research and diagnostics. Expert Rev Mol Diagn 2002 0.88
18 The hierarchically organized splitting of chromosomal bands for all human chromosomes. Mol Cytogenet 2009 0.87
19 Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpoints. Int J Oncol 2004 0.85
20 Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation. Am J Med Genet A 2006 0.85
21 Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter. Prenat Diagn 2003 0.85
22 Is 24-color FISH detection of in-vitro radiation-induced chromosomal aberrations suited to determine individual intrinsic radiosensitivity? Strahlenther Onkol 2002 0.85
23 Comet fluorescence in situ hybridization analysis for oxidative stress-induced DNA damage in colon cancer relevant genes. Toxicol Sci 2006 0.84
24 2-Dodecylcyclobutanone, a radiolytic product of palmitic acid, is genotoxic in primary human colon cells and in cells from preneoplastic lesions. Mutat Res 2005 0.84
25 Characterization of pepsinogen C as a potential biomarker for gastric cancer using a histo-proteomic approach. J Proteome Res 2005 0.84
26 A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injection. J Histochem Cytochem 2005 0.83
27 Microdissection-derived murine mcb probes from somatic cell hybrids. J Histochem Cytochem 2005 0.83
28 Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes. Int J Mol Med 2006 0.83
29 First postnatal case of mosaic del(22)/r(22). Prenat Diagn 2003 0.81
30 Karyotyping of human synaptonemal complexes by cenM-FISH. Eur J Hum Genet 2003 0.81
31 Synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases show chromosomal aberrations. Genes Chromosomes Cancer 2003 0.80
32 Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genes. Hum Mol Genet 2003 0.80
33 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 0.80
34 Characteristic genomic imbalances in pediatric pheochromocytoma. Genes Chromosomes Cancer 2006 0.79
35 Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia. Int J Oncol 2005 0.79
36 Uranyl nitrilotriacetate, a stabilized salt of uranium, is genotoxic in nontransformed human colon cells and in the human colon adenoma cell line LT97. Toxicol Sci 2006 0.79
37 Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal. Mutat Res 2003 0.78
38 First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16. Am J Med Genet A 2003 0.78
39 Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic Approaches. J Assoc Genet Technol 2003 0.78
40 Molecular characterization of head and neck tumors by analysis of telomerase activity and a panel of microsatellite markers. Int J Mol Med 2002 0.77
41 Precise breakpoint characterization of the colon adenocarcinoma cell line HT-29 clone 19A by means of 24-color fluorescence in situ hybridization and multicolor banding. Genes Chromosomes Cancer 2003 0.77
42 Residual chromosomal damage after radiochemotherapy with and without amifostine detected by 24-color FISH. Strahlenther Onkol 2003 0.77
43 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. Eur J Pediatr 2003 0.77
44 Telomerase activity in microdissected human breast cancer tissues: association with p53, p21 and outcome. Int J Oncol 2002 0.77
45 Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS. Oncol Rep 2003 0.77
46 New aspects of chromosomal evolution in the gorilla and the orangutan. Int J Mol Med 2007 0.76
47 First case of trisomy 13 plus mosaic trisomy 1q. Fetal Diagn Ther 2002 0.76
48 Identification of protein pattern in kidney cancer using ProteinChip arrays and bioinformatics. Int J Mol Med 2005 0.76
49 Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei. Prenat Diagn 2002 0.76
50 Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations. Cancer Genet Cytogenet 2003 0.75
51 Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells. Mol Cytogenet 2009 0.75
52 Dup(13)(q14.2-q14.3): yet another new differential diagnostic aspect for short stature-like phenotype. J Histochem Cytochem 2005 0.75
53 A complex translocation event between the two homologues of chromosomes 5 leading to a del(5)(q21q33) as a sole aberration in a case clinically diagnosed as CML: characterization of the aberration by multicolor banding. Int J Oncol 2002 0.75
54 Cultivation of fetal erythroid precursors from maternal blood: isolation and characterization by PCR and FISH. Int J Mol Med 2002 0.75
55 Increased efficiency of fluorescence in situ hybridization (FISH) using the microwave. J Histochem Cytochem 2005 0.75
56 Fluorescence in situ hybridization (FISH) on human chromosomes using photoprobe biotin-labeled probes. J Histochem Cytochem 2003 0.75
57 Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3. Int J Mol Med 2004 0.75
58 Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia. Genes Chromosomes Cancer 2002 0.75
59 TP53 alterations as a potential diagnostic marker in superficial bladder carcinoma and in patients serum, plasma and urine samples. Int J Oncol 2002 0.75
60 Characterization of a highly aberrant plasma cell leukemia karyotype: a case report. Oncol Rep 2004 0.75
61 Highly complex karyotypic changes in acute myelogenous leukemia: a case report. Int J Oncol 2003 0.75