The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting
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Citations
Cites
Statistical Methods for Rates and Proportions
Fleiss, J. L., Levin, B., & Paik, M. C. (2003) · Wiley Series in Probability and Statistics · doi:10.1002/0471445428 · Cited by 18,646
Cited by
Palomaki, G. E., Kloza, E. M., Lambert-Messerlian, G. M., Haddow, J. E., Neveux, L. M., Ehrich, M., van den Boom, D., Bombard, A. T., Deciu, C., Grody, W. W., et al. (2011) · Genetics in Medicine · doi:10.1097/gim.0b013e3182368a0e · Cited by 939
Self-citationNoninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population
Nicolaides, K. H., Syngelaki, A., Ashoor, G., Birdir, C., & Touzet, G. (2012) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2012.08.033 · Cited by 624
Pergament, E., Cuckle, H., Zimmermann, B., Banjevic, M., Sigurjonsson, S., Ryan, A., Hall, M. P., Dodd, M., Lacroute, P., Stosic, M., et al. (2014) · Obstetrics & Gynecology · doi:10.1097/aog.0000000000000363 · Cited by 284
Selective analysis of cell‐free DNA in maternal blood for evaluation of fetal trisomy
Sparks, A. B., Wang, E. T., Struble, C. A., Barrett, W., Stokowski, R., McBride, C., Zahn, J., Lee, K., Shen, N., Doshi, J., et al. (2012) · Prenatal Diagnosis · doi:10.1002/pd.2922 · Cited by 266
Thung, D. T., Beulen, L., Hehir-Kwa, J., & Faas, B. H. (2015) · Expert Review of Molecular Diagnostics · doi:10.1586/14737159.2015.973857 · Cited by 20
Metadata
- Authors
- Ehrich, M., Deciu, C., Zwiefelhofer, T., Tynan, J. A., Cagasan, L., Tim, R., Lu, V., McCullough, R., McCarthy, E., Nygren, A. O. H., Dean, J., Tang, L., Hutchison, D., Lu, T., Wang, H., Angkachatchai, V., Oeth, P., Cantor, C. R., Bombard, A., & van den Boom, D.
- Venue
- American Journal of Obstetrics and Gynecology
- Publisher
- Elsevier BV
- Published
- 2011-03
- Volume
- 204
- Issue
- 3
- Pages
- 205.e1-205.e11
- ISSN
- 0002-9378 (ISSN-L)
- OpenAlex
- W2132238722
- Cited by
- 472
- References
- 1
- FWCI
- 69.56
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting. https://app.cochat.ai/papers/10.1016/j.ajog.2010.12.060
- The paper
- Ehrich, M., Deciu, C., Zwiefelhofer, T., Tynan, J. A., Cagasan, L., Tim, R., Lu, V., McCullough, R., McCarthy, E., Nygren, A. O. H., Dean, J., Tang, L., Hutchison, D., Lu, T., Wang, H., Angkachatchai, V., Oeth, P., Cantor, C. R., Bombard, A., & van den Boom, D. (2011). Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting. American Journal of Obstetrics and Gynecology. https://doi.org/10.1016/j.ajog.2010.12.060
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.
