Gene · 6710
Papers1,578
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1 to 20 of 1,578
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Clinical characteristics, genotype-phenotype correlation, and prognostic follow-up of 48 Chinese children with hereditary spherocytosis. | Front Med (Lausanne) | 2026 | 42819045 | PubTator, text mining | PubMed |
| Case Report: A research on a case of hereditary spherocytosis with idiopathic pulmonary hemosiderosis. | Front Pediatr | 2026 | 42558654 | PubTator, text mining | PubMed |
| Decoding the Ektacytometric Landscape of Hereditary Spherocytosis: Insights from 204 Cases. | Diagnostics (Basel) | 2026 | 42510120 | PubTator, text mining | PubMed |
| Identification of a novel hereditary spherocytosis gene mutation in a Chinese child with α-globin gene triplication. | MedScience | 2026 | 42467362 | PubTator, text mining | PubMed |
| High-efficiency 14-plex cSNP SNaPshot assay for forensic peripheral blood identification. | BMC Genomics | 2026 | 42436368 | PubTator, text mining | PubMed |
| Screening of hereditary elliptocytosis caused by SPTB mutations and identification of its association with significant jaundice among Thai neonates. | BMJ Paediatr Open | 2026 | 42379836 | PubTator, text mining | PubMed |
| Hereditary Hemolytic Spherocytosis in the Active-Duty Population: A Unique Case. | Cureus | 2026 | 42326196 | PubTator, text mining | PubMed |
| Hereditary Spherocytosis: A Case Series Spanning Prenatal Detection to Neonatal Care. | Prenat Diagn | 2026 | 42175794 | PubTator, text mining | PubMed |
| Expanding the genetic spectrum of hereditary spherocytosis: novel mutations and phenotypic heterogeneity from a 55-patient cohort. | Ann Hematol | 2026 | 42126446 | PubTator, text mining | PubMed |
| Predictive functional profiling of 16S rRNA genes amplicons reveals bioremediation and sulfur metabolism capacity in thermophilic hot spring bacteriomes. | Sci Rep | 2026 | 42086823 | PubTator, text mining | PubMed |
| Clinicohematological and Genetic Profile of Hereditary Spherocytosis in Children: An Experience From a North Indian Center. | J Pediatr Hematol Oncol | 2026 | 42054241 | PubTator, text mining | PubMed |
| De novo mutations in ANK1 and SPTB cause hereditary spherocytosis: three case reports and literature review. | Ann Hematol | 2026 | 41920367 | PubTator, text mining | PubMed |
| In-depth analysis of osmotic gradient ektacytometry parameters across different genotypes in hereditary spherocytosis. | Br J Haematol | 2026 | 41914049 | PubTator, text mining | PubMed |
| Integrated transcriptome-proteome analysis in patients with myelofibrosis-related anemia. | Ann Hematol | 2026 | 41902926 | PubTator, text mining | PubMed |
| Moyamoya syndrome associated with hereditary spherocytosis: pathogenesis, management, and an illustrative case with rapid radiological progression. | Childs Nerv Syst | 2026 | 41879920 | PubTator, text mining | PubMed |
| Hereditary red cell defects as an underrecognized cause of neonatal jaundice. | J Perinatol | 2026 | 41840148 | PubTator, text mining | PubMed |
| [Analysis of the clinical application of next-generation sequencing in the diagnosis of neonatal hereditary spherocytosis]. | Zhonghua Er Ke Za Zhi | 2026 | 41834204 | PubTator, text mining | PubMed |
| A case report of lymphoplasmacytic lymphoma with spherocytosis. | Open Life Sci | 2026 | 41777550 | PubTator, text mining | PubMed |
| The Mystery of the Hidden Trace: Emerging Genetic Approaches to Improve Body Fluid Identification. | Genes (Basel) | 2026 | 41751530 | PubTator, text mining | PubMed |
| The Stiff Side of Cancer: How Matrix Mechanics Rewrites Non-Coding RNA Expression Programs. | Noncoding RNA | 2026 | 41745140 | 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
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