ConductScience.org, home
Papers
API referenceFor AI assistants

Paper · 41424170

Subclinical Telomere Biology Disorder in Cancer Patients Heterozygous for the RTEL1 R1264H Founder Variant.

Banaszak LG and 15 others. Am J Med Genet A, 2026. Cited by 0 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

Download JSON
Cite this record

ConductScience Library. Subclinical Telomere Biology Disorder in Cancer Patients Heterozygous for the RTEL1 R1264H Founder Variant. Papers, record 41424170. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/41424170

On this page

Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Subclinical Telomere Biology Disorder in Cancer Patients Heterozygous for the RTEL1 R1264H Founder Variant.
PubMed
Journal
Am J Med Genet A
PubMed
Year
2026
PubMed
Publication types
Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
0
iCite
Revised in PubMed
2026-08-13
PubMed

Authors16

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

OrderAuthorForenameKindORCID iD
1Banaszak LGLauren Ghttps://orcid.org/0000-0002-7682-0350
2Fiala EElise
3Ceyhan-Birsoy OOzge
4Khurram AAliya
5Kemel YMYelena M
6Walsh MFMichael F
7Liu YYinghttps://orcid.org/0000-0001-5790-851X
8Carlo MMaria
9Latham AAliciahttps://orcid.org/0000-0002-9758-713X
10Murciano-Goroff YRYonina R

1 to 10 of 16Source PubMed

See all 16 authors

Topics19

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

MeSH termMajor
NeoplasmsMajor topic
TelomereMajor topic
DNA HelicasesMajor topic
Humans
Female
Male
Heterozygote
Adult
Founder Effect
Middle Aged
Germ-Line Mutation
Genetic Predisposition to Disease
Child
Telomere Shortening
Adolescent
Telomere Homeostasis
Child, Preschool
Aged
Young Adult

Source PubMed

Grants3

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 bySource
P30 CA008748NCI NIH HHSUnited StatesP30CA008748PubMed and NIHNIH RePORTER
Robert and Kate Niehaus Center for Inherited Cancer GenomicsPubMedPubMed
P30 CA008748NCI NIH HHSUnited StatesP30CA008748PubMed and NIHNIH 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.

References44

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
127,418,648Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients.Haematologica2016https://conductscience.org/library/papers/27418648PubMed
225,607,374Rare variants in RTEL1 are associated with familial interstitial pneumonia.Am J Respir Crit Care Med2015https://conductscience.org/library/papers/25607374PubMed
325,741,868
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Genet Med2015https://conductscience.org/library/papers/25741868PubMed
434,340,209The Future of Parallel Tumor and Germline Genetic Testing: Is There a Role for All Patients With Cancer?J Natl Compr Canc Netw2021https://conductscience.org/library/papers/34340209PubMed
536,845,387Evaluation of genetic alterations in hereditary cancer susceptibility genes in the Ashkenazi Jewish women community of Mexico.Front Genet2023https://conductscience.org/library/papers/36845387PubMed
636,151,328Genetics of human telomere biology disorders.Nat Rev Genet2023https://conductscience.org/library/papers/36151328PubMed
730,272,225The Effect of Cancer Treatments on Telomere Length: A Systematic Review of the Literature.J Natl Cancer Inst2018https://conductscience.org/library/papers/30272225PubMed
832,561,545Human RTEL1 associates with Poldip3 to facilitate responses to replication stress and R-loop resolution.Genes Dev2020https://conductscience.org/library/papers/32561545PubMed
926,022,962Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis.Eur Respir J2015https://conductscience.org/library/papers/26022962PubMed
1032,923,861Pathogenic Loss-of-Function Germline TERT Mutations in Patients With Solid Tumors.JCO Precis Oncol2019https://conductscience.org/library/papers/32923861PubMed

1 to 10 of 44

See all 44 references

Cited by0

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 0 citations.

None in this release.

Genes1

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

GeneNCBI Gene IDLinked byIn Genes
RTEL151,750PubTator's text mininghttps://conductscience.org/library/genes/51750

Source 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.

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.

For software

Read this paper from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/papers/v1/41424170

GET https://conductscience.org/api/papers/v1/41424170/references?page=2

API referenceFor AI assistants