Evidence map›Paper›PMID 29162626›Full record

ArticleGenetics2018

Identification of

Lisa A Lansdon, Benjamin W Darbro, Aline L Petrin, Alissa M Hulstrand, Jennifer M Standley, Rachel B Brouillette, Abby Long, M Adela Mansilla, Robert A Cornell, Jeffrey C Murray and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. TheFrontiers in medicine · 2025
    Review
  5. Article
  6. Advances in research of biological functions of Isthmin-1.Journal of cell communication and signaling · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. ISM1 protects lung homeostasis via cell-surface GRP78-mediated alveolar macrophage apoptosis.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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

12 authors at 3 institutions in 2 countries.

Lisa A LansdonDepartment of Pediatrics.
Benjamin W DarbroDepartment of Pediatrics.
Aline L PetrinDepartment of Pediatrics.
Alissa M HulstrandDepartment of Biology, Northland College, Ashland, Wisconsin 54806.
Jennifer M StandleyDepartment of Pediatrics.
Rachel B BrouilletteDepartment of Biology.
Abby LongDepartment of Biology.
M Adela MansillaDepartment of Pediatrics.
Robert A CornellInterdisciplinary Graduate Program in Genetics.
Jeffrey C MurrayDepartment of Pediatrics.
Douglas W HoustonDepartment of Biology.
J Robert ManakDepartment of Pediatrics, john-manak@uiowa.edu.
University of Iowa · USInstitute of Cell Biology and Neurobiology · ITNorthland College · US

Funding

Molecular Genetic Epidemiology of Cleft Lip and PalateR37DE008559 · NIDCR · UNIVERSITY OF IOWA · PI MURRAY, JEFFREY C · 2004 to 2013
$6.8M
University of Iowa Institutional Training Program in Oral Health ResearchT90DE023520 · NIDCR · UNIVERSITY OF IOWA · PI STEVEN M. LEVY · 2013 to 2026
$5.6M
PREDOCTORAL TRAINING PROGRAM IN GENETICST32GM008629 · NIGMS · UNIVERSITY OF IOWA · PI EBERL, DANIEL F · 1997 to 2021
$4.1M
Genomic identification of copy number variants to identify clefting lociR01DE021071 · NIDCR · UNIVERSITY OF IOWA · PI MANAK, JOHN ROBERT · 2010 to 2014
$3.5M
Localized mRNAs in vertebrate axis formationR01GM083999 · NIGMS · UNIVERSITY OF IOWA · PI HOUSTON, DOUGLAS W · 2008 to 2016
$2.6M
NIDCR NIH HHS R01 DE021071NIDCR NIH HHS R37 DE008559NIDCR NIH HHS T90 DE023520NIGMS NIH HHS R01 GM083999NIGMS NIH HHS T32 GM008629
6 · The paper itself

Abstract

Orofacial clefts are one of the most common birth defects, affecting 1-2 per 1000 births, and have a complex etiology. High-resolution array-based comparative genomic hybridization has increased the ability to detect copy number variants (CNVs) that can be causative for complex diseases such as cleft lip and/or palate. Utilizing this technique on 97 nonsyndromic cleft lip and palate cases and 43 cases with cleft palate only, we identified a heterozygous deletion of

Indexed as

Case-Control StudiesCleft LipCleft PalateComparative Genomic HybridizationCraniofacial AbnormalitiesCRISPR-Cas SystemsDNA Copy Number VariationsGene DeletionHaploinsufficiencyHumansMorphogenesisOrganogenesisQuantitative Trait LociThrombospondinsISM1 protein, humanThrombospondinsbranchial archescleft lip and palatecopy number variationcraniofacial developmentXenopus laevis

Identifiers

PMID29162626
PMCPMC5753863
OpenAlexW2769248658

What OpenQuestion holds

Textmetadata
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.