Evidence map›Paper›PMID 39816865›Full record

ArticleFrontiers in child and adolescent psychiatry2023

Behavioral profiling in children and adolescents with Malan syndrome.

Paolo Alfieri, Federica Alice Maria Montanaro, Marina Macchiaiolo, Martina Collotta, Cristina Caciolo, Paolo Galassi, Filippo Maria Panfili, Fabiana Cortellessa, Marcella Zollino, Marcello Chinali and 7 more

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In one paragraph

Article in Frontiers in child and adolescent psychiatry, 2023. 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. Article
  2. Article
  3. 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

17 authors.

Paolo AlfieriChild and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Federica Alice Maria MontanaroChild and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Marina MacchiaioloRare Diseases and Medical Genetics Unit, University - Hospital Pediatric Department (DPUO), Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Martina CollottaChild and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Cristina CacioloChild and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Paolo GalassiChild and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Filippo Maria PanfiliSchool of Pediatrics, University Tor Vergata, Rome, Italy.
Fabiana CortellessaRare Diseases and Medical Genetics Unit, University - Hospital Pediatric Department (DPUO), Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Marcella ZollinoGenetica Medica, Fondazione Policlinico Universitario A. Gemelli, IRCCS, Roma, Italy.
Marcello ChinaliDepartment of Pediatric Cardiology, Bambino Gesù Children's Hospital, Rome, Italy.
Maria AccadiaMedical Genetics Service, Hospital "Cardinale G. Panico", Lecce, Italy.
Marco SeriUnit of Medical Genetics, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.
Andrea BartuliRare Diseases and Medical Genetics Unit, University - Hospital Pediatric Department (DPUO), Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Corrado MammìOperative Unit of Medical Genetics Bianchi - Melacrino- Morelli Hospital, Reggio Calabria, Italy.
Marco TartagliaGenetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Stefano VicariChild and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Manuela PrioloOperative Unit of Medical Genetics Bianchi - Melacrino- Morelli Hospital, Reggio Calabria, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malan syndrome (MALNS) is an ultra-rare genetic disorder caused by heterozygous chromosomal microdeletions involving the 19p13.2 region or loss-of-function variants in the

Indexed as

genotypeintellectual disabilitymalan syndromeneurobehavioralNFIX variantsphenotypepsychopathologyrare genetic syndromes

Identifiers

PMID39816865
PMCPMC11732151

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