Evidence map›Paper›PMID 42125600›Full record

ArticleJournal of clinical & translational endocrinology2026

Somatic genomic profiling reveals clinically relevant heterogeneity in

Edoardo Ruggeri, Simona Censi, Loris Bertazza, Andrea Benetti, Fausto Cortese, Ilaria Piva, Cristina Clausi, Vincenzo Marotta, Francesca Galuppini, Alessandra Giannella and 6 more

Abstract read
In one paragraph

Article in Journal of clinical & translational endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Edoardo RuggeriDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Simona CensiDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Loris BertazzaDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Andrea BenettiDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Fausto CorteseDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Ilaria PivaDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Cristina ClausiDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Vincenzo MarottaDepartment of Clinical Medicine and Surgery, University of Salerno, Italy.
Francesca GaluppiniDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Alessandra GiannellaDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Gianmaria PennelliDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Maurizio IacoboneDepartment of Surgical, Oncological and Gastroenterological Sciences (DiSCOG), University of Padua, Padua, Italy.
Mario VitaleDepartment of Clinical Medicine and Surgery, University of Salerno, Italy.
Giulio CeolottoDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Susi BarolloDepartment of Medicine (DIMED), University of Padua, Padua, Italy.
Caterina MianDepartment of Medicine (DIMED), University of Padua, Padua, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Sporadic medullary thyroid carcinoma (sMTC) is predominantly driven by somatic Methods: Deep targeted next-generation sequencing of 31 neuroendocrine- and cancer-related genes was performed on tumor samples from 94 patients with sMTC to characterize the somatic mutational landscape beyond canonical drivers. Results: Conclusions: Overall, these findings highlight additional oncogenic alterations potentially involved in tumor progression and suggest that extended targeted profiling may provide clinically relevant information on molecular heterogeneity in sMTC, particularly within

Indexed as

Biochemical cureNGS somatic panelPrecision medicine strategiesRAS-mutant tumorsT status

Identifiers

PMID42125600
PMCPMC13158359

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.