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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

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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.

Title
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients.
PubMed
Journal
Haematologica
PubMed
Year
2016
PubMed
Publication types
Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
126
iCite
Relative citation ratio, by iCite
4.07
iCite
Revised in PubMed
2018-11-13
PubMed

Authors10

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Keel SBSiobán B
2Scott AAngela
3Sanchez-Bonilla MMarilyn
4Ho PAPhoenix A
5Gulsuner SSuleyman
6Pritchard CCColin C
7Abkowitz JLJanis L
8King MCMary-Claire
9Walsh TTom
10Shimamura AAkiko

Source PubMed

Topics17

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
Anemia, AplasticMajor topic
Germ-Line MutationMajor topic
Myelodysplastic SyndromesMajor 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 itAgencyCountryNIH projectStated by
R24 DK099808NIDDK NIH HHSUnited StatesR24DK099808PubMed and NIH

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.

OrderPMIDTitleJournalYearIn PapersSource
112,676,774Mutations of the human telomerase RNA gene (TERC) in aplastic anemia and myelodysplastic syndrome.Blood2003https://conductscience.org/library/papers/12676774PubMed
225,239,263Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity.Haematologica2015https://conductscience.org/library/papers/25239263PubMed
319,282,459Cancer in dyskeratosis congenita.Blood2009https://conductscience.org/library/papers/19282459PubMed
412,393,398A novel diagnostic screen for defects in the Fanconi anemia pathway.Blood2002https://conductscience.org/library/papers/12393398PubMed
522,160,017Classification of childhood aplastic anemia and myelodysplastic syndrome.Hematology Am Soc Hematol Educ Program2011https://conductscience.org/library/papers/22160017PubMed
620,417,588Pathophysiology and management of inherited bone marrow failure syndromes.Blood Rev2010https://conductscience.org/library/papers/20417588PubMed
721,486,468Accurate and exact CNV identification from targeted high-throughput sequence data.BMC Genomics2011https://conductscience.org/library/papers/21486468PubMed
810,508,512Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia.Nat Genet1999https://conductscience.org/library/papers/10508512PubMed
916,825,992Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndrome.J Pediatr Hematol Oncol2006https://conductscience.org/library/papers/16825992PubMed
108,639,798The p53 gene in pediatric therapy-related leukemia and myelodysplasia.Blood1996https://conductscience.org/library/papers/8639798PubMed

Cited by93

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 126 citations.

PMIDTitleJournalYearIn PapersSource
41,924,923Preemptive hematopoietic stem cell transplantation in RUNX1 familial platelet disorder: a shared decision-making framework.Haematologica2026https://conductscience.org/library/papers/41924923PubMed
41,663,178[Chinese expert consensus on the clinical application of next-generation sequencing technology in myelodysplastic neoplasms (2026)].Zhonghua Xue Ye Xue Za Zhi2026https://conductscience.org/library/papers/41663178PubMed
41,624,889Hematological complications in solid organ transplant recipients with telomere biology disorders: a narrative review.Front Immunol2025https://conductscience.org/library/papers/41624889PubMed
41,424,170Subclinical Telomere Biology Disorder in Cancer Patients Heterozygous for the RTEL1 R1264H Founder Variant.Am J Med Genet A2026https://conductscience.org/library/papers/41424170PubMed
40,579,634Do Ethnicity/Caste-Based Disparities Influence Childhood Anemia in India?J Racial Ethn Health Disparities2026https://conductscience.org/library/papers/40579634PubMed
40,568,716Germline and somatic genetic landscape of pediatric myelodysplastic syndromes.Haematologica2025https://conductscience.org/library/papers/40568716PubMed
40,563,403Myelodysplastic Neoplasms (MDS): Pathogenesis and Therapeutic Prospects.Biomolecules2025https://conductscience.org/library/papers/40563403PubMed
40,562,847Hematopoietic stem cell transplantation outcomes in pediatric acquired aplastic anemia with inherited bone marrow failure syndrome-associated genes.Bone Marrow Transplant2025https://conductscience.org/library/papers/40562847PubMed
40,117,486[Diagnostic approaches and clinical relevance of hereditary hematological malignancies].Magy Onkol2025https://conductscience.org/library/papers/40117486PubMed
39,929,730Genetic Predisposition to Hematologic Malignancies.Cold Spring Harb Perspect Med2025https://conductscience.org/library/papers/39929730PubMed

1 to 10 of 93

See all 93 cited by

Genes10

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

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.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
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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