Evidence map›Paper›PMID 35720663›Full record

ArticleJBMR plus2022

Unusual Cortical Phenotype After Hematopoietic Stem Cell Transplantation in a Patient With Osteopetrosis.

Sonia Afshariyamchlou, Michelle Ng, Asmaa Ferdjallah, Stuart J Warden, Paul Niziolek, Imranul Alam, Lynda E Polgreen, Erik A Imel, Paul Orchard, Michael J Econs

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Autosomal Dominant Osteopetrosis (ADO) Caused by a Missense Variant in the TCIRG1 Gene.The Journal of clinical endocrinology and metabolism · 2024
    Article
  2. Correction of osteopetrosis in the neonateFrontiers in endocrinology · 2024
    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

10 authors at 4 institutions in 1 country.

Sonia AfshariyamchlouDepartment of Medicine Indiana University School of Medicine Indianapolis IN USA.ORCID https://orcid.org/0000-0002-0152-7280
Michelle NgDepartment of Pediatrics University of Minnesota Medical School Minneapolis MN USA.
Asmaa FerdjallahDepartment of Pediatrics University of Minnesota Medical School Minneapolis MN USA.
Stuart J WardenDepartment of Physical Therapy Indiana University School of Health and Human Sciences Indianapolis IN USA.ORCID https://orcid.org/0000-0002-6415-4936
Paul NiziolekDepartment of Radiology Indiana University School of Medicine Indianapolis IN USA.
Imranul AlamDepartment of Medicine Indiana University School of Medicine Indianapolis IN USA.ORCID https://orcid.org/0000-0002-8914-0610
Lynda E PolgreenThe Lundquist Institute at Harbor-UCLA Medical Center Torrance CA USA.
Erik A ImelDepartment of Medicine Indiana University School of Medicine Indianapolis IN USA.ORCID https://orcid.org/0000-0002-7284-3467
Paul OrchardDepartment of Pediatrics University of Minnesota Medical School Minneapolis MN USA.
Michael J EconsDepartment of Medicine Indiana University School of Medicine Indianapolis IN USA.
Indiana University School of MedicineUniversity of Minnesota Medical Center · USIndiana University Health · USUCLA Medical Center · US

Funding

Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
Resource CoreP30AR072581 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI Sharon M Moe · 2017 to 2026
$8.3M
GENETIC AND CLINICAL STUDIES OF AD02R01AR047866 · NIAMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI ECONS, MICHAEL J · 2002 to 2005
$1.4M
The Natural History of Autosomal Dominant Osteopetrosis Type 2R01AR077869 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI ECONS, MICHAEL J · 2020 to 2022
$632k
NCATS NIH HHS UL1 TR002529NIAMS NIH HHS P30 AR072581NIAMS NIH HHS R01 AR047866NIAMS NIH HHS R01 AR077869
6 · The paper itself

Abstract

The osteopetroses are a group of rare genetic diseases caused by osteoclast dysfunction or absence. The hallmark of osteopetrosis is generalized increased bone mineral density (BMD). However, the bone is fragile and fractures are common. Autosomal recessive osteopetrosis is usually a severe disorder and often life-threatening in childhood. We present male siblings with autosomal recessive osteopetrosis due to biallelic variants in

Indexed as

HIGH‐RESOLUTION PERIPHERAL QUANTITATIVE COMPUTED TOMOGRAPHY (HR‐pQCT)OSTEOPETROSISTCIRG1TRANSPLANTATION

Identifiers

PMID35720663
PMCPMC9189909
OpenAlexW4214734731

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.