The DOI matches its Crossref record; 72 of the 73 references it cites were found in a registry or an index.
Shortened Telomere Length Is Associated with Increased Risk of Cancer: A Meta-Analysis
Open accessAbstract
BACKGROUND: Telomeres play a key role in the maintenance of chromosome integrity and stability, and telomere shortening is involved in initiation and progression of malignancies. A series of epidemiological studies have examined the association between shortened telomeres and risk of cancers, but the findings remain conflicting. METHODS: A dataset composed of 11,255 cases and 13,101 controls from 21 publications was included in a meta-analysis to evaluate the association between overall cancer risk or cancer-specific risk and the relative telomere length. Heterogeneity among studies and their publication bias were further assessed by the χ(2)-based Q statistic test and Egger's test, respectively. RESULTS: The results showed that shorter telomeres were significantly associated with cancer risk (OR = 1.35, 95% CI = 1.14-1.60), compared with longer telomeres. In the stratified analysis by tumor type, the association remained significant in subgroups of bladder cancer (OR = 1.84, 95% CI = 1.38-2.44), lung cancer (OR = 2.39, 95% CI = 1.18-4.88), smoking-related cancers (OR = 2.25, 95% CI = 1.83-2.78), cancers in the digestive system (OR = 1.69, 95% CI = 1.53-1.87) and the urogenital system (OR = 1.73, 95% CI = 1.12-2.67). Furthermore, the results also indicated that the association between the relative telomere length and overall cancer risk was statistically significant in studies of Caucasian subjects, Asian subjects, retrospective designs, hospital-based controls and smaller sample sizes. Funnel plot and Egger's test suggested that there was no publication bias in the current meta-analysis (P = 0.532). CONCLUSIONS: The results of this meta-analysis suggest that the presence of shortened telomeres may be a marker for susceptibility to human cancer, but single larger, well-design prospective studies are warranted to confirm these findings.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Inter-individual variation in mean leukocyte telomere length (LTL) is associated with cancer and several age-associated diseases.”
From Identification of seven loci affecting mean telomere length and their association with disease (2013) · cites this paper as [4]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Bias in meta-analysis detected by a simple, graphical test
Egger, M., Smith, G. D., Schneider, M., & Minder, C. (1997) · BMJ · doi:10.1136/bmj.315.7109.629 · Cited by 56,722 · cited 1×
“The inverted funnel plots and Egger’s test (linear regression analysis) were used to investigate publication bias [49].”
Meta-analysis in clinical trials
DerSimonian, R., & Laird, N. (1986) · Controlled Clinical Trials · doi:10.1016/0197-2456(86)90046-2 · Cited by 39,552 · cited 1×
“The fixedeffects model and the random-effects model, based on the MantelHaenszel method [47] and the DerSimonian and Laird method [48], respectively, were used to combine values from different studies.”
Quantifying heterogeneity in a meta‐analysis
Higgins, J. P. T., & Thompson, S. G. (2002) · Statistics in Medicine · doi:10.1002/sim.1186 · Cited by 36,763 · cited 1×
“Heterogeneity was also quantified with the I(2) statistic, a value that indicates what proportion of the total variation across studies is beyond chance, where 0% indicates no observed heterogeneity and larger values show increasing heterogeneity [46].”
Statistical Aspects of the Analysis of Data From Retrospective Studies of Disease
(1959) · JNCI: Journal of the National Cancer Institute · doi:10.1093/jnci/22.4.719 · Cited by 14,689 · cited 1×
“The fixedeffects model and the random-effects model, based on the MantelHaenszel method [47] and the DerSimonian and Laird method [48], respectively, were used to combine values from different studies.”
Accelerated telomere shortening in response to life stress
Epel, E. S., Blackburn, E. H., Lin, J., Dhabhar, F. S., Adler, N. E., Morrow, J. D., & Cawthon, R. M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407162101 · Cited by 3,002
Oxidative stress shortens telomeres
von Zglinicki, T. (2002) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(02)02110-2 · Cited by 2,524 · cited 1×
“Firstly, several variables may affect the length of telomeres, such as age, sex, obesity, smoking, oxidative stress and chronic inflammation [12,64,65,66].”
Quantitative Synthesis in Systematic Reviews
Lau, J., Ioannidis, J. P. A., & Schmid, C. H. (1997) · Annals of Internal Medicine · doi:10.7326/0003-4819-127-9-199711010-00008 · Cited by 2,517 · cited 1×
“05 [45].”
Telomere length predicts replicative capacity of human fibroblasts.
Allsopp, R. C., Vaziri, H., Patterson, C., Goldstein, S., Younglai, E. V., Futcher, A. B., Greider, C. W., & Harley, C. B. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.21.10114 · Cited by 2,200 · cited 1×
“Thus, telomere length has been suggested as a ‘‘cellular mitotic clock’’ that defines the number of cell divisions and cellular life span [1,5].”
Switching and Signaling at the Telomere
Blackburn, E. H. (2001) · Cell · doi:10.1016/s0092-8674(01)00492-5 · Cited by 2,139 · cited 2×
“Thus, telomere length has been suggested as a ‘‘cellular mitotic clock’’ that defines the number of cell divisions and cellular life span [1,5].”
Telomere Shortening and Tumor Formation by Mouse Cells Lacking Telomerase RNA
Blasco, M. A., Lee, H.-W., Hande, M. P., Samper, E., Lansdorp, P. M., DePinho, R. A., & Greider, C. W. (1997) · Cell · doi:10.1016/s0092-8674(01)80006-4 · Cited by 2,108 · cited 1×
“For example, short telomeres cause an increased risk of developing epithelial cancers by the formation of complex non-reciprocal translocations [15,16], and telomeres in tumor cells and their precursor lesions are significantly shorter than that in surrounding non-tumor cells [17,18].”
Flagged first, then by citations
1 of the 73 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 301–375 of 375
Martino, P., Perez‐Alarcón, M., Deconinck, L., Raedt, R. D., Vanderhasselt, M., Kozusznik, M. W., Kooy, R. F., Hidalgo, V., Venero, C., Salvador, A., et al. (2025) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2025.107358 · Cited by 2
Role of Telomere Length in Cancer
Alotaibi, M. K. (2021) · Egyptian Academic Journal of Biological Sciences. C, Physiology and Molecular Biology/Egyptian Academic Journal of Biological Sciences. C, Physiology and Molecular Biology · doi:10.21608/eajbsc.2021.196932 · Cited by 2
Chen, C., Upton, C., Braidy, N., Khalil, J., Fang, Z., Xu, Y., & Chan, D. K. Y. (2014) · Journal of the American Geriatrics Society · doi:10.1111/jgs.12910 · Cited by 2
“Mental and physical engagements in complex environments may protect people from the development and progression of symptoms of neurodegenerative damage.(6) These positive effects may be related to the individuals’ levels of satisfaction with DS attendance.”
The correlation between iron homeostasis and telomere maintenance
Zhang, C. (2014) · Frontiers in Biology · doi:10.1007/s11515-014-1327-x · Cited by 2
“The pancreatic, prostate, bone, lung, bladder, and kidney cancer cells have been reported to exhibit shortened telomeres (Ma et al., 2011).”
BackgroundThe (A)Symmetry of the Male Graying Beard Hairs as an Indication of the Programmed Aging Process
Poljšak, B. (2020) · Acta Clinica Croatica · doi:10.20471/acc.2020.59.04.11 · Cited by 2
Perspectives to Modify and Counter Aging in the Frame of Subtelomere–Telomere Theory of Aging
Libertini, G. (2022) · OBM Geriatrics · doi:10.21926/obm.geriatr.2204208 · Cited by 2
Telomere Instability Induced by Anticancer Drugs in Mammalian Cells
Bolzán, A. D. (2016) · InTech eBooks · doi:10.5772/64928 · Cited by 2
“In addition, dysfunctional telomeres induce metabolic and mitochondrial compromise [37], promote carcinogenesis [38, 39], induce chromosome instability [27], and triggers cellular senescence [40].”
BackgroundCutaneous nevi and internal cancer risk: Results from two large prospective cohorts of US women
Li, X., Wu, W., Giovannucci, E. L., Stampfer, M. J., Gao, X., & Han, J. (2019) · International Journal of Cancer · doi:10.1002/ijc.32703 · Cited by 2
Libertini, G. (2019) · Springer eBooks · doi:10.1007/978-3-319-69892-2_26-2 · Cited by 2
Kleine-Gunk, B. (2022) · Springer eBooks · doi:10.1007/978-3-662-61417-4_1 · Cited by 1
Song, T., Liu, J., Zhao, K., Li, S., Qiu, M., Zhang, M., & Wang, H. (2024) · Medicine · doi:10.1097/md.0000000000039584 · Cited by 1
“[25,26] 29] An MR study indicated that the correlation between TL and tumor risk was significantly variable in multiple cancer categories, with increased TL significantly associated with a higher risk of glioma, lung adenocarcinoma, neuroblastoma, bladder cancer, melanoma, kidney cancer, and…”
BackgroundSteindorf, K., Clauss, D., Wiskemann, J., & Schmidt, M. E. (2015) · Sports · doi:10.3390/sports3030145 · Cited by 1
The Family System as a Unit of Clinical Care: The Role of Genetic Systems
Reiss, D. (2015) · Springer eBooks · doi:10.1007/978-1-4939-2923-8_10 · Cited by 1
Impact of Helicobacter pylori Eradication on Absolute Telomere Length in Gastric Mucosa
Omar, M., Aboelazm, A. A., & El-Glil, R. R. A. (2016) · Afro-Egyptian Journal of Infectious and Endemic Diseases · doi:10.21608/aeji.2016.9954 · Cited by 1
“0 fold increased risk of cancer for those with the shortest versus longest telomeres [16,5].”
BackgroundChild Telomere Length at 11–12 Years of Age Is Not Associated with Pregnancy Complications
Bianco‐Miotto, T., Hossain, S., Habibi, N., Haag, D. G., & Grieger, J. A. (2024) · DNA · doi:10.3390/dna4020011 · Cited by 1
“Shorter telomeres are associated with a 20–40% greater likelihood of developing diabetes and heart disease in adulthood [8,9].”
BackgroundTelomeres in Germ Line and Early Embryo: An Overview
Fernández, J. L., & González-Vasconcellos, I. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-812571-7.00006-x · Cited by 1
Independent Physics Researcher, R. 2.-4. 8., Pitkänen, M., Rastmanesh, R., & Member of The Nutrition Society, L. (2021) · Current Cancer Reports · doi:10.25082/ccr.2021.01.002 · Cited by 1
Telomere Length Inheritance throughout Generations: Role of Germ Cell Mortality
Rakha, A. (2021) · OALib · doi:10.4236/oalib.1107798 · Cited by 1
“have reported that long TL is associated with decreased risk of cancers or even has no any association with cancer development [66] [67].”
BackgroundSmith, J. S., & Weiderpass, E. (2013) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djt044 · Cited by 1
Telomere length as a putative biomarker of health and disease
Appleby, S. L. (2016) · Otago University Research Archive (University of Otago) · Cited by 1
Biomarkers for Assessing Risk of Cancer
Wu, X., & Gu, J. H. (2015) · Elsevier eBooks · doi:10.1016/b978-1-4557-4066-6.00021-4 · Cited by 1
Nuevas aportaciones a la caracterización del cáncer de mama en mujeres jóvenes
Pascual, A. (2017) · Gredos (University of Salamanca) · doi:10.14201/gredos.137119 · Cited by 1
Libertini, G. (2019) · Springer eBooks · doi:10.1007/978-3-319-69892-2_26-1 · Cited by 1
Wong, J., Blechter, B., Liu, Z., Shi, J.-X., & Roger, V. (2023) · medRxiv · doi:10.1101/2023.08.03.23293621
Self-citationWeiß, A. G. (2024) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10273 · Cited by 1
Han, L. (2015) · Digital Commons-TMC (Texas Medical Center)
Balducci, L. (2014) · doi:10.1002/9781118833391.ch19
Neighborhood cancerization: New approaches linking social and biological mechanisms of cancer
Lynch, S. M. (2015) · ScholarlyCommons (University of Pennsylvania)
Immune Surveillance and Cancer Pathogenesis
Mastrangelo, D. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1510-1_2
Exposure, telomere length, and cancer risk
Li, H. (2014) · Lund University Publications (Lund University)
The Influence of Biological Ageing in the Pathogenesis of Colorectal Cancer
Maxwell, F. (2013) · Enlighten: Theses (The University of Glasgow)
Wikgren, M. (2011) · DiVA at Umeå University (Umeå University)
The Role of Theory in Cancer Research
Pepper, J. W. (2016) · doi:10.1007/978-1-4939-6460-4_2
Neoplasia of the Gastrointestinal Tract
Margalit, O., & DuBois, R. N. (2015) · Wiley eBooks · doi:10.1002/9781118512074.ch31
Generation of knockout human iPSCs to investigate genes associated with telomere length
Shamkhi, N. (2017) · Figshare
Stochastic Telomere Shortening and the Route to Limitless Replicative Potential
Ye, Y., Yang, Z., & Lei, J. (2019) · Journal of Computational Biology · doi:10.1089/cmb.2018.0234
“Overexpression of telomerase often results in the elongation of telomere and prolongs replicative potential; however, shortened telomere length is often associated with increased cancer risk (Willeit et al., 2010; Ma et al., 2011; Savage et al., 2013).”
Welendorf, C. R. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.17.2019.tde-07022019-135007
Anti-Aging und Nahrungssupplemente — die nächste Generation
Kleine-Gunk, B. (2019) · gynäkologie + geburtshilfe · doi:10.1007/s15013-019-1845-3
Anti-Aging und Nahrungssupplemente — die nächste Generation
Kleine-Gunk, B. (2019) · ästhetische dermatologie & kosmetologie · doi:10.1007/s12634-019-0112-x
Leukocyte telomere length associated with glioma risk and survival
Shen, J., Song, R., Ye, Y., Gong, Y., & Zhao, H. (2020) · Aging and Cancer · doi:10.1002/aac2.12020
Subtelomere-Telomere Aging Theory
Libertini, G., Corbi, G., Conti, V., Shubernetskaya, O. S., & Ferrara, N. (2021) · Advances in studies of aging and health · doi:10.1007/978-3-030-73774-0_5
Saengmearnuparp, T., & Lojanapiwat, B. (2021) · Insight Urology · doi:10.52786/isu.a.19
최훈성 (2016) · Seoul National University Open Repository (Seoul National University)
叙述という行為におけるポリティクス--現代史・同時代史の叙述という問題構成を中心に
浅岡, 隆. (2011) · 立正大学文学部論叢
Joosten, T. K. (2007) · School for International Training Digital Collections (School for International Training)
Siwik, C. J. (2020) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/3477
Libertini, G. (2021) · Springer eBooks · doi:10.1007/978-3-030-22009-9_26
Telomeres and Early-Life Stress
Mayer, S. E., Conklin, Q. A., Ridout, S. J., & Ridout, K. K. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-813156-5.00027-3
Sung, K. W., Bae, J. S., Lee, J. W., Joung, J., Cho, H. W., Ju, H. Y., Yoo, K. H., & Koo, H. H. (2022) · Research Square · doi:10.21203/rs.3.rs-1360590/v1
Bae, J. S., Lee, J. W., Joung, J., Cho, H. W., Ju, H. Y., Yoo, K. H., Koo, H. H., & Sung, K. W. (2022) · Scientific Reports · doi:10.1038/s41598-022-17246-4
Kleine-Gunk, B. (2023) · gynäkologie + geburtshilfe · doi:10.1007/s15013-022-5094-5
Liu, Z., Ma, H., Wei, S., Li, G., Sturgis, E. M., & Wei, Q. (2023) · doi:10.1158/1055-9965.c.6514860
Self-citationLiu, Z., Ma, H., Wei, S., Li, G., Sturgis, E. M., & Wei, Q. (2023) · doi:10.1158/1055-9965.c.6514860.v1
Self-citationGramatges, M. M., Liu, Q., Yasui, Y., Okcu, M. F., Neglia, J. P., Strong, L. C., Armstrong, G. T., Robison, L. L., & Bhatia, S. (2023) · doi:10.1158/1078-0432.c.6521438
Age-related disease: Cancer, telomerase, and cell aging
Whittemore, K. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15500-0.00016-5
Alwehaidah, M. S., & Bakhiet, M. (2024) · Cytogenetic and Genome Research · doi:10.1159/000542323
“Meta-analysis studies based on human populations involving different types of cancer have concluded that shorter LTL is signi fi cantly associated with an increased risk of cancer and mortality [29].”
Libertini, G., Corbi, G., Shubernetskaya, O. S., Komici, K., & Ferrara, N. (2024) · Advances in studies of aging and health · doi:10.1007/978-3-031-84877-3_8
Pudjihartono, M., O'Sullivan, J. M., & Schierding, W. S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.25.640031
Figueroa, D., Mamun, M. M. A., Jung, D. K., Li, G., Tan, S. T., Jamshed, F., Butzin-Dozier, Z., Mertens, A., Lin, J., Pitchik, H. O., et al. (2025) · Scientific Reports · doi:10.1038/s41598-025-90505-2
Yang, B., Bi, J., Zeng, W., Chen, M., Yao, Z., Cheng, S., Jiang, Z., Zhang, C., Liao, H., Gu, X., et al. (2025) · Aging Clinical and Experimental Research · doi:10.1007/s40520-025-03046-z
“Nevertheless, our research on lung cancer frequently contradicts the findings of numerous prior studies, which commonly indicate a heightened likelihood of lung cancer in individuals with shorter TL [12, 40].”
Libertini, G. (2025) · OBM Geriatrics · doi:10.21926/obm.geriatr.2503325
Clarity, C., Trowbridge, J., Gerona, R. R. L., Ona, K., McMaster, M., Bessonneau, V., Rudel, R. A., Buren, H., & Morello-Frosch, R. A. (2021) · Figshare · doi:10.6084/m9.figshare.16530194
Limardi, P., Panigoro, S. S., Siregar, N. C., Sutandyo, N., Witjaksono, F., Priliani, L., Oktavianthi, S., & Malik, S. G. (2024) · Figshare · doi:10.6084/m9.figshare.26713690
Clarity, C., Trowbridge, J., Gerona, R. R. L., Ona, K., McMaster, M., Bessonneau, V., Rudel, R. A., Buren, H., & Morello-Frosch, R. A. (2021) · Figshare · doi:10.6084/m9.figshare.16530209
Carlund, O., Thörn, E., Osterman, P., Fors, M., Dernstedt, A., Forsell, M. N. E., Erlanson, M., Landfors, M., Degerman, S., & Hultdin, M. (2024) · Figshare · doi:10.6084/m9.figshare.25876255
Clarity, C., Trowbridge, J., Gerona, R., Ona, K., McMaster, M., Bessonneau, V., Rudel, R. A., Buren, H., & Morello-Frosch, R. A. (2021) · Figshare · doi:10.6084/m9.figshare.16530206
Clarity, C., Trowbridge, J., Gerona, R. R. L., Ona, K., McMaster, M., Bessonneau, V., Rudel, R. A., Buren, H., & Morello-Frosch, R. A. (2021) · Figshare · doi:10.6084/m9.figshare.16530200
Clarity, C., Trowbridge, J., Gerona, R., Ona, K., McMaster, M., Bessonneau, V., Rudel, R. A., Buren, H., & Morello-Frosch, R. A. (2021) · Figshare · doi:10.6084/m9.figshare.16530197
Sarkar, G., Chen, J., Sood, S., Fischer, K., Kossick, K., Schupack, D. A., Graham, R. P., Druliner, B. R., Heydari, Z., Helgeson, L., et al. (2026) · Cancers · doi:10.3390/cancers18030490
“Interestingly, peripheral blood leukocyte telomere length (LTL) can serve as an overall indicator of the telomere length of an individual and has shown association with multiple age-related conditions, including cancers [25,26].”
Telomere length dynamics in adults living with HIV: A systematic review
Massamba, M. K. Y., Madurai, L., Archary, D., & Mahomed, S. (2026) · BMC Infectious Diseases · doi:10.1186/s12879-026-13243-4
da Silva, I. M., Rocha, L. M. O., de Andrade, Q. G., de Lima, L. V. A., Vacario, B. G. L., de Almeida, T. M., Maraslis, F. T., Martínez‐López, W., Debia, N., de Sousa, A. A., et al. (2026) · Journal of Toxicology and Environmental Health Part B · doi:10.1080/10937404.2026.2707570
da Cunha, L. S., de Morais, G. P., Machado, C. B., Oliveira, D. D. S., Nogueira, B. M. D., Machado, A. K. D. C., Farias, I. C., Pessoa, F. M. C. D. P., Ribeiro, R. M., de Albuquerque, K. M. C., et al. (2026) · Blood Research · doi:10.1007/s44313-026-00157-y
DNA Telomere Electrostatic Fields: A Biophysical Hypothesis with Computational PredictionsPreprint
Rastmanesh, R., & Researcher, I. (2026) · Research Square · doi:10.21203/rs.3.rs-10557031/v1
Seguí, N. (2014) · Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona)
Metadata
- Authors
- Ma, H., Zhou, Z., Wei, S., Liu, Z., Pooley, K. A., Dunning, A. M., Svenson, U., Roos, G., Hosgood, H. D., Shen, M., & Wei, Q.
- Affiliations
- The University of Texas MD Anderson Cancer Center (US)
- University of Cambridge (GB)
- Umeå University (SE)
- National Institutes of Health (US)
- Corresponding author
- Wei, Qingyi
- ORCID
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2011-06-10
- Volume
- 6
- Issue
- 6
- Pages
- e20466
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC3112149
- OpenAlex
- W2136996519
- Cited by
- 376
- References
- 73
- Citations by year
- 2026: 6 · 2025: 10 · 2024: 21 · 2023: 16 · 2022: 19 · 2021: 24 · 2020: 25 · 2019: 32 · 2018: 34 · 2017: 27 · 2016: 33 · 2015: 34 · 2014: 35 · 2013: 36 · 2012: 18
- FWCI
- 3.27
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DiVA at Umeå University (Umeå University) (submittedVersion, other-oa)
- RePEc: Research Papers in Economics (submittedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Cancer Institute (R01CA131274, P30CA016672)
- National Institute of Environmental Health Sciences (R01ES011740)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Keywords
- telomere length, telomere shortening, cancer risk, cancer susceptibility, bladder cancer, lung cancer, tobacco-related cancer, gastrointestinal cancer, urogenital cancer, biomarkers
- MeSH terms
- Humans, Neoplasms, Risk Factors, Confidence Intervals, Odds Ratio, Telomere, Publication Bias, Genetic Predisposition to Disease
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review