Human genomics: A deep dive into genetic variation.

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.

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.

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

1. Evidence for penetrance in patients without a family history of disease: a systematic review.European journal of human genetics : EJHG · 2020
   Pooled it
2. Dilated cardiomyopathy.Nature reviews. Disease primers · 2019
   Review
3. Effects of allelic variations in the human myxovirus resistance protein A on its antiviral activity.The Journal of biological chemistry · 2018
   Article
4. A Novel STAT3 Gene Mutation Related Hyper-IgE Syndrome Misdiagnosed as Hidradenitis Suppurativa.Case reports in immunology · 2018
   Article
5. New insights into the generation and role of de novo mutations in health and disease.Genome biology · 2016
   Review

Corrections and comments

• Comment on
  Analysis of protein-coding genetic variation in 60,706 humans.2016

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as