Evidence map›Paper›PMID 33598243›Full record

ArticleClinical case reports2021

Prenatal characterization of a novel inverted

Cinthya J Zepeda-Mendoza, Anna Essendrup, Stephanie A Smoley, Sarah H Johnson, Nicole L Hoppman, George Vasmatzis, Daniel L Jackson, Hutton M Kearney, Linda B Baughn

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2021. 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
0.2field-weighted citation impact, top 37% 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, 2 citations in OpenAlex.

  1. Article
  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

9 authors at 3 institutions in 1 country.

Cinthya J Zepeda-MendozaCytogenetics and Genomic Microarray Laboratory ARUP Laboratories Salt Lake City UT USA.ORCID https://orcid.org/0000-0002-0434-4965
Anna EssendrupDivision of Laboratory Genetics Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester MN USA.
Stephanie A SmoleyDivision of Laboratory Genetics Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester MN USA.
Sarah H JohnsonCenter for Individualized Medicine-Biomarker Discovery, Mayo Clinic Rochester MN USA.
Nicole L HoppmanDivision of Laboratory Genetics Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester MN USA.
George VasmatzisCenter for Individualized Medicine-Biomarker Discovery, Mayo Clinic Rochester MN USA.
Daniel L JacksonDepartment of Obstetrics, Gynecology and Women's Health University of Missouri Health Columbia MO USA.
Hutton M KearneyDivision of Laboratory Genetics Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester MN USA.
Linda B BaughnDivision of Laboratory Genetics Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester MN USA.
Mayo Clinic · USARUP Laboratories (United States) · USUniversity of Missouri Health System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This case report underlines the importance of molecular characterization of genomic duplications and other structural variants in the prenatal setting to guide clinical interpretation, genetic counseling, and perinatal medical care.

Indexed as

dextrocardiaduplicationheterotaxymate pairSMAD2

Identifiers

PMID33598243
PMCPMC7869371
OpenAlexW3112323019

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.