Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

High resolution SNP array profiling identifies variability in retinoblastoma genome stability.

Genes, chromosomes & cancer - 1 Jan 2014

Mol Berber M, Massink Maarten P G, van der Hout Annemarie H, Dommering Charlotte J, Zaman Johannes M A, Bosscha Machteld I, Kors Wijnanda A, Meijers-Heijboer Hanne E, Kaspers Gertjan J L, Riele Hein te, Moll Annette C, Cloos Jacqueline, Dorsman Josephine C

Abstract excerpt

Both hereditary and nonhereditary retinoblastoma (Rb) are commonly initiated by loss of both copies of the retinoblastoma tumor suppressor gene (RB1), while additional genomic changes are required for tumor initiation and progression. Our aim was to determine whether there is genomic heterogeneit...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosomes, Human, Pair 13
Share to Chromosomes, Human, Pair 14

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Dosage

Share to Genes, Retinoblastoma

Share to Genomic Instability

Share to Loss of Heterozygosity

Share to Retinal Neoplasms

Share to Retinoblastoma

Source

Identifiers

PMID: 24249257
DOI: 10.1002/gcc.22111

Genes

AKT1
FUT8
MYCN
OTX2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24249257-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

High resolution SNP array profiling identifies variability in retinoblastoma genome stability.PMID 24249257Read ↗

Array comparative genomic hybridization in retinoma and retinoblastoma tissues.Semantic proximity Read ↗

Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changes.Semantic proximity Read ↗

High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization.Semantic proximity Read ↗

Comparative genomic hybridisation divides retinoblastomas into a high and a low level chromosomal instability groupSemantic proximity Read ↗

A novel retinoblastoma therapy from genomic and epigenetic analyses.Semantic proximity Read ↗

MYCN amplification levels in primary retinoblastoma tumors analyzed by Multiple Ligation-dependent Probe AmplificationSemantic proximity Read ↗

Genomic differences between retinoma and retinoblastomaSemantic proximity Read ↗

The genomic landscape of retinoblastoma: a review.Semantic proximity Read ↗

Comprehensive identification of pathogenic variants in retinoblastoma by long- and short-read sequencing.Semantic proximity Read ↗

SNP array profiling of childhood adrenocortical tumors reveals distinct pathways of tumorigenesis and highlights candidate driver genes.Semantic proximity Read ↗

One hit, two hits, three hits, more? Genomic changes in the development of retinoblastomaSemantic proximity Read ↗

Molecular karyotype of sporadic unilateral retinoblastoma tumors.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.