Evidence map›Paper›PMID 36253936›Full record

ArticleAmerican journal of medical genetics. Part A2023

Cornelia de Lange syndrome and cancer: An open question.

Maria M Pallotta, Maddalena Di Nardo, Raoul C M Hennekam, Frank J Kaiser, Ilaria Parenti, Juan Pié, Feliciano J Ramos, Antonie D Kline, Antonio Musio

Abstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in American journal of medical genetics. Part A, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Cornelia de Lange syndrome and cancer: An open question.American journal of medical genetics. Part A · 2023
    Article
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.

Maria M PallottaInstitute for Biomedical Technologies, National Research Council, Pisa, Italy.ORCID https://orcid.org/0000-0001-7731-8621
Maddalena Di NardoInstitute for Biomedical Technologies, National Research Council, Pisa, Italy.ORCID https://orcid.org/0000-0002-1481-2101
Raoul C M HennekamDepartment of Pediatrics, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Frank J KaiserInstitute for Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Ilaria ParentiInstitute for Human Genetics, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
Juan PiéUnit of Clinical Genetics and Functional Genomics, Department of Pharmacology-Physiology, School of Medicine, University of Zaragoza, CIBERER-GCV02 and ISS-Aragon, Zaragoza, Spain.
Feliciano J RamosUnit of Clinical Genetics and Functional Genomics, Department of Pharmacology-Physiology, School of Medicine, University of Zaragoza, CIBERER-GCV02 and ISS-Aragon, Zaragoza, Spain.
Antonie D KlineHarvey Institute for Human Genetics, Greater Baltimore Medical Center, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0002-7863-2994
Antonio MusioInstitute for Biomedical Technologies, National Research Council, Pisa, Italy.ORCID https://orcid.org/0000-0001-7701-6543

Funding

Associazione Italiana per la Ricerca sul Cancro IG23284
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

De Lange SyndromeNeoplasmsHumans

Identifiers

PMID36253936
PMCPMC10092277

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.