Ghent University Academic Bibliography

Journal Article
A1
open access

Pregnancy termination at a viable stage in daily clinical practice : a nationwide mortality follow‐back study in Flanders, Belgium

Ellen Roets (UGent) , Kim Beernaert (UGent) , Kenneth Chambaere (UGent) , Luc Deliens (UGent) , Kim van Berkel, Luc De Catte, Sophie Vanhaesebrouck (UGent) , Kristien Roelens (UGent) and Laure Dombrecht (UGent)

(2023) PRENATAL DIAGNOSIS. 43(6). p.781-791

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Do reproductive history and information given through genetic counselling influence patients' decisions on mosaic embryo transfer?

Lluc Coll, Monica Parriego, Gabriela Palacios, Sandra Garcia, Montserrat Boada, Buenaventura Coroleu, Nikolaos Polyzos (UGent) , Francesca Vidal and Anna Veiga

(2022) PRENATAL DIAGNOSIS. 42(13). p.1650-1657

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Journal Article
A1
open access

Enrichment of circulating trophoblasts from maternal blood using laminar microscale vortices

Ann-Sophie Vander Plaetsen, Jana Weymaere, Olivier Tytgat, Magaly Buyle (UGent) , Dieter Deforce (UGent) and Filip Van Nieuwerburgh (UGent)

(2021) PRENATAL DIAGNOSIS. 41(9). p.1171-1178

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Prenatally detected copy number variants in a national cohort : a postnatal follow-up study

Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Anne De Leener, Marjan De Rademaeker, Julie Desir, et al.

(2020) PRENATAL DIAGNOSIS. 40(10). p.1272-1283

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Journal Article
A1
open access

Preface : in silico pipeline for accurate cell-free fetal DNA fraction prediction

Lennart Raman, Machteld Baetens (UGent) , Matthias De Smet (UGent) , Annelies Dheedene (UGent) , Jo Van Dorpe (UGent) and Björn Menten (UGent)

(2019) PRENATAL DIAGNOSIS. 39(10). p.925-933

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The Belgian MicroArray Prenatal (BEMAPRE) database : a systematic nationwide repository of fetal genomic aberrations

Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker, et al.

(2018) PRENATAL DIAGNOSIS. 38(13). p.1120-1128

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Outcome after prenatal and postnatal diagnosis of complex congenital heart defects and the influence of genetic anomalies

Katya De Groote (UGent) , Ellen Vanhie, Ellen Roets (UGent) , Paul Ramaekers (UGent) , Hans De Wilde (UGent) , Joseph Panzer (UGent) , Kristof Vandekerckhove (UGent) , Thierry Bové (UGent) , Katrien Francois (UGent) , Koen Van Herck (UGent) , et al.

(2017) PRENATAL DIAGNOSIS. 37(10). p.983-991

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Journal Article
A1
open access

Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory

Annelies Dheedene (UGent) , Tom Sante (UGent) , Matthias De Smet (UGent) , Jean-François Vanbellinghen, Bernard Grisart, Sarah Vergult (UGent) , Sandra Janssens (UGent) and Björn Menten (UGent)

(2016) PRENATAL DIAGNOSIS. 36(8). p.699-707

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Role of CGH array in the diagnosis of autosomal recessive disease : a case of Ellis-van Creveld syndrome

Valentina D'Ambrosio, Carmela Votino, Teresa Cos, Sebastien Boulanger, Annelies Dheedene (UGent) , Jacques Jani and Kathelijn Keymolen

(2015) PRENATAL DIAGNOSIS. 35(1). p.97-99

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First trimester screening for intra-uterine growth restriction and early-onset pre-eclampsia

Griet Vandenberghe (UGent) , I Mensink, JWR Twisk, MA Blankenstein, AC Heijboer and JMG van Vugt

(2011) PRENATAL DIAGNOSIS. 31(10). p.955-961

Academic Bibliography

Pregnancy termination at a viable stage in daily clinical practice : a nationwide mortality follow‐back study in Flanders, Belgium

Do reproductive history and information given through genetic counselling influence patients' decisions on mosaic embryo transfer?

Enrichment of circulating trophoblasts from maternal blood using laminar microscale vortices

Prenatally detected copy number variants in a national cohort : a postnatal follow-up study

Preface : in silico pipeline for accurate cell-free fetal DNA fraction prediction

The Belgian MicroArray Prenatal (BEMAPRE) database : a systematic nationwide repository of fetal genomic aberrations

Outcome after prenatal and postnatal diagnosis of complex congenital heart defects and the influence of genetic anomalies

Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory

Role of CGH array in the diagnosis of autosomal recessive disease : a case of Ellis-van Creveld syndrome

First trimester screening for intra-uterine growth restriction and early-onset pre-eclampsia

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