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Items: 1 to 20 of 98

1.

Noninvasive fetal genome sequencing: a primer.

Snyder MW, Simmons LE, Kitzman JO, Santillan DA, Santillan MK, Gammill HS, Shendure J.

Prenat Diagn. 2013 Jun;33(6):547-54. doi: 10.1002/pd.4097. Review.

2.

Noninvasive whole-genome sequencing of a human fetus.

Kitzman JO, Snyder MW, Ventura M, Lewis AP, Qiu R, Simmons LE, Gammill HS, Rubens CE, Santillan DA, Murray JC, Tabor HK, Bamshad MJ, Eichler EE, Shendure J.

Sci Transl Med. 2012 Jun 6;4(137):137ra76. doi: 10.1126/scitranslmed.3004323.

3.

Probabilistic method for detecting copy number variation in a fetal genome using maternal plasma sequencing.

Rampášek L, Arbabi A, Brudno M.

Bioinformatics. 2014 Jun 15;30(12):i212-8. doi: 10.1093/bioinformatics/btu292.

4.

Noninvasive prenatal testing using cell-free fetal DNA in maternal plasma.

Dharajiya N, Zwiefelhofer T, Guan X, Angkachatchai V, Saldivar JS.

Curr Protoc Hum Genet. 2015 Jan 20;84:8.15.1-20. doi: 10.1002/0471142905.hg0815s84. Review.

PMID:
25599670
5.

Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA.

Lun FM, Chiu RW, Sun K, Leung TY, Jiang P, Chan KC, Sun H, Lo YM.

Clin Chem. 2013 Nov;59(11):1583-94. doi: 10.1373/clinchem.2013.212274.

6.

Fetal aneuploidy detection by maternal plasma DNA sequencing: a technology assessment.

Walsh JM, Goldberg JD.

Prenat Diagn. 2013 Jun;33(6):514-20. doi: 10.1002/pd.4109. Review.

PMID:
23686655
7.

Benefits and limitations of whole genome versus targeted approaches for noninvasive prenatal testing for fetal aneuploidies.

Boon EM, Faas BH.

Prenat Diagn. 2013 Jun;33(6):563-8. doi: 10.1002/pd.4111. Review.

PMID:
23613171
8.

Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease.

Chu T, Bunce K, Hogge WA, Peters DG.

Bioinformatics. 2009 May 15;25(10):1244-50. doi: 10.1093/bioinformatics/btp156.

9.

Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.

Lau TK, Cheung SW, Lo PS, Pursley AN, Chan MK, Jiang F, Zhang H, Wang W, Jong LF, Yuen OK, Chan HY, Chan WS, Choy KW.

Ultrasound Obstet Gynecol. 2014 Mar;43(3):254-64. doi: 10.1002/uog.13277. Review.

10.

Noninvasive prenatal molecular karyotyping from maternal plasma.

Yu SC, Jiang P, Choy KW, Chan KC, Won HS, Leung WC, Lau ET, Tang MH, Leung TY, Lo YM, Chiu RW.

PLoS One. 2013 Apr 17;8(4):e60968. doi: 10.1371/journal.pone.0060968.

11.

Maternal plasma sequencing: a powerful tool towards fetal whole genome recovery.

Papageorgiou EA, Patsalis PC.

BMC Med. 2013 Feb 27;11:56. doi: 10.1186/1741-7015-11-56.

12.

Noninvasive prenatal diagnosis of fetal trisomy 21 by allelic ratio analysis using targeted massively parallel sequencing of maternal plasma DNA.

Liao GJ, Chan KC, Jiang P, Sun H, Leung TY, Chiu RW, Lo YM.

PLoS One. 2012;7(5):e38154. doi: 10.1371/journal.pone.0038154.

13.

Non-invasive prenatal diagnostics of aneuploidy using next-generation DNA sequencing technologies, and clinical considerations.

Nepomnyashchaya YN, Artemov AV, Roumiantsev SA, Roumyantsev AG, Zhavoronkov A.

Clin Chem Lab Med. 2013 Jun;51(6):1141-54. Review.

PMID:
23023923
14.

Noninvasive prenatal diagnosis using next-generation sequencing.

Xu L, Shi R.

Gynecol Obstet Invest. 2014;77(2):73-7. doi: 10.1159/000355693. Review.

PMID:
24192219
15.

Noninvasive detection of a balanced fetal translocation from maternal plasma.

Jensen TJ, Kim SK, van den Boom D, Deciu C, Ehrich M.

Clin Chem. 2014 Oct;60(10):1298-305. doi: 10.1373/clinchem.2014.223198.

16.

Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing.

Chen EZ, Chiu RW, Sun H, Akolekar R, Chan KC, Leung TY, Jiang P, Zheng YW, Lun FM, Chan LY, Jin Y, Go AT, Lau ET, To WW, Leung WC, Tang RY, Au-Yeung SK, Lam H, Kung YY, Zhang X, van Vugt JM, Minekawa R, Tang MH, Wang J, Oudejans CB, Lau TK, Nicolaides KH, Lo YM.

PLoS One. 2011;6(7):e21791. doi: 10.1371/journal.pone.0021791.

17.

Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.

van den Veyver IB, Eng CM.

Cold Spring Harb Perspect Med. 2015 Aug 7;5(10). pii: a023077. doi: 10.1101/cshperspect.a023077. Review.

PMID:
26253094
18.

Non-invasive prenatal measurement of the fetal genome.

Fan HC, Gu W, Wang J, Blumenfeld YJ, El-Sayed YY, Quake SR.

Nature. 2012 Jul 19;487(7407):320-4. doi: 10.1038/nature11251. Erratum in: Nature. 2012 Sep 13;489(7415):326.

19.
20.

Maternal Plasma DNA and RNA Sequencing for Prenatal Testing.

Tamminga S, van Maarle M, Henneman L, Oudejans CB, Cornel MC, Sistermans EA.

Adv Clin Chem. 2016;74:63-102. doi: 10.1016/bs.acc.2015.12.004. Review.

PMID:
27117661
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