Evidence map›Paper›PMID 34087166›Full record

ArticleAmerican journal of human genetics2021

A form of muscular dystrophy associated with pathogenic variants in JAG2.

Sandra Coppens, Alison M Barnard, Sanna Puusepp, Sander Pajusalu, Katrin Õunap, Dorianmarie Vargas-Franco, Christine C Bruels, Sandra Donkervoort, Lynn Pais, Katherine R Chao and 48 more

Abstract readPublished Erratum
In one paragraph

Article in American journal of human genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Expert panel curation of 31 genes in relation to limb girdle muscular dystrophy.Annals of clinical and translational neurology · 2024
    Article
  3. Article
  4. Article
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

58 authors.

Sandra Coppens
Alison M Barnard
Sanna Puusepp
Sander Pajusalu
Katrin Õunap
Dorianmarie Vargas-Franco
Christine C Bruels
Sandra Donkervoort
Lynn Pais
Katherine R Chao
Julia K Goodrich
Eleina M England
Ben Weisburd
Vijay S Ganesh
Sanna Gudmundsson
Anne O'Donnell-Luria
Mait Nigul
Pilvi Ilves
Payam Mohassel
Teepu Siddique
Margherita Milone
Stefan Nicolau
Reza Maroofian
Henry Houlden
Michael G Hanna
Ros Quinlivan
Mehran Beiraghi Toosi
Ehsan Ghayoor Karimiani
Sabine Costagliola
Nicolas Deconinck
Hazim Kadhim
Erica Macke
Brendan C Lanpher
Eric W Klee
Anna Łusakowska
Anna Kostera-Pruszczyk
Andreas Hahn
Bertold Schrank
Ichizo Nishino
Masashi Ogasawara
Rasha El Sherif
Tanya Stojkovic
Isabelle Nelson
Gisèle Bonne
Enzo Cohen
Anne Boland-Augé
Jean-François Deleuze
Yao Meng
Ana Töpf
Catheline Vilain
Christina A Pacak
Marie L Rivera-Zengotita
Carsten G Bönnemann
Volker Straub
Penny A Handford
Isabelle Draper
Glenn A Walter
Peter B Kang

Funding

Molecular and Clinical Manifestations of Matrix and Aggregate MyopathiesZIANS003129 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI BÖNNEMANN, CARSTEN · 2011 to 2025
$52.8M
Joint Center for Mendelian GenomicsUM1HG008900 · NHGRI · BROAD INSTITUTE, INC. · PI O'DONNELL-LURIA, ANNE, REHM, HEIDI L · 2016 to 2020
$16.5M
Understanding and Improving Therapies for the Muscular Dystrophies through Noninvasive BiomarkersP50AR052646 · NIAMS · UNIVERSITY OF FLORIDA · PI SWEENEY, H LEE · 2021 to 2024
$6.2M
Partners Healthcare Training Program in Precision and Genomic MedicineT32HG010464 · NHGRI · MASSACHUSETTS GENERAL HOSPITAL · PI HEIDI L REHM, JORDAN W SMOLLER · 2019 to 2026
$3.1M
A powerful web-based discovery platform for rare disease geneticsR01HG009141 · NHGRI · BROAD INSTITUTE, INC. · PI QUINLAN, AARON R, REHM, HEIDI L · 2017 to 2020
$2.9M
NHGRI NIH HHS R01 HG009141NHGRI NIH HHS T32 HG010464NHGRI NIH HHS UM1 HG008900NIAMS NIH HHS P50 AR052646
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID34087166
PMCPMC8206378

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.