Evidence map›Paper›PMID 37216007›Full record

ArticleHGG advances2023

Genetic and clinical determinants of telomere length.

Patrick Allaire, Jing He, John Mayer, Luke Moat, Peter Gerstenberger, Reynor Wilhorn, Sierra Strutz, David S L Kim, Chenjie Zeng, Nancy Cox and 4 more

Open access · goldAbstract read
In one paragraph

Article in HGG advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  7. Identifying family structures from obituaries and matching them to patients in an electronic heath record.Journal of the American Medical Informatics Association : JAMIA · 2025
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 5 institutions in 1 country.

Patrick AllaireMarshfield Clinic Research Institute, Center for Precision Medicine Research, Marshfield, WI, USA.
Jing HeDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.
John MayerMarshfield Clinic Research Institute, Office of Research Computing and Analytics, Marshfield, WI, USA.
Luke MoatMarshfield Clinic Research Institute, Center for Precision Medicine Research, Marshfield, WI, USA.
Peter GerstenbergerMarshfield Clinic Research Institute, Center for Precision Medicine Research, Marshfield, WI, USA.
Reynor WilhornMarshfield Clinic Research Institute, Center for Precision Medicine Research, Marshfield, WI, USA.
Sierra StrutzMarshfield Clinic Research Institute, Center for Precision Medicine Research, Marshfield, WI, USA.
David S L KimMarshfield Clinic Health System, Pathology, Marshfield, WI, USA.
Chenjie ZengNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Nancy CoxVanderbilt Genetics Institute, Division of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Jerry W ShayUniversity of Texas Southwestern Medical Center, Department of Cell Biology and the Simmons Comprehensive Cancer Center, Dallas, TX, USA.
Joshua DennyNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
Lisa BastaracheCenter for Precision Medicine, Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.
Scott HebbringMarshfield Clinic Research Institute, Center for Precision Medicine Research, Marshfield, WI, USA.
Marshfield Clinic · USVanderbilt University Medical Center · USNational Institutes of Health · USMarshfield Clinic · USThe University of Texas Southwestern Medical Center · US

Funding

University of Wisconsin Institute for Clinical and Translational ResearchUL1TR002373 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI ELIZABETH S BURNSIDE, Allan R. Brasier · 2017 to 2026
$75.9M
From GWAS to PheWAS: Scanning the EMR Phenome for Gene-disease AssociationsR01LM010685 · NLM · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BASTARACHE, LISA · 2011 to 2022
$6.3M
PheWAS and GWAS of Telomere Length to Understand Human DiseaseR01GM130715 · NIGMS · MARSHFIELD CLINIC RESEARCH FOUNDATION · PI HEBBRING, SCOTT JOSEPH · 2020 to 2023
$1.8M
PheWAS of Loss-of-Function VariantsR01GM114128 · NIGMS · MARSHFIELD CLINIC RESEARCH FOUNDATION · PI HEBBRING, SCOTT JOSEPH · 2015 to 2019
$1.7M
NCATS NIH HHS UL1 TR002373NIGMS NIH HHS R01 GM114128NIGMS NIH HHS R01 GM130715NLM NIH HHS R01 LM010685
6 · The paper itself

Abstract

Many epidemiologic studies have identified important relationships between leukocyte telomere length (LTL) with genetics and health. Most of these studies have been significantly limited in scope by focusing predominantly on individual diseases or restricted to GWAS analysis. Using two large patient populations derived from Vanderbilt University and Marshfield Clinic biobanks linked to genomic and phenomic data from medical records, we investigated the inter-relationship between LTL, genomics, and human health. Our GWAS confirmed 11 genetic loci previously associated with LTL and two novel loci in

Indexed as

LeukocytesTelomereAgedCalcium-Binding ProteinsEye ProteinsHumansMembrane ProteinsCalcium-Binding ProteinsEye ProteinsMembrane ProteinsPITPNM1 protein, humanagingGWASPheWAStelomere

Identifiers

PMID37216007
PMCPMC10199259
OpenAlexW4367043745

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.