Evidence map›Paper›PMID 35168888›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2022

Correspondence on "Expanded phenotype of AARS1-related white matter disease" by Helman et al.

Alessia Leidi, Roberto Previtali, Cecilia Parazzini, Federico Raviglione, Stephana Carelli, Marisa I Mendes, Gajja S Salomons, Maria Iascone, Davide Tonduti

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Alessia LeidiDepartment of Biomedical and Clinical Sciences "L. Sacco", University of Milan, Milan, Italy.
Roberto PrevitaliDepartment of Biomedical and Clinical Sciences "L. Sacco", University of Milan, Milan, Italy.
Cecilia ParazziniPediatric Radiology and Neuroradiology Department, Vittore Buzzi Children's Hospital, Milan, Italy; COALA (Center for diagnosis and treatment of leukodystrophies), Vittore Buzzi Children's Hospital, Milan, Italy.
Federico RaviglioneChild Neuropsychiatry Unit, UONPIA ASST Rhodense, Milan, Italy.
Stephana CarelliDepartment of Biomedical and Clinical Sciences "L. Sacco", University of Milan, Milan, Italy; Pediatric Clinical Research Center Fondazione Romeo ed Enrica Invernizzi, University of Milan, Milan, Italy.
Marisa I MendesLaboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Vrije Universiteit Amsterdam, University of Amsterdam, Amsterdam, The Netherlands.
Gajja S SalomonsLaboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology Endocrinology Metabolism, Amsterdam UMC, Vrije Universiteit Amsterdam, University of Amsterdam, Amsterdam, The Netherlands.
Maria IasconeMolecular Genetics Section, Medical Genetics Laboratory, Papa Giovanni XXIII Hospital, Bergamo, Italy.
Davide TondutiCOALA (Center for diagnosis and treatment of leukodystrophies), Vittore Buzzi Children's Hospital, Milan, Italy; Child Neurology Unit, Vittore Buzzi Children's Hospital, Milan, Italy. Electronic address: davide.tonduti@asst-fbf-sacco.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

LeukoencephalopathiesHumansPhenotype

Identifiers

PMID35168888

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.