Evidence map›Paper›PMID 39590369›Full record

ArticleCurrent issues in molecular biology2024

Germline Variant Spectrum in Southern Italian High-Risk Hereditary Breast Cancer Patients: Insights from Multi-Gene Panel Testing.

Valentina Rocca, Elisa Lo Feudo, Francesca Dinatolo, Serena Marianna Lavano, Anna Bilotta, Rosario Amato, Lucia D'Antona, Francesco Trapasso, Francesco Baudi, Emma Colao and 3 more

Abstract read
In one paragraph

Article in Current issues in molecular biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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

13 authors.

Valentina RoccaMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.ORCID 0000-0002-8331-5723
Elisa Lo FeudoMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.
Francesca DinatoloMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.
Serena Marianna LavanoMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.
Anna BilottaMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.
Rosario AmatoMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.
Lucia D'AntonaDepartment of Health Sciences, Campus S. Venuta, University Magna Graecia of Catanzaro, 88100 Catanzaro, Italy.ORCID 0000-0002-8288-9784
Francesco TrapassoMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.
Francesco BaudiMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.ORCID 0000-0002-8976-8088
Emma ColaoMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.
Nicola PerrottiMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.ORCID 0000-0001-8836-5386
Francesco PaduanoStem Cells and Medical Genetics Units, Biomedical Section, Tecnologica Research Institute and Marrelli Health, 88900 Crotone, Italy.ORCID 0000-0003-0916-8101
Rodolfo IulianoMedical Genetics Unit, Renato Dulbecco University Hospital, 88100 Catanzaro, Italy.ORCID 0000-0002-8524-7402

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary breast cancer accounts for 5-10% of all cases, with pathogenic variants in

Indexed as

breast cancer (BC)cancer susceptibility genesfounder mutationsgenetic heterogeneitygermline variantsnext-generation sequencing (NGS)

Identifiers

PMID39590369
PMCPMC11592649

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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.