Evidence map›Paper›PMID 12014706›Full record

ReviewEndocrine2002

Role of genetics in osteoporosis.

Robert R Recker, Hong-Wen Deng

Abstract readReview
PubMed Publisher
In one paragraph

Review in Endocrine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 4 pooled it
5.1field-weighted citation impact, top 4% 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

49 citing papers in PubMed, 4 syntheses or guidelines pooled it, 120 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. The recurrence of osteoporotic fractures among first- and second-generation immigrants in Sweden.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Genomic structural variations link multiple genes to bone mineral density in a multi-ethnic cohort study: Louisiana osteoporosis study.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  10. Review
  11. Article
  12. Association betweenFrontiers in genetics · 2022
    Article
  13. Review
  14. Review
  15. Article
  16. A Statistical Approach to Fine Mapping for the Identification of Potential Causal Variants Related to Bone Mineral Density.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2017
    Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 2 institutions in 2 countries.

Robert R ReckerOsteoporis Research Center, Creighton University, Omaha, NE 68131, USA. rrecker@creighton.edu
Hong-Wen Deng
Creighton University · USHunan Normal University · CN

Funding

USHERIN--FUNCTION, EXPRESSION, AND ROLE IN PATHOGENESISP01DC001813 · NIDCD · FATHER FLANAGAN'S BOYS'HOME · PI KIMBERLING, WILLIAM J · 1993 to 2003
$4.7M
CHARACTERIZATION OF DELETERIOUS GENOMIC MUTATIONSR01GM060402 · NIGMS · UNIVERSITY OF MISSOURI KANSAS CITY · PI DENG, HONG-WEN · 2000 to 2005
$889k
Genetic Basis of Osteoporotic Fractures and Bone MassK01AR002170 · NIAMS · CREIGHTON UNIVERSITY · PI DENG, HONG-WEN · 2001 to 2005
$505k
GENETIC LINKAGE TO LOW PEAK BONE MASSR01AR045349 · NIAMS · CREIGHTON UNIVERSITY · PI RECKER, ROBERT R. · 1997 to 2000
$188k
NIAMS NIH HHS K01 AR02170-01NIAMS NIH HHS R01 AR45349-01NIDCD NIH HHS P01 DC01813-07NIGMS NIH HHS R01 GM60402-01A1
6 · The paper itself

Abstract

Osteoporosis is a disease characterized by fragile bones and high susceptibility to low-trauma fractures. It is a serious health problem, especially in elderly women. Bone mineral density (BMD) has been employed most commonly as the index for defining and studying osteoporosis. BMD has high genetic determination, with heritability ranging from 50 to 90%. Various gene-mapping approaches have been applied to identify specific genes underlying osteoporosis, largely using BMD as the study phenotype. We review here the genetic determination of osteoporosis as defined by BMD and discuss a fundamental issue we encounter in genetic research in osteoporosis: the choice of phenotype(s) to study. We briefly summarize and discuss advantages and disadvantages of various approaches used in genetic studies of osteoporosis. Finally, we review and discuss the current status for mapping and identification of genes for osteoporosis. We focus on linkage studies in humans and quantitative trait loci mapping in mice to supplement the already extensive reviews of association studies made by many investigators for candidate genes.

Indexed as

AnimalsChromosome MappingGenetic LinkageHumansLinkage DisequilibriumMiceMolecular BiologyOsteoporosisPedigreePhenotypeQuantitative Trait Loci

Identifiers

PMID12014706
OpenAlexW2028355948

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.