Evidence map›Paper›PMID 31980075›Full record

ArticleKidney international2020

Next-generation sequencing for detection of somatic mosaicism in autosomal dominant polycystic kidney disease.

Olivier Devuyst, York Pei

Abstract readComment
PubMed Publisher
In one paragraph

Article in Kidney international, 2020. 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
1.3field-weighted citation impact, top 20% 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, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Monogenic Kidney Diseases in Kidney Transplantation.Kidney international reports · 2024
    Review
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 2 institutions in 3 countries.

Olivier DevuystDepartment of Physiology, Mechanisms of Inherited Kidney Diseases Group, University of Zurich, Zurich, Switzerland; Division of Nephrology, UCLouvain Medical School, Brussels, Belgium. Electronic address: olivier.devuyst@uzh.ch.
York PeiDivision of Nephrology, University Health Network, Toronto, Ontario, Canada; Division of Nephrology, University of Toronto, Toronto, Ontario, Canada. Electronic address: york.pei@uhn.ca.
University Health Network · CAUniversity of Zurich · CH

Funding

CIHR
6 · The paper itself

Abstract

Mosaicism is defined as the presence of 2 genetically different populations of cells in a single organism, resulting from a mutation during early embryogenesis. Hopp et al. characterized mosaicism in 20 unresolved ADPKD families, using next-generation sequencing techniques with DNA isolated from blood cells. Mosaicism may be involved in 1% of ADPKD families, and it may explain some atypical disease phenotypes.

Indexed as

Polycystic Kidney, Autosomal DominantHigh-Throughput Nucleotide SequencingHumansMosaicismMutationTRPP Cation ChannelsTRPP Cation Channels

Identifiers

PMID31980075
OpenAlexW3002539520

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.