Evidence map›Paper›PMID 31879022›Full record

ArticleAmerican journal of human genetics2020

ZMIZ1 Variants Cause a Syndromic Neurodevelopmental Disorder.

Raphael Carapito, Ekaterina L Ivanova, Aurore Morlon, Linyan Meng, Anne Molitor, Eva Erdmann, Bruno Kieffer, Angélique Pichot, Lydie Naegely, Aline Kolmer and 51 more

Abstract readPublished Erratum
In one paragraph

Article in American journal of human genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Genome-wide association analysis identifies APOE as a mitophagy modifier in Lewy body disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

61 authors.

Raphael Carapito
Ekaterina L Ivanova
Aurore Morlon
Linyan Meng
Anne Molitor
Eva Erdmann
Bruno Kieffer
Angélique Pichot
Lydie Naegely
Aline Kolmer
Nicodème Paul
Antoine Hanauer
Frédéric Tran Mau-Them
Nolwenn Jean-Marçais
Susan M Hiatt
Gregory M Cooper
Tatiana Tvrdik
Alison M Muir
Clémantine Dimartino
Maya Chopra
Jeanne Amiel
Christopher T Gordon
Fabien Dutreux
Aurore Garde
Christel Thauvin-Robinet
Xia Wang
Magalie S Leduc
Meredith Phillips
Heather P Crawford
Mary K Kukolich
David Hunt
Victoria Harrison
Mira Kharbanda
Deciphering Developmental Disorders Study
University of Washington Center for Mendelian Genomics
Robert Smigiel
Nina Gold
Christina Y Hung
David H Viskochil
Sarah L Dugan
Pinar Bayrak-Toydemir
Géraldine Joly-Helas
Anne-Marie Guerrot
Caroline Schluth-Bolard
Marlène Rio
Ingrid M Wentzensen
Kirsty McWalter
Rhonda E Schnur
Andrea M Lewis
Seema R Lalani
Noël Mensah-Bonsu
Jocelyn Céraline
Zijie Sun
Rafal Ploski
Carlos A Bacino
Heather C Mefford
Laurence Faivre
Olaf Bodamer
Jamel Chelly
Bertrand Isidor
Seiamak Bahram

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID31879022
PMCPMC7042478

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.