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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 9
2003 9
2004 11
2005 18
2006 17
2007 16
2008 13
2009 15
2010 23
2011 15
2012 19
2013 24
2014 26
2015 32
2016 33
2017 27
2018 40
2019 30
2020 39
2021 36
2022 59
2023 42
2024 28

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497 results

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Page 1
Prenatal diagnosis by chromosomal microarray analysis.
Levy B, Wapner R. Levy B, et al. Among authors: wapner r. Fertil Steril. 2018 Feb;109(2):201-212. doi: 10.1016/j.fertnstert.2018.01.005. Fertil Steril. 2018. PMID: 29447663 Free PMC article. Review.
Preface.
Norton ME, Wapner RJ. Norton ME, et al. Among authors: wapner rj. Semin Perinatol. 2018 Aug;42(5):269. doi: 10.1053/j.semperi.2018.07.001. Epub 2018 Jul 25. Semin Perinatol. 2018. PMID: 30195988 Review. No abstract available.
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Petrovski S, Aggarwal V, Giordano JL, Stosic M, Wou K, Bier L, Spiegel E, Brennan K, Stong N, Jobanputra V, Ren Z, Zhu X, Mebane C, Nahum O, Wang Q, Kamalakaran S, Malone C, Anyane-Yeboa K, Miller R, Levy B, Goldstein DB, Wapner RJ. Petrovski S, et al. Among authors: wapner rj. Lancet. 2019 Feb 23;393(10173):758-767. doi: 10.1016/S0140-6736(18)32042-7. Epub 2019 Jan 31. Lancet. 2019. PMID: 30712878
Chromosomal microarray versus karyotyping for prenatal diagnosis.
Wapner RJ, Martin CL, Levy B, Ballif BC, Eng CM, Zachary JM, Savage M, Platt LD, Saltzman D, Grobman WA, Klugman S, Scholl T, Simpson JL, McCall K, Aggarwal VS, Bunke B, Nahum O, Patel A, Lamb AN, Thom EA, Beaudet AL, Ledbetter DH, Shaffer LG, Jackson L. Wapner RJ, et al. N Engl J Med. 2012 Dec 6;367(23):2175-84. doi: 10.1056/NEJMoa1203382. N Engl J Med. 2012. PMID: 23215555 Free PMC article. Clinical Trial.
Treatment of Subclinical Hypothyroidism or Hypothyroxinemia in Pregnancy.
Casey BM, Thom EA, Peaceman AM, Varner MW, Sorokin Y, Hirtz DG, Reddy UM, Wapner RJ, Thorp JM Jr, Saade G, Tita AT, Rouse DJ, Sibai B, Iams JD, Mercer BM, Tolosa J, Caritis SN, VanDorsten JP; Eunice Kennedy Shriver National Institute of Child Health and Human Development Maternal–Fetal Medicine Units Network. Casey BM, et al. Among authors: wapner rj. N Engl J Med. 2017 Mar 2;376(9):815-825. doi: 10.1056/NEJMoa1606205. N Engl J Med. 2017. PMID: 28249134 Free PMC article. Clinical Trial.
Cell-free DNA analysis for noninvasive examination of trisomy.
Norton ME, Jacobsson B, Swamy GK, Laurent LC, Ranzini AC, Brar H, Tomlinson MW, Pereira L, Spitz JL, Hollemon D, Cuckle H, Musci TJ, Wapner RJ. Norton ME, et al. Among authors: wapner rj. N Engl J Med. 2015 Apr 23;372(17):1589-97. doi: 10.1056/NEJMoa1407349. Epub 2015 Apr 1. N Engl J Med. 2015. PMID: 25830321 Free article. Clinical Trial.
Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Zhang J, Li J, Saucier JB, Feng Y, Jiang Y, Sinson J, McCombs AK, Schmitt ES, Peacock S, Chen S, Dai H, Ge X, Wang G, Shaw CA, Mei H, Breman A, Xia F, Yang Y, Purgason A, Pourpak A, Chen Z, Wang X, Wang Y, Kulkarni S, Choy KW, Wapner RJ, Van den Veyver IB, Beaudet A, Parmar S, Wong LJ, Eng CM. Zhang J, et al. Among authors: wapner rj. Nat Med. 2019 Mar;25(3):439-447. doi: 10.1038/s41591-018-0334-x. Epub 2019 Jan 28. Nat Med. 2019. PMID: 30692697
Introduction.
Wapner RJ, Goldberg JD. Wapner RJ, et al. Semin Perinatol. 2016 Feb;40(1):1-2. doi: 10.1053/j.semperi.2015.11.001. Epub 2015 Dec 22. Semin Perinatol. 2016. PMID: 26726137 No abstract available.
497 results