Evidence map›Paper›PMID 36833418›Full record

ArticleGenes2023

Stratification of a Phelan-McDermid Syndrome Population Based on Their Response to Human Growth Hormone and Insulin-like Growth Factor.

Bridgette A Moffitt, Sara M Sarasua, Diana Ivankovic, Linda D Ward, Kathleen Valentine, William E Bennett, Curtis Rogers, Katy Phelan, Luigi Boccuto

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. 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 at 4 institutions in 1 country.

Bridgette A MoffittSchool of Nursing, Healthcare Genetics Program, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0002-5906-2391
Sara M SarasuaSchool of Nursing, Healthcare Genetics Program, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0002-1625-7404
Diana IvankovicSchool of Nursing, Healthcare Genetics Program, Clemson University, Clemson, SC 29634, USA.
Linda D WardSchool of Nursing, Healthcare Genetics Program, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0002-5660-3594
Kathleen ValentineSchool of Nursing, Healthcare Genetics Program, Clemson University, Clemson, SC 29634, USA.
William E BennettDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Indiana University, Riley Hospital for Children, Indianapolis, IN 46202, USA.
Curtis RogersGreenwood Genetic Center, Greenwood, SC 29646, USA.
Katy PhelanGenetics Laboratory, Florida Cancer Specialists & Research Institute, Fort Myers, FL 33916, USA.
Luigi BoccutoSchool of Nursing, Healthcare Genetics Program, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0003-2017-4270
Clemson University · USFlorida Cancer Specialists & Research Institute · USGreenwood Genetic Center · USRiley Hospital for Children · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phelan-McDermid syndrome (PMS), caused by pathogenic variants in the

Indexed as

Human Growth HormoneInsulin-Like Growth Factor IChromosome DeletionChromosome DisordersChromosomes, Human, Pair 22HumansInfant, NewbornNerve Tissue ProteinsPhenotypeHuman Growth HormoneInsulin-Like Growth Factor INerve Tissue Proteins22q13.3 deletion syndromegrowth hormonehGHIGF-1insulin-like growth factor 1Phelan–McDermid syndromePMSSHANK3

Identifiers

PMID36833418
PMCPMC9956088
OpenAlexW4320917829

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.