Evidence map›Paper›PMID 30680360›Full record

ArticleJBMR plus2019

Genomewide Association Study of Fracture Nonunion Using Electronic Health Records.

Thomas H McCoy, Austin T Fragomen, Kamber L Hart, Amelia M Pellegrini, Kevin A Raskin, Roy H Perlis

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Genetic Influence of Fracture Nonunion (FNU): A Systematic Review.Pharmacogenomics and personalized medicine · 2023
    Review
  6. Review
  7. Article
  8. Review
  9. 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

6 authors at 3 institutions in 1 country.

Thomas H McCoyCenter for Quantitative Health Massachusetts General Hospital and Harvard Medical School Boston MA USA.
Austin T FragomenLimb Lengthening and Complex Reconstruction Service Hospital for Special Surgery and Weill Cornell Medical College New York NY USA.
Kamber L HartCenter for Quantitative Health Massachusetts General Hospital and Harvard Medical School Boston MA USA.
Amelia M PellegriniCenter for Quantitative Health Massachusetts General Hospital and Harvard Medical School Boston MA USA.
Kevin A RaskinDepartment of Orthopaedic Surgery Massachusetts General Hospital and Harvard Medical School Boston MA USA.
Roy H PerlisCenter for Quantitative Health Massachusetts General Hospital and Harvard Medical School Boston MA USA.
Harvard University · USMassachusetts General Hospital · USHospital for Special Surgery · US

Funding

Natural language processing for characterizing psychopathologyR01MH106577 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI PERLIS, ROY H. · 2016 to 2018
$1.2M
NIMH NIH HHS R01 MH106577
6 · The paper itself

Abstract

Nonunion is a clinically significant complication of fracture associated with worse outcomes, including increased pain, disability, and higher healthcare costs. The risk for nonunion is likely to be complex and multifactorial, and as such, the biology underlying such risk remains poorly understood. Genetic studies represent one approach to identify implicated biology for further investigation, but to date the lack of large cohorts for study has limited such efforts. We utilized the electronic health records of two large academic medical centers in Boston to identify individuals with fracture nonunion and control individuals with fracture but no evidence of nonunion. We conducted a genomewide association study among 1760 individuals of Northern European ancestry with upper or lower extremity fracture, including 131 with nonunion, to examine whether common variants were associated with nonunion in this cohort. In all, one locus in the Calcyon (CALY) gene exceeded a genomewide threshold for statistical significance (

Indexed as

CELL/TISSUE SIGNALINGEPIDEMIOLOGYFRACTURE PREVENTIONGENERAL POPULATION STUDIESGENETIC RESEARCHHUMAN ASSOCIATION STUDIESINJURY/FRACTURE HEALINGORTHOPEDICSPRACTICE/POLICY RELATED ISSUES

Identifiers

PMID30680360
PMCPMC6339539
OpenAlexW2805086047

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.