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Chromosomal mosaicism in human blastocysts: the ultimate challenge of preimplantation genetic testing?

Human reproduction (Oxford), 2018-07, Vol.33 (7), p.1342-1354

2018

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Extended in vitro culture of human embryos demonstrates the complex nature of diagnosing chromosomal mosaicism from a single trophectoderm biopsy

Human reproduction (Oxford), 2019-04, Vol.34 (4), p.758-769

2019

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CRISPR/Cas gene editing in the human germline

Seminars in cell & developmental biology, 2022-11, Vol.131, p.93-107

2022

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Direct comparison of distinct naive pluripotent states in human embryonic stem cells

Nature communications, 2017-04, Vol.8 (1), p.15055-15055, Article 15055

2017

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A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

Nature communications, 2019-10, Vol.10 (1), p.4779-16, Article 4779

2019

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Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin

Scientific reports, 2016-02, Vol.6 (1), p.21540-21540, Article 21540

2016

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TEAD4 regulates trophectoderm differentiation upstream of CDX2 in a GATA3-independent manner in the human preimplantation embryo

Human reproduction (Oxford), 2022-07, Vol.37 (8), p.1760-1773

2022

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GENType: all-in-one preimplantation genetic testing by pedigree haplotyping and copy number profiling suitable for third-party reproduction

Human reproduction (Oxford), 2022-06, Vol.37 (7), p.1678-1691

2022

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Characterization of ovarian tissue oocytes from transgender men reveals poor calcium release and embryo development, which might be overcome by spindle transfer

Human reproduction (Oxford), 2023-06, Vol.38 (6), p.1135-1150

2023

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Comparative analysis of mouse and human preimplantation development following POU5F1 CRISPR/Cas9 targeting reveals interspecies differences

Human reproduction (Oxford), 2021-04, Vol.36 (5), p.1242-1252

2021

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Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrest

Human reproduction (Oxford), 2020-07, Vol.35 (7), p.1562-1577

2020

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Various repair events following CRISPR/Cas9-based mutational correction of an infertility-related mutation in mouse embryos

Journal of assisted reproduction and genetics, 2024-06, Vol.41 (6), p.1605-1617

2024

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Comparison of the positivity rate of anti-spike and anti-nucleocapsid SARS-CoV-2 IgG in asymptomatic pregnant women

Journal of obstetrics and gynaecology, 2022-07, Vol.42 (5), p.1-1542

2022

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Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

Journal of medical genetics, 2006-08, Vol.43 (8), p.625-633

2006

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Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals

European journal of medical genetics, 2009-03, Vol.52 (2), p.77-87

2009

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Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

Nature communications, 2019-11, Vol.10 (1), p.5337-1, Article 5337

2019

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Array comparative genomic hybridization in male infertility

Human reproduction (Oxford), 2012-03, Vol.27 (3), p.921-929

2012

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An integrative genomics screen uncovers ncRNA T-UCR functions in neuroblastoma tumours

Oncogene, 2010-06, Vol.29 (24), p.3583-3592

2010

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Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

Nature genetics, 2004-11, Vol.36 (11), p.1213-1218

2004

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Extended In Vitro Culture of Human Embryos Demonstrates the Complex Nature of Diagnosing Chromosomal Mosaicism From a Single Trophectoderm Biopsy

Obstetrical & gynecological survey, 2019-07, Vol.74 (7), p.413-414

2019

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Mild early epileptic encephalopathy evolving to spastic paraplegia, neurogenic bladder and generalized slow colon transit in an 18-year old patient with pathogenic mutations in FARS2

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S175-S175

2016

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Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14

Journal of medical genetics, 2007-04, Vol.44 (4), p.264-268

2007

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OC06.04: The Belgian approach to meet the challenge in interpreting prenatal microarray results

Ultrasound in obstetrics & gynecology, 2016-09, Vol.48 (S1), p.11-11

2016

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A de novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features

Molecular syndromology, 2014-01, Vol.5 (1), p.32-35

2014

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Copy number alterations and copy number variation in cancer: close encounters of the bad kind

Cytogenetic and genome research, 2008-01, Vol.123 (1-4), p.176-182

2008

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Chromosomal mosaicism in human blastocysts: the ultimate challenge of preimplantation genetic testing?

Extended in vitro culture of human embryos demonstrates the complex nature of diagnosing chromosomal mosaicism from a single trophectoderm biopsy

CRISPR/Cas gene editing in the human germline

Direct comparison of distinct naive pluripotent states in human embryonic stem cells

A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

Zebrafish Collagen Type I: Molecular and Biochemical Characterization of the Major Structural Protein in Bone and Skin

TEAD4 regulates trophectoderm differentiation upstream of CDX2 in a GATA3-independent manner in the human preimplantation embryo

GENType: all-in-one preimplantation genetic testing by pedigree haplotyping and copy number profiling suitable for third-party reproduction

Characterization of ovarian tissue oocytes from transgender men reveals poor calcium release and embryo development, which might be overcome by spindle transfer

Comparative analysis of mouse and human preimplantation development following POU5F1 CRISPR/Cas9 targeting reveals interspecies differences

Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrest

Various repair events following CRISPR/Cas9-based mutational correction of an infertility-related mutation in mouse embryos

Comparison of the positivity rate of anti-spike and anti-nucleocapsid SARS-CoV-2 IgG in asymptomatic pregnant women

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals

Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

Array comparative genomic hybridization in male infertility

An integrative genomics screen uncovers ncRNA T-UCR functions in neuroblastoma tumours

Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis

Extended In Vitro Culture of Human Embryos Demonstrates the Complex Nature of Diagnosing Chromosomal Mosaicism From a Single Trophectoderm Biopsy

Mild early epileptic encephalopathy evolving to spastic paraplegia, neurogenic bladder and generalized slow colon transit in an 18-year old patient with pathogenic mutations in FARS2

Osteopoikilosis, short stature and mental retardation as key features of a new microdeletion syndrome on 12q14

OC06.04: The Belgian approach to meet the challenge in interpreting prenatal microarray results

A de novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features

Copy number alterations and copy number variation in cancer: close encounters of the bad kind

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