IGNATIA VAN DEN VEYVER to High-Throughput Nucleotide Sequencing
This is a "connection" page, showing publications IGNATIA VAN DEN VEYVER has written about High-Throughput Nucleotide Sequencing.
Connection Strength
0.419
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Use of amplicon-based sequencing for testing fetal identity and monogenic traits with Single Circulating Trophoblast (SCT) as one form of cell-based NIPT. PLoS One. 2021; 16(4):e0249695.
Score: 0.098
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The current and future impact of genome-wide sequencing on fetal precision medicine. Hum Genet. 2020 Sep; 139(9):1121-1130.
Score: 0.089
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Exome and genome sequencing in reproductive medicine. Fertil Steril. 2018 02; 109(2):213-220.
Score: 0.078
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Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women. Prenat Diagn. 2016 Dec; 36(12):1127-1134.
Score: 0.072
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Noninvasive prenatal screening by next-generation sequencing. Annu Rev Genomics Hum Genet. 2014; 15:327-47.
Score: 0.061
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Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA. Nat Med. 2019 03; 25(3):439-447.
Score: 0.021