Evidence map›Paper›PMID 35079678›Full record

ArticleJBMR plus2022

Parental Origin of

Patrick McMullan, Peter Maye, Qingfen Yang, David W Rowe, Emily L Germain-Lee

Registry-linked trialOpen 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. It is linked to trial NCT00209235 (Natural History Study of Albright Hereditary Osteodystrophy), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 17% 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.

NCT00209235 naactive not recruitingnot on this map

Natural History Study of Albright Hereditary Osteodystrophy: Includes Substudies on Effects of Growth Hormone in Patients With Pseudohypoparathyroidism Type 1A and Cognitive & Behavioral Studies in Albright Hereditary Osteodystrophy

TypeinterventionalSponsorConnecticut Children's Medical CenterRan2003 to 2030Enrolled600ConditionsPseudohypoparathyroidism Type 1A, Albright Hereditary Osteodystrophy, PseudopseudohypoparathyroidismArmsNeurocognitive and psychosocial testing
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Frontiers in endocrinology · 2023
    Review
  5. 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 1 institution in 1 country.

Patrick McMullanDepartment of Pediatrics University of Connecticut School of Medicine Farmington CT USA.
Peter MayeDepartment of Reconstructive Sciences University of Connecticut School of Dental Medicine Farmington CT USA.
Qingfen YangDepartment of Pediatrics University of Connecticut School of Medicine Farmington CT USA.
David W RoweDepartment of Reconstructive Sciences University of Connecticut School of Dental Medicine Farmington CT USA.
Emily L Germain-LeeDepartment of Pediatrics University of Connecticut School of Medicine Farmington CT USA.ORCID https://orcid.org/0000-0002-5727-610X
University of Connecticut · US

Funding

Skeletal, Craniofacial and Oral Biology Training GrantT90DE021989 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MINA, MINA · 2011 to 2022
$4.5M
Extracellular regulation of bone mass by transforming growth factor-ß-related ligands and their binding proteinsR01AR081659 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI EMILY L GERMAIN-LEE, Se-Jin Lee · 2022 to 2026
$3.1M
Skeletal Phenotyping of Heterozygotes from IMPC Embryonic Lethal LinesR01HD098636 · NICHD · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI MAYE, PETER, ROWE, DAVID W. · 2019 to 2023
$2.8M
The role of G protein-coupled signaling in neurocognitive and psychosocialabnormalitiesR21HD078864 · NICHD · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI GERMAIN-LEE, EMILY L · 2016 to 2017
$451k
NIAMS NIH HHS R01 AR081659NICHD NIH HHS R01 HD098636NICHD NIH HHS R21 HD078864NIDCR NIH HHS T90 DE021989
6 · The paper itself

Abstract

Albright hereditary osteodystrophy (AHO) is caused by heterozygous inactivation of

Indexed as

BONEDISEASES AND DISORDERS OF/RELATED TO BONE – OTHERGENETIC ANIMAL MODELSGnasMOLECULAR PATHWAYS – REMODELINGOSTEOBLASTSOSTEOCLASTS

Identifiers

PMID35079678
PMCPMC8771002
OpenAlexW3205391120

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.