NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder-Reference-Cited by-同舟云学术

NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder

Published:2018-07-10 Issue:2 Volume:94 Page:264-268
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Lévy J.¹²^ORCID,Grotto S.¹,Mignot C.³⁴,Maruani A.⁵⁶,Delahaye-Duriez A.²⁷⁸,Benzacken B.²⁷,Keren B.³,Haye D.³,Xavier J.⁹,Heulin M.¹⁰,Charles E.¹⁰,Verloes A.¹²^ORCID,Dupont C.¹,Pipiras E.²⁷,Tabet A.-C.¹⁶^ORCID

Affiliation:

1. Genetics Department, AP-HP; Robert-Debré University Hospital; Paris France

2. INSERM UMR1141, Paris Diderot University, AP-HP, Robert-Debré Hospital; Paris France

3. Genetics Department, AP-HP; Pitié-Salpêtrière Hospital; Paris France

4. Centre de Référence Déficience Intellectuelle de Causes Rares; GRC Université Pierre et Marie Curie « Déficience Intellectuelle et Autisme », Pitié-Salpêtrière Hospital; Paris France

5. Child and Adolescent Psychiatry Department; Robert-Debré Hospital, AP-HP; Paris France

6. Neuroscience Department, Génétique Humaine et Fonction Cognitive Unit; Pasteur Institute; Paris France

7. Department of Cytogenetics, Jean-Verdier Hospital; Paris 13 University, Embryology and Histology, AP-HP; Bondy France

8. Division of Brain Sciences; Imperial College Faculty of Medicine; London

9. Department of Child and Adolescent Psychiatry; Pitié-Salpêtrière Hospital, AP-HP; Paris France

10. Unité de Diagnostic et d'Evaluation Pluriprofessionnelle de l'autisme et des troubles apparentés, Etablissement publique de santé de Ville-Evrard; Neuilly Sur Marne France

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.13383/fullpdf

Reference16 articles.

1. Structure and function of Nurr1 identifies a class of ligand-independent nuclear receptors;Wang;Nature,2003

2. Nuclear receptor 4A (NR4A) family - orphans no more;Safe;J Steroid Biochem Mol Biol,2016

3. The role of Nurr1 in the development of dopaminergic neurons and Parkinson's disease;Jankovic;Prog Neurobiol,2005

4. Intellectual disability and hemizygous GPD2 mutation;Barge-Schaapveld;Am J Med Genet A,2013

5. Rare inherited and de novo CNVs reveal complex contributions to ASD risk in multiplex families;Leppa;Am J Hum Genet,2016

Cited by 25 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The NR4A2/VGF pathway fuels inflammation-induced neurodegeneration via promoting neuronal glycolysis;Journal of Clinical Investigation;2024-06-18

2. NR4A2 as a Novel Target Gene for Developmental and Epileptic Encephalopathy: A Systematic Review of Related Disorders and Therapeutic Strategies;International Journal of Molecular Sciences;2024-05-10

3. Albiflorin ameliorates thioacetamide-induced hepatic fibrosis: The involvement of NURR1-mediated inflammatory signaling cascades in hepatic stellate cells activation;Ecotoxicology and Environmental Safety;2024-05

4. lncRNA Sequencing Reveals Neurodegeneration-Associated FUS Mutations Alter Transcriptional Landscape of iPS Cells That Persists in Motor Neurons;Cells;2023-10-16

5. Genome-wide DNA methylation analysis in families with multiple individuals diagnosed with schizophrenia and intellectual disability;The World Journal of Biological Psychiatry;2023-04-18