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

Rethinking pheochromocytomas and paragangliomas from a genomic perspective.

Oncogene - 3 Mar 2016

Castro-Vega L J, Lepoutre-Lussey C, Gimenez-Roqueplo A-P, Favier J

Abstract excerpt

Pheochromocytomas (PCC) and paragangliomas (PGL) are rare neuroendocrine tumors of neural crest origin. These tumors are caused by germline or somatic mutations in known susceptibility genes in up to 70% of cases. Over the past few years, the emergence of high-throughput technologies has enabled the unprecedented characterization of genomic alterations in PCC/PGL, and has improved our understanding of the...

Read the complete abstract on PubMed

Topics

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

Share to Mutation
Share to Neuroendocrine Tumors
Share to Adrenal and Paraganglionic Tumors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Predisposition to Disease

Share to Genomics

Share to Paraganglioma

Share to Pheochromocytoma

Source

Identifiers

PMID: 26028031
DOI: 10.1038/onc.2015.172

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Rethinking pheochromocytomas and paragangliomas from a genomic perspective.PMID 26028031Read ↗

Multi-omics analysis defines core genomic alterations in pheochromocytomas and paragangliomas.Semantic proximity Read ↗

Update on the genetics of paragangliomas.Semantic proximity Read ↗

The genomic landscape of phaeochromocytoma.Semantic proximity Read ↗

Pheochromocytoma and paraganglioma: germline genetics and hereditary syndromesSemantic proximity Read ↗

Current Management of Pheochromocytoma/Paraganglioma: A Guide for the Practicing Clinician in the Era of Precision MedicineSemantic proximity Read ↗

Pheochromocytoma and paraganglioma: molecular testing and personalized medicine.Semantic proximity Read ↗

Genetic bases of pheochromocytoma and paraganglioma.Semantic proximity Read ↗

Clinical and molecular markers guide the genetics of pheochromocytoma and paraganglioma.Semantic proximity Read ↗

Comprehensive Molecular Characterization of Pheochromocytoma and Paraganglioma.Semantic proximity Read ↗

Genetics of pheochromocytoma and paraganglioma.Semantic proximity Read ↗

New Insights on the Genetics of Pheochromocytoma and Paraganglioma and Its Clinical ImplicationsSemantic proximity Read ↗

Pheochromocytomas and Paragangliomas: From Genetic Diversity to Targeted TherapiesSemantic proximity Read ↗

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