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 paragraphArticle 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 itWhat 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 registryThe 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 literatureWho cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
4 · The recordCorrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
5 · Who and what moneyAuthors 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 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.
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 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 itselfAbstract
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
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