Evidence map›Paper›PMID 40225157›Full record

ArticleHuman mutation2023

Quantitative Phenotype Morbidity Description of

Yuri A Zarate, Katherine Bosanko, Amrit Kannan, Ashlen Thomason, Beth Nutt, Nihit Kumar, Kirt Simmons, Aaron Hiegert, Larry Hartzell, Adam Johnson and 6 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Human mutation, 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
–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

2 citing papers in PubMed.

  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

16 authors.

Yuri A ZarateDivision of Genetics and Metabolism, University of Kentucky, Lexington, KY, USA.ORCID 0000-0001-8235-6200
Katherine BosankoSection of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, AR, USA.
Amrit KannanUniversity of Arkansas for Medical Sciences School of Medicine, Little Rock, AR, USA.
Ashlen ThomasonAudiology/Speech Pathology Department, Arkansas Children's Hospital, Little Rock, AR, USA.
Beth NuttAudiology/Speech Pathology Department, Arkansas Children's Hospital, Little Rock, AR, USA.
Nihit KumarDivision of Child and Adolescent Psychiatry, University of Arkansas for Medical Sciences, Little Rock, AR, USA.ORCID 0000-0002-3728-6335
Kirt SimmonsDepartment of Pediatric and Special Needs Dentistry, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Aaron HiegertDepartment of Pediatric and Special Needs Dentistry, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Larry HartzellDepartment of Otolaryngology, Head and Neck Surgery, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.ORCID 0000-0003-0625-221X
Adam JohnsonDepartment of Otolaryngology, Head and Neck Surgery, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.ORCID 0000-0002-8694-8665
Tabitha PraterDepartment of Clinical Nutrition, Arkansas Children's Hospital, Little Rock, AR, USA.
Eduardo Pérez-PalmaUniversidad del Desarrollo, Centro de Genética y Genómica, Facultad de Medicina Clínica Alemana, Santiago, Chile.ORCID 0000-0003-0546-5141
Tobias BrüngerCologne Center for Genomics, University of Cologne, Cologne, NRW, Germany.
Arthur StefanskiGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, USA.
Dennis LalCologne Center for Genomics, University of Cologne, Cologne, NRW, Germany.ORCID 0000-0002-5173-9636
Aisling R CaffreyHealth Outcomes, College of Pharmacy, University of Rhode Island, Kingston, RI, USA.ORCID 0000-0002-4180-027X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Characterized by developmental delay with severe speech delay, dental anomalies, cleft palate, skeletal abnormalities, and behavioral difficulties,

Indexed as

Developmental DisabilitiesMatrix Attachment Region Binding ProteinsPhenotypeTranscription FactorsChildChild, PreschoolFemaleGenetic Association StudiesHumansMaleSeverity of Illness IndexSyndromeMatrix Attachment Region Binding ProteinsSATB2 protein, humanTranscription Factors

Identifiers

PMID40225157
PMCPMC11918880

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.