Onderzoeker
Paul Brady
- Disciplines:Genetica, Systeembiologie, Moleculaire en celbiologie
Affiliaties
- Laboratorium voor Cytogenetica en Genoomonderzoek (Afdeling)
Lid
Vanaf1 apr 2009 → 30 apr 2016
Projecten
1 - 1 of 1
- Prenatale Chromosomale Microarray Analyse en Identificatie van Genetische Variaties bij Congenitale Hernia Diafragmatica.Vanaf1 jun 2009 → 14 apr 2014Financiering: Eigen Middelen zoals patrimonium, inschrijvingsgelden, giften, ....
Publicaties
11 - 20 van 29
- Real-time PCR evaluation of cell-free DNA subjected to various storage and shipping conditions(2015)
Auteurs: Paul Brady, Joris Vermeesch
Pagina's: 12797 - 804 - Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management(2015)
Auteurs: Baran Bayindir, Nathalie Brison, Paul Brady, Simon Ardui, Molka Kammoun, Kris Van Den Bogaert, Jeroen Van Houdt, Hilde Peeters, Hilde Van Esch, Thomy de Ravel de l'Argentière, et al.
Pagina's: 1286 - 1293 - Prenatal management of the fetus with isolated congenital diaphragmatic hernia in the era of the TOTAL trial(2014)
Auteurs: Jan Deprest, Paul Brady, Joris Vermeesch
Pagina's: 338 - 348 - Exome Sequencing Identifies a recessive PIGN splice site mutation as a cause of Syndromic Congenital Diaphragmatic Hernia(2014)
Auteurs: Paul Brady, Philippe Moerman, Luc De Catte, Jan Deprest, Koenraad Devriendt, Joris Vermeesch
Pagina's: 487 - 93 - 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(2014)
Auteurs: Paul Brady, Gabrielle Christenhusz, Kris Dierickx, Kris Van Den Bogaert, Luc De Catte, Jan Deprest, Thomy de Ravel de l'Argentière, Hilde Van Esch, Jean-Pierre Frijns, Koenraad Devriendt, et al.
Pagina's: 469 - 76 - Prenatal Chromosomal Microarray Analysis and Identification of Genetic Variants in Congenital Diaphragmatic Hernia.(2014)
Auteurs: Paul Brady, Joris Vermeesch, Koenraad Devriendt, Jan Deprest
- Exome sequencing identifies ZFPM2 as a cause of familial isolated Congenital Diaphragmatic Hernia and possibly cardiovascular malformations(2014)
Auteurs: Paul Brady, Jeroen Van Houdt, Jan Deprest, Koenraad Devriendt, Joris Vermeesch
Pagina's: 247 - 252 - Identification of dosage sensitive genes in foetuses referred with severe isolated congenital diaphragmatic hernia(2013)
Auteurs: Paul Brady, Philip DeKoninck, Jean-Pierre Frijns, Koenraad Devriendt, Jan Deprest, Joris Vermeesch
Pagina's: 1283 - 92 - The future of prenatal cytogenetics: from copy number variations to non-invasive prenatal testing(2013)
Auteurs: Paul Brady, Simon Ardui, Joris Vermeesch
Pagina's: 91 - 98 - Congenital diaphragmatic hernia interval on chromosome 8p23.1 characterized by genetics and protein interaction networks(2012)
Auteurs: Mauro Longoni, Kasper Lage, Meaghan K Russell, Maria Loscertales, Omar A Abdul-Rahman, Gareth Baynam, Steven B Bleyl, Paul Brady, Jeroen Breckpot, Chih P Chen, et al.
Pagina's: 3148 - 3158