Evidence map›Paper›PMID 31645974›Full record

ArticleHuman genome variation2019

Diamond-Blackfan anemia caused by chromosome 1p22 deletion encompassing

Makiko Tominaga, Satoshi Hamanoue, Hiroaki Goto, Toshiyuki Saito, Jun-Ichi Nagai, Mitsuo Masuno, You Umeda, Kenji Kurosawa

Open access · goldAbstract read
PubMed Full text at PMC Publisher
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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. 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.

Makiko Tominaga1Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
Satoshi Hamanoue3Division of Hematology and Oncology, Kanagawa Children's Medical Center, Yokohama, Japan.
Hiroaki Goto3Division of Hematology and Oncology, Kanagawa Children's Medical Center, Yokohama, Japan.
Toshiyuki Saito4Department of Clinical Laboratory, Kanagawa Children's Medical Center, Yokohama, Japan.
Jun-Ichi Nagai4Department of Clinical Laboratory, Kanagawa Children's Medical Center, Yokohama, Japan.
Mitsuo Masuno5Genetic Counseling Program, Kawasaki University of Medical Welfare, Kurashiki, Japan.
You Umeda2Children's Medical Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Kenji Kurosawa1Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.ORCID 0000-0002-6817-7748
Kanagawa Children's Medical Center · JPShowa University Northern Yokohama Hospital · JPKawasaki University of Medical Welfare · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diamond-Blackfan anemia (DBA) is an inherited anemia with multiple congenital malformations, and mutations in ribosomal protein genes have been identified as the underlying cause. We describe a female patient with mild DBA due to 1p22 deletion, encompassing the gene encoding 60S ribosomal protein L5 (

Indexed as

AnaemiaGenetics research

Identifiers

PMID31645974
PMCPMC6804687
OpenAlexW2964947101

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.