| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/S41436-019-0748-Y |
| P698 | PubMed publication ID | 32024963 |
| P50 | author | Olga Tšuiko | Q89214134 |
| Thierry Voet | Q91106775 | ||
| Joris R Vermeesch | Q60061382 | ||
| P2093 | author name string | Koen Devriendt | |
| Kris Van Den Bogaert | |||
| Eric Legius | |||
| Eftychia Dimitriadou | |||
| Masoud Zamani Esteki | |||
| Cindy Melotte | |||
| Nathalie Brison | |||
| Maria Neofytou | |||
| Darine Villela | |||
| Huiwen Che | |||
| P2860 | cites work | Sequencing of Circulating Cell-free DNA during Pregnancy | Q90691273 |
| In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages | Q91106778 | ||
| Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA | Q91259903 | ||
| Risk of miscarriage following amniocentesis or chorionic villus sampling: systematic review of literature and updated meta-analysis | Q92262131 | ||
| Expanded carrier screening: A review of early implementation and literature | Q26771546 | ||
| Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management | Q27324761 | ||
| The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data | Q27860742 | ||
| Fast and accurate long-read alignment with Burrows-Wheeler transform | Q29547193 | ||
| Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma | Q33682367 | ||
| Non-invasive prenatal measurement of the fetal genome | Q34286073 | ||
| Haplotype phasing: existing methods and new developments | Q35554981 | ||
| Concurrent whole-genome haplotyping and copy-number profiling of single cells | Q35759080 | ||
| Haplotyping germline and cancer genomes with high-throughput linked-read sequencing | Q35909792 | ||
| Global Carrier Rates of Rare Inherited Disorders Using Population Exome Sequences | Q36027898 | ||
| Noninvasive whole-genome sequencing of a human fetus. | Q36048523 | ||
| Proof-of-principle rapid noninvasive prenatal diagnosis of autosomal recessive founder mutations | Q36165615 | ||
| Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma | Q37000915 | ||
| Carrier testing for severe childhood recessive diseases by next-generation sequencing | Q37086582 | ||
| Clinical utility and cost of non-invasive prenatal testing with cfDNA analysis in high-risk women based on a US population | Q37089135 | ||
| Non-invasive prenatal diagnosis by single molecule counting technologies | Q37525261 | ||
| Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage | Q37745036 | ||
| Population-based impact of noninvasive prenatal screening on screening and diagnostic testing for fetal aneuploidy. | Q38778126 | ||
| Prenatal and pre-implantation genetic diagnosis | Q38954748 | ||
| Modeled Fetal Risk of Genetic Diseases Identified by Expanded Carrier Screening | Q39482038 | ||
| Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNA. | Q39967854 | ||
| Digital PCR analysis of maternal plasma for noninvasive detection of sickle cell anemia | Q40028010 | ||
| Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma. | Q41475376 | ||
| The causes of misdiagnosis and adverse outcomes in PGD. | Q45717027 | ||
| Universal Haplotype-Based Noninvasive Prenatal Testing for Single Gene Diseases | Q45862706 | ||
| Non-invasive prenatal diagnosis (NIPD) for single gene disorders: cost analysis of NIPD and invasive testing pathways. | Q45885294 | ||
| Carrier Screening: Past, Present, and Future. | Q46330110 | ||
| cfDNA screening and diagnosis of monogenic disorders - where are we heading? | Q47191639 | ||
| Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping | Q47900162 | ||
| Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing. | Q48127306 | ||
| Principles guiding embryo selection following genome-wide haplotyping of preimplantation embryos | Q48702835 | ||
| Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the Fetus | Q56937251 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| ‘Designer babies’ almost thirty years on | Q60018988 | ||
| P577 | publication date | 2020-02-06 | |
| P1433 | published in | Genetics in Medicine | Q15765508 |
| P1476 | title | Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA |
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