Evidence map›Paper›PMID 32397577›Full record

ArticleHigh-throughput2020

Genetic Counseling and NGS Screening for Recessive LGMD2A Families.

Claudia Strafella, Valerio Caputo, Giulia Campoli, Rosaria Maria Galota, Julia Mela, Stefania Zampatti, Giulietta Minozzi, Cristina Sancricca, Serenella Servidei, Emiliano Giardina and 1 more

Open access · goldAbstract read
In one paragraph

Article in High-throughput, 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
0.2field-weighted citation impact, top 51% 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, 3 citations in OpenAlex.

  1. Limb-girdle muscular dystrophy in pregnancy: a narrative review.Archives of gynecology and obstetrics · 2024
    Review
  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

11 authors at 5 institutions in 2 countries.

Claudia StrafellaGenomic Medicine Laboratory UILDM, Santa Lucia Foundation, 00179 Rome, Italy.
Valerio CaputoGenomic Medicine Laboratory UILDM, Santa Lucia Foundation, 00179 Rome, Italy.
Giulia CampoliGenomic Medicine Laboratory UILDM, Santa Lucia Foundation, 00179 Rome, Italy.
Rosaria Maria GalotaGenomic Medicine Laboratory UILDM, Santa Lucia Foundation, 00179 Rome, Italy.
Julia MelaGenomic Medicine Laboratory UILDM, Santa Lucia Foundation, 00179 Rome, Italy.
Stefania ZampattiGenomic Medicine Laboratory UILDM, Santa Lucia Foundation, 00179 Rome, Italy.
Giulietta MinozziDepartment of Veterinary Medicine, University of Milan, 20133 Milan, Italy.
Cristina SancriccaFondazione Policlinico Universitario A. Gemelli IRCCS, UOC Neurofisiopatologia, 00168 Rome, Italy.
Serenella ServideiFondazione Policlinico Universitario A. Gemelli IRCCS, UOC Neurofisiopatologia, 00168 Rome, Italy.
Emiliano GiardinaGenomic Medicine Laboratory UILDM, Santa Lucia Foundation, 00179 Rome, Italy.
Raffaella CascellaGenomic Medicine Laboratory UILDM, Santa Lucia Foundation, 00179 Rome, Italy.
Fondazione Santa Lucia · ITUniversity of Rome Tor Vergata · ITAgostino Gemelli University Polyclinic · ITCatholic University Our Lady of Good Counsel · ALUniversity of Milan · IT

Funding

Italian Ministry of Health 5X1000-2016 and 5x2017 MINSAL.3
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

CAPN3data analysisfamily historygenetic counselingLGMD2Anext-generation sequencingrecurrence/reproductive risk

Identifiers

PMID32397577
PMCPMC7349198
OpenAlexW3023637597

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.