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Single molecule real-time (SMRT) sequencing comes of age: applications and utilities for medical diagnostics.
Nucleic Acids Res. 2018 Mar 16;46(5):2159-2168. doi: 10.1093/nar/gky066.
Nucleic Acids Res. 2018.
PMID: 29401301
Free PMC article.
Review.
Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management.
Bayindir B, Dehaspe L, Brison N, Brady P, Ardui S, Kammoun M, Van der Veken L, Lichtenbelt K, Van den Bogaert K, Van Houdt J, Peeters H, Van Esch H, de Ravel T, Legius E, Devriendt K, Vermeesch JR.
Bayindir B, et al. Among authors: ardui s.
Eur J Hum Genet. 2015 Oct;23(10):1286-93. doi: 10.1038/ejhg.2014.282. Epub 2015 Jan 14.
Eur J Hum Genet. 2015.
PMID: 25585704
Free PMC article.
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Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing.
Ardui S, Race V, Zablotskaya A, Hestand MS, Van Esch H, Devriendt K, Matthijs G, Vermeesch JR.
Ardui S, et al.
Hum Mutat. 2017 Mar;38(3):324-331. doi: 10.1002/humu.23150. Epub 2017 Jan 17.
Hum Mutat. 2017.
PMID: 27883256
Free article.
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Detecting AGG Interruptions in Females With a FMR1 Premutation by Long-Read Single-Molecule Sequencing: A 1 Year Clinical Experience.
Ardui S, Race V, de Ravel T, Van Esch H, Devriendt K, Matthijs G, Vermeesch JR.
Ardui S, et al.
Front Genet. 2018 May 16;9:150. doi: 10.3389/fgene.2018.00150. eCollection 2018.
Front Genet. 2018.
PMID: 29868108
Free PMC article.
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Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells.
Dastidar S, Ardui S, Singh K, Majumdar D, Nair N, Fu Y, Reyon D, Samara E, Gerli MFM, Klein AF, De Schrijver W, Tipanee J, Seneca S, Tulalamba W, Wang H, Chai YC, In't Veld P, Furling D, Tedesco FS, Vermeesch JR, Joung JK, Chuah MK, VandenDriessche T.
Dastidar S, et al. Among authors: ardui s.
Nucleic Acids Res. 2018 Sep 19;46(16):8275-8298. doi: 10.1093/nar/gky548.
Nucleic Acids Res. 2018.
PMID: 29947794
Free PMC article.
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MSH2 knock-down shows CTG repeat stability and concomitant upstream demethylation at the DMPK locus in myotonic dystrophy type 1 human embryonic stem cells.
Franck S, Barbé L, Ardui S, De Vlaeminck Y, Allemeersch J, Dziedzicka D, Spits C, Vanroye F, Hilven P, Duqué G, Vermeesch JR, Gheldof A, Sermon K.
Franck S, et al. Among authors: ardui s.
Hum Mol Genet. 2021 Jan 6;29(21):3566-3577. doi: 10.1093/hmg/ddaa250.
Hum Mol Genet. 2021.
PMID: 33242073
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