Evidence map›Paper›PMID 33630210›Full record

ArticleGeroScience2021

Lack of resemblance between Myhre syndrome and other "segmental progeroid" syndromes warrants restraint in applying this classification.

Angela E Lin, Nicola Brunetti-Pierri, Bert Callewaert, Valérie Cormier-Daire, Sofia Douzgou, T Bernard Kinane, Mark E Lindsay, Lois J Starr, Myhre Syndrome Foundation Professional Advisory Board

Abstract readLetterComment
PubMed Full text at PMC Publisher
In one paragraph

Article in GeroScience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Angela E LinMedical Genetics, Department of Pediatrics, Massachusetts General Hospital for Children, Boston, MA, USA. lin.angela@mgh.harvard.edu.ORCID http://orcid.org/0000-0002-1145-4572
Nicola Brunetti-PierriDepartment of Translational Medicine, Federico II University of Naples, Naples, Italy.
Bert CallewaertCenter for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
Valérie Cormier-DaireClinical Genetics, Paris Centre University, INSERM UMR 1163, Imagine Institute, Hôpital Necker enfants, Malades, Paris, France.
Sofia DouzgouDepartment of Medical Genetics, Haukeland University Hospital, Bergen, Norway.
T Bernard KinanePediatric Pulmonary, Department of Pediatrics, Massachusetts General Hospital for Children, Boston, MA, USA.
Mark E LindsayCardiovascular Genetics Program, Division of Cardiology and Pediatric Cardiology, Departments of Medicine and Pediatrics, Massachusetts General Hospital, Boston, MA, USA.
Lois J StarrMedical Genetics, Department of Pediatrics, University of Nebraska Medical Center, Omaha, NE, USA.
Myhre Syndrome Foundation Professional Advisory Board

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Cellular SenescenceDNA DamageCryptorchidismFaciesGrowth DisordersHand Deformities, CongenitalHumansIntellectual DisabilityMaleMutationSmad4 ProteinSyndromeTransforming Growth Factor betaSmad4 ProteinSMAD4 protein, humanTransforming Growth Factor beta

Identifiers

PMID33630210
PMCPMC8110621

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.