I. Veyver

发表

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization

P. Stankiewicz, A. C. Chinault, Ankita Patel, 2006, Genetics in Medicine.

V. Sutton, I. Veyver, Bret L. Bostwick, 2019, Harper's Textbook of Pediatric Dermatology.

Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasia

Ankita Patel, C. Thaller, V. Sutton, 2007, Nature Genetics.

Microphthalmia with linear skin defects (MLS), Aicardi, and Goltz syndromes: are they related X-linked dominant male-lethal disorders?

I. Veyver, 2002 .

Cerebral Vasospasm in Eclampsia: Transcranial Doppler Ultrasound Findings

M. Belfort, K. Moise, I. Veyver, 1994 .

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

I. Veyver, 2022, Prenatal Diagnosis.

GENETIC EFFECTS OF METHYLATION DIETS

I. Veyver, 2002 .

Recent advances in prenatal genetic screening and testing

I. B. Van den Veyver, I. Veyver, Ignatia B. Van den Veyver, 2016, F1000Research.

Clinical application of microarray-based comparative genomic hybridization in prenatal diagnosis

I. Veyver, H. Peng, 2009 .

The human homologue (PEG3) of the mouse paternally expressed gene 3 (Peg3) is maternally imprinted but not mutated in women with familial recurrent hydatidiform molar pregnancies.

R. Slim, I. Veyver, Charles Q. Tran, 2001 .

Improving the prenatal diagnosis of Beckwith–Wiedemann syndrome

I. Veyver, 2021, Prenatal Diagnosis.

Prenatal Genetic Testing and Screening

I. Veyver, 2018 .

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

Ripudaman Singh, Niels Uldbjerg, Rui Chen, 2016, Prenatal diagnosis.

New technologies for the assessment of chromosomes in prenatal diagnosis

L. Shaffer, I. Veyver, 2012, Prenatal diagnosis.

Multiplex ligation‐dependent probe amplification (MLPA) and prenatal diagnosis

A. Willis, C. Eng, I. Veyver, 2012, Prenatal diagnosis.

Skewed X inactivation in X-linked disorders.

I. Veyver, 2001 .

Detection of ≥1 Mb microdeletions and microduplications in a single cell using custom oligonucleotide arrays

P. Stankiewicz, A. Breman, C. Shaw, 2012, Prenatal diagnosis.

Tooth Enamel Defects in Mice with a Deletion at the Arhgap6/AmelX Locus

C. Gibson, J. T. Wright, R. Sierra, 2005, Calcified Tissue International.

Advances in Molecular Genetics Including Fetal Sequencing

M. Walkiewicz, I. Veyver, 2020, Fetal Medicine.

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

I. B. Van den Veyver, I. Veyver, 2019, Prenatal diagnosis.

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

Z. Deans, Y. Yaron, I. Veyver, 2023 .

Next-Generation Sequencing for Gene Panels and Clinical Exomes

I. B. Van den Veyver, I. Veyver, Elizabeth A. Normand, 2019, Human Reproductive and Prenatal Genetics.

Chronic maternal protein deprivation in mice is associated with overexpression of the cohesin-mediator complex in liver of their offspring.

M. Fiorotto, B. Sadikovic, H. Sangi-Haghpeykar, 2011, The Journal of nutrition.

Evidence for Feasibility of Fetal Trophoblastic Cell-Based Noninvasive Prenatal Testing

Jeffrey L. Werbin, A. Breman, C. Shaw, 2017 .

Characterization and physical mapping in human and mouse of a novel RING finger gene in Xp22.

H. Zoghbi, A. Baldini, I. B. Van den Veyver, 1998, Genomics.

73: Metagenomic-based approach to a comprehensive characterization of the vaginal microbiome signature in pregnancy

A. Milosavljevic, J. Petrosino, C. Coarfa, 2011 .

Detection of intrauterine viral infection using the polymerase chain reaction.

J. Towbin, N. Bowles, K. Moise, 1998, Molecular genetics and metabolism.

Genetic mapping of a maternal locus responsible for familial hydatidiform moles.

M. Seoud, R. Slim, I. B. Van den Veyver, 1999, Human molecular genetics.

A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles.

L. Shao, D. del Gaudio, I. B. Van den Veyver, 2008, Molecular human reproduction.

Terminal osseous dysplasia and pigmentary defects: clinical characterization of a novel male lethal X-linked syndrome.

D. Stockton, C. Bacino, I. B. Van den Veyver, 2000, American journal of medical genetics.

The product of the imprinted gene IPL marks human villous cytotrophoblast and is lost in complete hydatidiform mole.

B. Tycko, A. Saxena, D. Frank, 2003, Placenta.