CDKN2B gene

Aliases

CDNK2B, cdkn2b

External links

NCBI Gene · Ensembl · GeneCards · UniProt

Related entities (1)

Mentioned in (29)

Papers in which this entity is mentioned.

• Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. (2024)
• Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme. (2024)
• Heritable defects in telomere and mitotic function selectively predispose to sarcomas. (2023)
• Integrating molecular profiles into clinical frameworks through the Molecular Oncology Almanac to prospectively guide precision oncology. (2021)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Whole-exome sequencing of cervical carcinomas identifies activating ERBB2 and PIK3CA mutations as targets for combination therapy. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes. (2018)
• Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes (2018)
• The 3D Genome Browser: a web-based browser for visualizing 3D genome organization and long-range chromatin interactions. (2018)
• Patterns and mechanisms of structural variations in human cancer. (2018)
• Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma. (2017)
• Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors. (2017)
• Truncating Erythropoietin Receptor Rearrangements in Acute Lymphoblastic Leukemia. (2016)
• Integrative clinical genomics of advanced prostate cancer. (2015)
• Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia. (2015)
• Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth. (2015)
• Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping Microarrays. (2014)
• RNA in unexpected places: long non-coding RNA functions in diverse cellular contexts. (2013)
• The genomic landscape of hypodiploid acute lymphoblastic leukemia. (2013)
• Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. (2012)
• Molecular genetics of B-precursor acute lymphoblastic leukemia. (2012)
• Genome-wide association study of primary open angle glaucoma risk and quantitative traits. (2012)
• VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. (2012)
• Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. (2011)
• Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. (2010)
• Perinatal choline deficiency produces abnormal sensory inhibition in Sprague-Dawley rats. (2008)
• Heterogeneity in meta-analyses of genome-wide association investigations. (2007)
• Dietary choline deficiency alters global and gene-specific DNA methylation in the developing hippocampus of mouse fetal brains. (2006)

Merged raw entities (2)

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