Evidence map›Paper›PMID 28235191›Full record

ArticleCell2017

Mutational Processes Shaping the Genome in Early Human Embryos.

Thierry Voet, Joris R Vermeesch

Open access · bronzeAbstract readComment
PubMed Publisher
In one paragraph

Article in Cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

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

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 2 countries.

Thierry VoetDepartment of Human Genetics, University of Leuven, KU Leuven, Herestraat 49, 3000 Leuven, Belgium; Wellcome Trust Sanger Institute, Hinxton CB10 1SA, UK. Electronic address: thierry.voet@kuleuven.be.
Joris R VermeeschDepartment of Human Genetics, University of Leuven, KU Leuven, Herestraat 49, 3000 Leuven, Belgium. Electronic address: joris.vermeesch@kuleuven.be.
KU Leuven · BEWellcome Sanger Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In-vitro-fertilized human embryos often acquire large structural and numerical chromosomal abnormalities. Liu et al. now show that multiple smaller copy number variations may also arise in in-vivo-conceived embryos. Analysis of these variations provides insight into the DNA mutational processes occurring in early embryos and the mechanisms underlying them.

Indexed as

DNA Copy Number VariationsFertilization in VitroChromosome AberrationsGenomeHumansMutation

Identifiers

PMID28235191
OpenAlexW2591791065

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.