Gene · 55636
Papers2,784
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
161 to 180 of 2,784
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Systematic Ultrasound Evaluation of Olfactory Sulci in Fetuses with Congenital Heart Defects: A Clue for CHARGE Syndrome Diagnosis. | Fetal Diagn Ther | 2025 | 39809240 | PubTator, text mining | PubMed |
| Genetic landscape in undiagnosed patients with syndromic hearing loss revealed by whole exome sequencing and phenotype similarity search. | Hum Genet | 2025 | 39755840 | PubTator, text mining | PubMed |
| Novel insights into cuproptosis in alcoholic liver disease using bioinformatics analysis and experimental validation. | Int Immunopharmacol | 2025 | 39709914 | PubTator, text mining | PubMed |
| Autosomally dominantly inherited isolated gonadotropin deficiency via maternal assisted reproduction due to SOX10 mutation. | J Pediatr Endocrinol Metab | 2025 | 39680495 | PubTator, text mining | PubMed |
| Let-7c-5p Targeting CHD7 Hinders Cervical Cancer Migration and Invasion by Regulating Cell Adhesion. | Biochem Genet | 2025 | 39680330 | PubTator, text mining | PubMed |
| Whole-genome sequencing analysis of Japanese autism spectrum disorder trios. | Psychiatry Clin Neurosci | 2025 | 39610113 | PubTator, text mining | PubMed |
| Deciphering HMGB1: Across a spectrum of DNA and nucleosome dynamics. | Cell Biol Int | 2025 | 39551968 | PubTator, text mining | PubMed |
| Genetic burden in neonatal and pediatric-onset pulmonary hypertension: A single-center retrospective study using exome sequencing in a Chinese population. | Pediatr Neonatol | 2025 | 39542781 | PubTator, text mining | PubMed |
COMPREHENSIVE CHARACTERIZATION OF CYTOKINES IN PATIENTS UNDER EXTRACORPOREAL MEMBRANE OXYGENATION: EVIDENCE FROM INTEGRATED BULK AND SINGLE-CELL RNA SEQUENCING DATA USING MULTIPLE MACHINE LEARNING APPROACHES. | Shock | 2025 | 39503329 | PubTator, text mining | PubMed |
| A Novel Cuproptosis-Related Gene Signature Predicts Prognosis in Papillary Thyroid Carcinoma Patients. | Comb Chem High Throughput Screen | 2025 | 39253931 | PubTator, text mining | PubMed |
| Genetic Variants Can Predict the Outcome of Brace Treatment in Patients With Adolescent Idiopathic Scoliosis. | Spine (Phila Pa 1976) | 2025 | 39206768 | PubTator, text mining | PubMed |
| Kismet/CHD7/CHD8 affects gut microbiota, mechanics, and the gut-brain axis in Drosophila melanogaster. | Biophys J | 2025 | 38902926 | PubTator, text mining | PubMed |
| Genetic analysis of congenital unilateral renal agenesis in children based on next-generation sequencing. | Pediatr Res | 2025 | 38849481 | PubTator, text mining | PubMed |
| Cuproptosis-related Gene Signatures and Immunological Characterization in Sepsis-associated Acute Lung Injury. | Comb Chem High Throughput Screen | 2025 | 38779731 | PubTator, text mining | PubMed |
| Hybrid peripheral nerve sheath tumours - A Review. | J Oral Maxillofac Pathol | 2024 | 39949689 | PubTator, text mining | PubMed |
| Identification of Cuproptosis-Related Patterns Predict Prognosis and Immunotherapy Response in Hepatocellular Carcinoma. | J Cell Mol Med | 2024 | 39663596 | PubTator, text mining | PubMed |
| A case report of CHARGE syndrome caused by a de novo CHD7 gene mutation. | SAGE Open Med Case Rep | 2024 | 39618705 | PubTator, text mining | PubMed |
| Kallmann Syndrome: Functional Analysis of a CHD7 Missense Variant Shows Aberrant RNA Splicing. | Int J Mol Sci | 2024 | 39596130 | PubTator, text mining | PubMed |
| [CHARGE syndrome in a neonate]. | Zhongguo Dang Dai Er Ke Za Zhi | 2024 | 39587755 | PubTator, text mining | PubMed |
| Analysis of TRIOBP gene in non-syndromic deafness: A case report. | Medicine (Baltimore) | 2024 | 39533558 | 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/v1/55636/papers?page=9