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

[Novel methods and their applicability in the evaluation of the genetic background of endocrine system tumours].

Orvosi hetilap - 20 Dec 2015

Patócs Attila, Likó István, Butz Henriett, Baghy Kornélia, Rácz Károly

Abstract excerpt

The technical developments leading to revolution in clinical genetic testing offer new approaches for patients with cancer. From one mutation or one gene approach the scale of genetic testing moved to whole exome or whole genome scale. It is well known that many tumours are genetically determined and they are part of familial tumour syndromes. In addition, some mutations indicate specific molecular targeted...

Read the complete abstract on PubMed

Topics

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

Share to Adrenal Gland Neoplasms
Share to DNA, Neoplasm
Share to Endocrine Gland Neoplasms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Testing

Share to High-Throughput Nucleotide Sequencing

Share to Neoplastic Syndromes, Hereditary

Share to Paraganglioma

Share to Pheochromocytoma

Source

Identifiers

PMID: 26654542
DOI: 10.1556/650.2015.30316

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

[Novel methods and their applicability in the evaluation of the genetic background of endocrine system tumours].PMID 26654542Read ↗

Molecular genetic testing strategies used in diagnostic flow for hereditary endocrine tumour syndromes.Semantic proximity Read ↗

[Next generation sequencing - application in clinical practice].Semantic proximity Read ↗

Advancing Precision Medicine: The Role of Genetic Testing and Sequencing Technologies in Identifying Biological Markers for Rare CancersSemantic proximity Read ↗

Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN).Semantic proximity Read ↗

[Molecular tests for (early) recognition of endocrine disorders - towards a sophisticated management of complex endocrine and metabolic diseases].Semantic proximity Read ↗

HEREDITARY ENDOCRINE TUMOURS: CURRENT STATE-OF-THE-ART AND RESEARCH OPPORTUNITIES: Challenges and opportunities in genetic counseling for hereditary endocrine neoplasia syndromes.Semantic proximity Read ↗

Next generation sequencing in endocrine practice.Semantic proximity Read ↗

Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancer.Semantic proximity Read ↗

Molecular Pathology of Endocrine Gland Tumors.Semantic proximity Read ↗

Molecular pathology of endocrine gland tumors: genetic alterations and clinicopathologic relevance.Semantic proximity Read ↗

[A consensus on the standardization of the next generation sequencing process for the diagnosis of genetic diseases (1) - Procedures prior to genetic testing].Semantic proximity Read ↗

CCMG practice guideline: laboratory guidelines for next-generation sequencingSemantic proximity Read ↗

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