Evidence map›Paper›PMID 29388939›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2018

Correction: Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases.

Kelly D Farwell Hagman, Deepali N Shinde, Cameron Mroske, Erica Smith, Kelly Radtke, Layla Shahmirzadi, Dima El-Khechen, Zöe Powis, Elizabeth C Chao, Wendy A Alcaraz and 9 more

Abstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Kelly D Farwell HagmanDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA. kfarwell@ambrygen.com.
Deepali N ShindeDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Cameron MroskeDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Erica SmithDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Kelly RadtkeDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Layla ShahmirzadiDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Dima El-KhechenDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Zöe PowisDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Elizabeth C ChaoDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Wendy A AlcarazDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Katherine L HelbigDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Samin A SajanDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Mari RossiDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Hsiao-Mei LuDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Robert HuetherDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Shuwei LiDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Sitao WuDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.
Mark E NuñesDepartment of Genetics, Kaiser Permanente, San Diego, California, USA.
Sha TangDepartment of Clinical Genomics, Ambry Genetics, Aliso Viejo, California, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the published version of this paper, some of the columns in the last three rows of Table 3 were mistakenly transposed. The corrected table appears below. In col. 6 of the row for DNMT3A, "S3" was published in the original article. However, in the revised table for the corrigendum, it has been corrected to "S1". In col. 6 of the row for SON, "S3" was published in the original article. However, in the revised table for the corrigendum, it has been corrected to "S2".

Identifiers

PMID29388939
PMCPMC7608241

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.