Paper · 27418648
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients.
Keel SB and 9 others. Haematologica, 2016. Cited by 126 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
Cite this record
ConductScience Library. Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients. Papers, record 27418648. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/27418648
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
Topics17
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Anemia, Aplastic | Major topic |
| Germ-Line Mutation | Major topic |
| Myelodysplastic Syndromes | Major topic |
| Adolescent | |
| Adult | |
| Child | |
| Child, Preschool | |
| Core Binding Factor Alpha 2 Subunit | |
| Family | |
| Female | |
| Genetic Testing | |
| Humans | |
| Infant | |
| Male | |
| Mutation | |
| Sequence Analysis, DNA | |
| Young Adult |
Source PubMed
Grants1
Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.
| Grant, as the record writes it | Agency | Country | NIH project | Stated by |
|---|---|---|---|---|
| R24 DK099808 | NIDDK NIH HHS | United States | R24DK099808 | PubMed and NIH |
Source NIH RePORTER
Trials0
The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.
None in this release.
Comments and corrections0
PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.
None in this release.
References29
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 12,676,774 | Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome. | Blood | 2003 | https://conductscience.org/library/papers/12676774 | PubMed |
| 2 | 25,239,263 | Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity. | Haematologica | 2015 | https://conductscience.org/library/papers/25239263 | PubMed |
| 3 | 19,282,459 | Cancer in dyskeratosis congenita. | Blood | 2009 | https://conductscience.org/library/papers/19282459 | PubMed |
| 4 | 12,393,398 | A novel diagnostic screen for defects in the Fanconi anemia pathway. | Blood | 2002 | https://conductscience.org/library/papers/12393398 | PubMed |
| 5 | 22,160,017 | Classification of childhood aplastic anemia and myelodysplastic syndrome. | Hematology Am Soc Hematol Educ Program | 2011 | https://conductscience.org/library/papers/22160017 | PubMed |
| 6 | 20,417,588 | Pathophysiology and management of inherited bone marrow failure syndromes. | Blood Rev | 2010 | https://conductscience.org/library/papers/20417588 | PubMed |
| 7 | 21,486,468 | Accurate and exact CNV identification from targeted high-throughput sequence data. | BMC Genomics | 2011 | https://conductscience.org/library/papers/21486468 | PubMed |
| 8 | 10,508,512 | Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. | Nat Genet | 1999 | https://conductscience.org/library/papers/10508512 | PubMed |
| 9 | 16,825,992 | Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndrome. | J Pediatr Hematol Oncol | 2006 | https://conductscience.org/library/papers/16825992 | PubMed |
| 10 | 8,639,798 | The p53 gene in pediatric therapy-related leukemia and myelodysplasia. | Blood | 1996 | https://conductscience.org/library/papers/8639798 | PubMed |
1 to 10 of 29
See all 29 referencesCited by93
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 126 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 41,924,923 | Preemptive hematopoietic stem cell transplantation in RUNX1 familial platelet disorder: a shared decision-making framework. | Haematologica | 2026 | https://conductscience.org/library/papers/41924923 | PubMed |
| 41,663,178 | [Chinese expert consensus on the clinical application of next-generation sequencing technology in myelodysplastic neoplasms (2026)]. | Zhonghua Xue Ye Xue Za Zhi | 2026 | https://conductscience.org/library/papers/41663178 | PubMed |
| 41,624,889 | Hematological complications in solid organ transplant recipients with telomere biology disorders: a narrative review. | Front Immunol | 2025 | https://conductscience.org/library/papers/41624889 | PubMed |
| 41,424,170 | Subclinical Telomere Biology Disorder in Cancer Patients Heterozygous for the RTEL1 R1264H Founder Variant. | Am J Med Genet A | 2026 | https://conductscience.org/library/papers/41424170 | PubMed |
| 40,579,634 | Do Ethnicity/Caste-Based Disparities Influence Childhood Anemia in India? | J Racial Ethn Health Disparities | 2026 | https://conductscience.org/library/papers/40579634 | PubMed |
| 40,568,716 | Germline and somatic genetic landscape of pediatric myelodysplastic syndromes. | Haematologica | 2025 | https://conductscience.org/library/papers/40568716 | PubMed |
| 40,563,403 | Myelodysplastic Neoplasms (MDS): Pathogenesis and Therapeutic Prospects. | Biomolecules | 2025 | https://conductscience.org/library/papers/40563403 | PubMed |
| 40,562,847 | Hematopoietic stem cell transplantation outcomes in pediatric acquired aplastic anemia with inherited bone marrow failure syndrome-associated genes. | Bone Marrow Transplant | 2025 | https://conductscience.org/library/papers/40562847 | PubMed |
| 40,117,486 | [Diagnostic approaches and clinical relevance of hereditary hematological malignancies]. | Magy Onkol | 2025 | https://conductscience.org/library/papers/40117486 | PubMed |
| 39,929,730 | Genetic Predisposition to Hematologic Malignancies. | Cold Spring Harb Perspect Med | 2025 | https://conductscience.org/library/papers/39929730 | PubMed |
1 to 10 of 93
See all 93 cited byGenes10
The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.
| Gene | NCBI Gene ID | Linked by | In Genes | Source |
|---|---|---|---|---|
| DKC1 | 1,736 | PubTator's text mining | https://conductscience.org/library/genes/1736 | NCBI Gene |
| FANCA | 2,175 | PubTator's text mining | https://conductscience.org/library/genes/2175 | NCBI Gene |
| GATA2 | 2,624 | PubTator's text mining | https://conductscience.org/library/genes/2624 | NCBI Gene |
| MPL | 4,352 | PubTator's text mining | https://conductscience.org/library/genes/4352 | NCBI Gene |
| RTEL1 | 51,750 | PubTator's text mining | https://conductscience.org/library/genes/51750 | NCBI Gene |
| RUNX1 | 861 | PubTator's text mining | https://conductscience.org/library/genes/861 | NCBI Gene |
| SBDS | 51,119 | PubTator's text mining | https://conductscience.org/library/genes/51119 | NCBI Gene |
| TERT | 7,015 | PubTator's text mining | https://conductscience.org/library/genes/7015 | NCBI Gene |
| TINF2 | 26,277 | PubTator's text mining | https://conductscience.org/library/genes/26277 | NCBI Gene |
| TP53 | 7,157 | PubTator's text mining | https://conductscience.org/library/genes/7157 | NCBI Gene |
Drugs0
The drugs whose trials, in the Pipelines release, list the paper.
None in this release.
Data0
The data bank entries PubMed's record names. Trial numbers are under Trials.
None in this release.
Data dates
The date of each source this release read.
- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- 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
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- 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 RePORTER's grant and 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
- PMC's ID fileNone 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/
- 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.
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