Evidence map›Paper›PMID 24687084›Full record

ArticleThe Journal of investigative dermatology2014

A new lamin a mutation associated with acrogeria syndrome.

Smail Hadj-Rabia, Jacob Mashiah, Patrice Roll, Amandine Boyer, Patrice Bourgeois, Philippe Khau Van Kien, Nicolas Lévy, Annachiara De Sandre-Giovannoli, Christine Bodemer, Claire Navarro

Open access · greenAbstract readLetter
PubMed Publisher
In one paragraph

Article in The Journal of investigative dermatology, 2014. 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
0.4field-weighted citation impact, top 36% 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, 11 citations in OpenAlex.

  1. Article
  2. 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 5 institutions in 1 country.

Smail Hadj-RabiaDepartment of Dermatology, Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), INSERM U781, Université Paris Descartes-Sorbonne Paris Cité, Paris, France; Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France. Electronic address: smail.hadj@inserm.fr.
Jacob MashiahDepartment of Dermatology, Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), INSERM U781, Université Paris Descartes-Sorbonne Paris Cité, Paris, France; Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.
Patrice RollAix Marseille Université, GMGF, INSERM, UMR_S 910, Marseille, France; Laboratoire de Biologie Cellulaire, Assistance Publique-Hôpitaux de Marseille, Hôpital d'Enfants La Timone, Marseille, France.
Amandine BoyerLaboratoire de Génétique Moléculaire, Assistance Publique-Hôpitaux de Marseille, Hôpital d'Enfants La Timone, Marseille, France.
Patrice BourgeoisLaboratoire de Génétique Moléculaire, Assistance Publique-Hôpitaux de Marseille, Hôpital d'Enfants La Timone, Marseille, France.
Philippe Khau Van KienLaboratoire de Génétique Moléculaire, Centre de Compétences Maladies Vasculaires Rares, CHU de Montpellier, Montpellier, France; Laboratoire de Cytologie Clinique et Cytogénétique, UF Génétique Médicale, CHU de Nîmes, Nîmes, France.
Nicolas LévyAix Marseille Université, GMGF, INSERM, UMR_S 910, Marseille, France; Laboratoire de Génétique Moléculaire, Assistance Publique-Hôpitaux de Marseille, Hôpital d'Enfants La Timone, Marseille, France.
Annachiara De Sandre-GiovannoliAix Marseille Université, GMGF, INSERM, UMR_S 910, Marseille, France; Laboratoire de Génétique Moléculaire, Assistance Publique-Hôpitaux de Marseille, Hôpital d'Enfants La Timone, Marseille, France.
Christine BodemerDepartment of Dermatology, Reference Center for Genodermatoses and Rare Skin Diseases (MAGEC), INSERM U781, Université Paris Descartes-Sorbonne Paris Cité, Paris, France; Institut Imagine, Hôpital Universitaire Necker-Enfants Malades, Assistance Publique-Hôpitaux de Paris, Paris, France.
Claire NavarroAix Marseille Université, GMGF, INSERM, UMR_S 910, Marseille, France. Electronic address: claire.navarro@univ-amu.fr.
Inserm · FRDélégation Paris 5 · FRCentre Hospitalier Universitaire de Nîmes · FRGénétique Médicale & Génomique Fonctionelle · FRHôpital de la Timone · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MutationAdultCollagen Type IIIHumansLamin Type AProgeriaCOL3A1 protein, humanCollagen Type IIILamin Type A

Identifiers

PMID24687084
OpenAlexW2044782755

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.