Ghent University Academic Bibliography

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A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis

Allan Thomas Højland, Lisse J. M. Tavernier, Isabelle Schrauwen, Manou Sommen, Vedat Topsakal, Isabelle Schatteman, Ingeborg Dhooge (UGent) , Alex Huber, Diego Zanetti, Henricus P. M. Kunst, et al.

(2022) HUMAN GENETICS. 141. p.951-963
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- Journal Article
- A1
- open access
Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes

Aleksandra Nijak, Eline Simons, Bert Vandendriessche, Dieter Van de Sande, Erik Fransen, Ewa Sieliwonczyk, Ilse Van Gucht, Emeline Van Craenenbroeck, Johan Saenen, Hein Heidbuchel, et al.

(2022) BIOLOGY OPEN. 11(2).
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Luminescent human iPSC-derived neurospheroids enable modeling of neurotoxicity after oxygen-glucose deprivation

Elise Van Breedam, Aleksandra Nijak, Tamariche Buyle-Huybrecht, Julia Di Stefano, Marlies Boeren, Jonas Govaerts, Alessandra Quarta, Tine Swartenbroekx, Eva Jacobs, Björn Menten (UGent) , et al.

(2022) NEUROTHERAPEUTICS. 19(2). p.550-569
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Atmospheric deposition of elements and its relevance for nutrient budgets of tropical forests

Leandro Van Langenhove, Lore T. Verryckt, Laëtitia Bréchet, Elodie A. Courtois, Clement Stahl, Florian Hofhansl, Marijn Bauters (UGent) , Jordi Sardans, Pascal Boeckx (UGent) , Erik Fransen, et al.

(2020) BIOGEOCHEMISTRY. 149(2). p.175-193
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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
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- open access
Enrichment of rare variants in Loeys-Dietz syndrome genes in spontaneous coronary artery dissection but not in severe fibromuscular dysplasia

Aline Verstraeten, Melanie H.A.M. Perik, Anna A. Baranowska, Josephina A.N. Meester, Lotte Van Den Heuvel, Jarl Bastianen, Marlies Kempers, Ingrid P.C. Krapels, Angela Maas, Andrea Rideout, et al.

(2020) CIRCULATION. 142(10). p.1021-1024
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Insufficient evidence for a role of SERPINF1 in otosclerosis

Hanne Valgaeren, Manou Sommen, Matthias Beyens, Geert Vandeweyer, Isabelle Schrauwen, Anne Schepers, Isabelle Schatteman, Vedat Topsakal, Ingeborg Dhooge (UGent) , Henricus Kunst, et al.

(2019) MOLECULAR GENETICS AND GENOMICS. 294(4). p.1001-1006
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State-associated changes in longitudinal [18F]-PBR111 TSPO PET imaging of psychosis patients : evidence for the accelerated ageing hypothesis?

Livia De Picker, Julie Ottoy, Jeroen Verhaeghe, Steven Deleye, Leonie Wyffels, Erik Fransen, Lauren Kosten, Bernard Sabbe, Violette Coppens, Maarten Timmers, et al.

(2019) BRAIN BEHAVIOR AND IMMUNITY. 77. p.46-54
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Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis

Isabelle Schrauwen, Hanne Valgaeren, Laura Tomas-Roca, Manou Sommen, Umut Altunoglu, Mieke Wesdorp, Matthias Beyens, Erik Fransen, Abdul Nasir, Geert Vandeweyer, et al.

(2019) GENETICS IN MEDICINE. 21(5). p.1199-1208
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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

Academic Bibliography

A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis

Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes

Luminescent human iPSC-derived neurospheroids enable modeling of neurotoxicity after oxygen-glucose deprivation

Atmospheric deposition of elements and its relevance for nutrient budgets of tropical forests

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

Enrichment of rare variants in Loeys-Dietz syndrome genes in spontaneous coronary artery dissection but not in severe fibromuscular dysplasia

Insufficient evidence for a role of SERPINF1 in otosclerosis

State-associated changes in longitudinal [18F]-PBR111 TSPO PET imaging of psychosis patients : evidence for the accelerated ageing hypothesis?

Variants affecting diverse domains of MEPE are associated with two distinct bone disorders, a craniofacial bone defect and otosclerosis

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

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