PubRank

Anja Weise

Author PubWeight™ 61.04‹?›

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 Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics. Int J Mol Med 2007 1.78
3 Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification. Hum Genet 2003 1.57
4 Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male. Mol Cytogenet 2009 1.43
5 Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones. Int J Oncol 2010 1.33
6 Early embryonic chromosome instability results in stable mosaic pattern in human tissues. PLoS One 2010 1.32
7 Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity? Mol Cytogenet 2008 1.07
8 Chromosome distribution in human sperm - a 3D multicolor banding-study. Mol Cytogenet 2008 1.06
9 Small supernumerary marker chromosomes and uniparental disomy have a story to tell. J Histochem Cytochem 2011 1.03
10 Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC. Am J Med Genet A 2006 1.02
11 Centromere activity in dicentric small supernumerary marker chromosomes. Chromosome Res 2010 0.96
12 Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature. Int J Mol Med 2008 0.93
13 Molecular cytogenetic characterization of epithelioid hemangioendothelioma. Cancer Genet 2011 0.92
14 Somatic mosaicism in cases with small supernumerary marker chromosomes. Curr Genomics 2010 0.92
15 Heteromorphic variants of chromosome 9. Mol Cytogenet 2013 0.92
16 Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair. Mol Cytogenet 2010 0.92
17 Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients. J Appl Genet 2007 0.91
18 Insertional translocation leading to a 4q13 duplication including the EPHA5 gene in two siblings with attention-deficit hyperactivity disorder. Am J Med Genet A 2013 0.90
19 Characterization of sSMC by FISH and molecular techniques. Eur J Med Genet 2011 0.90
20 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
21 Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-R. Int J Oncol 2007 0.90
22 Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences. Eur J Hum Genet 2005 0.89
23 A new multicolor fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH. J Histochem Cytochem 2012 0.89
24 A parallel approach for subwavelength molecular surgery using gene-specific positioned metal nanoparticles as laser light antennas. Nano Lett 2007 0.88
25 The human genome puzzle - the role of copy number variation in somatic mosaicism. Curr Genomics 2010 0.87
26 Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon. Mol Cytogenet 2008 0.87
27 The hierarchically organized splitting of chromosomal bands for all human chromosomes. Mol Cytogenet 2009 0.87
28 Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics. Int J Mol Med 2009 0.87
29 Handling small supernumerary marker chromosomes in prenatal diagnostics. Expert Rev Mol Diagn 2009 0.87
30 Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome. Eur J Med Genet 2009 0.87
31 Multicolor FISH methods in current clinical diagnostics. Expert Rev Mol Diagn 2013 0.87
32 Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier. Fertil Steril 2011 0.87
33 t(11;19)(q21;p12~p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinoma. J Pediatr Surg 2007 0.86
34 Further delineation of complex chromosomal rearrangements in fertile male using multicolor banding. Mol Cytogenet 2008 0.85
35 Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report. Mol Cytogenet 2008 0.85
36 Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances. J Appl Genet 2011 0.84
37 Comet fluorescence in situ hybridization analysis for oxidative stress-induced DNA damage in colon cancer relevant genes. Toxicol Sci 2006 0.84
38 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
39 FISH banding in tumor cytogenetics. Cancer Genet Cytogenet 2006 0.83
40 An interstitial 4q31.21q31.22 microdeletion associated with developmental delay: case report and literature review. Cytogenet Genome Res 2014 0.83
41 Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype. Int J Oncol 2009 0.83
42 New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank. J Histochem Cytochem 2007 0.83
43 A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report. Mol Cytogenet 2009 0.83
44 Presence of harmless small supernumerary marker chromosomes hampers molecular genetic diagnosis: a case report. Mol Med Rep 2011 0.82
45 Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. Eur J Hum Genet 2008 0.82
46 Partial 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 literature. Mol Cytogenet 2008 0.82
47 Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies. Arch Gynecol Obstet 2013 0.81
48 New aspects on chromosomal instability: chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sites. Int J Oncol 2010 0.81
49 Molecular cytogenetic characterisation of the colorectal cancer cell line SW480. Oncol Rep 2004 0.80
50 Parental origin and functional relevance of a de novo UBE3A variant. Eur J Med Genet 2010 0.80
51 Characterization of chromosomal rearrangements using multicolor-banding (MCB/m-band). Methods Mol Biol 2010 0.80
52 Impact of polyphenol metabolites produced by colonic microbiota on expression of COX-2 and GSTT2 in human colon cells (LT97). Nutr Cancer 2011 0.79
53 Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report. Mol Cytogenet 2012 0.79
54 Molecular cytogenetic characterisation of a mosaic add(12)(p13.3) with an inv dup(3)(q26.31 --> qter) detected in an autistic boy. Mol Cytogenet 2009 0.79
55 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
56 Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal. Mutat Res 2003 0.78
57 Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH. Prenat Diagn 2009 0.78
58 Small supernumerary marker chromosomes 1 with a normal phenotype. J Chin Med Assoc 2010 0.78
59 Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic Approaches. J Assoc Genet Technol 2003 0.78
60 BAC-probes applied for characterization of fragile sites (FS). Methods Mol Biol 2015 0.77
61 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
62 How to narrow down chromosomal breakpoints in small and large derivative chromosomes--a new probe set. J Appl Genet 2012 0.77
63 Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report. Mol Cytogenet 2009 0.77
64 Breakpoint locations within chromosomes 1, 2, and 4 of patients with increased radiosensitivity. Cancer Genet Cytogenet 2006 0.76
65 Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male. Mol Cytogenet 2009 0.75
66 Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation? Mol Cytogenet 2010 0.75
67 Loss of chromosome 4 correlates with better long-term survival and lower relapse rate after R0-resection of colorectal liver metastases. J Cancer Res Clin Oncol 2013 0.75
68 Comparative analysis of proliferative and genetic alterations in a primary chordoid meningioma and its recurrence using locus-specific probes and AgNOR. Mol Med Rep 2011 0.75
69 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
70 A case of aggressive medulloblastoma with multiple recurrent chromosomal alterations. Cancer Genet Cytogenet 2010 0.75
71 A 33-year-old male patient with paternal derived duplication of 14q11.2-14q22.1~22.3: clinical course, phenotypic and genotypic findings. J Pediatr Endocrinol Metab 2016 0.75