Gene · 85358
Papers2,252
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
281 to 300 of 2,252
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Identification of Extremely Rare Pathogenic CNVs by Array CGH in Saudi Children with Developmental Delay, Congenital Malformations, and Intellectual Disability. | Children (Basel) | 2023 | 37189911 | PubTator, text mining | PubMed |
| Sleep disturbances in autism spectrum disorder: Animal models, neural mechanisms, and therapeutics. | Neurobiol Sleep Circadian Rhythms | 2023 | 37188242 | PubTator, text mining | PubMed |
| The emerging roles of Shank3 in cardiac function and dysfunction. | Front Cell Dev Biol | 2023 | 37187620 | PubTator, text mining | PubMed |
| Case report: Treatment-resistant depression, multiple trauma exposure and suicidality in an adolescent female with previously undiagnosed Autism Spectrum Disorder. | Front Psychiatry | 2023 | 37181890 | PubTator, text mining | PubMed |
| Functional and phosphoproteomic analysis of β-adrenergic receptor signaling at excitatory synapses in the CA1 region of the ventral hippocampus. | Sci Rep | 2023 | 37161045 | PubTator, text mining | PubMed |
| Gene copy number variation and pediatric mental health/neurodevelopment in a general population. | Hum Mol Genet | 2023 | 37154571 | PubTator, text mining | PubMed |
| Involvement of oxytocin receptor deficiency in psychiatric disorders and behavioral abnormalities. | Front Cell Neurosci | 2023 | 37153633 | PubTator, text mining | PubMed |
| De novo 11q13.3q13.4 deletion in a patient with Fanconi renotubular syndrome and intellectual disability: Case report and review of literature. | Front Pediatr | 2023 | 37152320 | PubTator, text mining | PubMed |
| Neurodevelopmental disorders, like cancer, are connected to impaired chromatin remodelers, PI3K/mTOR, and PAK1-regulated MAPK. | Biophys Rev | 2023 | 37124926 | PubTator, text mining | PubMed |
| Parental perspectives on Phelan-McDermid syndrome: Results of a worldwide survey. | Eur J Med Genet | 2023 | 37120079 | PubTator, text mining | PubMed |
| Consensus recommendations on counselling in Phelan-McDermid syndrome, with special attention to recurrence risk and to ring chromosome 22. | Eur J Med Genet | 2023 | 37120077 | PubTator, text mining | PubMed |
| Magnetic Resonance Imaging in Autism Spectrum Disorders: clinical and neuroradiological phenotypes. | Acta Biomed | 2023 | 37092643 | PubTator, text mining | PubMed |
| Thrombospondin1 mimics rapidly relieve depression via Shank3 dependent uncoupling between dopamine D1 and D2 receptors. | iScience | 2023 | 37091229 | PubTator, text mining | PubMed |
| A clinically relevant selective ERK-pathway inhibitor reverses core deficits in a mouse model of autism. | EBioMedicine | 2023 | 37088035 | PubTator, text mining | PubMed |
| Consensus recommendations on mental health issues in Phelan-McDermid syndrome. | Eur J Med Genet | 2023 | 37085014 | PubTator, text mining | PubMed |
| High-content synaptic phenotyping in human cellular models reveals a role for BET proteins in synapse assembly. | Elife | 2023 | 37083703 | PubTator, text mining | PubMed |
| Editorial: Pain, immunity, and neurological and autoimmune disorders. | Front Immunol | 2023 | 37081877 | PubTator, text mining | PubMed |
| Axin2 coupled excessive Wnt-glycolysis signaling mediates social defect in autism spectrum disorders. | EMBO Mol Med | 2023 | 37078424 | PubTator, text mining | PubMed |
| Pathology and Astrocytes in Autism. | Neuropsychiatr Dis Treat | 2023 | 37077706 | PubTator, text mining | PubMed |
| Consensus recommendations on lymphedema in Phelan-McDermid syndrome. | Eur J Med Genet | 2023 | 37075886 | PubTator, text mining | PubMed |
gene-search-2026-11-11-0.2.0
Sources 12
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
- GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
- HGNCCC0
- NCBI GenePublic domain (US government)
- NIH's project files and grant-paper linksPublic domain
- Open TargetsCC0 1.0
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
- GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
- HGNCCC0: https://www.genenames.org/about/license/
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
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GET https://conductscience.org/api/genes/v1/85358/papers?page=15