Ghent University Academic Bibliography

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Outcome of publicly funded nationwide first-tier noninvasive prenatal screening

Kris Van den Bogaert, Lore Lannoo, Nathalie Brison, Vincent Gatinois, Machteld Baetens (UGent) , Bettina Blaumeiser, Francois Boemer, Laura Bourlard, Vincent Bours, Anne De Leener, et al.

(2021) GENETICS IN MEDICINE. 23(6). p.1137-1142
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- Conference Paper
- C3
Exome-based panel testing as an efficient method to diagnose the highly heterogeneous ocular disorder spectrum Microphthalmia, Anophthalmia, Coloboma and Anterior Segment Dysgenesis (MAC-ASD)

Hannah Verdin (UGent) , Toon Rosseel (UGent) , Sascha Vermeer, Irina Balikova (UGent) , Philippe Kestelyn (UGent) , Colombine Meunier, Françoise Meire (UGent) , Julie Van De Velde (UGent) , Olivier Vanakker (UGent) , Jenneke Van Den Ende, et al.

(2020) Belgian Society for Human Genetics, 20th Annual meeting, Abstracts.
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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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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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- Conference Paper
- C3
An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

Miriam Bauwens (UGent) , Julie De Zaeytijd (UGent) , Nicole Weisschuh, Susanne Kohl, Thomy de Ravel de l'Argentière, Marjan De Rademaeker, Bart Loeys, Frauke Coppieters (UGent) , Bart Leroy (UGent) and Elfride De Baere (UGent)

(2015) EUROPEAN JOURNAL OF HUMAN GENETICS. 23(suppl. 1).
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- Conference Paper
- C3
An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

Miriam Bauwens (UGent) , Julie De Zaeytijd (UGent) , Nicole Weisschuh, Susanne Kohl, Thomy de Ravel de l'Argentière, Marjan De Rademaeker, Bart Loeys, Frauke Coppieters (UGent) , Bart Leroy (UGent) and Elfride De Baere (UGent)

(2015) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 56(7).
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An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

Miriam Bauwens (UGent) , Julie De Zaeytijd (UGent) , Nicole Weisschuh, Susanne Kohl, Thomy de Ravel de l'Argentière, Marjan De Rademaeker, Bart Loeys, Frauke Coppieters (UGent) , Bart Leroy (UGent) and Elfride De Baere (UGent)

(2015) BeMGI Annual meeting, Abstracts.
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- Conference Paper
- C3
An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

Miriam Bauwens (UGent) , Julie De Zaeytijd (UGent) , Nicole Weisschuh, Susanne Kohl, Thomy de Ravel de l'Argentière, Marjan De Rademaeker, Bart Loeys, Frauke Coppieters (UGent) , Bart Leroy (UGent) and Elfride De Baere (UGent)

(2015) Pro Retina, 10th Research colloquium, Abstracts.
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An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

Miriam Bauwens (UGent) , Julie De Zaeytijd (UGent) , Nicole Weisschuh, Susanne Kohl, Thomy de Ravel de l'Argentière, Marjan De Rademaeker, Bart Loeys, Frauke Coppieters (UGent) , Bart Leroy (UGent) and Elfride De Baere (UGent)

(2015) Science Day, Faculty of Medicine and Health Science, Ghent University, Abstracts.
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Exploring the role of non-coding variation in hereditary blindness : Stargardt disease as a model

Miriam Bauwens (UGent) , Julie De Zaeytijd (UGent) , Nicole Weisschuh, Susanne Kohl, Thomy de Ravel de l'Argentière, Marjan De Rademaeker, Bart Loeys, Frauke Coppieters (UGent) , Bart Leroy (UGent) and Elfride De Baere (UGent)

(2015) Science Day, Faculty of Medicine and Health Science, Ghent University, Abstracts.

Academic Bibliography

Outcome of publicly funded nationwide first-tier noninvasive prenatal screening

Exome-based panel testing as an efficient method to diagnose the highly heterogeneous ocular disorder spectrum Microphthalmia, Anophthalmia, Coloboma and Anterior Segment Dysgenesis (MAC-ASD)

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

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

An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

An augmented ABCA4 screen targeting non-coding regions reveals a deep intronic founder causal variant in Belgian Stargardt patients

Exploring the role of non-coding variation in hereditary blindness : Stargardt disease as a model

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