Evidence map›Paper›PMID 31645981›Full record

ArticleHuman genome variation2019

A novel

Yuji Nakamura, Yusuke Okuno, Hideki Muramatsu, Tomoko Kawai, Kazuhito Satou, Daisuke Ieda, Ikumi Hori, Kei Ohashi, Yutaka Negishi, Ayako Hattori and 3 more

Abstract read
In one paragraph

Article in Human genome variation, 2019. 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
–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

5 citing papers in PubMed.

  1. Article
  2. Case Report: Cabezas syndrome caused byFrontiers in neuroscience · 2025
    Article
  3. Article
  4. Article
  5. CUL4The American journal of pathology · 2021
    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

13 authors.

Yuji Nakamura1Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Yusuke Okuno2Center for Advanced Medicine and Clinical Research, Nagoya University Hospital, Nagoya, Japan.ORCID 0000-0003-3139-9272
Hideki Muramatsu3Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Tomoko Kawai4Department of Maternal-Fetal Biology, National Research Institute for Child Health and Development, Tokyo, Japan.ORCID 0000-0001-8137-0334
Kazuhito Satou5Department of Genome Medicine, National Research Institute for Child Health and Development, Tokyo, Japan.
Daisuke Ieda1Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Ikumi Hori1Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID 0000-0003-4481-0673
Kei Ohashi1Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Yutaka Negishi1Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Ayako Hattori1Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
Yoshiyuki Takahashi3Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Seiji Kojima3Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Shinji Saitoh1Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.ORCID 0000-0001-6911-3351

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients with variants in

Indexed as

Genetics researchOutcomes research

Identifiers

PMID31645981
PMCPMC6804535

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.