Evidence map›Paper›PMID 39518056›Full record

ArticleCancers2024

Clinical Assessment and Genetic Testing for Hereditary Polyposis Syndromes in an Italian Cohort of Patients with Colorectal Polyps.

Candida Fasano, Filomena Cariola, Giovanna Forte, Antonia Lucia Buonadonna, Paola Sanese, Andrea Manghisi, Martina Lepore Signorile, Katia De Marco, Valentina Grossi, Vittoria Disciglio and 1 more

Abstract 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. 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

11 authors.

Candida FasanoMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.
Filomena CariolaMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.
Giovanna ForteMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.
Antonia Lucia BuonadonnaMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.
Paola SaneseMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.
Andrea ManghisiMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.
Martina Lepore SignorileMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.
Katia De MarcoMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.
Valentina GrossiMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.ORCID 0000-0003-3843-1618
Vittoria DisciglioMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.
Cristiano SimoneMedical Genetics, National Institute of Gastroenterology, IRCCS "Saverio de Bellis" Research Hospital, 70013 Castellana Grotte, Italy.

Funding

Italian Association for Cancer Research (AIRC) AIRC Fellowship for Italy ID26678-2021 to M.L.S.Italian Association for Cancer Research (AIRC) IG23794 to C.S.Italian Ministry of Health Ricerca Corrente 2023-2025 to V.G.Italian Ministry of Health Ricerca Corrente 2024-2026 to C.F. and V.D.Italian Ministry of Health Ricerca Corrente 2024-2026 to C.S.Italian Ministry of Health Starting Grant SG-2019-12371540
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

APCBMPR1Aclinical eligibility criteriagenetic testinghereditary polyposis syndromesMUTYHpathogenic variant (PV)SMAD4STK11variant of uncertain significance (VUS)

Identifiers

PMID39518056
PMCPMC11544946

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.