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Cited by 596

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18

Norton, Mary E., Brar, Herb, Weiss, Jonathan, Karimi, Ardeshir, Laurent, Louise C., Caughey, Aaron B., Rodriguez, M. Hellen, Williams, John, Mitchell, Michael E., Adair, Charles D., Lee, Hanmin, Jacobsson, Bo, Tomlinson, Mark W., Oepkes, Dick, Hollemon, Desiree, Sparks, Andrew B., Oliphant, Arnold, Song, Ken·2012·American Journal of Obstetrics and Gynecology
DOI 10.1016/j.ajog.2012.05.021
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Research works printed but not linked: 23

  1. 2007, ACOG practice bulletin no. 77: screening for fetal chromosomal abnormalities, Obstet Gynecol, 109, 217, 10.1097/00006250-200701000-00054 · DOI · Paper page
  2. Malone, 2005, First-trimester or second-trimester screening, or both, for Down's syndrome, N Engl J Med, 353, 2001, 10.1056/NEJMoa043693 · DOI · Paper page
  3. Rozenberg, 2006, Screening for Down syndrome using first-trimester combined screening followed by second-trimester ultrasound examination in an unselected population, Am J Obstet Gynecol, 195, 1379, 10.1016/j.ajog.2006.02.046 · DOI
  4. 2007, ACOG practice bulletin No. 88, December 2007: invasive prenatal testing for aneuploidy, Obstet Gynecol, 110, 1459, 10.1097/01.AOG.0000291570.63450.44 · DOI · Paper page
  5. Alfirevic, 2003, Amniocentesis and chorionic villus sampling for prenatal diagnosis, Cochrane Database Syst Rev, 3
  6. Shulman, 2011, One small step and one giant leap for non-invasive prenatal screening: an editorial, Am J Obstet Gynecol, 204, 183, 10.1016/j.ajog.2011.01.042 · doi:10.1016/j.ajog.2011.01.042
  7. Chiu, 2011, Non-invasive prenatal assessment of trisomy 21 by multiplexed plasma DNA sequencing: large scale validity study, BMJ, 342, 1, 10.1136/bmj.c7401 · DOI · Paper page
  8. Ehrich, 2011, Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting, Am J Obstet Gynecol, 204, 205.e1, 10.1016/j.ajog.2010.12.060 · DOI · Paper page
  9. Palomaki, 2011, DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study, Genet Med, 13, 913, 10.1097/GIM.0b013e3182368a0e · DOI · Paper page
  10. Bianchi, 2012, Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing, Obstet Gynecol, 119, 1, 10.1097/AOG.0b013e318258c419 · doi:10.1097/aog.0b013e318258c419
  11. Chitty, 2012, Noninvasive prenatal testing for aneuploidy–ready for prime time?, Am J Obstet Gynecol, 206, 269, 10.1016/j.ajog.2012.02.021 · DOI
  12. Palomaki, 2012, DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study, Genet Med, 14, 296, 10.1038/gim.2011.73 · DOI · Paper page
  13. Chen, 2011, Non-invasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing, PLoS One, 6, e21791, 10.1371/journal.pone.0021791 · DOI · Paper page
  14. Sparks, 2012, Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy, Prenat Diagn, 32, 1, 10.1002/pd.2922 · DOI · Paper page
  15. Sparks, 2012, Non-invasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18, Am J Obstet Gynecol, 206, 319.e1, 10.1016/j.ajog.2012.01.030 · DOI · Paper page
  16. Ashoor, 2012, Chromosome-selective sequencing of maternal plasma cell-free DNA for first-trimester detection of trisomy 21 and trisomy 18, Am J Obstet Gynecol, 206, 322.e1, 10.1016/j.ajog.2012.01.029 · DOI · Paper page
  17. Wilson, 1927, Probable inference, the law of succession, and statistical inference, J Am Stat Assoc, 22, 209, 10.1080/01621459.1927.10502953 · DOI · Paper page
  18. Fernando, 2010, A new methodology to preserve the original proportion and integrity of cell-free fetal DNA in maternal plasma during sample processing and storage, Prenat Diagn, 30, 418, 10.1002/pd.2484 · DOI
  19. Lun, 2008, Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasma, Clin Chem, 54, 1664, 10.1373/clinchem.2008.111385 · DOI · Paper page
  20. Ashoor, 2012, Fetal fraction in maternal plasma cell-free DNA at 11-13 weeks' gestation: effect of maternal and fetal factors, Fetal Diagn Ther, 10.1159/000337373 · DOI
  21. Fang, 2009, Down syndrome screening in the United States in 2001 and 2007: a survey of maternal-fetal medicine specialists, Am J Obstet Gynecol, 201, 97.e1, 10.1016/j.ajog.2009.02.029 · DOI
  22. Norton, 2012, Effect of changes in prenatal screening and diagnostic testing policies on resources utilization in a large, integrated health care system, Am J Obstet Gynecol, 206, S317, 10.1016/j.ajog.2011.10.731 · doi:10.1016/j.ajog.2011.10.731
  23. Goldman, 2012, Trends in prenatal diagnosis in CA over a decade, 1998-2009, Am J Obstet Gynecol, 206, S321, 10.1016/j.ajog.2011.10.741 · doi:10.1016/j.ajog.2011.10.741

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Metadata

Authors
Norton, M. E., Brar, H., Weiss, J., Karimi, A., Laurent, L. C., Caughey, A. B., Rodriguez, M. H., Williams, J., Mitchell, M. E., Adair, C. D., Lee, H., Jacobsson, B., Tomlinson, M. W., Oepkes, D., Hollemon, D., Sparks, A. B., Oliphant, A., & Song, K.
Venue
American Journal of Obstetrics and Gynecology
Publisher
Elsevier BV
Published
2012-08
Volume
207
Issue
2
Pages
137.e1-137.e8
ISSN
0002-9378 (ISSN-L)
DOI
10.1016/j.ajog.2012.05.021
OpenAlex
W1984290204
Cited by
596
References
1
FWCI
71.51
Type
journal article
Language
en
Open access
closed
Licence

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CoChat. (2026). Citation check: Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18. https://app.cochat.ai/papers/10.1016/j.ajog.2012.05.021
The paper
Norton, M. E., Brar, H., Weiss, J., Karimi, A., Laurent, L. C., Caughey, A. B., Rodriguez, M. H., Williams, J., Mitchell, M. E., Adair, C. D., Lee, H., Jacobsson, B., Tomlinson, M. W., Oepkes, D., Hollemon, D., Sparks, A. B., Oliphant, A., & Song, K. (2012). Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18. American Journal of Obstetrics and Gynecology. https://doi.org/10.1016/j.ajog.2012.05.021

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.