The DOI matches its Crossref record; 21 of the 21 references it cites were found in a registry or an index.
Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation
Open accessOverview
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.
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
Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning
Cokus, S. J., Feng, S., Zhang, X., Chen, Z., Merriman, B., Haudenschild, C. D., Pradhan, S., Nelson, S. F., Pellegrini, M., & Jacobsen, S. E. (2008) · Nature · doi:10.1038/nature06745 · Cited by 2,256
Widespread Monoallelic Expression on Human Autosomes
Gimelbrant, A., Hutchinson, J. N., Thompson, B. R., & Chess, A. (2007) · Science · doi:10.1126/science.1148910 · Cited by 655
Discovery of expression QTLs using large-scale transcriptional profiling in human lymphocytes
Göring, H. H. H., Curran, J. E., Johnson, M. P., Dyer, T. D., Charlesworth, J., Cole, S. A., Jowett, J. B. M., Abraham, L. J., Rainwater, D. L., Comuzzie, A. G., et al. (2007) · Nature Genetics · doi:10.1038/ng2119 · Cited by 504
dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data
Lin, M., Wei, L.-J., Sellers, W. R., Lieberfarb, M., Wong, W. H., & Li, C. (2004) · Bioinformatics · doi:10.1093/bioinformatics/bth069 · Cited by 374
Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancer
Chan, T. L., Yuen, S. T., Kong, C. K., Chan, Y. W., Chan, A. S., Ng, W. F., Tsui, W. Y., Lo, M. W., Tam, W. Y., Li, V. S., et al. (2006) · Nature Genetics · doi:10.1038/ng1866 · Cited by 324
Genetics of alcohol and tobacco use in humans
Tyndale, R. F. (2003) · Annals of Medicine · doi:10.1080/07853890310010014 · Cited by 217
Boccaccio, I., Glatt-Deeley, H., Watrin, F., Roeckel, N., Lalande, M., & Muscatelli, F. (1999) · Human Molecular Genetics · doi:10.1093/hmg/8.13.2497 · Cited by 184
A Comprehensive Analysis of Allelic Methylation Status of CpG Islands on Human Chromosome 21q
Yamada, Y., Watanabe, H., Miura, F., Soejima, H., Uchiyama, M., Iwasaka, T., Mukai, T., Sakaki, Y., & Ito, T. (2004) · Genome Research · doi:10.1101/gr.1351604 · Cited by 171
Inheritance of allelic blueprints for methylation patterns
SILVA, A. (1988) · Cell · doi:10.1016/0092-8674(88)90546-6 · Cited by 168
Murrell, A. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddh013 · Cited by 160
Cited by
Epigenetics and the environment: emerging patterns and implications
Feil, R., & Fraga, M. F. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3142 · Cited by 1,929
Interplay between the Cancer Genome and Epigenome
Shen, H., & Laird, P. W. (2013) · Cell · doi:10.1016/j.cell.2013.03.008 · Cited by 910
DNA methylation patterns associate with genetic and gene expression variation in HapMap cell lines
Bell, J. T., Pai, A. A., Pickrell, J. K., Gaffney, D. J., Pique-Regi, R., Degner, J. F., Gilad, Y., & Pritchard, J. K. (2011) · Genome Biology · doi:10.1186/gb-2011-12-1-r10 · Cited by 838
Beyond GWASs: Illuminating the Dark Road from Association to Function
Edwards, S. L., Beesley, J., French, J. D., & Dunning, A. M. (2013) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2013.10.012 · Cited by 784
Epigenetics as a unifying principle in the aetiology of complex traits and diseases
Petronis, A. (2010) · Nature · doi:10.1038/nature09230 · Cited by 687
Metadata
- Authors
- Kerkel, K., Spadola, A., Yuan, E., Kosek, J., Jiang, L., Hod, E., Li, K., Murty, V. V., Schupf, N., Vilain, E., Morris, M., Haghighi, F., & Tycko, B.
- Venue
- Nature Genetics
- Published
- 2008-06-22
- Volume
- 40
- Issue
- 7
- Pages
- 904-908
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- OpenAlex
- W1995008831
- Cited by
- 441
- References
- 21
- FWCI
- 15.14
- 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: Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation. https://app.cochat.ai/papers/10.1038/ng.174
- The paper
- Kerkel, K., Spadola, A., Yuan, E., Kosek, J., Jiang, L., Hod, E., Li, K., Murty, V. V., Schupf, N., Vilain, E., Morris, M., Haghighi, F., & Tycko, B. (2008). Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation. Nature Genetics. https://doi.org/10.1038/ng.174
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.
