Evidence map›Paper›PMID 29654772›Full record

ArticleNeuron2015

Mutations in KATNB1 Cause Complex Cerebral Malformations by Disrupting Asymmetrically Dividing Neural Progenitors.

Ketu Mishra-Gorur, Ahmet Okay Çağlayan, Ashleigh E Schaffer, Chiswili Chabu, Octavian Henegariu, Fernando Vonhoff, Gözde Tuğce Akgümüş, Sayoko Nishimura, Wenqi Han, Shu Tu and 30 more

Abstract readPublished Erratum
PubMed Publisher
In one paragraph

Article in Neuron, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. The Mammalian Family of Katanin Microtubule-Severing Enzymes.Frontiers in cell and developmental biology · 2021
    Review
  5. Review
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

40 authors.

Ketu Mishra-Gorur
Ahmet Okay Çağlayan
Ashleigh E Schaffer
Chiswili Chabu
Octavian Henegariu
Fernando Vonhoff
Gözde Tuğce Akgümüş
Sayoko Nishimura
Wenqi Han
Shu Tu
Burçin Baran
Hakan Gümüş
Cengiz Dilber
Maha S Zaki
Heba A A Hossni
Jean-Baptiste Rivière
Hülya Kayserili
Emily G Spencer
Rasim Ö Rosti
Jana Schroth
Hüseyin Per
Caner Çağlar
Çağri Çağlar
Duygu Dölen
Jacob F Baranoski
Sefer Kumandaş
Frank J Minja
E Zeynep Erson-Omay
Shrikant M Mane
Richard P Lifton
Tian Xu
Haig Keshishian
William B Dobyns
Neil C Chi
Nenad Šestan
Angeliki Louvi
Kaya Bilgüvar
Katsuhito Yasuno
Joseph G Gleeson
Murat Günel

Funding

Molecular Mechanisms of Intellectual DisabilityR00HD082337 · NICHD · CASE WESTERN RESERVE UNIVERSITY · PI SCHAFFER, ASHLEIGH E · 2017 to 2019
$662k
Molecular Mechanisms of Intellectual DisabilityK99HD082337 · NICHD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SCHAFFER, ASHLEIGH E · 2015 to 2016
$268k
NICHD NIH HHS K99 HD082337
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

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.