Evidence map›Paper›PMID 37895195›Full record

ReviewGenes2023

LRP5, Bone Mass Polymorphisms and Skeletal Disorders.

Jake Littman, Wentian Yang, Jon Olansen, Chanika Phornphutkul, Roy K Aaron

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Case Report: Expanding theFrontiers in pediatrics · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. 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

5 authors at 2 institutions in 1 country.

Jake LittmanDepartment of Orthopedic Surgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.ORCID 0000-0002-7122-2423
Wentian YangDepartment of Orthopedic Surgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.ORCID 0000-0002-2127-6239
Jon OlansenDepartment of Orthopedic Surgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.ORCID 0000-0003-2391-5185
Chanika PhornphutkulDivision of Human Genetics, Department of Pediatrics, Hasbro Children's Hospital, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.
Roy K AaronDepartment of Orthopedic Surgery, Warren Alpert Medical School of Brown University, Providence, RI 02903, USA.ORCID 0000-0002-0745-2267
Brown University · USUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The formation and maintenance of the gross structure and microarchitecture of the human skeleton require the concerted functioning of a plethora of morphogenic signaling processes. Through recent discoveries in the field of genetics, numerous genotypic variants have been implicated in pathologic skeletal phenotypes and disorders arising from the disturbance of one or more of these processes. For example, total loss-of-function variants of

Indexed as

Osteogenesis ImperfectaOsteoporosisBone and BonesBone DensityHumansLow Density Lipoprotein Receptor-Related Protein-5Low Density Lipoprotein Receptor-Related Protein-5LRP5 protein, humanhigh bone masslow bone masslow-density lipoprotein receptor-related protein 5LRP5OPPGosteoporosis-pseudoglioma syndromeskeletal dysmorphogenesisskeletal phenotype

Identifiers

PMID37895195
PMCPMC10606254
OpenAlexW4386996827

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.