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

EIF1AX mutation in thyroid nodules: a histopathologic analysis of 56 cases in the context of institutional practices.

Virchows Archiv : an international journal of pathology - 1 Nov 2024

Abi-Raad Rita, Xu Bin, Gilani Syed, Ghossein Ronald A, Prasad Manju L

Abstract excerpt

EIF1AX mutation has been identified as a driver mutation for papillary thyroid carcinoma (PTC) by The Cancer Genome Atlas (TCGA) study. Subsequent studies confirmed this mutation in PTC and Anaplastic Thyroid Carcinoma (ATC) but also reported EIF1AX mutation in Follicular nodular disease (FND) and benign thyroid nodules. In this study, we review thyroid nodules with EIF1AX mutation from two institutions: a...

Read the complete abstract on PubMed

Topics

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

Share to Adenocarcinoma, Follicular
Share to Aged

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to Thyroid Neoplasms

Share to Thyroid Nodule

Source

Identifiers

PMID: 39225726
DOI: 10.1007/s00428-024-03914-5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

EIF1AX mutation in thyroid nodules: a histopathologic analysis of 56 cases in the context of institutional practices.PMID 39225726Read ↗

Prevalence and phenotypic correlations of EIF1AX mutations in thyroid nodules.Semantic proximity Read ↗

Clinicopathological features and outcomes of thyroid nodules with EIF1AX mutations.Semantic proximity Read ↗

Characterization and Clinical Significance of EIF1AX Mutations and Co-Mutations in Cytologically Indeterminate Thyroid Nodules: A 5-Year Retrospective Analysis.Semantic proximity Read ↗

EIF1AX mutation in thyroid tumors: a retrospective analysis of cytology, histopathology and co-mutation profiles.Semantic proximity Read ↗

Molecular findings in thyroid tumors: Practical diagnostic, prognostic, and therapeutic insights.Semantic proximity Read ↗

Mutation profiles of follicular thyroid tumors by targeted sequencingSemantic proximity Read ↗

Patient with multiple genetically distinct thyroid nodules including papillary thyroid carcinoma harboring novel YWHAG-BRAF fusion.Semantic proximity Read ↗

Reappraisal of BRAFK601E-positive thyroid tumors in the NIFTP era.Semantic proximity Read ↗

Molecular Markers in Follicular and Oncocytic Thyroid Carcinomas: Clinical Application of Molecular Genetic TestingSemantic proximity Read ↗

Does Noninvasive Follicular Thyroid Neoplasm With Papillary-Like Nuclear Features (NIFTP) Have a Unique Molecular Profile?Semantic proximity Read ↗

Impact of Co-Mutations and Genetic Variations on Malignancy Risk in RAS-Positive Indeterminate Thyroid Nodules: an Institutional Experience.Semantic proximity Read ↗

TERT, HRAS, and EIF1AX Mutations in a Patient with Follicular Adenoma.Semantic proximity Read ↗

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