PubRank

E Schröck

Author PubWeight™ 75.00‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Role of chromosome territories in the functional compartmentalization of the cell nucleus. Cold Spring Harb Symp Quant Biol 1993 3.38
2 Comparative genomic hybridization reveals a specific pattern of chromosomal gains and losses during the genesis of colorectal tumors. Genes Chromosomes Cancer 1996 3.30
3 Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3. Nat Genet 1997 3.11
4 Comprehensive and definitive molecular cytogenetic characterization of HeLa cells by spectral karyotyping. Cancer Res 1999 3.06
5 Multicolour spectral karyotyping of mouse chromosomes. Nat Genet 1996 2.90
6 Gain of chromosome 3q defines the transition from severe dysplasia to invasive carcinoma of the uterine cervix. Proc Natl Acad Sci U S A 1996 2.81
7 Centrosome amplification and instability occurs exclusively in aneuploid, but not in diploid colorectal cancer cell lines, and correlates with numerical chromosomal aberrations. Genes Chromosomes Cancer 2000 2.73
8 Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Hum Genet 1993 2.64
9 Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma. Blood 1998 2.36
10 Mapping of multiple DNA gains and losses in primary small cell lung carcinomas by comparative genomic hybridization. Cancer Res 1994 2.31
11 Genomic changes defining the genesis, progression, and malignancy potential in solid human tumors: a phenotype/genotype correlation. Genes Chromosomes Cancer 1999 2.19
12 Advanced-stage cervical carcinomas are defined by a recurrent pattern of chromosomal aberrations revealing high genetic instability and a consistent gain of chromosome arm 3q. Genes Chromosomes Cancer 1997 2.06
13 Comparative genomic hybridization of formalin-fixed, paraffin-embedded breast tumors reveals different patterns of chromosomal gains and losses in fibroadenomas and diploid and aneuploid carcinomas. Cancer Res 1995 2.04
14 Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification. Hum Mol Genet 1993 1.91
15 Three-dimensional reconstruction of painted human interphase chromosomes: active and inactive X chromosome territories have similar volumes but differ in shape and surface structure. J Cell Biol 1996 1.82
16 Multiple putative oncogenes at the chromosome 20q amplicon contribute to colorectal adenoma to carcinoma progression. Gut 2008 1.77
17 Quantitative analysis of comparative genomic hybridization. Cytometry 1995 1.72
18 Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in chromophobe renal cell carcinomas revealed by comparative genomic hybridization. Am J Pathol 1994 1.62
19 Hidden chromosome abnormalities in haematological malignancies detected by multicolour spectral karyotyping. Nat Genet 1997 1.57
20 Jumping translocations are common in solid tumor cell lines and result in recurrent fusions of whole chromosome arms. Genes Chromosomes Cancer 2001 1.38
21 Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK). Nat Genet 1994 1.36
22 Specific chromosomal aberrations and amplification of the AIB1 nuclear receptor coactivator gene in pancreatic carcinomas. Am J Pathol 1999 1.36
23 A recurring pattern of chromosomal aberrations in mammary gland tumors of MMTV-cmyc transgenic mice. Genes Chromosomes Cancer 1999 1.26
24 Primary small-cell lung carcinomas and their metastases are characterized by a recurrent pattern of genetic alterations. Int J Cancer 1997 1.16
25 Identification of de novo chromosomal markers and derivatives by spectral karyotyping. Hum Genet 1998 1.11
26 Tumor cytogenetics revisited: comparative genomic hybridization and spectral karyotyping. J Mol Med (Berl) 1998 1.07
27 Spectral karyotyping, a 24-colour FISH technique for the identification of chromosomal rearrangements. Histochem Cell Biol 1998 1.06
28 Comparative genomic hybridization analysis of human parathyroid tumors. Cancer Genet Cytogenet 1998 1.04
29 Previously hidden chromosome aberrations in T(12;15)-positive BALB/c plasmacytomas uncovered by multicolor spectral karyotyping. Cancer Res 1997 1.00
30 Identification and chromosomal localization of Atm, the mouse homolog of the ataxia-telangiectasia gene. Genomics 1996 0.99
31 Cytogenetic and molecular characterization of random chromosomal rearrangements activating the drug resistance gene, MDR1/P-glycoprotein, in drug-selected cell lines and patients with drug refractory ALL. Genes Chromosomes Cancer 1998 0.99
32 Chromosome painting: a useful art. Hum Mol Genet 1998 0.98
33 Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2. Br J Haematol 2001 0.97
34 Application of confocal laser microscopy and three-dimensional Voronoi diagrams for volume and surface estimates of interphase chromosomes. J Microsc 1995 0.93
35 Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instability. J Med Genet 2005 0.93
36 Prenatal diagnosis of a mosaic extra structurally abnormal chromosome by spectral karyotyping. Prenat Diagn 1999 0.93
37 Analysis of B-cell neoplasias by spectral karyotyping (SKY). Curr Top Microbiol Immunol 1999 0.91
38 Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 by spectral karyotyping. Genes Chromosomes Cancer 1999 0.89
39 Analysis of ovarian borderline tumors using comparative genomic hybridization and fluorescence in situ hybridization. Genes Chromosomes Cancer 1999 0.88
40 A recurrent pattern of chromosomal aberrations and immunophenotypic appearance defines anal squamous cell carcinomas. Br J Cancer 1997 0.86
41 Core binding factor beta-smooth muscle myosin heavy chain chimeric protein involved in acute myeloid leukemia forms unusual nuclear rod-like structures in transformed NIH 3T3 cells. Proc Natl Acad Sci U S A 1996 0.86
42 Spectral karyotypic study of the HL-60 cell line: detection of complex rearrangements involving chromosomes 5, 7, and 16 and delineation of critical region of deletion on 5q31.1. Cancer Genet Cytogenet 1999 0.85
43 Primary carcinoma of the fallopian tube: comparative genomic hybridization reveals high genetic instability and a specific, recurring pattern of chromosomal aberrations. Int J Gynecol Pathol 1998 0.83
44 Characterization of 5q deletions by subtelomeric probes and spectral karyotyping. Cancer Genet Cytogenet 1998 0.82
45 Multicolor fluorescence in situ hybridization on metaphase chromosomes and interphase Halo-preparations using cosmid and YAC clones for the simultaneous high resolution mapping of deletions in the dystrophin gene. Hum Genet 1994 0.80
46 [Function-controlled neurosurgery. Neurophysiologic and neuropsychological monitoring during surgery of the nervous system]. Nervenarzt 1995 0.80
47 Selection of a highly invasive neuroblastoma cell population through long-term human cytomegalovirus infection. Oncogenesis 2012 0.80
48 Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping. Prenat Diagn 1999 0.79
49 Extensive splice variation and localization of the EHK-1 receptor tyrosine kinase in adult human brain and glial tumors. Brain Res Mol Brain Res 1997 0.76
50 Assignment of a human homolog of the mouse Htr3 receptor gene to chromosome 11q23.1-q23.2. Genomics 1995 0.76
51 A mosaic extra ring chromosome 4 in a female patient with postnatal overgrowth. Genet Couns 1999 0.75
52 Spectral Karyotyping (SKY) of Hematologic Malignancies. Methods Mol Med 2001 0.75
53 Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term culture. Prenat Diagn 1996 0.75
54 [News from allied medical fields. Medical genetics. Possibilities of computer-assisted phenotype diagnosis in human genetic counseling]. Padiatr Grenzgeb 1993 0.75
55 [Genetic alterations in sinonasal adenocarcinoma in wood workers studies with comparative genomic hybridization]. Acta Otorrinolaringol Esp 2003 0.75
56 Molecular cytogenetics of brain tumors. J Neuropathol Exp Neurol 1997 0.75