Evidence map›Paper›PMID 33382938›Full record

ArticleThe New England journal of medicine2020

Causal Genetic Variants in Stillbirth. Reply.

Kate E Stanley, Ronald J Wapner, David B Goldstein

Abstract readLetterComment
PubMed Publisher
In one paragraph

Article in The New England journal of medicine, 2020. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Essential genes: a cross-species perspective.Mammalian genome : official journal of the International Mammalian Genome Society · 2023
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Kate E StanleyColumbia University Vagelos College of Physicians and Surgeons, New York, NY rw2191@cumc.columbia.edu.
Ronald J WapnerColumbia University Vagelos College of Physicians and Surgeons, New York, NY rw2191@cumc.columbia.edu.
David B GoldsteinColumbia University Vagelos College of Physicians and Surgeons, New York, NY rw2191@cumc.columbia.edu.

Funding

Prenatal Genetic Diagnosis by Genomic Sequencing: A Prospective EvaluationR01HD055651 · NICHD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Wendy K Chung, Vaidehi Jobanputra · 2007 to 2026
$16.5M
NICHD NIH HHS R01 HD055651
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

StillbirthCausalityFemaleHumansPregnancy

Identifiers

PMID33382938

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.