Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 195

The DOI matches its Crossref record; 10 of the 10 references it cites were found in a registry or an index.

Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis From the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

Open access
Smith, Nicholas L., Felix, Janine F., Morrison, Alanna C., Demissie, Serkalem, Glazer, Nicole L., Loehr, Laura R., Cupples, L. Adrienne, Dehghan, Abbas, Lumley, Thomas, Rosamond, Wayne D., Lieb, Wolfgang, Rivadeneira, Fernando, Bis, Joshua C., Folsom, Aaron R., Benjamin, Emelia, Aulchenko, Yurii S., Haritunians, Talin, Couper, David, Murabito, Joanne, Wang, Ying A., Stricker, Bruno H., Gottdiener, John S., Chang, Patricia P., Wang, Thomas J., Rice, Kenneth M., Hofman, Albert, Heckbert, Susan R., Fox, Ervin R., O'Donnell, Christopher J., Uitterlinden, Andre G., Rotter, Jerome I., Willerson, James T., Levy, Daniel, van Duijn, Cornelia M., Psaty, Bruce M., Witteman, Jacqueline C.M., Boerwinkle, Eric, Vasan, Ramachandran S.·2010·Circulation: Cardiovascular Genetics

Abstract

Background—: Although genetic factors contribute to the onset of heart failure (HF), no large-scale genome-wide investigation of HF risk has been published to date. We have investigated the association of 2 478 304 single-nucleotide polymorphisms with incident HF by meta-analyzing data from 4 community-based prospective cohorts: the Atherosclerosis Risk in Communities Study, the Cardiovascular Health Study, the Framingham Heart Study, and the Rotterdam Study. Methods and Results—: Eligible participants for these analyses were of European or African ancestry and free of clinical HF at baseline. Each study independently conducted genome-wide scans and imputed data to the ≈2.5 million single-nucleotide polymorphisms in HapMap. Within each study, Cox proportional hazards regression models provided age- and sex-adjusted estimates of the association between each variant and time to incident HF. Fixed-effect meta-analyses combined results for each single-nucleotide polymorphism from the 4 cohorts to produce an overall association estimate and P value. A genome-wide significance P value threshold was set a priori at 5.0×10 −7 . During a mean follow-up of 11.5 years, 2526 incident HF events (12%) occurred in 20 926 European-ancestry participants. The meta-analysis identified a genome-wide significant locus at chromosomal position 15q22 (1.4×10 −8 ), which was 58.8 kb from USP3 . Among 2895 African-ancestry participants, 466 incident HF events (16%) occurred during a mean follow-up of 13.7 years. One genome-wide significant locus was identified at 12q14 (6.7×10 −8 ), which was 6.3 kb from LRIG3 . Conclusions—: We identified 2 loci that were associated with incident HF and exceeded genome-wide significance. The findings merit replication in other community-based settings of incident HF.

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.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1161/circgenetics.109.895763

Cites

10 of 10 references verified0 citation errors · 0 not checkable

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.

A few free checks a day · papers already verified open instantly · results are public

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

Show all 10 references

Cited by

See all 195

Metadata

Authors
Smith, N. L., Felix, J. F., Morrison, A. C., Demissie, S., Glazer, N. L., Loehr, L. R., Cupples, L. A., Dehghan, A., Lumley, T., Rosamond, W. D., Lieb, W., Rivadeneira, F., Bis, J. C., Folsom, A. R., Benjamin, E., Aulchenko, Y. S., Haritunians, T., Couper, D., Murabito, J., Wang, Y. A., Stricker, B. H., Gottdiener, J. S., Chang, P. P., Wang, T. J., Rice, K. M., Hofman, A., Heckbert, S. R., Fox, E. R., O'Donnell, C. J., Uitterlinden, A. G., Rotter, J. I., Willerson, J. T., Levy, D., van Duijn, C. M., Psaty, B. M., Witteman, J. C. M., Boerwinkle, E., & Vasan, R. S.
Venue
Circulation: Cardiovascular Genetics
Published
2010-06
Volume
3
Issue
3
Pages
256-266
ISSN
  • 1942-325X (ISSN-L)
  • 1942-3268
OpenAlex
W2110624042
Cited by
195
References
10
FWCI
9.05
Type
journal article
Language
en
Open access
green

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

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis From the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. https://app.cochat.ai/papers/10.1161/circgenetics.109.895763
The paper
Smith, N. L., Felix, J. F., Morrison, A. C., Demissie, S., Glazer, N. L., Loehr, L. R., Cupples, L. A., Dehghan, A., Lumley, T., Rosamond, W. D., Lieb, W., Rivadeneira, F., Bis, J. C., Folsom, A. R., Benjamin, E., Aulchenko, Y. S., Haritunians, T., Couper, D., Murabito, J., . . . Vasan, R. S. (2010). Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis From the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. Circulation: Cardiovascular Genetics. https://doi.org/10.1161/circgenetics.109.895763

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.