The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy
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In the citing paper
“The phenotypic heterogeneity among patients with similar gene variants likely relates, in part, to the effect of functional “modifier” variants in other genes that influence the penetrance and phenotypic expression of the main pathogenic variants.83”
From Current management of hypertrophic cardiomyopathy (2025) · cites this paper as [83]
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Citations
Cites
Levy, D., Garrison, R. J., Savage, D. D., Kannel, W. B., & Castelli, W. P. (1990) · New England Journal of Medicine · doi:10.1056/nejm199005313222203 · Cited by 5,699
Hypertrophic Cardiomyopathy: A Systematic Review
Maron, B. J. (2002) · JAMA · doi:10.1001/jama.287.10.1308 · Cited by 2,224
Research works printed but not linked: 3
- Igo, R.P., Jr., Chapman, N.H., Berninger, V.W., Matsushita, M., Brkanac, Z., Rothstein, J.H., Holzman, T., Nielsen, K., Raskind, W.H. and Wijsman, E.M. (2006) Genomewide scan for real-word reading 2470 Human Molecular Genetics, 2007, Vol. 16, No. 20 subphenotypes of dyslexia: novel chromosome 13 locus and genetic complexity. Am. J. Med. Genet. B Neuropsychiatr. Genet., 141, 15-27.
- Shmulewitz, D., Heath, S.C., Blundell, M.L., Han, Z., Sharma, R., Salit, J., Auerbach, S.B., Signorini, S., Breslow, J.L., Stoffel, M. and Friedman, J.M. (2006) Linkage analysis of quantitative traits for obesity, diabetes, hypertension, and dyslipidemia on the island of Kosrae, Federated States of Micronesia. Proc. Natl. Acad. Sci USA., 103, 3502-3509.
- Ma, J., Amos, C.I. and Daw, E.W. (2007). Ascertainment correction for Markov Chain Monte Carlo segregation and linkage analysis of a quantitative trait. Genet. Epidemiol., doi: 10.1002/gepi.20231. · DOI
Cited by
Sorted by citations
Hypertrophic Cardiomyopathy: Genetics, Pathogenesis, Clinical Manifestations, Diagnosis, and Therapy
Marian, A. J., & Braunwald, E. (2017) · Circulation Research · doi:10.1161/circresaha.117.311059 · Cited by 1,403
Self-citationGenetics and Genomics of Single-Gene Cardiovascular Diseases
Marian, A. J., van Rooij, E., & Roberts, R. (2016) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2016.09.968 · Cited by 48
Self-citationCurrent management of hypertrophic cardiomyopathy
Sikand, N., Stendahl, J., Sen, S., Lampert, R., & Day, S. (2025) · BMJ · doi:10.1136/bmj-2023-077274 · Cited by 26
Genomic Analysis of Left Ventricular Remodeling
Sarwar, R., & Cook, S. A. (2009) · Circulation · doi:10.1161/circulationaha.108.797225 · Cited by 13
Metadata
- Authors
- Daw, E. W., Chen, S. N., Czernuszewicz, G., Lombardi, R., Lu, Y., Ma, J., Roberts, R., Shete, S., & Marian, A. J.
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2007-04-05
- Volume
- 16
- Issue
- 20
- Pages
- 2463-2471
- ISSN
- 0964-6906
- 1460-2083
- Cited by
- 70
- References
- 2
- Language
- en
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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.
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- CoChat. (2026). Citation check: Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy. https://app.cochat.ai/papers/10.1093/hmg/ddm202
- The paper
- Daw, E. W., Chen, S. N., Czernuszewicz, G., Lombardi, R., Lu, Y., Ma, J., Roberts, R., Shete, S., & Marian, A. J. (2007). Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy. Human Molecular Genetics. https://doi.org/10.1093/hmg/ddm202
