Evidence map›Paper›PMID 34234302›Full record

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

Correspondence on "Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities," by Carmignac et al.

Nicoletta Resta, Olga Calabrese, Valentina Grossi, Licia Lugli, Cristiano Simone, Carlotta Ranieri, Marilidia Piglionica, Martina Lepore Signorile, Katia Rossi, Diana Carli and 1 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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Response to Resta et al.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Nicoletta RestaDepartment of Biomedical Sciences and Human Oncology (DIMO), Medical Genetics, University of Bari "Aldo Moro", Bari, Italy. nicoletta.resta@uniba.it.ORCID http://orcid.org/0000-0001-8640-5532
Olga CalabreseMedical Genetic Unit, Mother-Child Department, University Hospital of Modena, Modena, Italy.
Valentina GrossiMedical Genetics, National Institute for Gastroenterology, IRCCS "S. de Bellis" Research Hospital, Castellana Grotte (Ba), Italy.
Licia LugliNeonatal Intensive Care Unit, Mother-Child Department, University Hospital of Modena and Reggio Emilia, Modena, Italy.
Cristiano SimoneDepartment of Biomedical Sciences and Human Oncology (DIMO), Medical Genetics, University of Bari "Aldo Moro", Bari, Italy.
Carlotta RanieriDepartment of Biomedical Sciences and Human Oncology (DIMO), Medical Genetics, University of Bari "Aldo Moro", Bari, Italy.
Marilidia PiglionicaDepartment of Biomedical Sciences and Human Oncology (DIMO), Medical Genetics, University of Bari "Aldo Moro", Bari, Italy.
Martina Lepore SignorileMedical Genetics, National Institute for Gastroenterology, IRCCS "S. de Bellis" Research Hospital, Castellana Grotte (Ba), Italy.
Katia RossiNeonatal Intensive Care Unit, Mother-Child Department, University Hospital of Modena and Reggio Emilia, Modena, Italy.
Diana CarliPediatric Clinical Genetics Unit, Department of Public Health and Pediatric Sciences, University of Torino, and Regina Margherita Children's Hospital, Città della Salute e della Scienza di Torino, Torino, Italy.
Alessandro MussaPediatric Clinical Genetics Unit, Department of Public Health and Pediatric Sciences, University of Torino, and Regina Margherita Children's Hospital, Città della Salute e della Scienza di Torino, Torino, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

HypopigmentationHumansMosaicismTOR Serine-Threonine KinasesMTOR protein, humanTOR Serine-Threonine Kinases

Identifiers

PMID34234302

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.