The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.
Genome-Wide Association Study of Coronary Heart Disease and Its Risk Factors in 8,090 African Americans: The NHLBI CARe Project
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?
The RNF130 locus was previously linked with plasma LDL-C levels in a small population (8,090 individuals) of African Americans.
“The RNF130 locus was previously linked with plasma LDL-C levels in a small population (8,090 individuals) of African Americans33.”
From RNF130 Regulates LDLR Availability and Plasma LDL Cholesterol Levels (2023) · cites this paper as [33]
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
PLINK: a tool set for whole-genome association and population-based linkage analyses.
Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A. R., Bender, D., Maller, J., Sklar, P., de Bakker, P. I. W., Daly, M. J., et al. (2007) · The American Journal of Human Genetics · doi:10.1086/519795 · Cited by 34,089
Principal components analysis corrects for stratification in genome-wide association studies
Price, A. L., Patterson, N. J., Plenge, R. M., Weinblatt, M. E., Shadick, N. A., & Reich, D. (2006) · Nature Genetics · doi:10.1038/ng1847 · Cited by 10,248
Self-citationGenome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
The Wellcome Trust Case Control Consortium, Management Committee, Burton, P. R., Clayton, D. G., Cardon, L. R., Craddock, N., Deloukas, P., Duncanson, A., Kwiatkowski, D. P., McCarthy, M. I., et al. (2007) · Nature · doi:10.1038/nature05911 · Cited by 9,442
METAL: fast and efficient meta-analysis of genomewide association scans
Willer, C. J., Li, Y., & Abecasis, G. R. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btq340 · Cited by 5,205
Hindorff, L. A., Sethupathy, P., Junkins, H. A., Ramos, E. M., Mehta, J. P., Collins, F. S., & Manolio, T. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0903103106 · Cited by 4,013
Biological, clinical and population relevance of 95 loci for blood lipids
Teslovich, T. M., Musunuru, K., Smith, A. V., Edmondson, A. C., Stylianou, I. M., Koseki, M., Pirruccello, J. P., Ripatti, S., Chasman, D. I., Willer, C. J., et al. (2010) · Nature · doi:10.1038/nature09270 · Cited by 3,487
Self-citationLocusZoom: regional visualization of genome-wide association scan results
Pruim, R. J., Welch, R. P., Sanna, S., Teslovich, T. M., Chines, P. S., Gliedt, T. P., Boehnke, M., Abecasis, G. R., & Willer, C. J. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btq419 · Cited by 2,707
Genomewide Association Analysis of Coronary Artery Disease
Samani, N. J., Erdmann, J., Hall, A. S., Hengstenberg, C., Mangino, M., Mayer, B., Dixon, R. J., Meitinger, T., Braund, P., Wichmann, H.-E., et al. (2007) · New England Journal of Medicine · doi:10.1056/nejmoa072366 · Cited by 2,044
A Common Variant on Chromosome 9p21 Affects the Risk of Myocardial Infarction
Helgadottir, A., Thorleifsson, G., Manolescu, A., Gretarsdottir, S., Blondal, T., Jonasdottir, A., Jonasdottir, A., Sigurdsson, A., Baker, A., Palsson, A., et al. (2007) · Science · doi:10.1126/science.1142842 · Cited by 1,594
Self-citationA Common Allele on Chromosome 9 Associated with Coronary Heart Disease
McPherson, R., Pertsemlidis, A., Kavaslar, N., Stewart, A., Roberts, R., Cox, D. R., Hinds, D. A., Pennacchio, L. A., Tybjaerg-Hansen, A., Folsom, A. R., et al. (2007) · Science · doi:10.1126/science.1142447 · Cited by 1,587
Self-citationCommon variants at 30 loci contribute to polygenic dyslipidemia
Kathiresan, S., Willer, C. J., Peloso, G. M., Demissie, S., Musunuru, K., Schadt, E. E., Kaplan, L., Bennett, D., Li, Y., Tanaka, T., et al. (2009) · Nature Genetics · doi:10.1038/ng.291 · Cited by 1,364
Self-citationMyocardial Infarction Genetics Consortium (2009) · Nature Genetics · doi:10.1038/ng.327 · Cited by 1,088
New susceptibility locus for coronary artery disease on chromosome 3q22.3
Italian Atherosclerosis, T., Erdmann, J., Myocardial Infarction Genetics Consortium, Wellcome Trust Case Control Consortium, Cardiogenics Consortium, Großhennig, A., Braund, P. S., König, I. R., Hengstenberg, C., Hall, A. S., et al. (2009) · Nature Genetics · doi:10.1038/ng.307 · Cited by 484
Self-citation
Flagged first, then by citations
Research works printed but not linked: 19
- J Thomas, 1997, Cardiovascular disease in African American and white physicians: the Meharry Cohort and Meharry-Hopkins Cohort Studies., J Health Care Poor Underserved, 8, 270, 10.1353/hpu.2010.0526 · DOI
- DW Jones, 2002, Risk factors for coronary heart disease in African Americans: the atherosclerosis risk in communities study, 1987–1997., Arch Intern Med, 162, 2565, 10.1001/archinte.162.22.2565 · DOI
- R Cooper, 1997, Hypertension in blacks., Am J Hypertens, 10, 804, 10.1016/S0895-7061(97)00211-2 · DOI
- RS Cooper, 2001, Racial differences and the genetics of hypertension., Curr Hypertens Rep, 3, 19, 10.1007/s11906-001-0073-z · DOI
- PT Katzmarzyk, 2000, Familial resemblance for coronary heart disease risk: the HERITAGE Family Study., Ethn Dis, 10, 138
- CJ Willer, 2008, Newly identified loci that influence lipid concentrations and risk of coronary artery disease., Nat Genet, 40, 161, 10.1038/ng.76 · DOI · Paper page
- DF Gudbjartsson, 2009, Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction., Nat Genet, 41, 342, 10.1038/ng.323 · DOI
- K Musunuru, 2010, Candidate gene association resource (CARe): design, methods, and proof of concept., Circ Cardiovasc Genet, 3, 267, 10.1161/CIRCGENETICS.109.882696 · DOI
- JM Korn, 2008, Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs., Nat Genet, 40, 1253, 10.1038/ng.237 · DOI · Paper page
- Y Li, 2009, Genotype imputation., Annu Rev Genomics Hum Genet, 10, 387, 10.1146/annurev.genom.9.081307.164242 · DOI · Paper page
- SJ Kang, 2010, Genome-wide association of anthropometric traits in African- and African-derived populations., Hum Mol Genet, 19, 2725, 10.1093/hmg/ddq154 · DOI
- MH Chen, 2009, GWAF: an R package for genome-wide association analyses with family data., Bioinformatics
- A Adeyemo, 2009, A genome-wide association study of hypertension and blood pressure in African Americans., PLoS Genet, 5, e1000564, 10.1371/journal.pgen.1000564 · DOI
- A Helgason, 2007, Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution., Nat Genet, 39, 218, 10.1038/ng1960 · DOI
- N Patterson, 2004, Methods for high-density admixture mapping of disease genes., Am J Hum Genet, 74, 979, 10.1086/420871 · DOI
- MH Chen, 2010, GWAF: an R package for genome-wide association analyses with family data., Bioinformatics, 26, 580, 10.1093/bioinformatics/btp710 · DOI · Paper page
- E Zeggini, 2008, Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes., Nat Genet, 40, 638, 10.1038/ng.120 · DOI · Paper page
- YS Aulchenko, 2009, Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts., Nat Genet, 41, 47, 10.1038/ng.269 · DOI
- S Kathiresan, 2008, Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans., Nat Genet, 40, 189, 10.1038/ng.75 · DOI · Paper page
Cited by
Sorted by citations
Innate Immune Activity Conditions the Effect of Regulatory Variants upon Monocyte Gene Expression
Fairfax, B. P., Humburg, P., Makino, S., Naranbhai, V., Wong, D., Lau, E., Jostins, L., Plant, K., Andrews, R., McGee, C., et al. (2014) · Science · doi:10.1126/science.1246949 · Cited by 764
An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people
Nelson, M. R., Wegmann, D., Ehm, M. G., Kessner, D., St. Jean, P., Verzilli, C., Shen, J., Tang, Z., Bacanu, S.-A., Fraser, D., et al. (2012) · Science · doi:10.1126/science.1217876 · Cited by 647
Taking race out of human genetics
Yudell, M., Roberts, D., DeSalle, R., & Tishkoff, S. (2016) · Science · doi:10.1126/science.aac4951 · Cited by 631
Natarajan, P., Young, R., Stitziel, N. O., Padmanabhan, S., Baber, U., Mehran, R., Sartori, S., Fuster, V., Reilly, D. F., Butterworth, A., et al. (2017) · Circulation · doi:10.1161/circulationaha.116.024436 · Cited by 570
Self-citationGromovsky, A. D., Schugar, R. C., Brown, A. L., Helsley, R. N., Burrows, A. C., Ferguson, D., Zhang, R., Sansbury, B. E., Lee, R. G., Morton, R. E., et al. (2018) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.117.309660 · Cited by 115
Transferability and Fine Mapping of Type 2 Diabetes Loci in African Americans
Ng, M. C. Y., Saxena, R., Li, J., Palmer, N. D., Dimitrov, L., Xu, J., Rasmussen-Torvik, L. J., Zmuda, J. M., Siscovick, D. S., Patel, S. R., et al. (2013) · Diabetes · doi:10.2337/db12-0266 · Cited by 62
Self-citationAherrahrou, R., Reinberger, T., Hashmi, S., & Erdmann, J. (2024) · Cardiovascular Research · doi:10.1093/cvr/cvae161 · Cited by 25
RNF130 Regulates LDLR Availability and Plasma LDL Cholesterol Levels
Clifford, B. L., Jarrett, K. E., Cheng, J., Cheng, A., Seldin, M., Morand, P., Lee, R., Chen, M., Baldan, A., de Aguiar Vallim, T. Q., et al. (2023) · Circulation Research · doi:10.1161/circresaha.122.321938 · Cited by 20
Cheng, C.-Y., Reich, D., Haiman, C. A., Tandon, A., Patterson, N., Elizabeth, S., Akylbekova, E. L., Brancati, F. L., Coresh, J., Boerwinkle, E., et al. (2012) · PLoS ONE · doi:10.1371/annotation/52e53d8e-a4bd-4419-951a-75ddcbaf6c5d · Cited by 2
Self-citation
Metadata
- Authors
- Lettre, G., Palmer, C. D., Young, T., Ejebe, K. G., Allayee, H., Benjamin, E. J., Bennett, F., Bowden, D. W., Chakravarti, A., Dreisbach, A., Farlow, D. N., Folsom, A. R., Fornage, M., Forrester, T., Fox, E., Haiman, C. A., Hartiala, J., Harris, T. B., Hazen, S. L., Heckbert, S. R., Henderson, B. E., Hirschhorn, J. N., Keating, B. J., Kritchevsky, S. B., Larkin, E., Li, M., Rudock, M. E., McKenzie, C. A., Meigs, J. B., Meng, Y. A., Mosley, T. H., Newman, A. B., Newton-Cheh, C. H., Paltoo, D. N., Papanicolaou, G. J., Patterson, N., Post, W. S., Psaty, B. M., Qasim, A. N., Qu, L., Rader, D. J., Redline, S., Reilly, M. P., Reiner, A. P., Rich, S. S., Rotter, J. I., Liu, Y., Shrader, P., Siscovick, D. S., Tang, W. H. W., Taylor, H. A., Tracy, R. P., Vasan, R. S., Waters, K. M., Wilks, R., Wilson, J. G., Fabsitz, R. R., Gabriel, S. B., Kathiresan, S., & Boerwinkle, E.
- Venue
- PLoS Genetics
- Publisher
- Public Library of Science (PLoS)
- Published
- 2011-02-10
- Volume
- 7
- Issue
- 2
- Pages
- e1001300
- ISSN
- 1553-7404
- PMC
- PMC3037413
- Cited by
- 272
- References
- 13
- Language
- en
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