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Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screening

Reproductive biomedicine online, 2024-09, Vol.49 (3), p.104294, Article 104294

2024

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Polygenic embryo screening: quo vadis?

Journal of assisted reproduction and genetics, 2024-07, Vol.41 (7), p.1719-1726

2024

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Are we not going too far?“: Socio-ethical considerations of preimplantation genetic testing using polygenic risk scores according to healthcare professionals

Social science & medicine (1982), 2024-02, Vol.343, p.116599-116599, Article 116599

2024

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Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores

European journal of human genetics : EJHG, 2023-10, Vol.31 (10), p.1133-1138

2023

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Simultaneous genome-wide haplotyping and copy number detection enabling PGT-A and PGT-M testing in equine in vitro produced embryos

Journal of equine veterinary science, 2023-06, Vol.125, p.104642, Article 104642

2023

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TET2-Driver and NLRC4-Passenger Variants in Adult-Onset Autoinflammation

The New England journal of medicine, 2023-04, Vol.388 (17), p.1626-1629

2023

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Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing

Human reproduction (Oxford), 2023-03, Vol.38 (3), p.511-519

2023

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Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge

European journal of human genetics : EJHG, 2022-12, Vol.30 (12), p.1323-1330

2022

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Parental genomes segregate into distinct blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts

Genome Biology, 2022-10, Vol.23 (1), p.201-29, Article 201

2022

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Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing

Nucleic acids research, 2022-06, Vol.50 (11), p.e63-e63

2022

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A review of normative documents on preimplantation genetic testing: Recommendations for PGT-P

Genetics in medicine, 2022-06, Vol.24 (6), p.1165-1175

2022

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A systematic review of the views of healthcare professionals on the scope of preimplantation genetic testing

Journal of community genetics, 2022-02, Vol.13 (1), p.1-11

2022

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Haplotyping-based preimplantation genetic testing reveals parent-of-origin specific mechanisms of aneuploidy formation

Npj genomic medicine, 2021-10, Vol.6 (1), p.81-81, Article 81

2021

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Polygenic risk scoring of human embryos: a qualitative study of media coverage

BMC medical ethics, 2021-09, Vol.22 (1), p.125-125, Article 125

2021

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Genome‐wide abnormalities in embryos: Origins and clinical consequences

Prenatal diagnosis, 2021-04, Vol.41 (5), p.554-563

2021

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PREIMPLANTATION GENETIC TESTING: Single-cell technologies at the forefront of PGT and embryo research

Reproduction (Cambridge, England), 2020-11, Vol.160 (5), p.A19-A31

2020

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Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA

Genetics in medicine, 2020-05, Vol.22 (5), p.962-973

2020

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Identity-by-state-based haplotyping expands the application of comprehensive preimplantation genetic testing

Human reproduction (Oxford), 2020-03, Vol.35 (3), p.718-726

2020

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Novel Methods in Preimplantation Genetic Testing: Comprehensive Preimplantation Genetic Testing

Preimplantation Genetic Testing, 2020, p.87-95

1, 2020

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In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages

Nature medicine, 2019-11, Vol.25 (11), p.1699-1705

2019

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Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing

Human reproduction (Oxford), 2019-08, Vol.34 (8), p.1608-1619

2019

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Detection of a balanced translocation carrier through trophectoderm biopsy analysis: a case report

Molecular cytogenetics, 2019-06, Vol.12 (1), p.28-6, Article 28

2019

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A speculative outlook on embryonic aneuploidy: Can molecular pathways be involved?

Developmental biology, 2019-03, Vol.447 (1), p.3-13

2019

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Demographic and evolutionary trends in ovarian function and aging

Human reproduction update, 2019-01, Vol.25 (1), p.34-50

2019

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Chromosomal scan of single sperm cells by combining fluorescence-activated cell sorting and next-generation sequencing

Journal of assisted reproduction and genetics, 2019-01, Vol.36 (1), p.91-97

2019

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Perspectives of preimplantation genetic testing patients in Belgium on the ethics of polygenic embryo screening

Polygenic embryo screening: quo vadis?

Are we not going too far?“: Socio-ethical considerations of preimplantation genetic testing using polygenic risk scores according to healthcare professionals

Limitations, concerns and potential: attitudes of healthcare professionals toward preimplantation genetic testing using polygenic risk scores

Simultaneous genome-wide haplotyping and copy number detection enabling PGT-A and PGT-M testing in equine in vitro produced embryos

TET2-Driver and NLRC4-Passenger Variants in Adult-Onset Autoinflammation

Preclinical workup using long-read amplicon sequencing provides families with de novo pathogenic variants access to universal preimplantation genetic testing

Rare autosomal trisomies detected by non-invasive prenatal testing: an overview of current knowledge

Parental genomes segregate into distinct blastomeres during multipolar zygotic divisions leading to mixoploid and chimeric blastocysts

Single-cell genome-wide concurrent haplotyping and copy-number profiling through genotyping-by-sequencing

A review of normative documents on preimplantation genetic testing: Recommendations for PGT-P

A systematic review of the views of healthcare professionals on the scope of preimplantation genetic testing

Haplotyping-based preimplantation genetic testing reveals parent-of-origin specific mechanisms of aneuploidy formation

Polygenic risk scoring of human embryos: a qualitative study of media coverage

Genome‐wide abnormalities in embryos: Origins and clinical consequences

PREIMPLANTATION GENETIC TESTING: Single-cell technologies at the forefront of PGT and embryo research

Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA

Identity-by-state-based haplotyping expands the application of comprehensive preimplantation genetic testing

Novel Methods in Preimplantation Genetic Testing: Comprehensive Preimplantation Genetic Testing

In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages

Multi-centre evaluation of a comprehensive preimplantation genetic test through haplotyping-by-sequencing

Detection of a balanced translocation carrier through trophectoderm biopsy analysis: a case report

A speculative outlook on embryonic aneuploidy: Can molecular pathways be involved?

Demographic and evolutionary trends in ovarian function and aging

Chromosomal scan of single sperm cells by combining fluorescence-activated cell sorting and next-generation sequencing

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