Evidence map›Paper›PMID 34079076›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2021

Correspondence on "De novo variants in MED12 cause X-linked syndromic neurodevelopmental disorders in 18 females" by Polla et al.

Florence Riccardi, Alexandre Astier, Margot Grisval, Arnaud Maillard, Vincent Michaud, Catherine Badens, Christopher T Gordon, Aurélien Trimouille, Laurence Faivre, Jeanne Amiel and 2 more

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2021. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Florence RiccardiCentre de Référence Anomalies du développement et syndromes malformatifs Sud-Est PACA, Département de Génétique Médicale, APHM, Marseille, France.
Alexandre AstierCentre de Référence Anomalies du développement et syndromes malformatifs Sud-Est PACA, Département de Génétique Médicale, APHM, Marseille, France.
Margot GrisvalCentre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon, Dijon, France.
Arnaud MaillardService de Génétique Médicale, Hôpital Necker-Enfants Malades, AP-HP, Paris, France.
Vincent MichaudService de Génétique médicale, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
Catherine BadensAix Marseille Université, MMG, Inserm, Marseille, France.
Christopher T GordonInserm UMR 1163 Institut Imagine, Université de Paris, Paris, France.
Aurélien TrimouilleService de Génétique médicale, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
Laurence FaivreCentre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon, Dijon, France.
Jeanne AmielService de Génétique Médicale, Hôpital Necker-Enfants Malades, AP-HP, Paris, France.
Sabine SigaudyCentre de Référence Anomalies du développement et syndromes malformatifs Sud-Est PACA, Département de Génétique Médicale, APHM, Marseille, France.
Svetlana GorokhovaCentre de Référence Anomalies du développement et syndromes malformatifs Sud-Est PACA, Département de Génétique Médicale, APHM, Marseille, France. svetlana.gorokhova@univ-amu.fr.ORCID 0000-0001-6870-4061

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Genes, X-LinkedNeurodevelopmental DisordersFemaleHumansMediator ComplexSyndromeMED12 protein, humanMediator Complex

Identifiers

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.