Evidence map›Paper›PMID 33412162›Full record

ArticleKidney international2021

Rho-GTPase Activating Protein myosin MYO9A identified as a novel candidate gene for monogenic focal segmental glomerulosclerosis.

Qi Li, Ashima Gulati, Mathieu Lemaire, Timothy Nottoli, Allen Bale, Alda Tufro

Open access · bronzeAbstract read
In one paragraph

Article in Kidney international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
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  5. The CaPediatric nephrology (Berlin, Germany) · 2025
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  7. Article
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  9. Cytoskeleton Rearrangement in Podocytopathies: An Update.International journal of molecular sciences · 2024
    Review
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  11. Store-operated CaExperimental biology and medicine (Maywood, N.J.) · 2023
    Review
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  17. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Qi LiDepartment of Pediatrics, Nephrology Section, Yale School of Medicine, New Haven, Connecticut, USA.
Ashima GulatiDepartment of Internal Medicine, Nephrology Section, Yale School of Medicine, New Haven, Connecticut, USA.
Mathieu LemaireDepartment of Genetics, Yale School of Medicine, New Haven, Connecticut, USA.
Timothy NottoliYale Gene Editing Center, Yale School of Medicine, New Haven, Connecticut, USA.
Allen BaleDepartment of Genetics, Yale School of Medicine, New Haven, Connecticut, USA.
Alda TufroDepartment of Pediatrics, Nephrology Section, Yale School of Medicine, New Haven, Connecticut, USA; Department of Cell and Molecular Physiology, Yale School of Medicine, New Haven, Connecticut, USA. Electronic address: alda.tufro@yale.edu.
Yale University · USYale Cancer Center · US

Funding

Yale Center for Mendelian DisordersU54HG006504 · NHGRI · YALE UNIVERSITY · PI GERSTEIN, MARK BENDER, GUNEL, MURAT · 2012 to 2015
$11.0M
Molecular characterization of a novel cause of human FSGSR01DK109434 · NIDDK · YALE UNIVERSITY · PI TUFRO, ALDA · 2017 to 2020
$2.0M
NHGRI NIH HHS U54 HG006504NIDDK NIH HHS R01 DK109434
6 · The paper itself

Abstract

Focal segmental glomerulosclerosis (FSGS) is a podocytopathy leading to kidney failure, whose molecular cause frequently remains unresolved. Here, we describe a rare MYO9A loss of function nonsense heterozygous mutation (p.Arg701

Indexed as

Glomerulosclerosis, Focal SegmentalPodocytesAnimalsGTPase-Activating ProteinsHumansMiceMyosinsPhenotypeGTPase-Activating ProteinsMYO9A protein, humanMyosinsFSGSMyo9A-actin-calmodulin interactionMYO9A variantsRhoA activity

Identifiers

PMID33412162
PMCPMC8076076
OpenAlexW3120676362

What OpenQuestion holds

Textmetadata
LicenceTDM
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.