P. Brady

发表

Presymptomatic Identification of Cancers in Pregnant Women During Noninvasive Prenatal Testing.

P. Neven, J. Vermeesch, L. Dehaspe, 2015, JAMA oncology.

Targeted array comparative genomic hybridisation (array CGH) identifies genomic imbalances associated with isolated congenital diaphragmatic hernia (CDH)

K. Devriendt, J. Vermeesch, J. Deprest, 2010, Prenatal diagnosis.

Expanding the phenotypic spectrum of PORCN variants in two males with syndromic microphthalmia

K. Devriendt, J. Vermeesch, J. Deprest, 2014, European Journal of Human Genetics.

Trends in the pharmacological management of atrial fibrillation in UK general practice 2008–2018

K. Phillips, G. Thomas, L. Fabritz, 2021, Heart.

Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management

H. Peeters, K. Devriendt, J. Vermeesch, 2015, European Journal of Human Genetics.

Exome sequencing identifies ZFPM2 as a cause of familial isolated congenital diaphragmatic hernia and possibly cardiovascular malformations.

K. Devriendt, J. Vermeesch, J. Deprest, 2014, European journal of medical genetics.

A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors

Gabrielle M. Christenhusz, K. Devriendt, B. Menten, 2013, Genetics in Medicine.

Array technology in prenatal diagnosis.

J. Vermeesch, O. Zuffardi, A. Vetro, 2011, Seminars in fetal & neonatal medicine.

Prenatal management of the fetus with isolated congenital diaphragmatic hernia in the era of the TOTAL trial.

J. Vermeesch, K. Nicolaides, A. Benachi, 2014, Seminars in fetal & neonatal medicine.

Identification of dosage‐sensitive genes in fetuses referred with severe isolated congenital diaphragmatic hernia

K. Devriendt, J. Deprest, P. Brady, 2013, Prenatal diagnosis.

The Future of Prenatal Cytogenetics: From Copy Number Variations to Non-invasive Prenatal Testing

J. Vermeesch, S. Ardui, P. Brady, 2013, Current Genetic Medicine Reports.

Genome‐wide arrays: Quality criteria and platforms to be used in routine diagnostics

J. Vermeesch, K. Kok, R. Hastings, 2012, Human mutation.

Genomic microarrays: a technology overview

J. Vermeesch, P. Brady, 2012, Prenatal diagnosis.

Array-based approaches in prenatal diagnosis.

K. Devriendt, J. Vermeesch, J. Deprest, 2012, Methods in molecular biology.

Recent Developments in the Genetic Factors Underlying Congenital Diaphragmatic Hernia

K. Devriendt, J. Vermeesch, J. Deprest, 2010, Fetal Diagnosis and Therapy.

Clinical implementation of NIPT – technical and biological challenges

H. Peeters, T. de Ravel, K. Devriendt, 2016, Clinical genetics.

Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic hernia.

K. Devriendt, J. Vermeesch, J. Deprest, 2014, European journal of medical genetics.

Fetal surgery is a clinical reality.

Zeger Debyser, Joris Vermeesch, Gunnar Naulaers, 2010, Seminars in fetal & neonatal medicine.

Congenital diaphragmatic hernia as a part of Nance–Horan syndrome?

K. Devriendt, J. Vermeesch, J. Deprest, 2018, European Journal of Human Genetics.

Clinically relevant discordances identified after tertiary reassessment of fetuses with isolated congenital diaphragmatic hernia

K. Devriendt, J. Deprest, L. Lewi, 2017, Prenatal diagnosis.

A Novel Biomarker Model for Detecting Patients With Atrial Fibrillation: A Development and Validation Study

H. Crijns, P. Kirchhof, U. Schotten, 2021 .

Quantification of fibroblast growth factor 23 and N-terminal pro-B-type natriuretic peptide to identify patients with atrial fibrillation using a high-throughput platform: A validation study

P. Kirchhof, G. Gkoutos, P. Kastner, 2021, PLoS medicine.

Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks

E. Zackai, K. Lage, P. Donahoe, 2012, American journal of medical genetics. Part A.

Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury

J. Deprest, J. Richter, J. Vanoirbeek, 2016, Journal of Translational Medicine.

Transcriptome Analysis of the Preterm Rabbit Lung after Seven Days of Hyperoxic Exposure

J. Deprest, J. Richter, T. Salaets, 2015, PloS one.

Proton-pump inhibitor omeprazole attenuates hyperoxia induced lung injury

J. Deprest, J. Richter, J. Vanoirbeek, 2016, Journal of Translational Medicine.

Pulmonary transcriptome analysis in the surgically induced rabbit model of diaphragmatic hernia treated with fetal tracheal occlusion

J. Vermeesch, J. Deprest, J. Toelen, 2016, Disease Models & Mechanisms.

Title : Pulmonary transcriptome analysis in the rabbit model of surgically-induced diaphragmatic hernia treated with fetal tracheal occlusion

J. Vermeesch, J. Deprest, J. Toelen, 2016 .

Genome‐wide arrays: Quality criteria and platforms to be used in routine diagnostics

J. Vermeesch, K. Kok, R. Hastings, 2012, Human mutation.

Genetic profile of isolated congenital diaphragmatic hernia revealed by targeted next‐generation sequencing

K. Devriendt, J. Vermeesch, J. Deprest, 2018, Prenatal diagnosis.