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Publisher Correction: Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Nat Med. 2019 Apr;25(4):701-702. doi: 10.1038/s41591-019-0391-9.
Nat Med. 2019.
PMID: 30787481
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: saucier jb.
Nat Med. 2019 Mar;25(3):439-447. doi: 10.1038/s41591-018-0334-x. Epub 2019 Jan 28.
Nat Med. 2019.
PMID: 30692697
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Correction: Clinical experience with carrier screening in a general population: support for a comprehensive pan-ethnic approach.
Westemeyer M, Saucier J, Wallace J, Prins SA, Shetty A, Malhotra M, Demko ZP, Eng CM, Weckstein L, Boostanfar R, Rabinowitz M, Benn P, Keen-Kim D, Billings P.
Westemeyer M, et al.
Genet Med. 2020 Jul;22(7):1282. doi: 10.1038/s41436-020-0853-y.
Genet Med. 2020.
PMID: 32483296
Free PMC article.
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Clinical experience with carrier screening in a general population: support for a comprehensive pan-ethnic approach.
Westemeyer M, Saucier J, Wallace J, Prins SA, Shetty A, Malhotra M, Demko ZP, Eng CM, Weckstein L, Boostanfar R, Rabinowitz M, Benn P, Keen-Kim D, Billings P.
Westemeyer M, et al.
Genet Med. 2020 Aug;22(8):1320-1328. doi: 10.1038/s41436-020-0807-4. Epub 2020 May 5.
Genet Med. 2020.
PMID: 32366966
Free PMC article.
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Non-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach.
Hall MP, Hill M, Zimmermann B, Sigurjonsson S, Westemeyer M, Saucier J, Demko Z, Rabinowitz M.
Hall MP, et al.
PLoS One. 2014 May 7;9(5):e96677. doi: 10.1371/journal.pone.0096677. eCollection 2014.
PLoS One. 2014.
PMID: 24805989
Free PMC article.
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SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy.
Samango-Sprouse C, Banjevic M, Ryan A, Sigurjonsson S, Zimmermann B, Hill M, Hall MP, Westemeyer M, Saucier J, Demko Z, Rabinowitz M.
Samango-Sprouse C, et al.
Prenat Diagn. 2013 Jul;33(7):643-9. doi: 10.1002/pd.4159. Epub 2013 Jun 20.
Prenat Diagn. 2013.
PMID: 23712453
Free PMC article.
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Letter to the editor by megan Hall.
Saucier J, Merrion K, Mash J, Pettersen B, Hall M, Demko Z.
Saucier J, et al.
Curr Genomics. 2013 Apr;14(2):79. doi: 10.2174/1389202911314020001.
Curr Genomics. 2013.
PMID: 24082818
Free PMC article.
No abstract available.
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Racial-ethnic differences in genetic amniocentesis uptake.
Saucier JB, Johnston D, Wicklund CA, Robbins-Furman P, Hecht JT, Monga M.
Saucier JB, et al.
J Genet Couns. 2005 Jun;14(3):189-95. doi: 10.1007/s10897-005-0641-5.
J Genet Couns. 2005.
PMID: 15959650
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