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DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting

Genes, 2021-08, Vol.12 (8), p.1214

2021

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Recent advances in prenatal genetic screening and testing

F1000 research, 2016, Vol.5, p.2591-2591

Van den Veyver, Ignatia B

2016

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Prenatally diagnosed developmental abnormalities of the central nervous system and genetic syndromes: A practical review

Prenatal diagnosis, 2019-08, Vol.39 (9), p.666-678

Van den Veyver, Ignatia B.

2019

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The current and future impact of genome-wide sequencing on fetal precision medicine

Human genetics, 2020-09, Vol.139 (9), p.1121-1130

2020

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Overview and recent developments in cell‐based noninvasive prenatal testing

Prenatal diagnosis, 2021-09, Vol.41 (10), p.1202-1214

2021

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Prenatal exomes and genomes – so much new and so much more to learn

Prenatal diagnosis, 2022-05, Vol.42 (6), p.659-661

Veyver, Ignatia B.

2022

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Parental mosaicism for apparent de novo genetic variants: Scope, detection, and counseling challenges

Prenatal diagnosis, 2022-06, Vol.42 (7), p.811-821

2022

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International Society for Prenatal Diagnosis 2022 debate 3—Fetal genome sequencing should be offered to all pregnant patients

Prenatal diagnosis, 2023-04, Vol.43 (4), p.428-434

2023

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Take your mother's ferry: preimplantation embryo development requires maternal karyopherins for nuclear transport

The Journal of clinical investigation, 2023-01, Vol.133 (2), p.1-3

2023

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Deletion of Porcn in Mice Leads to Multiple Developmental Defects and Models Human Focal Dermal Hypoplasia (Goltz Syndrome)

PloS one, 2012-03, Vol.7 (3), p.e32331

2012

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Improving the prenatal diagnosis of Beckwith–Wiedemann syndrome

Prenatal diagnosis, 2021-06, Vol.41 (7), p.795-797

Veyver, Ignatia B.

2021

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Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis

Prenatal diagnosis, 2022-11, Vol.42 (12), p.1479-1480

2022

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International Society for Prenatal Diagnosis Updated Position Statement on the use of genome‐wide sequencing for prenatal diagnosis

Prenatal diagnosis, 2022-05, Vol.42 (6), p.796-803

2022

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Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming

Scientific reports, 2017-03, Vol.7 (1), p.44667-44667, Article 44667

2017

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Current controversies in prenatal diagnosis 2: The 59 genes ACMG recommends reporting as secondary findings when sequencing postnatally should be reported when detected on fetal (and parental) sequencing

Prenatal diagnosis, 2020-12, Vol.40 (12), p.1508-1514

2020

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Lower fetal fraction in clinical cell‐free DNA screening results is associated with increased risk of hypertensive disorders of pregnancy

Prenatal diagnosis, 2022-09, Vol.42 (10), p.1253-1261

2022

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Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles

American journal of human genetics, 2018-11, Vol.103 (5), p.740-751

2018

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The uptake of pan‐ethnic expanded carrier screening is higher when offered during preconception or early prenatal genetic counseling

Prenatal diagnosis, 2019-03, Vol.39 (4), p.319-323

2019

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Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women

Prenatal diagnosis, 2016-12, Vol.36 (12), p.1127-1134

2016

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Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder

Genome medicine, 2018-09, Vol.10 (1), p.74-74, Article 74

2018

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Chromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions

Prenatal diagnosis, 2018-10, Vol.38 (11), p.858-865

2018

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Obituary: Laird Jackson

Prenatal diagnosis, 2020-03, Vol.40 (4), p.395-397

2020

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Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies

Prenatal diagnosis, 2022-06, Vol.42 (7), p.947-954

2022

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DNA Methylation Dynamics in the Female Germline and Maternal-Effect Mutations That Disrupt Genomic Imprinting

Recent advances in prenatal genetic screening and testing

Prenatally diagnosed developmental abnormalities of the central nervous system and genetic syndromes: A practical review

The current and future impact of genome-wide sequencing on fetal precision medicine

Overview and recent developments in cell‐based noninvasive prenatal testing

Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA

Prenatal exomes and genomes – so much new and so much more to learn

Parental mosaicism for apparent de novo genetic variants: Scope, detection, and counseling challenges

International Society for Prenatal Diagnosis 2022 debate 3—Fetal genome sequencing should be offered to all pregnant patients

Take your mother's ferry: preimplantation embryo development requires maternal karyopherins for nuclear transport

Deletion of Porcn in Mice Leads to Multiple Developmental Defects and Models Human Focal Dermal Hypoplasia (Goltz Syndrome)

Improving the prenatal diagnosis of Beckwith–Wiedemann syndrome

Facilitating variant curation sharing for fetal precision genomics: A new venture for prenatal diagnosis

International Society for Prenatal Diagnosis Updated Position Statement on the use of genome‐wide sequencing for prenatal diagnosis

Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming

Current controversies in prenatal diagnosis 2: The 59 genes ACMG recommends reporting as secondary findings when sequencing postnatally should be reported when detected on fetal (and parental) sequencing

Lower fetal fraction in clinical cell‐free DNA screening results is associated with increased risk of hypertensive disorders of pregnancy

Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles

The uptake of pan‐ethnic expanded carrier screening is higher when offered during preconception or early prenatal genetic counseling

Genome-wide copy number analysis on DNA from fetal cells isolated from the blood of pregnant women

Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder

Chromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions

Multicenter clinical experience with non‐invasive cell‐free DNA screening for monosomy X and related X‐chromosome variants

Obituary: Laird Jackson

Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies

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