Evidence map›Paper›PMID 31645982›Full record

ArticleHuman genome variation2019

Novel

Yaeko Ichikawa, Masaki Tanaka, Eriko Kurita, Masanori Nakajima, Masaki Tanaka, Chizuko Oishi, Jun Goto, Shoji Tsuji, Atsuro Chiba

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Primary Familial Brain Calcification WithJournal of clinical neurology (Seoul, Korea) · 2024
    Article
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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

9 authors at 3 institutions in 1 country.

Yaeko Ichikawa1Department of Neurology, Kyorin University School of Medicine, Tokyo, Japan.
Masaki Tanaka2Department of Neurology, The University of Tokyo Hospital, Tokyo, Japan.
Eriko Kurita1Department of Neurology, Kyorin University School of Medicine, Tokyo, Japan.
Masanori Nakajima1Department of Neurology, Kyorin University School of Medicine, Tokyo, Japan.
Masaki Tanaka1Department of Neurology, Kyorin University School of Medicine, Tokyo, Japan.
Chizuko Oishi1Department of Neurology, Kyorin University School of Medicine, Tokyo, Japan.
Jun Goto4Department of Neurology, International University of Health and Welfare Mita Hospital, Tokyo, Japan.
Shoji Tsuji2Department of Neurology, The University of Tokyo Hospital, Tokyo, Japan.ORCID 0000-0001-5602-5686
Atsuro Chiba1Department of Neurology, Kyorin University School of Medicine, Tokyo, Japan.
Kyorin University · JPMita Hospital · JPUniversity of Tokyo Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic basal ganglia calcification-1 (IBGC1) is an autosomal dominant disorder characterized by calcification in the basal ganglia, which can manifest a range of neuropsychiatric symptoms, including parkinsonism. We herein describe a 64-year-old Japanese IBGC1 patient with bilateral basal ganglia calcification carrying a novel

Indexed as

Medical geneticsNeurological disorders

Identifiers

PMID31645982
PMCPMC6804589
OpenAlexW2971944684

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.