Evidence map›Paper›PMID 41751586›Full record

ArticleGenes2026

Behavioral Features in Phelan-McDermid Syndrome: Characteristics and Genetic and Metabolic Contributions in a Cohort of 56 Individuals.

Emily Payne, Bridgette A Moffitt, Lindsay M Oberman, Laura Beamer, Sujata Srikanth, Lauren Nicole Cascio, Kelly Jones, Lavanya Jain, Rini Pauly, Melanie May and 9 more

Abstract read
In one paragraph

Article in Genes, 2026. 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

19 authors.

Emily PayneHealthcare Genetics and Genomics Program, School of Nursing, Clemson University, Clemson, SC 29634, USA.ORCID 0009-0005-0836-6095
Bridgette A MoffittHealthcare Genetics and Genomics Program, School of Nursing, Clemson University, Clemson, SC 29634, USA.
Lindsay M ObermanNational Institute of Mental Health, National Institutes of Health, Bethesda, MD 20892, USA.
Laura BeamerGreenwood Genetic Center, Greenwood, SC 29646, USA.
Sujata SrikanthHealthcare Genetics and Genomics Program, School of Nursing, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0001-9962-2800
Lauren Nicole CascioGreenwood Genetic Center, Greenwood, SC 29646, USA.ORCID 0000-0001-6086-4140
Kelly JonesGreenwood Genetic Center, Greenwood, SC 29646, USA.
Lavanya JainDepartment of Biomedical Engineering, Cleveland Clinic Research, Cleveland, OH 44195, USA.ORCID 0000-0003-0454-5019
Rini PaulyGreenwood Genetic Center, Greenwood, SC 29646, USA.
Melanie MayGreenwood Genetic Center, Greenwood, SC 29646, USA.
Cindy SkinnerGreenwood Genetic Center, Greenwood, SC 29646, USA.ORCID 0000-0002-7841-8277
Carrie BuchananGreenwood Genetic Center, Greenwood, SC 29646, USA.
Barbara G DuPontGreenwood Genetic Center, Greenwood, SC 29646, USA.
Rebekah R MartinHealthcare Genetics and Genomics Program, School of Nursing, Clemson University, Clemson, SC 29634, USA.
R Curtis RogersGreenwood Genetic Center, Greenwood, SC 29646, USA.
Katy PhelanGenetics Department, Florida Cancer Specialists & Research Institute, Fort Myers, FL 33905, USA.ORCID 0000-0003-2457-6226
Sara M SarasuaHealthcare Genetics and Genomics Program, School of Nursing, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0002-1625-7404
Walter E KaufmannGreenwood Genetic Center, Greenwood, SC 29646, USA.ORCID 0000-0002-8561-8453
Luigi BoccutoHealthcare Genetics and Genomics Program, School of Nursing, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0003-2017-4270

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Chromosome DisordersNerve Tissue ProteinsAdolescentAdultAutism Spectrum DisorderChildChild, PreschoolChromosome DeletionChromosomes, Human, Pair 22Cross-Sectional StudiesFemaleGenetic Association StudiesHumansMalePhenotypeYoung AdultNerve Tissue ProteinsSHANK3 protein, humanautism spectrum disordermetabolomicsPhelan–McDermid syndromeSHANK3

Identifiers

PMID41751586
PMCPMC12940330

What OpenQuestion holds

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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.