Evidence map›Paper›PMID 31204721›Full record

ArticleJournal of genetics2019

Victoria Vlachou, Line Larsen, Efterpi Pavlidou, Naila Ismayilova, N D Mazarakis, Marcello Scala, Mantha Pantazi, Kshitij Mankad, Maria Kinali

Abstract readCase Reports
PubMed
In one paragraph

Article in Journal of genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Structural brain MRI abnormalities inFrontiers in neurology · 2025
    Article
  5. Article
  6. Article
  7. Article
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

9 authors at 6 institutions in 2 countries.

Victoria VlachouDepartment of Paediatric Neurology, Chelsea and Westminster NHS Foundation Trust, London SW10 9NH, UK. victoria.vlachou@nhs.net.
Line Larsen
Efterpi Pavlidou
Naila Ismayilova
N D Mazarakis
Marcello Scala
Mantha Pantazi
Kshitij Mankad
Maria Kinali
Chelsea and Westminster Hospital NHS Foundation Trust · GBAHEPA University Hospital · GRGeneral Hospital of Ioannina G. Hatzikosta · GRGreat Ormond Street Hospital · GBHammersmith Hospital · GBThe Portland Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuronal migration disorders (NMDs) are a heterogeneous group of conditions caused by the abnormal migration of neuroblasts in the developing brain and nervous system, resulting in severe developmental impairment, intractable epilepsy and intellectual disability (Spalice

Indexed as

MutationNeuroimagingPhenotypeAmino Acid SequenceDiagnosis, DifferentialHumansInfantMagnetic Resonance ImagingMaleMalformations of Cortical Development, Group IINAV1.2 Voltage-Gated Sodium ChannelSpasms, InfantileNAV1.2 Voltage-Gated Sodium ChannelSCN2A protein, human

Identifiers

PMID31204721
OpenAlexW2947946042

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.