The DOI matches its Crossref record; 13 of the 13 references it cites were found in a registry or an index.
Deep Whole-Genome Sequencing of 100 Southeast Asian Malays
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Cites
A method and server for predicting damaging missense mutations.
Adzhubei, I. A., Schmidt, S., Peshkin, L., Ramensky, V. E., Gerasimova, A., Bork, P., Kondrashov, A. S., & Sunyaev, S. R. (2010) · Nature Methods · doi:10.1038/nmeth0410-248 · Cited by 13,194
Principal components analysis corrects for stratification in genome-wide association studies
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A map of human genome variation from population-scale sequencing.
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The International HapMap Project
†The International HapMap Consortium, Genotyping centres: Baylor College of Medicine and ParAllele BioScience, Gibbs, R. A., Belmont, J. W., Hardenbol, P., Willis, T. D., Yu, F., Chinese HapMap Consortium, Yang, H., Ch'ang, L.-Y., et al. (2003) · Nature · doi:10.1038/nature02168 · Cited by 6,057
Self-citationA second generation human haplotype map of over 3.1 million SNPs
The International HapMap Consortium (2007) · Nature · doi:10.1038/nature06258 · Cited by 4,438
Accurate whole human genome sequencing using reversible terminator chemistry
Bentley, D. R., Balasubramanian, S., Swerdlow, H. P., Smith, G. P., Milton, J., Brown, C. G., Hall, K. P., Evers, D. J., Barnes, C. L., Bignell, H. R., et al. (2008) · Nature · doi:10.1038/nature07517 · Cited by 3,684
Self-citationIntegrating common and rare genetic variation in diverse human populations
The International HapMap 3 Consortium (2010) · Nature · doi:10.1038/nature09298 · Cited by 3,026
A genome-wide association study identifies novel risk loci for type 2 diabetes
Sladek, R., Rocheleau, G., Rung, J., Dina, C., Shen, L., Serre, D., Boutin, P., Vincent, D., Belisle, A., Hadjadj, S., et al. (2007) · Nature · doi:10.1038/nature05616 · Cited by 2,993
Genome-wide association study identifies novel breast cancer susceptibility loci
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Targeted capture and massively parallel sequencing of 12 human exomes
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Cited by
A copy number variation map of the human genome
Zarrei, M., MacDonald, J. R., Merico, D., & Scherer, S. W. (2015) · Nature Reviews Genetics · doi:10.1038/nrg3871 · Cited by 921
Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals
Nagasaki, M., Yasuda, J., Katsuoka, F., Nariai, N., Kojima, K., Kawai, Y., Yamaguchi-Kabata, Y., Yokozawa, J., Danjoh, I., Saito, S., et al. (2015) · Nature Communications · doi:10.1038/ncomms9018 · Cited by 400
Ishigaki, K., Sakaue, S., Terao, C., Luo, Y., Sonehara, K., Yamaguchi, K., Amariuta, T., Too, C. L., Laufer, V. A., Scott, I. C., et al. (2022) · Nature Genetics · doi:10.1038/s41588-022-01213-w · Cited by 341
Self-citationHigasa, K., Miyake, N., Yoshimura, J., Okamura, K., Niihori, T., Saitsu, H., Doi, K., Shimizu, M., Nakabayashi, K., Aoki, Y., et al. (2016) · Journal of Human Genetics · doi:10.1038/jhg.2016.12 · Cited by 304
Privacy risks from genomic data-sharing beacons
Shringarpure, S. S., & Bustamante, C. D. (2015) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2015.09.010 · Cited by 211
Metadata
- Authors
- Wong, L.-P., Ong, R. T.-H., Poh, W.-T., Liu, X., Chen, P., Li, R., Lam, K. K.-Y., Pillai, N. E., Sim, K.-S., Xu, H., Sim, N.-L., Teo, S.-M., Foo, J.-N., Tan, L. W.-L., Lim, Y., Koo, S.-H., Gan, L. S.-H., Cheng, C.-Y., Wee, S., Yap, E. P.-H., Ng, P. C., Lim, W.-Y., Soong, R., Wenk, M. R., Aung, T., Wong, T.-Y., Khor, C.-C., Little, P., Chia, K.-S., & Teo, Y.-Y.
- Venue
- The American Journal of Human Genetics
- Publisher
- Elsevier BV
- Published
- 2013-01
- Volume
- 92
- Issue
- 1
- Pages
- 52-66
- ISSN
- 0002-9297 (ISSN-L)
- OpenAlex
- W1995964126
- Cited by
- 183
- References
- 13
- FWCI
- 10.72
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: Deep Whole-Genome Sequencing of 100 Southeast Asian Malays. https://app.cochat.ai/papers/10.1016/j.ajhg.2012.12.005
- The paper
- Wong, L.-P., Ong, R. T.-H., Poh, W.-T., Liu, X., Chen, P., Li, R., Lam, K. K.-Y., Pillai, N. E., Sim, K.-S., Xu, H., Sim, N.-L., Teo, S.-M., Foo, J.-N., Tan, L. W.-L., Lim, Y., Koo, S.-H., Gan, L. S.-H., Cheng, C.-Y., Wee, S., . . . Teo, Y.-Y. (2013). Deep Whole-Genome Sequencing of 100 Southeast Asian Malays. The American Journal of Human Genetics. https://doi.org/10.1016/j.ajhg.2012.12.005
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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.
