Evidence map›Paper›PMID 34782469›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

De novo germline mutation in the dual specificity phosphatase 10 gene accelerates autoimmune diabetes.

Anne-Perrine Foray, Sophie Candon, Sara Hildebrand, Cindy Marquet, Fabrice Valette, Coralie Pecquet, Sebastien Lemoine, Francina Langa-Vives, Michael Dumas, Peipei Hu and 12 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. MAP kinase phosphatases in metabolic diseases.Trends in endocrinology and metabolism: TEM · 2026
    Review
  2. Review
  3. Article
  4. Applications of Genome-Editing Technologies for Type 1 Diabetes.International journal of molecular sciences · 2023
    Review
  5. Article
  6. Review
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

22 authors at 4 institutions in 5 countries.

Anne-Perrine ForayInstitut Necker-Enfants Malades, Université de Paris, 75015 Paris, France.
Sophie CandonInstitut Necker-Enfants Malades, Université de Paris, 75015 Paris, France.
Sara HildebrandCenter for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Cindy MarquetInstitut Necker-Enfants Malades, Université de Paris, 75015 Paris, France.
Fabrice ValetteInstitut Necker-Enfants Malades, Université de Paris, 75015 Paris, France.
Coralie PecquetInstitut Necker-Enfants Malades, Université de Paris, 75015 Paris, France.
Sebastien LemoineInstitut Necker-Enfants Malades, Université de Paris, 75015 Paris, France.
Francina Langa-VivesMouse Genetics Engineering Center, Institut Pasteur, 75724 Paris, France.
Michael DumasCNRS UMR7242, Biotechnology and Cell Signaling, University of Strasbourg, 67412 Illkirch Cedex, France.
Peipei HuInstitut Necker-Enfants Malades, Université de Paris, 75015 Paris, France.
Pere SantamariaJulia McFarlane Diabetes Research Centre, Department of Microbiology, Immunology, and Infectious Diseases, Snyder Institute for Chronic Diseases and Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary AB T2N 4N1, Canada.
Sylvaine YouInstitut Necker-Enfants Malades, Université de Paris, 75015 Paris, France.
Stephen LyonCenter for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0002-6198-3827
Lindsay ScottCenter for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0003-4243-4010
Chun Hui BuCenter for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Tao WangCenter for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, TX 75390.
Darui XuCenter for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0003-1117-966X
Eva Marie Y MorescoCenter for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, TX 75390.ORCID 0000-0002-2049-7291
Claudio ScazzocchioSection of Microbiology, Department of Infectious Diseases, Imperial College London, London SW7 2AZ, United Kingdom.ORCID 0000-0001-8800-2534
Jean-François BachInstitut Necker-Enfants Malades, Université de Paris, 75015 Paris, France; jean-francois.bach@academie-sciences.fr Bruce.Beutler@UTSouthwestern.edu lucienne.chatenoud@inserm.fr.
Bruce BeutlerCenter for the Genetics of Host Defense, University of Texas Southwestern Medical Center, Dallas, TX 75390; jean-francois.bach@academie-sciences.fr Bruce.Beutler@UTSouthwestern.edu lucienne.chatenoud@inserm.fr.ORCID 0000-0002-3639-246X
Lucienne ChatenoudInstitut Necker-Enfants Malades, Université de Paris, 75015 Paris, France; jean-francois.bach@academie-sciences.fr Bruce.Beutler@UTSouthwestern.edu lucienne.chatenoud@inserm.fr.
Centre National de la Recherche Scientifique · FRThe University of Texas Southwestern Medical Center · USGeneralitat de Catalunya · ESInstitut Pasteur · FR

Funding

Systems Biology CoreU19AI100627 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI ULEVITCH, RICHARD J · 2012 to 2021
$49.1M
Automated Forward Genetic Analysis of Adaptive ImmunityR01AI125581 · NIAID · UT SOUTHWESTERN MEDICAL CENTER · PI BRUCE A BEUTLER · 2016 to 2026
$19.5M
NIAID NIH HHS R01 AI125581NIAID NIH HHS U19 AI100627
6 · The paper itself

Abstract

Insulin-dependent or type 1 diabetes (T1D) is a polygenic autoimmune disease. In humans, more than 60 loci carrying common variants that confer disease susceptibility have been identified by genome-wide association studies, with a low individual risk contribution for most variants excepting those of the major histocompatibility complex (MHC) region (40 to 50% of risk); hence the importance of missing heritability due in part to rare variants. Nonobese diabetic (NOD) mice recapitulate major features of the human disease including genetic aspects with a key role for the MHC haplotype and a series of

Indexed as

Germ-Line MutationAnimalsAutoimmune DiseasesDiabetes Mellitus, Type 1Dual-Specificity PhosphatasesFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHaplotypesHumansIslets of LangerhansMajor Histocompatibility ComplexMaleMiceMice, Inbred C57BLMice, Inbred NODDual-Specificity PhosphatasesDUSP10 protein, humanMitogen-Activated Protein Kinase Phosphatasesautoimmunitygenetic mappingNOD mousetype 1 diabetes

Identifiers

PMID34782469
PMCPMC8617500
OpenAlexW3212775966

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.