Evidence map›Paper›PMID 19169714›Full record

ArticlePediatric nephrology (Berlin, Germany)2009

Detection by multiplex ligation-dependent probe amplification of large deletion mutations in the COL4A5 gene in female patients with Alport syndrome.

Kandai Nozu, Rafal Przybyslaw Krol, Koichi Nakanishi, Norishige Yoshikawa, Yoshimi Nozu, Yasufumi Ohtsuka, Kazumoto Iijima, Masafumi Matsuo

Abstract readLetter
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2009. 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
0.4field-weighted citation impact, top 41% 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, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Recurrent deep intronic mutations in the SLC12A3 gene responsible for Gitelman's syndrome.Clinical journal of the American Society of Nephrology : CJASN · 2011
    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

8 authors at 3 institutions in 1 country.

Kandai Nozu
Rafal Przybyslaw Krol
Koichi Nakanishi
Norishige Yoshikawa
Yoshimi Nozu
Yasufumi Ohtsuka
Kazumoto Iijima
Masafumi Matsuo
Kobe University · JPWakayama Medical University · JPSaga Medical School Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Gene DeletionCollagen Type IVFemaleHumansMolecular Diagnostic TechniquesNephritis, HereditaryNucleic Acid Amplification TechniquesCOL4A5 protein, humanCollagen Type IV

Identifiers

PMID19169714
OpenAlexW1970949504

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.