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Cindy Postma

Researcher at VU University Medical Center

Publications -  19
Citations -  1695

Cindy Postma is an academic researcher from VU University Medical Center. The author has contributed to research in topics: Cancer & Chromosome instability. The author has an hindex of 17, co-authored 19 publications receiving 1639 citations. Previous affiliations of Cindy Postma include VU University Amsterdam.

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Colorectal adenoma to carcinoma progression follows multiple pathways of chromosomal instability

TL;DR: Evidence was found that these chromosomal abnormalities occurred in specific combinations of a few abnormalities rather than as a mere accumulation of events, indicating the existence of multiple independent chromosomal instability pathways of colorectal cancer progression.
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MiR-17-92 cluster is associated with 13q gain and c-myc expression during colorectal adenoma to adenocarcinoma progression.

TL;DR: Increased expression of the miR-17-92 cluster during colorectal adenoma to adenocarcinoma progression is associated to DNA copy number gain of miR 17-92 locus on 13q31 and c-myc expression.
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Multiple putative oncogenes at the chromosome 20q amplicon contribute to colorectal adenoma to carcinoma progression

TL;DR: C20orf24, AURKA, RNPC1, TH1L, ADRM1, C20orf20 and TCFL5 genes are revealed to be important in chromosomal instability-related adenoma to carcinoma progression and may serve as highly specific biomarkers for colorectal cancer with potential clinical applications.
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Genomic Alterations in Primary Gastric Adenocarcinomas Correlate with Clinicopathological Characteristics and Survival

TL;DR: Microarray CGH has revealed several chromosomal regions that have not been described before in gastric cancer at this frequency and resolution, such as amplification of at 7q21–q22 and 12q14.1, as well as gains at 1q32.1.
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Genomic profiling of gastric cancer predicts lymph node status and survival.

TL;DR: Genomic profiling of gastric adenocarcinomas based on microarray analysis of chromosomal copy number changes predicted lymph node status and survival and the possibility to discriminate between patients with a high risk of lymph node metastasis could clinically be helpful for selecting patients for extended lymph node resection.