Evidence mapPaperPMID 35216282Full record

ArticleInternational journal of molecular sciences2022

Utilizing Genomically Targeted Molecular Data to Improve Patient-Specific Outcomes in Autism Spectrum Disorder.

Sharon Hausman-Cohen, William LaValley, Heather Way, Emily Gutierrez, Jordan Reeder

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Decoding microRNAs in autism spectrum disorder.Molecular therapy. Nucleic acids · 2022
    Review
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

5 authors at 2 institutions in 2 countries.

Sharon Hausman-CohenIntellxxDNA, Austin, TX 78731, USA.
William LaValleyLaValley MD Protocols, Austin, TX 78759, USA.ORCID 0000-0002-4570-7419
Heather WayThe Australian Center for Genomic Analysis, Kenmore, QLD 4069, Australia.
Emily GutierrezNeuronutrition Associates, Austin, TX 78730, USA.
Jordan ReederIntellxxDNA, Austin, TX 78731, USA.
Intel (United States) · USAGRF Ltd · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Molecular biology combined with genomics can be a powerful tool for developing potential intervention strategies for improving outcomes in children with autism spectrum disorders (ASD). Monogenic etiologies rarely cause autism. Instead, ASD is more frequently due to many polygenic contributing factors interacting with each other, combined with the epigenetic effects of diet, lifestyle, and environment. One limitation of genomics has been identifying ways of responding to each identified gene variant to translate the information to something clinically useful. This paper will illustrate how understanding the function of a gene and the effects of a reported variant on a molecular level can be used to develop actionable and targeted potential interventions for a gene variant or combinations of variants. For illustrative purposes, this communication highlights a specific genomic variant, SHANK3. The steps involved in developing molecularly genomically targeted actionable interventions will be demonstrated. Cases will be shared to support the efficacy of this strategy and to show how clinicians utilized these targeted interventions to improve ASD-related symptoms significantly. The presented approach demonstrates the utility of genomics as a part of clinical decision-making.

Indexed as

Autism Spectrum DisorderAutistic DisorderChromosome DisordersChildChromosome DeletionHumansNerve Tissue ProteinsNerve Tissue Proteinsautism spectrum disorder (ASD)clinical decision support tool (CDS tool)genomicsglutamatemolecular biologyPDD (pervasive developmental disorder)personalized medicinePMS (Phelan-McDermid syndrome)SHANK3 (SH3 and multiple ankyrin repeat domains 3)SNP (small nucleic polymorphism)variant

Identifiers

PMID35216282
PMCPMC8879068
OpenAlexW4212930079

What Socratic 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 Socratic graph.