Evidence map›Paper›PMID 40611650›Full record

ArticleThe Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association2026

Multimodality Craniofacial Phenotyping of Congenital Facial Weakness Disorders.

Konstantinia Almpani, Katelin R Devine, Denise K Liberton, Rashmi Mishra, Carol Bassim, Carol Van Ryzin, Flavia M Facio, Bryn D Webb, Brenda J Barry, Elizabeth C Engle and 5 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2026. 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
–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

1 citing paper in PubMed.

  1. 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

15 authors.

Konstantinia AlmpaniCraniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA.ORCID 0000-0001-7558-6796
Katelin R DevineCraniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA.
Denise K LibertonCraniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA.
Rashmi MishraCraniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA.
Carol BassimCraniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA.
Carol Van RyzinMedical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA.
Flavia M FacioMedical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA.
Bryn D WebbDepartment of Genetics and Genomic Sciences and Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Brenda J BarryDepartment of Neurology, Boston Children's Hospital, Boston, MA, USA.
Elizabeth C EngleDepartment of Neurology, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0001-8194-7738
Ethylin Wang JabsDepartment of Genetics and Genomic Sciences and Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Francis S CollinsMedical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA.
Irini ManoliMedical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA.
Janice S LeeCraniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA.ORCID 0000-0001-5164-5958
Moebius Syndrome Research Consortium

Funding

Craniofacial Anomalies and RegenerationZIADE000746 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI LEE, JANICE · 2015 to 2025
$12.3M
Genetics of Moebius syndrome and other congenital facial weakness disordersZIAHG200389 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI COLLINS, FRANCIS S. · 2013 to 2024
$4.9M
Birth Defects: Moebius syndrome and related facial weakness disordersU01HD079068 · NICHD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BROOKS, BRIAN PATRICK, ENGLE, ELIZABETH C. · 2014 to 2016
$1.1M
Intramural NIH HHS Z99 DE999999Intramural NIH HHS ZIA DE000746Intramural NIH HHS ZIA HG200389NICHD NIH HHS U01 HD079068
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Craniofacial AbnormalitiesFacial ParalysisAdolescentAdultCephalometryChildCohort StudiesCone-Beam Computed TomographyFemaleHumansImaging, Three-DimensionalMaleMobius SyndromePhenotype3D facial surfaceCAPSCarey-Fineman-Ziter syndromeCBCTcephalometric analysisclinical phenotypingcone-beam computed tomographycongenital facial weaknesscraniofacial anomalies prevalence scoregeometric morphometric analysishereditary congenital facial palsyMoebius syndromemultimodality craniofacial phenotypingoral-dental anomaliesTUBB3β-tubulin isotype 3 syndrome

Identifiers

PMID40611650
PMCPMC12826332

What OpenQuestion holds

Textmetadata
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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.