Evidence map›Paper›PMID 37102214›Full record

ArticleDisease models & mechanisms2023

Facial analytics based on a coordinate extrapolation system (zFACE) for morphometric phenotyping of developing zebrafish.

Lorena Maili, Oscar E Ruiz, Philip H Kahan, Frankie Chiu, Stephen T Larson, S Shahrukh Hashmi, Jacqueline T Hecht, George T Eisenhoffer

Open access · goldAbstract read
In one paragraph

Article in Disease models & mechanisms, 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
0.8field-weighted citation impact, top 28% 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. Disruption ofFrontiers in cell and developmental biology · 2023
    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

8 authors at 2 institutions in 1 country.

Lorena MailiPediatric Research Center, Department of Pediatrics, McGovern Medical School University of Texas Health Science Center-Houston, Houston, TX 77030, USA.ORCID 0000-0001-7695-4319
Oscar E RuizDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Philip H KahanDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Frankie ChiuPediatric Research Center, Department of Pediatrics, McGovern Medical School University of Texas Health Science Center-Houston, Houston, TX 77030, USA.
Stephen T LarsonDepartment of Genetics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
S Shahrukh HashmiPediatric Research Center, Department of Pediatrics, McGovern Medical School University of Texas Health Science Center-Houston, Houston, TX 77030, USA.ORCID 0000-0001-8758-8254
Jacqueline T HechtPediatric Research Center, Department of Pediatrics, McGovern Medical School University of Texas Health Science Center-Houston, Houston, TX 77030, USA.ORCID 0000-0002-9087-3379
George T EisenhofferGenetics and Epigenetics Graduate Program, The University of Texas MD Anderson Cancer Center UTHealth Houston Graduate School of Biomedical Sciences, Houston, TX 77030, USA.ORCID 0000-0003-0188-6782
The University of Texas MD Anderson Cancer Center · USTexas Children's Hospital · US

Funding

MOLECULAR STUDIES IN NONSYNDROMIC CLEFT LIP AND PALATER01DE011931 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BLANTON, SUSAN HALLORAN, HECHT, JACQUELINE T · 1999 to 2017
$7.6M
Regulation of Cell Turnover During Epithelial Tissue HomeostasisR01GM124043 · NIGMS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI EISENHOFFER, GEORGE THOMAS · 2018 to 2022
$2.0M
The role of regulatory variants in FZD6 and interacting genes in nonsyndromic cleft lip and palateF31DE028187 · NIDCR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MAILI, LORENA · 2019 to 2020
$65k
NIDCR NIH HHS F31 DE028187NIDCR NIH HHS R01 DE011931NIGMS NIH HHS R01 GM124043
6 · The paper itself

Abstract

Facial development requires a complex and coordinated series of cellular events that, when perturbed, can lead to structural birth defects. A quantitative approach to quickly assess morphological changes could address how genetic or environmental inputs lead to differences in facial shape and promote malformations. Here, we report on a method to rapidly analyze craniofacial development in zebrafish embryos using facial analytics based on a coordinate extrapolation system, termed zFACE. Confocal images capture facial structures and morphometric data are quantified based on anatomical landmarks present during development. The quantitative morphometric data can detect phenotypic variation and inform on changes in facial morphology. We applied this approach to show that loss of smarca4a in developing zebrafish leads to craniofacial anomalies, microcephaly and alterations in brain morphology. These changes are characteristic of Coffin-Siris syndrome, a rare human genetic disorder associated with mutations in SMARCA4. Multivariate analysis of zFACE data facilitated the classification of smarca4a mutants based on changes in specific phenotypic characteristics. Together, zFACE provides a way to rapidly and quantitatively assess the impact of genetic alterations on craniofacial development in zebrafish.

Indexed as

Abnormalities, MultipleIntellectual DisabilityMicrognathismAnimalsDNA HelicasesFaceHumansNuclear ProteinsTranscription FactorsZebrafishDNA HelicasesNuclear ProteinsSMARCA4 protein, humanTranscription FactorsCraniofacial developmentGeometric morphometricssmarca4aZebrafish

Identifiers

PMID37102214
PMCPMC10245138
OpenAlexW4367174821

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.