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Ronald Simon

Researcher at University of Münster

Publications -  19
Citations -  1719

Ronald Simon is an academic researcher from University of Münster. The author has contributed to research in topics: Comparative genomic hybridization & Ductal carcinoma. The author has an hindex of 13, co-authored 19 publications receiving 1695 citations.

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Comparative genomic hybridization of ductal carcinoma in situ of the breast-evidence of multiple genetic pathways.

TL;DR: Analysis of paraffin‐embedded specimens of DCIS and six associated invasive carcinomas revealed a genetic pattern almost identical to the one seen in the DCIS counterpart, characterize DCIS as a genetically far‐advanced, heterogeneous lesion and as a direct precursor of invasive breast cancer.
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Different genetic pathways in the evolution of invasive breast cancer are associated with distinct morphological subtypes.

TL;DR: Data demonstrate the close genetic similarity of well‐, intermediately, and poorly differentiated DCIS and distinct morphological types of invasive breast carcinoma, providing further evidence that DCIS is a direct precursor lesion ofvasive breast cancer and that various evolutionary genetic pathways exist.
Journal Article

Length and Loss of Heterozygosity of an Intron 1 Polymorphic Sequence of egfr Is Related to Cytogenetic Alterations and Epithelial Growth Factor Receptor Expression

TL;DR: It is concluded that the CA repeat status in intron 1 of the egfr gene also modulates the intratumoral EGFR content in vivo and is associated with genetically advanced tumors.
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Ductal invasive G2 and G3 carcinomas of the breast are the end stages of at least two different lines of genetic evolution.

TL;DR: The findings of this study demonstrate that ductal invasive G2 carcinomas have to be interpreted as the morphological end stage resulting from two different cytogenetics and morphological pathways; the loss of 16q material is the cytogenetic key event in the evolution of a subgroup of this entity.
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Chromosomal aberrations associated with invasion in papillary superficial bladder cancer.

TL;DR: These data show characteristic chromosomal aberrations associated with invasion in superficial bladder cancer.