Evidence map›Paper›PMID 38339246›Full record

ArticleCancers2024

Does Genotype-Specific Phenotype in Patients with Multiple Endocrine Neoplasia Type 2 Occur as Current Guidelines Predict?

Teresa Binter, Sabina Baumgartner-Parzer, Marie Helene Schernthaner-Reiter, Melisa Arikan, Lindsay Hargitai, Martin Bruno Niederle, Bruno Niederle, Christian Scheuba, Philipp Riss

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.6field-weighted citation impact, top 5% of its field
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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Hereditary Medullary Thyroid Cancer: Genotype-Phenotype Correlation.Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer · 2025
    Review
  5. Epidemiology, Clinical Presentation, and Diagnosis of Medullary Thyroid Carcinoma.Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer · 2025
    Review
  6. Neuroendocrine Tumors: Germline Genetics and Hereditary Syndromes.Current treatment options in oncology · 2025
    Review
  7. Article
  8. Observational
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

9 authors at 1 institution in 1 country.

Teresa BinterDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-9930-2767
Sabina Baumgartner-ParzerDivision of Endocrinology and Metabolism, Department of Medicine III, Medical University of Vienna, 1090 Vienna, Austria.
Marie Helene Schernthaner-ReiterDivision of Endocrinology and Metabolism, Department of Medicine III, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0002-7972-7610
Melisa ArikanDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Lindsay HargitaiDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Martin Bruno NiederleDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, 1090 Vienna, Austria.ORCID 0000-0003-0450-6132
Bruno NiederleDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Christian ScheubaDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Philipp RissDivision of Visceral Surgery, Department of General Surgery, Medical University of Vienna, 1090 Vienna, Austria.
Medical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The clinical manifestation of multiple endocrine neoplasia type 2 (MEN2) in terms of developing medullary thyroid cancer (MTC), pheochromocytoma (PCC), and/or primary hyperparathyroidism (PHPT) is related to the respective pathogenic variant of the

Indexed as

c-cell hyperplasiagermline mutationhereditary medullary thyroid carcinomamultiple endocrine neoplasia type 2pheochromocytomaprimary hyperparathyroidismRET mutation

Identifiers

PMID38339246
PMCPMC10854710
OpenAlexW4391157102

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.