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107 results

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Page 1
Cell-free DNA screening for prenatal detection of 22q11.2 deletion syndrome.
Dar P, Jacobsson B, Clifton R, Egbert M, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Edwards L, Strong N, Haeri S, Silver R, Vohra N, Hyett J, Demko Z, Martin K, Rabinowitz M, Flood K, Carlsson Y, Doulaveris G, Daly S, Hallingström M, MacPherson C, Kao C, Hakonarson H, Norton ME. Dar P, et al. Among authors: vohra n. Am J Obstet Gynecol. 2022 Jul;227(1):79.e1-79.e11. doi: 10.1016/j.ajog.2022.01.002. Epub 2022 Jan 13. Am J Obstet Gynecol. 2022. PMID: 35033576 Free article.
Cell-free DNA screening for trisomies 21, 18, and 13 in pregnancies at low and high risk for aneuploidy with genetic confirmation.
Dar P, Jacobsson B, MacPherson C, Egbert M, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Edwards L, Haeri S, Silver R, Vohra N, Hyett J, Clunie G, Demko Z, Martin K, Rabinowitz M, Flood K, Carlsson Y, Doulaveris G, Malone C, Hallingstrom M, Klugman S, Clifton R, Kao C, Hakonarson H, Norton ME. Dar P, et al. Among authors: vohra n. Am J Obstet Gynecol. 2022 Aug;227(2):259.e1-259.e14. doi: 10.1016/j.ajog.2022.01.019. Epub 2022 Jan 25. Am J Obstet Gynecol. 2022. PMID: 35085538 Free article.
Obstetrical, perinatal, and genetic outcomes associated with nonreportable prenatal cell-free DNA screening results.
Norton ME, MacPherson C, Demko Z, Egbert M, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Strong N, Haeri S, Silver R, Vohra N, Hyett J, Martin K, Rabinowitz M, Jacobsson B, Dar P. Norton ME, et al. Among authors: vohra n. Am J Obstet Gynecol. 2023 Sep;229(3):300.e1-300.e9. doi: 10.1016/j.ajog.2023.03.026. Epub 2023 Mar 23. Am J Obstet Gynecol. 2023. PMID: 36965866 Free article.
Performance of prenatal cfDNA screening for sex chromosomes.
Martin K, Dar P, MacPherson C, Egbert M, Demko Z, Parmar S, Hashimoto K, Haeri S, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Strong N, Silver RM, Vohra N, Hyett J, Rabinowitz M, Kao C, Hakonarson H, Jacobsson B, Norton ME. Martin K, et al. Among authors: vohra n. Genet Med. 2023 Aug;25(8):100879. doi: 10.1016/j.gim.2023.100879. Epub 2023 May 5. Genet Med. 2023. PMID: 37154148 Free article.
Impact of high-risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study.
Martin K, Norton ME, MacPherson C, Demko Z, Egbert M, Haeri S, Malone F, Wapner RJ, Roman AS, Khalil A, Faro R, Madankumar R, Strong N, Silver R, Vohra N, Hyett J, Kao C, Hakonarson H, Jacobson B, Dar P. Martin K, et al. Among authors: vohra n. Prenat Diagn. 2023 Dec;43(13):1574-1580. doi: 10.1002/pd.6483. Epub 2023 Dec 8. Prenat Diagn. 2023. PMID: 38066724
The role of cell-free DNA biomarkers and patient data in the early prediction of preeclampsia: an artificial intelligence model.
Khalil A, Bellesia G, Norton ME, Jacobsson B, Haeri S, Egbert M, Malone FD, Wapner RJ, Roman A, Faro R, Madankumar R, Strong N, Silver RM, Vohra N, Hyett J, MacPherson C, Prigmore B, Ahmed E, Demko Z, Ortiz JB, Souter V, Dar P. Khalil A, et al. Among authors: vohra n. Am J Obstet Gynecol. 2024 Nov;231(5):554.e1-554.e18. doi: 10.1016/j.ajog.2024.02.299. Epub 2024 Mar 2. Am J Obstet Gynecol. 2024. PMID: 38432413
Trends in nuchal translucency measurement at late first trimester ultrasound, and prenatal diagnostic testing after the introduction of cell-free fetal DNA screening: data from a large health system in New York from 2010-2023.
Jackson FI, Kouba I, Keller NA, Bracero LA, Vohra N, Blitz MJ. Jackson FI, et al. Among authors: vohra n. Am J Obstet Gynecol MFM. 2024 Sep 19;6(11):101499. doi: 10.1016/j.ajogmf.2024.101499. Online ahead of print. Am J Obstet Gynecol MFM. 2024. PMID: 39299501 No abstract available.
107 results