Gene · 9378
Papers2,134
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
81 to 100 of 2,134
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Phenotypic complexities of rare heterozygous neurexin-1 deletions. | Nature | 2025 | 40205044 | PubTator, text mining | PubMed |
| Evaluación de siete programas bioinformáticos para el análisis terciario de datos genómicos generados a partir de la secuenciación del exoma completo en un grupo piloto de pacientes. | Adv Lab Med | 2025 | 40160392 | PubTator, text mining | PubMed |
| A review of antipsychotic therapy effectiveness and tolerability among individuals with copy number variants relevant to schizophrenia. | Psychiatr Genet | 2025 | 40145886 | PubTator, text mining | PubMed |
| Identification and characterization of mitochondrial autophagy-related genes in osteosarcoma and predicting clinical prognosis. | Sci Rep | 2025 | 40128298 | PubTator, text mining | PubMed |
| Clinical phenotypic spectrum of NRXN1 microdeletions and their association with epilepsy: A systematic review and meta-analysis. | Epilepsia | 2025 | 40126490 | PubTator, text mining | PubMed |
| Evolutionary constrained genes associated with autism spectrum disorder across 2,054 nonhuman primate genomes. | Mol Autism | 2025 | 39849619 | PubTator, text mining | PubMed |
| Integrating genetics and transcriptomics to characterize shared mechanisms in digestive diseases and psychiatric disorders. | Commun Biol | 2025 | 39809838 | PubTator, text mining | PubMed |
| Uncovering potential causal genes for undiagnosed congenital anomalies using an in-house pipeline for trio-based whole-genome sequencing. | Hum Genomics | 2025 | 39762984 | PubTator, text mining | PubMed |
| Neuron-like lineage differentiation induced by exogenous Neurexin-1 as a potential therapeutic strategy for glioma. | Cancer Lett | 2025 | 39657829 | PubTator, text mining | PubMed |
| Neurexin1 level in Huntington's Disease and decreased Neurexin1 in disease progression. | Neurosci Res | 2025 | 39481547 | PubTator, text mining | PubMed |
| Bi-allelic NRXN1α deletion in microglia derived from iPSC of an autistic patient increases interleukin-6 production and impairs supporting function on neuronal networking. | Brain Behav Immun | 2025 | 39243986 | PubTator, text mining | PubMed |
| Multiomic analysis reveals cellular, transcriptomic and epigenetic changes in intestinal pouches of ulcerative colitis patients. | medRxiv | 2025 | 38014192 | PubTator, text mining | PubMed |
| SOX7: Autism Associated Gene Identified by Analysis of Multi-Omics Data. | bioRxiv | 2025 | 37292933 | PubTator, text mining | PubMed |
| Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology. | NPJ Genom Med | 2024 | 39695155 | PubTator, text mining | PubMed |
| NRXN1-related disorders, attempt to better define clinical assessment. | Open Med (Wars) | 2024 | 39655047 | PubTator, text mining | PubMed |
| NRXN1 as a Prognostic Biomarker: Linking Copy Number Variation to EMT and Survival in Colon Cancer. | Int J Mol Sci | 2024 | 39518976 | PubTator, text mining | PubMed |
| SNAP25-induced MYC upregulation promotes high-grade neuroendocrine lung carcinoma progression. | Front Immunol | 2024 | 39430761 | PubTator, text mining | PubMed |
| starTracer is an accelerated approach for precise marker gene identification in single-cell RNA-Seq analysis. | Commun Biol | 2024 | 39266658 | PubTator, text mining | PubMed |
| scTab: Scaling cross-tissue single-cell annotation models. | Nat Commun | 2024 | 39098889 | PubTator, text mining | PubMed |
| Beneath HMGA2 alterations in pleomorphic adenomas: Pathological, immunohistochemical, and molecular insights. | Hum Pathol | 2024 | 39089476 | 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/v1/9378/papers?page=5