Evidence map›Paper›PMID 25655944›Full record

ArticleAmerican journal of medical genetics. Part A2015

Phenotypic sub-grouping in microtia using a statistical and a clinical approach.

Daniela V Luquetti, Babette S Saltzman, Carrie L Heike, Kathleen C Sie, Craig B Birgfeld, Kelly N Evans, Brian G Leroux

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In one paragraph

Article in American journal of medical genetics. Part A, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 pooled it
–field-weighted citation impact, top 97% 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

3 citing papers in PubMed, 2 syntheses or guidelines pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. 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

7 authors at 2 institutions in 1 country.

Daniela V LuquettiDepartment of Pediatrics, University of Washington, Seattle, Washington; Craniofacial Center, Seattle Children's Hospital, Seattle, Washington; Center of Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington.
Babette S Saltzman
Carrie L Heike
Kathleen C Sie
Craig B Birgfeld
Kelly N Evans
Brian G Leroux
Seattle Children's Hospital · USUniversity of Washington · US

Funding

Phenotypic and Genomic Characterization of Microtia in the Andean PopulationR00DC011282 · NIDCD · SEATTLE CHILDREN'S HOSPITAL · PI LUQUETTI, DANIELA VARELA · 2013 to 2015
$739k
NIDCD NIH HHS R00 DC011282NIDCD NIH HHS R00DC011282
6 · The paper itself

Abstract

The clinical presentation of microtia varies widely from minimal morphological abnormalities to complete absence of the ear. In this study we sought to identify and characterize sub-groups of microtia using a statistical and a clinical approach. Photographs of 86 ears were classified in relation to all the external ear components. We used cluster analysis and rater's clinical opinion to identify groups with similar phenotypes in two separate analyses. We used Cramer's Phi coefficient of association to assess the similarity among the clinician's groupings as well as among the statistical sub-phenotypic groups and each of the clinician's groupings. The cluster analysis initially divided the 86 ears into a more and a less severe group. The less severe group included two sub-groups that included ears classified as normal and a group that had very few anomalous components. The group of 48 more affected ears all had abnormalities of the helix crus; antihelix-stem, -superior crus and -inferior crus; and antitragus. These were further divided into 4 sub-phenotypes. There was a moderate degree of association among the raters' groupings (Cramer's Phi: 0.64 to 0.73). The statistical and clinical groupings had a lower degree of association (Cramer's Phi: 0.49 to 0.58). Using standardized characterization of structural abnormalities of the ear we identified six distinct phenotypic groups; correlations with clinicians' groupings were moderate. These clusters may represent groups of ear malformations associated with the same etiology, similar time of insult or target cell population during embryonic development. The results will help inform investigations on etiology.

Indexed as

AdolescentCase-Control StudiesChildChild, PreschoolCluster AnalysisCongenital MicrotiaEar, ExternalFemaleHumansInfantInfant, NewbornMalePhenotypeear morphologymicrotiaphenotype

Identifiers

PMID25655944
PMCPMC5730095
OpenAlexW1559035660

What OpenQuestion holds

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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.