Evidence map›Paper›PMID 34532616›Full record

ArticleJBMR plus2021

CRISPR-Cas9-Mediated Genome Editing Confirms

James A Pippin, Alessandra Chesi, Yadav Wagley, Chun Su, Matthew C Pahl, Kenyaita M Hodge, Matthew E Johnson, Andrew D Wells, Kurt D Hankenson, Struan F A Grant

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
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

10 authors at 3 institutions in 1 country.

James A PippinCenter for Spatial and Functional Genomics Children's Hospital of Philadelphia Philadelphia PA USA.ORCID https://orcid.org/0000-0002-6850-8164
Alessandra ChesiCenter for Spatial and Functional Genomics Children's Hospital of Philadelphia Philadelphia PA USA.ORCID https://orcid.org/0000-0002-0954-7446
Yadav WagleyDepartment of Orthopedic Surgery University of Michigan Medical School Ann Arbor MI USA.
Chun SuCenter for Spatial and Functional Genomics Children's Hospital of Philadelphia Philadelphia PA USA.
Matthew C PahlCenter for Spatial and Functional Genomics Children's Hospital of Philadelphia Philadelphia PA USA.
Kenyaita M HodgeGenetics and Molecular Biology Graduate Program, Laney Graduate School Emory University Atlanta GA USA.
Matthew E JohnsonCenter for Spatial and Functional Genomics Children's Hospital of Philadelphia Philadelphia PA USA.
Andrew D WellsCenter for Spatial and Functional Genomics Children's Hospital of Philadelphia Philadelphia PA USA.ORCID https://orcid.org/0000-0002-3630-2145
Kurt D HankensonDepartment of Orthopedic Surgery University of Michigan Medical School Ann Arbor MI USA.ORCID https://orcid.org/0000-0001-6361-143X
Struan F A GrantCenter for Spatial and Functional Genomics Children's Hospital of Philadelphia Philadelphia PA USA.ORCID https://orcid.org/0000-0003-2025-5302
Children's Hospital of Philadelphia · USUniversity of Michigan · USEmory University · US

Funding

Genomics of bone and body composition traits in childrenR01HD100406 · NICHD · CHILDREN'S HOSP OF PHILADELPHIA · PI GRANT, STRUAN F A, ZEMEL, BABETTE S · 2020 to 2024
$3.4M
Network-based algorithms for target identification and drug repositioning from genetic associationsR01HG010067 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI GREENE, CASEY S · 2018 to 2022
$3.2M
Regulators of Ischemic Fracture HealingR01AR066028 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HANKENSON, KURT DAVID · 2015 to 2020
$2.7M
NHGRI NIH HHS R01 HG010067NIAMS NIH HHS R01 AR066028NICHD NIH HHS R01 HD100406
6 · The paper itself

Abstract

Genome-wide-association studies (GWASs) have discovered genetic signals robustly associated with BMD, but typically not the precise localization of effector genes. By intersecting genome-wide promoter-focused Capture C and assay for transposase-accessible chromatin using sequencing (ATAC-seq) data generated in human mesenchymal progenitor cell (hMSC)-derived osteoblasts, consistent contacts were previously predicted between the

Indexed as

BONE MINERAL DENSITY (BMD)CHROMATIN CAPTURECRISPROSTEOBLAST DIFFERENTIATIONOSTEOBLAST PROGENITOR

Identifiers

PMID34532616
PMCPMC8441377
OpenAlexW3177558710

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.