Evidence map›Paper›PMID 32714618›Full record

ArticleJournal of pediatric genetics2020

Primary Microcephaly with Novel Variant of

Piero Pavone, Xena Giada Pappalardo, Andrea Domenico Praticò, Agata Polizzi, Martino Ruggieri, Maria Piccione, Giovanni Corsello, Raffaele Falsaperla

Open access · greenAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of pediatric genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Prenatal Identification of a Novel Mutation in theChildren (Basel, Switzerland) · 2022
    Article
  4. 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

8 authors at 3 institutions in 1 country.

Piero PavoneDepartment of Clinical and Experimental Medicine, Pediatric Clinic, University Hospital, A.U.O. "Policlinico-Vittorio Emanuele," Catania, Italy.ORCID 0000-0002-5600-9560
Xena Giada PappalardoNational Council of Research, Institute for Biomedical Research and Innovation (IRIB), Unit of Catania, Catania, Italy.ORCID 0000-0002-4640-6677
Andrea Domenico PraticòDepartment of Clinical and Experimental Medicine, Pediatric Clinic, University Hospital, A.U.O. "Policlinico-Vittorio Emanuele," Catania, Italy.
Agata PolizziDepartment of Educational Sciences, Chair of Pediatrics, University of Catania, Catania, Italy.
Martino RuggieriDepartment of Clinical and Experimental Medicine, Pediatric Clinic, University Hospital, A.U.O. "Policlinico-Vittorio Emanuele," Catania, Italy.
Maria PiccioneOperative Unit of Pediatrics and Neonatal Intensive Therapy, Department of Mother and Child, University of Palermo, Palermo, Italy.
Giovanni CorselloOperative Unit of Pediatrics and Neonatal Intensive Therapy, Department of Mother and Child, University of Palermo, Palermo, Italy.
Raffaele FalsaperlaDepartment of Pediatrics and Pediatric Emergency, University Hospital, A.U.O. "Policlinico Vittorio Emanuele," Catania, Italy.
Azienda Ospedaliero-Universitaria Policlinico - Vittorio Emanuele · ITUniversity of Catania · ITUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study is a clinical report on twin females affected by primary microcephaly who displayed at molecular analysis of heterozygous novel

Indexed as

autoimmune juvenile thyroiditisHashimoto's thyroiditisMCPH1 variantsprimary microcephalytwins

Identifiers

PMID32714618
PMCPMC7375846
OpenAlexW3017867294

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.